Abstract
Background
Medicinal plants have been used countless times for curing diseases mainly in developing countries. They are easily available with little to no side effects when compared to modern medicine. This manuscript encompasses information on ethnomedicinal plants in Champhai district, located in the North East Region (NER) of India. The region lies within Indo-Burma biodiversity hotspot. This study will be the first quantitative report on the ethnomedicinal plants used by the local tribes of this region. Knowledge of medicinal plants is mostly acquired by word of mouth, and the knowledge is dying among the local youths with the prevalence of modern medicine. Hence, there is urgency in deciphering and recording such information.
Methods
Information was gathered through interviews with 200 informants across 15 villages of the Champhai district. From the data obtained, we evaluate indices such as used report (UR), frequency of citation (FC), informant consensus factor (Fic), cultural values (CVs) and relative importance (RI) for all the plant species. Secondary data were obtained from scientific databases such as Pubmed, Sci Finder and Science Direct. The scientific name of the plants was matched and arranged in consultation with the working list of all plant species (http://www.theplantlist.org).
Results
Totally, 93 plant species from 53 families and 85 genera were recorded. The most common families are Euphorbiaceae and Asteraceae with six and five species representatives, respectively. Leaves were the most frequently used part of a plant and were usually used in the form of decoction. Curcuma longa has the most cultural value (27.28 CVs) with the highest used report (136 FC), and the highest RI value was Phyllanthus emblica. The main illness categories as per Frequency of citation were muscle/bone problem (0.962 Fic), gastro-intestinal disease (0.956 Fic) and skin care (0.953 Fic).
Conclusion
The people of Mizoram living in the Champhai district have an immense knowledge of ethnomedicinal plants. There were no side effects recorded for consuming ethnomedicinal plants. We observed that there is a scope of scientific validation of 10 plant species for their pharmacological activity and 13 species for the phytochemical characterisation or isolation of the phytochemicals. This might pave the path for developing a scientifically validated botanical or lead to semisyntheic derivatives intended for modern medicine.
Keywords: Ayurveda, Champhai, Ethnomedicinal, Indo-Burma hotspot, Tribal
Background
Plants have been known to be a major source of diverse chemical compounds possessing both medicinal properties and commercial value. There have been several reports on medicinal plants as a source for drug discovery. However, new diseases will likely continue to emerge along with drug-resistant pathogens. This dynamic nature of pathogens has constantly challenged researchers to look for alternatives. The past few decades have witnessed the surge in ethnomedicinal plant research [1], one of the reasons being that the natural products have played an important role in the development of drugs, contributing more than 50% of clinical drugs in the pharmaceutical industry [2]. Further, the rapid growth in human population has raised the demand which in turn has increased the quest for novel plant resources, triggering a threat to natural resources [3].
Traditional knowledge and practices of herbal remedies have been passed on to new generations over the centuries and will continue to do so, with some variations taking place every generation. Plants have been the essential source for therapeutic regimes since ages, and traditional practices are proved to have little known side effects besides their low cost and easy availability. India has been well known worldwide for its indigenous traditional pieces of knowledge and practices from ancient times, through different systems of medicine such as Ayurveda, Siddha and Unani [4]. Although more than 427 tribal communities are having vast diversity of ancient traditions, still there has been criticism of ethnomedicines due to regional variation, political and socio-economic challenges [5]. Reports are stating that several plants have been increasingly utilised by the indigenous people of India [1]. Generally, in India, it was estimated that 6,000 species are used in traditional and herbal medicine which represent about 75% of the needs of the third world, and meanwhile, 3,000 plants were officially acknowledged due to their medicinal values [6].
The healthcare system of India witnesses a wide variation encompassing urban and rural populations which rely on both modern and traditional systems of medicine. The recently implemented Ayushman Bharat Pradhan Mantri Jan Arogya Yojana from the Commonwealth Fund enables cashless secondary and tertiary care at private facilities [7]. Besides, health insurance schemes also exist for institutions and factories. Catering to the huge population has its limitations, and thus, many of the ailments are treated either by traditional healers or through traditional knowledge and practices, especially in remote areas. One such state in the North-Eastern part of India is Mizoram.
Although some researchers [8–13] have documented and identified several ethnomedicinal plants of Mizoram mentioning their mode of preparation, usage, distribution and habitat, they mostly reported from the core areas of the cities. Their studies highlighted the qualitative data. However, there are no in-depth ethnobotanical studies recorded in Champhai district. Therefore, the present study aims to carry out a quantitative study using different cultural importance indices to assess the most valued plants and document the ethnomedicinal practices involving medicinal plants of the Champhai district of Mizoram, India. Their practical knowledge has been established based on more than a century of credence and observation.
Methods
Description of the study area
Mizoram lies within the Indo-Burma biodiversity hotspot region and shares two international borders with Bangladesh in the west and Myanmar in the east. According to Champion and Seth (1968), Mizoram forests are classified into Tropical semi-evergreen forests, tropical wet evergreen forests and mountain sub-tropical pine forests [14]. The study area, i.e. the Champhai district, is classified as a rural area where healthcare facilities are relatively poor which drives the people to rely on traditional medicines. The traditional healers using medicinal plant-based formulations for various ailments indicate that traditional medicines are still one of the mainstays in their contemporary health care. It is felt that prospection and research on the medicinal plants that play such an important role in the health care of Mizo tribes need a more intensified effort.
Champhai is one of the 8 districts in Mizoram, amidst the North-East Region of India. It is located in the eastern part of Mizoram, internationally bordered by Myanmar and therefore becoming the main gate of trading for India and Myanmar. It lies between 23.456° N latitude and 93.328°E longitude. The average annual rainfall is approximately 1814 mm, and the temperature remains around 18.6 °C which is slightly colder than the rest of the state during winter. The total land area is 3185.83 sq kilometres at an elevation around 1678 m above sea level, population density is 10 per sq kilometres (32,734). According to an official Census (2011), Champhai reported a population of 1,26,000, of which male and female were 62,357 and 63,388, respectively [15]. The study area was divided into 15 village council areas (Vengthlang, Vengthlang North, Venglai, Vengsang, Electric veng, Kanan, Kahrawt, Bethel, New Champhai, Zotlang, Hmunhmeltha, Tualcheng, Ngopa, Khawzawl and East Lungdar) for extensive data collection (Fig. 1). The majority of people living in this area are Mizo tribe and use the Mizo dialect in common.
Fig. 1.
Location of the present study area: Champhai district, Mizoram, India
Investigative method
In the field study, formal questionnaires were distributed to each participant while having face to face interviews at their residence. At least 16 people were interviewed in each village council area. Only those people who have knowledge in the art of preparing medicines either for their families or their neighbourhood were considered for the interaction. The interactions primarily focussed on their experience, type of dosage form, duration of usage, any adverse effects observed and the source of their knowledge about the plant and their parts used. This information was then correlated with the scientific data curated from related databases (Pubmed, SciFinder and Science Direct). In most of the cases, the voucher specimens were deposited (Herbarium, Mizoram University, Aizawl, Mizoram, India) for their authentication and archiving.
Characteristics of demographic data
This demonstrated the socio-economic information of the informant including qualities like age, sex, education level and occupation. Using random sampling method, 200 people (12–14 individuals from each village) in the ages group of 18–71 years were interviewed, of which 112 and 82 were males and females, respectively. Respondents belonged to various professions while some were students. Most of the informants do not engage in full-time ethnomedicinal practice or as a profession. The feature of demographical characteristics obtained in the study is tabulated below (Table 1).
Table 1.
Demographic characteristics of informants (n = 200)
| Age | Number | In percent (%) |
|---|---|---|
| Demographic characteristics | ||
| 18–30 | 42 | 21 |
| 31–50 | 69 | 34.5 |
| 51–70 | 76 | 38 |
| 71 above | 13 | 6.5 |
| Sex | ||
| Male | 112 | 56 |
| Female | 88 | 44 |
| Educational level | ||
| Primary | 30 | 15 |
| Middle | 44 | 22 |
| High School | 56 | 28 |
| Higher Secondary | 32 | 16 |
| University | 38 | 19 |
| Occupation | ||
| Self Employed (farmer, carpenter, bussiness) | 70 | 35 |
| Govt. Employed (teacher, bank, officer) | 65 | 32.5 |
| Unemployed Student, housewives) | 65 | 32.5 |
Quantitative analysis
Frequency of citation
Frequency of citation was used to further examine the primary data by finding the sum of total citations/usage reports for a particular species. The usage report is the quotation of one plant by an informant [16].
Use value
Use value or UV is used to express the correlative importance of each particular plant species locally known and was calculated by the following equation [17].
where ‘Ui’ represents the number of citations of each species by the informants and ‘n’ represents the total number of informants in the study area. The larger the number of citations, the greater is the use-value.
Informant consensus factor
Fic or ICF is used to represent the consistency of the information among the informants, indicating whether there were shared knowledge and concurrence in the use of plants for treating the ailment category among the plant’s users in the study area. It was calculated by the following equation [18].
where ‘Nur’ refers to the number of users reports in each illness category and ‘Nt’ refers to the number of plant species used for a particular illness category by all the informants.
Further, Fic value with 1 or either close to 1 indicates that a large number of informants had agreed on using few plants for curing an illness category while low Fic value signified that there was an argument on using medicinal plants to treat illness amidst the category.
Relative importance
When calculating RI, both the informants who mentioned the useful plant species and their various kinds of uses are considered. So, it was calculated by the following equation [19].
where ‘NUC’ refers to the number of illnesses use category of each species divided by the total number of most use categories among the species and ‘NT’ refers to the number of illness types of uses of each species divided by the total number of most types of uses among the species.
Cultural values
In this index, the use category is taken into account and it was calculated by using the following equation [20].
where ‘UCs’ is the number of the used reports for each species divided by the total number of use categories of that species. ‘ICs’ is the number of informants who mention each plant as effective divided by the total number of informants, and ∑IUCs is the number of informants who report the use of each species divided by the total number of informants.
Results
Demographic characteristics
All the 200 respondents were randomly selected from 15 village council areas interviewing at least 16 persons in each area with no equal separation of male–female ratio. Amongst them, the elderly in their seventies and above occupied 6.5% only, while people between 31 and 50 years old occupied 34.5%. The average age among the informants was 54 years. Mizoram is the second most literate state in the country (2011 census), and all the informants were literate having at least primary school level education. Out of the total informants, 32.5% were engaged in government jobs like teachers, officers, while 35% were self-employed like farmers, carpenters, skilled workers, small businesses and the rest 32.5% of the informants were unemployed including students and housewives (Table 1).
Taxonomy identification
In the present study, 93 medicinal plant species belonging to 53 families and 85 genera have been reported for treating various kinds of ailments. The most prominent families were Euphorbiaceae with 6 plant species followed by Asteraceae with 5 plant species and 4 species each among Cucurbitaceae and Zingiberaceae. Liliaceae, Fabaceae, Verbenaceae, Solanaceae, Rutaceae, Anacardiaceae are with 3 species each while Orchidaceae, Combrethaceae Theaceae, Arecaceae, Apocynaceae, Musaceae, Rubiaceae, Scrophulariaceae, Lamiaceace, Mimosaceae, Smilacaceae are with 2 species each and other 34 families with one species each as shown in Table 2. The high usage report of this large family like Euphorbiaceae (6 species), Asteraceae (5 species) and Zingiberaceae (4 species) occupied 10.8%, 9.2% and 8.35% of the total used report, respectively, indicating that most people in the study area are inclined to use plants that are easily available and abundant around them (Table 2).
Table 2.
Name of plant families with number of species and used report
| Family | No of species | No of used report | % |
|---|---|---|---|
| Euphorbiaceae | 6 | 294 | 10.8 |
| Asteraceae | 5 | 250 | 9.2 |
| Cucurbitaceae | 4 | 82 | 3.02 |
| Zingiberaceae | 4 | 227 | 8.35 |
| Liliaceae | 3 | 76 | 2.8 |
| Fabaceae | 3 | 56 | 2.06 |
| Verbenaceae | 3 | 78 | 2.87 |
| Solanaceae | 3 | 83 | 3.05 |
| Rutaceae | 3 | 120 | 4.42 |
| Musaceae | 3 | 80 | 2.94 |
| Anacardiaceae | 3 | 79 | 2.91 |
| Apocynaceae | 2 | 53 | 1.95 |
| Orchidaceae | 2 | 14 | 0.52 |
| Combretaceae | 2 | 55 | 1.66 |
| Meliaceae | 2 | 54 | 1.99 |
| Theaceae | 2 | 28 | 1.03 |
| Arecaceae | 2 | 86 | 3.17 |
| Rubiaceae | 2 | 38 | 1.4 |
| Scrophulariaceae | 2 | 48 | 1.77 |
| Lamiaceae | 2 | 40 | 1.47 |
| Mimosaceae | 2 | 53 | 1.95 |
| Smilacaceae | 2 | 26 | 0.96 |
| Bromeliaceae | 1 | 49 | 1.8 |
| Begoniaceae | 1 | 37 | 1.36 |
| Amaranthaceae | 1 | 15 | 0.55 |
| Betulaceae | 1 | 7 | 0.26 |
| Cannabinaceae | 1 | 36 | 1.32 |
| Apiaceae | 1 | 29 | 1.07 |
| Caricaceae | 1 | 53 | 1.95 |
| Fagaceae | 1 | 17 | 0.63 |
| Araceae | 1 | 2 | 0.07 |
| Dilleniaceae | 1 | 22 | 0.81 |
| Discoreaceae | 1 | 27 | 0.99 |
| Caryophyllaceae | 1 | 28 | 1.03 |
| Eleagnaceae | 1 | 31 | 1.14 |
| Proteaceae | 1 | 15 | 0.55 |
| Malvaceae | 1 | 4 | 0.15 |
| Saururaceae | 1 | 16 | 0.59 |
| Convulvulaceae | 1 | 37 | 1.36 |
| Rosaceae | 1 | 14 | 0.52 |
| Campanulaceae | 1 | 25 | 0.92 |
| Myrsinaceae | 1 | 4 | 0.15 |
| Magnoliaceae | 1 | 18 | 0.66 |
| Clusiaceae | 1 | 18 | 0.66 |
| Moraceae | 1 | 2 | 0.07 |
| Bignoliaceae | 1 | 37 | 1.36 |
| Pandanaceae | 1 | 24 | 0.88 |
| Phyllanthaceae | 1 | 48 | 1.77 |
| Plantaginaceae | 1 | 36 | 1.32 |
| Myrtaceae | 1 | 98 | 3.61 |
| Polypodiaceae | 1 | 12 | 0.44 |
| Punicaceae | 1 | 31 | 1.14 |
| Poaceae | 1 | 15 | 0.55 |
Frequency of usage of parts of plants
The most commonly used medicinal plants fell under herbs (35.5%) followed by trees (33.3%), shurbs (18.3%) and creepers (12.9%) as shown in (Fig. 2). Among the parts, leaves, fruits and barks were mainly utilised by the informants (Fig. 3). A detailed analysis concluded that leaves (47%) followed by fruits (14%), barks (11%), seeds (10%), rhizomes (6%), stems (4%), young shoot (2%), oil (1%) and in some cases the whole plant (3%) were used for ethnomedicinal purposes.
Fig. 2.

Percentage of plants habit
Fig. 3.

Percentage of parts used
Mode of preparation and administration
The mode of formulation preparation or administration was observed to be in the form of decoction (44.2%) followed by paste (23%), raw (19.5%), juice (9.73%), powder (1.77%) and others like maceration and oil (1.77%) (Fig. 4.).
Fig. 4.

Distribution of formulation usage
Usage analysis based on the treatment of ailments
The total number of user reports documented in this study was 2717, in which all different illnesses were categorised into 16 groups using International Classification of Primary Care (ICPC) with a slight modification. Among the illness category, the gastro-intestinal disease has the highest usage report (940) followed by skincare (259) cardiovascular (222), kidney disease (196), hyperglycaemia (175), ENT (159), genito-urinary disease (139) and so on as shown in Table 3.
Table 3.
Usage analysis with illness category and their term
| Illness categories | Medical term | Local term | Frequency of usage |
|---|---|---|---|
| Dental Care (DC) |
Tooth decay Toothpaste |
Hamuat/Hanget Hanawhna |
57 |
| Skin Care (SC) | Pimple, burn, Face pack, boil, chickenpox, Measles, Herpes | Bawl, Kang, Sentut, Khawihli, Awmvel, Tangseh Hmai chiahna, | 259 |
| Hair Care (HC) | Growth enhances, shining, hair fall | Sam thatna, Sam tletna, Sam tla | 16 |
| Eyes/Nose/Ears/Mouth (ENT) | Otorrhoea, eye itching, Sinusitis, Tonsilitis | Beng kherh, Mit thak, Sinus, Tonsil | 159 |
| Genito-urinary Disease (GUD) | Delivery pain, placenta discharge, urine retention | Nau neih zawh hlam tlakna / na, Zun in | 139 |
| Kidney Disease (KD) | Nephrolithiasis, kidney failure | Kal a lungte awm, Kalna, Kal a hnai awm | 196 |
| High glucose level (HGL) | Diabetes type I & II | Zunthlum | 175 |
| Cancer Disease (CD) | Breast cancer, Leukaemia, lung cancer, etc. | Hnute Cancer, Thisen cancer, Chuap cancer leh dangte | 75 |
| Liver Problem (LP) | Jaundice, Hepatitis B & C, cholelithiasis, Malaria | Thinlian, Hepatitis, Malaria, Mit a lungte awm | 100 |
| Cardiovascular Problem (CP) | Hypertension, Heart problem | Bp sang leh hniam, lung thalo | 222 |
| Muscular/Bone Problem (MBP) | Rheumatoid, Arthritis, Sciatica | Ruh seh/Sehpui, thana, Scaitica | 81 |
| Respiratory System illness (RSI) | Cold, Cough, Asthma, lung disease | Hritlang, Awmna, Khuh, Thawhah | 42 |
| Gastro-intestinal Disease (GID) | Ulcer, stomach pain, Dysentry, Diarrhoea, Digestion, Hemorrhoid, Constipation, Intestinal worms, internal bleeding | Ulcer, Pumna, Ek khal, Pile na, Puar nuamlo, Khawthalo, Santen, Rul hlut, Internal bleeding | 940 |
| Wound healing (WH) | Inflammation | Pem thar /Pilh damdawi, Pan, vung | 126 |
| Poisonous Bites (PB) | Snake bite, Scorpion bite, dog bite, Wasp sting | Rul chuk, Ui seh, Khuai zuk, Khawmual kaikuang seh | 45 |
| General Health (GH) | Fever, Headache, cold, Immuno-booster, Energy booster, etc | Luna, Khawsik, Taksa chakna, Hriselna | 81 |
| Total | 2717 |
Data analysis
Frequency of citation
Among the total number of user reports (UR) cited, Curcuma longa L. (136 FC), Flueggea virosa (Roxb. ex Willd.) Royle (126 FC), Psidium guajava L. (98 FC), Chromolaena odorata (L.) R.M. King & H. Rob. (87 FC), Mikania micrantha Kunth. (82 FC), Citrus limon (L.) Osbeck (68 FC), Carica papaya L. (53 FC), Ananas comosus (L.) Merr. (49 FC), Sarcococca pruniformis Lindl. (49 FC), Phyllanthus emblica L. (48 FC), Rhus chinensis Mill. (45 FC), Clerodendrum glandulosum Lindl. (44 FC), Senecio scandens Buch- Ham. ex D. Don (43 FC) were those species having the highest FC (Table 4).
Table 4.
List of plant species with their use value (UV)
| Sl. no | Species name; voucher no | Family name | Local name | aHabit | bPart Use | Mode of administration | Ailments & UR | FC | UV | Isolated chemical compounds | Bioactivity |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | Allium cepa L. (HAMP20045) | Liliaceae | Purun sen | H | Rt (Bulb) | Raw | Hair care (12), headache (1) | 13 | 0.065 | S-alk(en)yl-substituted cysteine sulphoxides, quercetin, kaempferol [21] | Antioxidant, appetiser Antimicrobial, Hypertension, hair regrowth [22, 23] |
| 2 | Allium sativum L. (HAMP20046) | Liliaceae | Purun var | H | Rt (Bulb) | Raw | Tension (10), toothache (2), cold (12), pimple (7) | 31 | 0.155 | S-allyl-cysteine, Allyl thiosulfinate (Allicin), S-ally-mercapto cysteine [24, 25] | Fever, hypertension, antitumor, antioxidant, antimicrobial, tooth disease, immune boost, etc. [26–28] |
| 3 | Aloe vera (L.) Burm.f. (HAMP20047) | Liliaceae | Rul lei | H | Lf | Raw | Burn (21), Stomachache (2), skin care (9) | 32 | 0.16 | Vitamin E, Sulfuric acid, butyl heptadecylic ester, 1-Tetradecyne [29] | Antimicrobial, anti- inflammatory, laxative, antidiarrhoea, wound healing, antiaging, antioxidant, etc. [30, 31] |
| 4 | Alstonia scholaris (L.) R. Br. (HAMP20006) | Apocynaceae | Thuamriat | T | Br | Decoction | Ulcer (15) | 15 | 0.075 | Alstonine, picrinine, akuammicine, echitamine [32] | Antimicrobial, anti-asthmatic, antioxidant, anti-ulcers, anticancer, rheumatic, inflammatory, wound healing, etc. [33, 34] |
| 5 | Ananas comosus (L.) Merr. (HAMP20019) | Bromeliaceae | Lakhuihthei | Sh | Lf, Fr | Raw, paste | Ulcer (12), seizure (1), Hypertension (10), urinary infection (16), lung disease (10) | 49 | 0.245 | 1-O-feruloylglycerol, tricin, 2, 4-dichlorobenzoic acid, etc. [35] | Anti-inflammatory, anti-thrombotic, antioxidant, antiedematous, anthelminthic, diuretic, rheumatoid, anticancer, antimicrobial, etc. [36, 37] |
| 6 | Anoectochilus brevilabris Lindl. (HAMP20062) | Orchidaceae | Hnah mawi | H | Lf | Paste | Pile problem (12) | 12 | 0.06 | Not reported | Not reported |
| 7 | Anogeissus acuminata (Roxb. ex DC.) Wall. Ex Guillem. &Perr. (HAMP20023) | Combretaceae | Zairum | T | Br | Decoction, | Ulcer (26) | 26 | 0.13 | Castamollilin, Grandinin, (-)-Secoisolariciresinol, 2,3-bis-(4-Hydroxybenzyl butadiene [38] | Hypoglycemic, wound healing, cytoxicity, antibacterial, etc. [39, 40] |
| 8 | Aporosa octandra (Buch-Ham. ex D. Don) Vickery (HAMP20035) | Euphorbiaceae | Chhawntual | T | Lf, Br | Decoction | Ulcer (5), uterus problem (11) | 16 | 0.08 | 2-Methyl-3-en-butyl-cyclohexyl Phthalate, (R)-Coclaurine (AO-5) [41] | Antioxidant, anthelmintic, oxidative stress, D-galactose induce protectivity, etc. [42, 43] |
| 9 | Azadirachta indica A. Juss (HAMP20052) | Meliaceae | Neem | T | Lf | Decoction | Malaria (16), jaundice (8) | 24 | 0.12 | Diepoxyazadirol, flowerine, flowerone, O-methylazadir-onolide [44] | Immunostimulant, antiviral, analgesic, anti-inflammatory, antiulcer, antioxidant, antimicrobial, hepatoprotective, antimalarial, antipyretic, hypoglycemic, etc. [45] |
| 10 | Begonia inflata C.B. Clark. (HAMP20016) | Begoniaceae | Sekhupthur | H, Cr | Lf | Paste, juice | Pile problem (12), diarrhoea (11), dysentery (14) | 37 | 0.185 | Not reported | Not reported |
| 11 | Benincasa hispida (Thunb.) Cogn. (HAMP20028) | Cucurbitaceae | Maipawl | H, Cr | Fr | Decoction | Stomach problem (4), digestion (10), diarrhoea (15) | 29 | 0.145 | Pentanoic acid, 5-hydroxy-2,4- dibutyl phenyl esters, Palmitic acid, 9,12-Octadeca-dienylchloride [46] | Anti-obesity; anti-ulcer; anti-inflammatory; antioxidant; anti-diarrhoeal; anxiolytic; antidiabetic, antinociceptive, etc. [47, 48] |
| 12 | Beta vulgaris L. (HAMP20001) | Amaranthaceae | Beet root | H | Rh | Raw, juice | Aneamia (3), immuno- booster (8), cancer (4) | 15 | 0.075 | Apigenin, Luteolin, Isoscutellarein 7-O-glucosyl, 8-O-xylosid, Caffeoyl-6-(3,4-dihydroxy benzoyl) β-D-glucoside [49] | Antioxidant, anticancer, hepatoprotective, anti-inflammatory, antimicrobial, anti-hypertension, hypoglycemic [50, 51] |
| 13 | Betula alnoides Buch-Ham. ex D. Don (HAMP20017) | Betulaceae | Hriang | T | Lf | Paste | Tooth paste (7) | 7 | 0.035 | α-pinene; a-terpineol; limonene; camphor; β-pinene [52] | Cytotoxicity, anti-inflammatory, antioxidant, antimicrobial, etc. [2, 53] |
| 14 | Bischofia javanica Blume (HAMP20036) | Euphorbiaceae | Khuang thli | T | Lf | Paste | Toothache (13) | 13 | 0.065 | 3,4-dihydroxyphenylethyl alcohol, isotachioside, catechin, epicatechin, gallocatechin [54] | Antimicrobial, antiulcer, cytoxicity, antidysentry, anthelminthic, etc. [55, 56] |
| 15 | Cajanus cajan (L.) Millsp. (HAMP20041) | Fabaceae | Behliang | Sh | Lf | Decoction | Jaundice (25), intestinal worms (3) | 28 | 0.14 | 3,5-bis1,1-dimethylethyl, Tetradecanoic acid, allyl hexadecyl, ester, n-Hexadecanoic acid [57] | Antimicrobial, antidiabetic, antioxidant, glycemic, anthelmintic, hepatoprotective, etc. [58] |
| 16 | Callicarpa arborea Roxb. (HAMP20087) | Verbenaceae | Hnah kiah | T | Lf, Br | Decoction | Stomach ache (9), diabetes (16), convulsion (7) | 32 | 0.16 | Martynoside, Isomartynoside, Ursolic acid, Antiarol rutinoside [59] | Antioxidant, antimicrobial, analgesic, anti-inflammatory, neuroprotective, antidiabetic, etc. [59] |
| 17 | Camellia sinensis (L.) Kuntze (HAMP20082) | Theaceae | Thingpuife | Sh | Lf | Raw, Decoction | Toothace (7), itchy eye (7) | 14 | 0.07 | Caffeine, Theobromine, Gallic acid, Ampelopsin, epicatechin-3-O-gallate, catechin-3-O-gallate [60] | Antimicrobial, tooth decay, antioxidant, anticancer, anti-obesity, antidiabetic, anti-inflammatory, etc. [61, 62] |
| 18 | Cannabis sativa L. (HAMP20021) | Cannabinaceae | Trip/ Kanza | H | Lf | Raw, | Stomach ache (12), diarrhoea (24) | 36 | 0.18 | Cannabigerol, cannabichromene, cannabidiol, cannabisativa, delta 9-Tetrahydrocannabinol [63] | Antioxidant, anti-allergic, anti-inflammatory, analgesic, anti-tumour, anti-diabetic, antibiotic [64] |
| 19 | Centella asiatica (L.) Urb. (HAMP20005) | Apiaceae | Darbengbur /lambak | H | WP | Decoction | Stomach ache (8), urinary infection (17), kidney disease (2), eye pain (2) | 29 | 0.145 | Centellin, asiaticin, centellicin [65] | Ati-ulcer, neuroprotective, antidepressant, anticonvulsion, immunostimulating, antioxidant, antibacterial, kidney injury protectivity, etc. [66, 67] |
| 20 | Capsicum annuum L. (HAMP20084) | Solanaceae | Hmarhcha | H | Fr | Paste | Wasp sting (9), burn (3), toothache (4), boil (2) | 18 | 0.09 | Ascorbic acids, quercetin, luteolin, chrysoeriol, hydroxycinnamic acids [68] | Anti-inflammatory, antimicrobial, antiviral, anticancer, analgesic, etc. [69] |
| 21 | Carica papaya L. (HAMP20026) | Caricaceae | Thingfanghma | T | Lf, Fr sap | Paste, raw | Tonsil (1), face pack (3), cancer (16), diabetes (11), dog bite (17), milk booster in mother (5) | 53 | 0.265 | Benzyl-β-d glucoside, β-sistosterol, β-sistosterol, oleic acids [70] | Antimalaria, antidiuretic, antimicrobial, anthelminthic, hepatoprotective, immunomodulatory, etc. [71, 72] |
| 22 | Castanopsis tribuloides (Sm.) A. DC. (HAMP20044) | Fagaceae | Thingsia | T | Br | Paste | Toothache (17) | 17 | 0.085 | Not reported | Antioxidant [73] |
| 23 | Catharanthus roseus (L.) G. Don (HAMP20007) | Apocynaceae | Kumtluang | T | Lf | Decoction | Hypertension (18), diabetes (20) | 38 | 0.19 | 4-O-caffeoylquinic acid, quercetin-3- O-(6-O-rhamnosyl-glucoside), kaempferol-3-O- (6-O-rhamnosyl-glucoside) [74] | Antihypercholesterollemi, antideuretic, antibacterial, antimalaria, antiviral, cytotoxic, antidiabetic, antihyperglycemic antidiarrhoeal, antioxidant, anthelminthic, etc. [75, 76] |
| 24 | Cheilocostus speciosus (J. Koenig) C.D. Specht (HAMP20090) | Zingiberaceae | Sumbul | Sh | Rh | Decoction | Kidney disease (5), urinary problem (16), stomach ache (18) | 39 | 0.195 | 24-hydroxytriacontan-26-one, sitosterol, cyloartanol, methyl triacontanoate [77] | Antifungal, insecticidal, antioxidant [78, 79] |
| 25 | Chromolaena odorata (L.) R.M. King & H. Rob. (HAMP20011) | Asteraceae | Tlangsam | H | Lf | Decoction, raw | Kidney disease (18), diarrhoea (13), stomach, ache (8), jaundice (14), wound (34) | 87 | 0.435 | α & β-pinenes,1,8-Cineole, β-Calacorene, β-Copaen-4α-ol [80] | Antipyretic, analgesic, anti-inflammatory, antispasmodiac, antimalaria, antioxidant, antimicrobial, etc. [81, 82] |
| 26 | Citrus aurantiifolia (Christm.) Swingle (HAMP20074) | Rutaceae | Champara | T | Fr | Juice | Stomach problem (7), digestion (9) | 16 | 0.08 | Pinene, Sabinene limonene, Myrcene, Telinene [83] | Antimicrobial, antioxidant, antiobesity, anthelminthic [84, 85] |
| 27 | Citrus maxima (Burm.) Merr. (HAMP20075) | Rutaceae | Sertawk | Sh | S | Raw | Hypertension (36) | 36 | 0.18 | Naringenin,5,7-dihydroxylcoumarin, 1, 3,5-trihydroxyhenzene, xanthotoxol [86] | Antimicrobial, analgesic, antioxidant, anti-obesity, anti-inflammatory, etc. [87, 88] |
| 28 | Citrus limon (L.) Osbeck (HAMP20076) | Rutaceae | Nimbu | T | Fr | Juice | Stomach problem (24), digestion (44) | 68 | 0.34 | Ascorbic acid, y-Aminobutyric acid, alanine, aspartic acid, arginine [89] | Anticancer, antiparasitic anti-inflammatory, antimicrobial, [90] |
| 29 | Clerodendrum glandulosum Lindl. (HAMP20088) | Verbenaceae | Phuihnam | Sh | Lf | Decoction | Hypertension (44) | 44 | 0.22 | Strongyloster, lupeol, n hentriacontane, palmitic acid, 2-pentadecyn-1-ol, hexacosane, vitamin E [91] | 2-pentadecyn-1-ol, hexacosane, vitamin E [91] |
| 30 | Colocasia esculenta (L.) Schott (HAMP20008) | Araceae | Dawl | H | St sap | Juice | Vaginal discharge/ Lochia (2) | 2 | 0.01 | 14α-methyl-5α-cholesta-9, 24-diene-3b, 7α-diol; 9, 12, cyanidin 3-glucoside; 9, 12, 13-trihydroxy-(E)- 10-octadecenoic acid [92] | Antihepatotoxicity, anthelminthic, anticancer, antimicrobial, antioxidant, anti-inflammatory, etc. [92–95] |
| 31 | Combretum wallichii DC (HAMP20024) | Combretaceae | Leihruisen | Sh | Sh | Raw | Tonsil (19) | 19 | 0.095 | Not reported | Anthelminthic [96] |
| 32 | Crassocephalum crepidioides (Benth.) S. Moore (HAMP20012) | Asteraceae | Buar thau | H | Lf | Paste | Wound bleeding (14) | 14 | 0.07 | (E)-β-farnesene, α-humulene, cis-β-guaiene, α-bulnesene [97] | Anti-tumour, cytoxicity, antidiabetic [98, 99] |
| 33 | Cucurbita maxima Duchesne (HAMP20029) | Cucurbitaceae | Mai | H, Cr | S | Raw | Instestinl worm (15) | 15 | 0.075 | Oleic acid, linoleic acid, palmitic acid, caffeic, syringic, vanillic, p-coumaric [100] | Antidiabetic, anticancer, antiobesity, antihelmintic, cytotoxicity, antibacterial, anti-inflammatory, anti-parasitic [101] |
| 34 | Curcuma caesia Roxb. (HAMP20091) | Zingiberaceae | Ailaidum | H | Rh | Raw, juice | Stomach ache (4), diarrhoea (18) | 22 | 0.11 | α, β-pineneeucalyptol, camphor, camphene, gallic acid, quercetin [102] | Antimicrobial, analgesic, antioxidant, antiulcer, antimutagenic, anti-asthmatic, anthelminthic, etc. [103] |
| 35 | Curcuma longa L. (HAMP20092) | Zingiberaceae | Aieng | H | Rh | Powder, juice | Ulcer (67), diarrhoea (4), derma care (30), stomach ache (35) | 136 | 0.68 | Curcumin, ar-turmerone, β-sesquiphellandrene, curcumenol [104] | Antimicrobial, anticancer gastrointestinal and respiratory disorder, anti-inflammatory, anti-diabetic, anti-allergic, hepatoprotective, anti-dermatophytic, neuroprotective, etc. [105] |
| 36 | Cucumis sativus L.h (HAMP20030) | Cucurbitaceae | Fanghma | H, Cr | Lf | Decoction, raw | Malaria (8), derma care (17) | 25 | 0.125 | Myristic acid, karounidiol, avenasterol, palmitoleic acid, alpha-linolenic acid [106] | Antimicrobial, antiulcer, antitumour, wound healing, hypoglycemic, hypolipidemic, anti-inflammatory, antioxidant, etc. [107] |
| 37 | Dichrocephala integrifolia (L.f.) Kuntze (HAMP20013) | Asteraceae | Vawkek tumtual | H | Lf | Decoction | Kidney disease (24) | 24 | 0.12 | Stearic acid, stigmasta-7,22-dien-3-ol, epifriedelanol, Methyl stearate, tritetracontane [108] | Antimicrobial, cytotoxity, antidiarhoeal, antioxidant, anti-inflammatory, neuroprotectivity [109–111] |
| 38 | Dillenia pentagyna Roxb. (HAMP20032) | Dilleniaceae | Kaihzawl | T | Lf, Br | Decoction | Diarrhoea (21), kidney disease (1) | 22 | 0.11 | Dillenetin, betunaldehyde, betulinic acid, quercetin, kaempferol glucoside, lupeol [112] | Antimicrobial, antiviral antioxidant, anticancer, antidiabetic, anti-inflammatory [112] |
| 39 | Dioscorea alata L. (HAMP20033) | Discoreaceae | Bachhim | H, Cr | Fr | Decoction | Cancer (27) | 27 | 0.135 | Hydro-Q9 chromene, γ-tocopherol-9, 1-feruloylglycerol, RRR-α-tocopherol [113] | Antimicrobial, antioxidant, anti-inflammatory, antidiabetic, etc. [114, 115] |
| 40 | Drymaria cordata (L.) Willd. ex Schult. (HAMP20027) | Caryophyllaceae | Changkal rit | H, Cr | Lf | Decoction, paste | Rheumatism (24), dysentery (4) | 28 | 0.14 | Stigmasterol, cerebroside [116] | Analgesic, anxiolytic, antipyretic, antitussive, antibacterial, anti-inflammatory [116] |
| 41 | Dysoxylum excelsum Blume. (HAMP20051) | Meliaceae | Thingthupui | T | YS | Decoction | Diarrhoea (18), hyper tension (12) | 30 | 0.15 | Isodauc-6-ene-10β,14-diol; 4-epi-isodauc-6-ene-10β,14-diol; 4-epi-6α,10β-dihydroxy-artabotrol [117] | Not reported |
| 42 | Elaeagnus caudata Schltdl. ex Momiy. (HAMP20034) | Elaegnaceae | Sarzuk | T | Lf | Decoction | Vaginal discharge/ Lochia (31) | 31 | 0.155 | Not reported | Expelling placenta, miscarriage, jaundice [118, 119] |
| 43 | Elaeis guineensis Jacq. (HAMP20009) | Arecaceae | Oil palm | T | Oil | Oil | Wound (1), burn (1), hair care (3) | 5 | 0.025 | 3-isobutyl-2-methoxypyrazine; acetoin; 2-acetyl-1-pyrroline; ethyl hexanoate; 3-methylbutyl xacetate [120] | Antioxidant, wound healing, antimicrobial, anti-inflammatory, cardiovascular effect, antidiabetic, anticancer, etc. [121, 122] |
| 44 | Embelia vestita Roxb. (HAMP20010) | Arecaceae | Tling | Sh | Lf | Decoction | Measles (16), chickenpox (65) | 81 | 0.405 | Not reported | Not reported |
| 45 | Ensete glaucum (Roxb.) Cheesman (HAMP20057) | Musaceae | Saisu | H | St | Decoction | Nephrolithiasis (34) | 34 | 0.17 | Not reported | Not reported |
| 46 | Ensete superbum (Roxb.) Cheesman (HAMP20058) | Musaceae | Changel/ Tumbu | H | St sap, Fr | Juice | Snake bite (6), kidney disease (1), diabetes (4), WBC deficiency (23) | 34 | 0.17 | Pentadecanoic acid; 4H-Pyran-4-one, 2,3-dihydro-3, 5-dihydroxy-6-methyl-; 2-Furancarboxaldehyde, 5-(hydroxymethyl) [123] | Kidney stone preventivity, antioxidant, etc. [124] |
| 47 | Erythrina stricta Roxb. (HAMP20042) | Fabaceae | Fartuah | T | Br | Decoction | Ulcer (8), kidney disease (2) | 10 | 0.05 | β-caryophyllene; δ-cadenine; alpinum isoflavone; obovatin; isovanillin [125] | Antimicrobial, epilepsy, antioxidant, leprosy, anti-inflammatory, etc. [126, 127] |
| 48 | Eulophia nuda Lindl. (HAMP20062) | Orchidaceae | Nauban | H | WP | Decoction | Diarrhoea (2) | 2 | 0.01 | Eulophiol;3,4-dihydroxy-3,5,5- trimethoxybibenzyl; nudol; lupeol [128] | Antimicrobial, anti-inflammatory, cytotoxic, antioxidant, anticancer, antiasthmatic/ antibronchitis [128, 129] |
| 49 | Euphorbia milii Des Moul. (HAMP20037) | Euphorbiaceae | Hlinglukhum | H | Lf | Raw | Diarrhoea (52) | 52 | 0.26 | Abruquinone B; eremopetasitenin A; ellagic acid; isopetasoside; 7,8-Dihydroxycoumarin; [130] | Antimicrobial, antioxidant, cytoxicity, antinociceptive, anthelmintic, etc. [131, 132] |
| 50 | Euphorbia royleana Boiss. (HAMP20038) | Euphorbiaceae | Chawng | Sh | Lf sap | Juice | Otorrhoea (38) | 38 | 0.19 | Antiquorine A; Eurifoloid D; sandaracopimaradienolal; 15-isopimaradien-18-a [133] | Antitumour, anti-arthritic, antimicrobial, antioxidant, cytotoxicity, anti-inflammatory, etc. [134, 135] |
| 51 | Flueggea virosa (Roxb. ex Willd.) Royle (HAMP20039) | Euphorbiaceae | Saisiak | Sh | Lf | Decoction | Diabetes (59), stomach ache (17), chicken pox (50) | 126 | 0.63 | 11-O-acetyl bergenin; gallic acid; virosecurinine; kaempferol; β-sitosterol; quercetin [136] | Anti-inflammatory, anti-pyretic, anti-hepatitis C, etc. [137, 138] |
| 52 | Gomphogyne cissiformis Griff. (HAMP20031) | Cucurbitaceae | Lalruanga dawi bur | H, Cr | Fr | Juice | Hypertension (6), diabetes (7) | 13 | 0.065 | Not reported | Not reported |
| 53 | Hedyotis scandens Roxb. (HAMP20072) | Rubiaceae | Kelhnam tur | H | Lf | Decoction | Kidney disease (4), pain relief (7), diabetes (10) | 21 | 0.105 | Hedyotoside A; hedyotoside B; hedyotoside C, D & E [139] | Antimicrobial, abdominal pain [140, 141] |
| 54 | Helicia robusta (Roxb.) R.Br. ex Blume (HAMP20069) | Proteaceae | Pasal-taka-za | T | Lf | Decoction | Placenta discharge (6), stomach pain (8), kidney disorder (1) | 15 | 0.075 | Not reported | Not reported |
| 55 | Hibiscus sinensis Mill. (HAMP20052) | Malvaceae | Midum par | Sh | Lf | Paste | Boil (4) | 4 | 0.02 | Quercetin-3,5-diglucoside, undecanoic acid, cyanidin chorides, rachidic acid, cyanin [142] | Antioxidant, antipyretic, antimicrobial, antifertility, anticonvulsive, etc. [142, 143] |
| 56 | Houttuynia cordata Thunb. (HAMP20077) | Saururaceae | Ui thinthang | H | Lf | Juice | Sainus problem (16) | 16 | 0.08 | Quercetin-3-O-β-D-galactoside-7-O-β-D-glucoside, aristolactam A & B, β-Sitosterol, N-phenethyl-benzamide [144] | Antiviral, antitumour, antioxidant, anti-inflammatory, antimicrobial, anti-SARS, immunomodulator, etc. [144] |
| 57 | Ipomoea batatas (L.) Lam. (HAMP20025) | Convovulaceae | Kawl-ba-hra | H, Cr | YS | Raw | Digestion (37) | 37 | 0.185 | 3-mono-O-caffeoylquinic acid; caffeic acid; vitamin C; kaempferol [145] [145] | Antidiabetic, anticancer, antioxidant, antiulcer, cardiovascular effect [145] |
| 58 | Lablab purpureus (L.) Sweet (HAMP20043) | Fabaceae | Bepui | Sh | Lf | Paste | Vaccine pain relief (18) | 18 | 0.09 | Phytic acid, linoleic acid, linolenic acid [146] | Antidiabetic, anti-inflammatory, analgesic, cytotoxicity, antimicrobial, antioxidant, hypolipidemic [147] |
| 59 | Laurocerasus undulata (Buch-Ham. ex D. Don) M. Roem. (HAMP20071) | Rosaceae | Thei-ar-lung | H | Lf | Decoction | Heart disease (14) | 14 | 0.07 | Not reported | Not reported |
| 60 | Lindernia ruellioides (Colsm.) Pennell (HAMP20078) | Scrophulariaceae | Thasuih | H | WP | Paste | Sciatica (24) | 24 | 0.12 | Linderruelliosides A & B; plantainoside A; acteoside, desrhamnosylverbascoside [148] | Anti-inflammatory, antitumour, antiulcer, analgesic [149] |
| 61 | Lobelia angulata G. Forst. (HAMP20020) | Campanulaceae | Choak-a-thi | H | WP | Decoction | Tonsil (9), gallstone (16) | 25 | 0.125 | Not reported | Not reported |
| 62 | Maesa indica (Roxb.) A. DC. (HAMP20060) | Myrsinaceae | Arngeng | Sh | Lf | Paste | Toothache (4) | 4 | 0.02 | 2 5 dihydroxy-6-methyl 3 (hemeos 16-enyl)-1 4benzoquinone [150] | Hypoglycemic, [151] |
| 63 | Magnolia champaca (L.) Baill. ex Pierre (HAMP20050) | Magnoliaceae | Ngiau | T | Lf | Miceration | Itchy eyes (18) | 18 | 0.09 | Butanoic acid, 2-methyl-3-oxo-, ethyl ester; Camphorsulfonic acid [152] | Anti-inflammatory, antipyretic, antimicrobial, anticancer [152, 153] |
| 64 | Mangifera indica L. (HAMP20002) | Anacardiaceae | Theihai | T | YS | Decoction | Diarrhoea (5), diabetes (10), hypertension (10), asthma (6) | 31 | 0.155 | Quercetin-3-O-β-L-rhamnopyranoside; maclurin-3-C-β-glucoside; amentoflavone; mangiferin [154] | Antidiabetic, antiviral, antiulcer, antimalarial, hepatoprotective, anti-inflammatory, antibacterial [155] |
| 65 | Mentha arvensis L. (HAMP20048) | Lamiaceae | Pudina | H | Lf | Decoction | Stomach problem (38) | 38 | 0.19 | Menthol, p-menthone, neo-menthone, iso-menthone [156] | Antioxidant, analgesic, antibacterial, cytotoxic, antifertility, anti-inflammatory, antiallergic [157] |
| 66 | Mesua ferrea L. (HAMP20022) | Clusiaceae | Herhse | T | Lf | Paste, decoction | Wound (8), stomachache (7), diarrhoea (3) | 18 | 0.09 | 1,5-dihydroxyxanthone; euxanthone, 7-methyl ether; β-sitosterol [158] | Antimicrobial, anti-inflammatory, antiulcer, anti-arthritis, analgesic, analgesic, hepatoprotective, antioxidant [159] |
| 67 | Mikania micrantha Kunth. (HAMP20014) | Asteraceae | Japan Hlo | H, Cr | Lf | Paste, decoction | Wound (52), diarrhoea (8), dysentery (6), stomach ache (16) | 82 | 0.41 | β-cubebene; 1H-inden-1-one, 5-(1, 1-dimethylethyl)-2, 3-; allo-aromadendrene; β-caryophyllene [160] | Antimicrobial, antioxidant, anthelminthic [161, 162] |
| 68 | Mimosa pudica L. (HAMP20054) | Mimosaceae | Hlonuar | H | Lf | Decoction | Kidney disease (37) | 37 | 0.185 | 7, 8, 3', 4'-tetrahydroxyl-6-C [alpha- L-rhamnopyranosyl-(1 – > 2)]-beta- D-glucopyranosyl flavone; catcher; 5, 7,3', 4'-tetrahydroxyl-6-C [alpha-L- rhamnopyranosyl-(1 – > 2)]-beta- D-glucopyranosyl flavone [163] | Wound healing, antimicrobial, analgesic, antimalaria, anti-inflammatory, hepatotoxicity, antidiarrhoeal, anthelminthes [164] |
| 69 | Morus macroura Miq. (HAMP20056) | Moraceae | Lung-li | T | Lf | Raw | Cut / wound (22) | 2 | 0.01 | Gallic acid, catechin, p-hydroxy benzoic, ellagic acid,3,4,5- methoxy cinnamic [165] | Anti-inflammatory, antioxidative, antiulcer [165] |
| 70 | Musa acuminata Colla (HAMP20059) | Musaceae | Balhla | H | Fr, sap | Paste, Decoction | Diabetic wound (6), lung disease (2), snake bite (4) | 12 | 0.06 | Pantothenic acid (B5), ferulic acid-hexoside, Vitamin C, provitamin A, lycopene [166] | Antioxidant, antidiarrhoea, immunomodulatory, anti-HIV, antidiabetic, hypolipidemic, anticancer, antimicrobial [167, 168] |
| 71 | Mussaenda macrophylla Wall. (HAMP20072) | Rubiaceae | Va-kep | Sh | Lf | Decoction | Internal bleeding (17) | 17 | 0.085 | 3-O-β-d-glucopyranosyl-28-O-α-l-rhamnopyranosyl-16α-hydroxy-23-deoxyprotobassic acid; 16α-hydroxyprotobassic acid; 3-O-acetyldaturadiol; rotundic acid [169] | Antimicrobial [170] |
| 72 | Ocimum americanum L. (HAMP20049) | Lamiaceae | Runhmui | H | Lf, St | Paste | Pile problem (2) | 2 | 0.01 | á-pinene; farnesene; terpineol; farnesol; limonen [171] | Antioxidant, antimicrobial, [172, 173] |
| 73 | Oroxylum indicum (L.) Kurz (HAMP20018) | Bignoniaceae | Ar-chang- kawm | T | Br, Lf | Paste, decoction | Ulcer (6), arthritis (13), diarrhoea (3), dysentry (6), hepatitis C (9) | 37 | 0.185 | Ellagic acid; oroxylin-A; 7-o-methyl chrysin; palmitoleic; linoleic acids [174] | Anticancer, antimicrobial, hepatoprotective, antiulcer, amtiarthritic, anti-inflammatory, antioxidant, immunostimulatant, cardioprotective [175] |
| 74 | Pandanus odorifer (Forssk.) Kuntze (HAMP20064) | Pandanaceae | Ram-la-kuih | Sh | Lf | Decoction | Kidney disease 24 | 24 | 0.12 | Not reported | Anticancer, antimicrobial [176] |
| 75 | Parkia timoriana (DC.) Merr. (HAMP20055) | Mimosaceae | Zawngtah | T | Fr, peel, Br | Paste, raw | Diabetes (10), baby umblical care (2), hypertension (4) | 16 | 0.08 | β-sitostero; javanicoside A; epigallocatechin gallate; ursolic acid; hyperin [177] | Antioxidant, antidiabetic, antiproliferative, antibacterial, anti-insecticidal [177] |
| 76 | Phyllanthus emblica L. (HAMP20065) | Phyllanthaceae | Sunhlu | T | Fr | Raw, juice | Diarrhoea (2), skincare (12), stomach problem (8), energybooster (7), diabetes (9), hypertension (6), jaundice (4) | 48 | 0.24 | Ascorbic acids, gallic acids, quercetin, punigluconin, emblicanin A&B, citric acids [178] | Antimicrobial, analgesic, antioxidant, antipyretic, hepatoprotective, antiulcer, antitumour, anti-inflammatory, immunostimulant [178] |
| 77 | Picria fel-terrae Lour. (HAMP20079) | Scrophulariaceae | Khatual | H | Lf | Decoction | Hypertension (24) | 24 | 0.12 | Rosmarinic acid; apigenin-7-O-β-D-glucuronide; picfeltarraegenin IV; acteoside; apigenin [179] | Antioxidant, anthelmintic, antiproliferative [180, 181] |
| 78 | Plantago major L. (HAMP20066) | Plantaginaceae | Kelba-an | H | Lf | Decoction | Kidney disease (2), urinary problem (34) | 36 | 0.18 | Plantaginin; plantagonin; ursolic acid; aucubin; palmitic acid, ascorbic acid [182] | Immunomodulator, antioxidant, analgesic, antiulcer, antibiotic, antiviral, cytotoxicity, hepatoprotective [182] |
| 79 | Psidium guajava L. (HAMP20061) | Myrtaceae | Kawl-thei | T | Lf | Decoction | Diarrhoea (97), hair fall (1) | 98 | 0.49 | β-sitosterol; guajanoic acid; oleanolic acid; uvaol; ursolic acid [183] | Anti-allergy, antioxidant, antimicrobial, anticough, antinogenetic, analgesic, cytotoxicity, antidiabetic, anti-inflammator [184] |
| 80 | Pseudodrynaria coronans (Wall. ex Mett.) Ching (HAMP20067) | Polypodiaceae | Awmvel | H | Lf | Paste | Herpes (12) | 12 | 0.06 | Kaempferol-3-O-(6'' -O-acetyl)-β-D-glucopyranoside; astragalin; isoquercitrin; kaempferol3-O-(6'' -O-feruloyl-4'' -O-acetyl)-β-D-glucopyranoside [185] | Antioxidant [185] |
| 81 | Punica granatum L. (HAMP20068) | Punicaceae | Thei-buh-fai | T | Fr | Raw, juice | Anemia (5), immuno- booster (21), cancer (5) | 31 | 0.155 | Ellagic acid; kaempferol; anthocyanins; punicalagin; quercetin; luteolin; ellagitannins [186] | Antiepileptic, antimicrobial, antiviral antidiabetic, antioxidant, anticancer, anti-inflammatory, hepatoprotective [186] |
| 82 | Rhus chinensis Mill. (HAMP20003) | Anacardiaceae | Khawmhma | T | Fr | Raw, powder | Diarrhoea (27), stomach ache (18) | 45 | 0.225 | Moronic acid; gallicin; 3-oxo-6β-hydroxyolean-12-en-28-oic; aciddimethyl caffic acid; phytol [187] | Antidiarrhoeal, anticancer, anti-HIV, antidiabetic, hepatoprotective [187] |
| 83 | Sarcococca pruniformis Lindl. (HAMP20040) | Euphorbiaceae | Pawhrual | H | Lf | Raw, decoction | Tonsil (49) | 49 | 0.245 | Not reported | Not reported |
| 84 | Schima wallichii Choisy (HAMP20083) | Theaceae | Khiang | T | Br/ St | Paste | Insect bite (9), wound (5) | 14 | 0.07 | Phenylpropanolamine; rotenone; glycidol; 2, 3-benzofurandione [188] | Anti-inflammatory, antioxidant, antimicrobial, analgesic, anti-pyretic [189, 190] |
| 85 | Senecio scandens Buch- Ham. ex D. Don (HAMP20015) | Asteraceae | Sai-ek-hlo | H, Cr | Lf | Decoction, paste | Ulcer (17), diabetes (13), Hypertension (8), toothache (3), wound (2) | 43 | 0.215 | Quercetin; kaempferol; luteolin; rutin; phytol, palmitic acid; β-Amyrin; β-Sitosterol [191] | Anti-inflammatory, analgesic, mutagenic, antimicrobial, antiviral, anti-tumour, anti-leptospirosis, antioxidant [191] |
| 86 | Smilax glabra Roxb. (HAMP20081) | Smilacaceae | Kai-tluang | H, Cr | Lf | Paste | Arthritis (20) | 20 | 0.1 | Palmitic acid; β-sitosterol; quercetin; apigenin; 3-methoxygallic acid; lignoceric acid [192] | Antimicrobial, antioxidant, cytotoxicity, anti-inflammatory, hepatoprotective, antiviral [192] |
| 87 | Smilax perfoliata Lour. (HAMP20080) | Smilacaceae | Kai-ha | Sh, Cr | Lf | Decoction | Dysentry (6) | (6) | 0.03 | Rutin,1; 6-O-diferuloyl-(3-O-p-coumaroyl)-b-D-fructofuranosyl-(2 → 1)-2-O-acetyl-a-D-glucopyranoside; cassiamin A & B; narcissin [193] | Antioxidant, antimicrobial [194] |
| 88 | Solanum americanum Mill. (HAMP20085) | Solanaceae | Anhling | Sh | Lf | Decoction | Nephrolithiasis (15), urinary retention (6), Kidney disease (11) | 32 | 0.16 | Pinoresinol; tetracosanoic acid; syringaresinol; β-sitosterol; scopoletin; medioresinol [195] | Antimicrobial, hepatoprotectivity, anti-inflammatory, anti-seizure, antioxidant, antipyretic, antitumour [196, 197] |
| 89 | Solanum violaceum Ortega (HAMP20086) | Solanaceae | Tawkte | Sh | Fr | Decoction, paste | Hypertension (20), diabetes (6), burn (4), boil (1), herpes (2) | 33 | 0.165 | 7-oxositosterol; yamogenin; 7-oxostigmasteroldiosgenin [198] | Antioxidant, antiobesity. anthelminthic, cytotoxity, anti-inflammatory, analgesic, antinociceptive, antipyretic [199, 200] |
| 90 | Spondias pinnata (L. f.) Kurz (HAMP20004 | Anacardiaceae | Tawi-taw | T | Br | Decoction | Diarrhoea (3) | 3 | 0.015 | Ellagitannins, galloylgeranin, lignoseric acid, β -carotein, oleanic acid [201] | Antimicrobial, cytoxicity, anti-cancer, antioxidant, anthelmintic, thrombolytic activity, antidiarrhoeal [201] |
| 91 | Tectona grandis L.f. (HAMP20089) | Verbenaceae | Teak | T | Br, Lf | Paste | Wound bleeding (2) | 2 | 0.01 | Gallic acid; β-sitosterol; betulinic acid; tectoquinone; squalene; lauric acid [202] | Antibacterial, anti-diabetic, antioxidant, antiulcer, antipyretic, anti-inflammatory, analgesic, antiviral, cytotoxic activity [202, 203] |
| 92 | Zea mays L. (HAMP20070) | Poaceae | Vaimim | H | Lf | Decoction | Kidney disease (15) | 15 | 0.075 | Eugenol; cis-α-terpineol; citronellol; 6,11-oxidoacor-4-ene [204] | Antimcrobial, antioxidant, antimutagen [205, 206] |
| 93 | Zingiber officinale Roscoe (HAMP20093) | Zingiberaceae | Sawhthing | H | Rh | Raw, decoction | Cold / cough (12), digestion (18) | 30 | 0.15 | Zingiberene; gingerols; farnesene; curcumene; zingerone; vitamins [207] | Appetiser, antimicrobial, immunostimulant, analgesic, anticancer antioxidant, antidiabetic, anti-inflammatory, antiarthritis, etc. [208] |
aHabit: H, herbs; Sh, shrubs; Cr, creeper; T, tree; UR, used reports; FC, frequency of citation; UV, use value
bPart used, Lf, leaf; Br, bark; Fr, fruit, Rh, rhizome; St, stem; S, seed; WP, whole plants; YS, Young shoot
Plant use value
From the UV value evaluation, Curcuma longa L. (0.68), Flueggea virosa (Roxb. ex Willd.) Royle (0.63), Psidium guajava L. (0.49), Chromolaena odorata (L.) R.M. King & H. Rob. (0.43), Mikania micrantha Kunth. (0.41), Citrus limon (L.) Osbeck (0.34), Carica papaya L. (0.26), Ananas comosus (L.) Merr. (0.24), Sarcococca pruniformis Lindl. (0.24), Phyllanthus emblica L. (0.24), Clerodendrum glandulosum Lindl. (0.22), Rhus chinensis Mill. (0.22), Senecio scandens Buch- Ham. ex D. Don (0.21) were reported to have the highest use value (UV).
Informant consensus factor
We calculated the informant consensus factor by categorising the reported illness into 16 ailment groups along with the number of users report and taxa (Table 5). In our study, Fic values ranged from 0.866 to 0.962 which were all close to 1.
Table 5.
Informant consensus factor with their used report in each of an ailment category
| Illness categories | No. of used report | No of taxa | Fic |
|---|---|---|---|
| Dental Care (DC) | 57 | 8 | 0.875 |
| Skin Care (SC) | 259 | 13 | 0.953 |
| Hair Care (HC) | 16 | 3 | 0.866 |
| Eyes/Nose/ Ears/Mouth (ENT) | 159 | 9 | 0.949 |
| Genito-urinary Disease (GUD) | 139 | 9 | 0.942 |
| Kidney Disease (KD) | 196 | 15 | 0.928 |
| Endocrinal Disorder (ED) | 175 | 12 | 0.936 |
| Cancer Disease (CD) | 75 | 5 | 0.945 |
| Liver Problem (LP) | 100 | 7 | 0.939 |
| Cardiovascular Problem (CP) | 222 | 14 | 0.941 |
| Muscle/Bone Problem (MBP) | 81 | 4 | 0.962 |
| Respiratory System illness (RSI) | 42 | 5 | 0.902 |
| Gastro-intestinal Disease (GID) | 940 | 42 | 0.956 |
| Wound healing (WH) | 126 | 10 | 0.928 |
|
Poisonous Bites (PB) |
45 | 5 | 0.909 |
| General Health (GH) | 81 | 10 | 0.887 |
| 2717 |
Relative importance and cultural value
Results of top-ranking species in terms of both indices of relative importance and cultural value are given in Table 6. This study elucidates the highest cultural valued species and relative importance species utilised by the inhabitants of the study area. In general, the evaluated values were quite high in case of CVs and an average value of RI (0.607 ± 0.38) clarified that the versatile species, i.e. Phyllanthus emblica (RI = 2) was 3.3 times more relevant than the rest of the listed species.
Table 6.
Species with high cultural values and relative importance
| CVs | RI |
|---|---|
| Curcuma longa (27.28) | Phyllanthus emblica (2) |
| Flueggea virosa (16.0) | Carica papya (1.85) |
| Embelia vestita (13.12) | Senecio scandens (1.54) |
| Psidium guajava (11.64) | Ananas comosus (1.54) |
| Citrus limon (7.16) | Oroxylum indicum (1.38) |
| Mikania micrantha (6.72) | Chromolaena odorata (1.37) |
| Chromolaena odorata (3.40) | Allium sativum (1.23) |
| Euphorbia milii (3.17) | Ensete superbum (1.23) |
| Sarcococca pruniformis (2.82) | Centella asiatica (1.23) |
| Clerodendrum glandulosum (1.93) | Measia indica (1.23) |
| Rhus chinensis (1.82) | Solanum violaceum (1.21) |
| Mimosa pudica (1.129) | Capsicum annuum (1.07) |
CVs, caltural value; RI, relative importance
Correlation and validation studies
An attempt was made to compare the use of all the medicinal plants reported by the informants with the previous papers published for their biological activity or ethnomedicines (Table 4). According to the studies conducted by Cakilcioglu et al., 2011, it was stated that if a medicinal plant has been reported for similar use in other parts of the world, its pharmacological effect could be more easily known [209].
The use of crude juice of Allium cepa L. showed a significantly higher hair growth rate than tap water when applied twice a day for two months which corroborated the present report of hair regrowth [22]. Metallothionein, an antioxidant protein present in Aloe vera (L.) gel, has been reported to have a protective effect against UV and gamma radiation damage to the skin. It scavenges free radicals by preventing the suppression of glutathione peroxidase and superoxide dismutase in the skin [30]. So, this validated the used of A. vera for skin care and burning by the Mizo tribes. In the present study, Betula alnoides Buch- Ham. ex D. Don has been used as toothpaste for whitening teeth while it was proved that 80% methanolic bark extract had the potential α-glucosidase inhibitory effect that prevent the (98.4%) at 40 µg/mL concentration [2]. Cajanus cajan (L.) Millsp is used effectively in Champhai district to treat jaundice and intestinal worms. To certify this, the methanolic extracts showed hepatoprotective activity in Swiss albino mice by inducing carbon tetrachloride (CCl4) that cause liver damage. It lowers the serum levels of glutamate pyruvate transaminase (SGPT), or alanine aminotransferase (ALT) aspartate aminotransferase (AST) or serum glutamate oxaloacetate transaminase (SGOT) significantly [58].
When the aqueous extracts of Carica papaya L. and Ananas comosus L. were given to Spraque Dawley rats orally at doses of 5 and 10 mg/kg, both possessed mild to strong diuretic activity. Careful measure should be taken when using these plants as increase in the level of urinary K+, serum BUN and creatinine were mentioned [71]. This validated the used of C. papaya and A. comosus in kidney disease and urinary infection. The contemporary reports showed that Drymaria cordata (L.) was used as an instant pain killer for rheumatism; meanwhile, the scientific study also demonstrated that the aqueous whole plant extract exhibited analgesic and antipyretic properties at doses of 100, 200, and 400 mg/kg p.o mediated through peripheral and central mechanisms [210]. The latex water-soluble fraction of Euphorbia royleana Boiss. showed dose-dependent anti-arthritic and anti-inflammatory effects in rats and mice administered through gavage at doses of 50–200 mg/kg having more than 1500 mg/kg oral LD50 in both [135]. Dose-dependent and significant decline in the number of abdominal constrictions induced by intraperitoneal administration of acetic acid was observed in methanol extract of Lablab purpureus (L.) Sweet. at a dose of 200 mg and 400 mg exhibited far better analgesic activity than 200 mg aspirin per kg of body weight [211].
Colocasia esculenta (L.) Schott and Elaeagnus caudata Schltdl. ex Momiy. were declared to use to discharge placenta after birth and to treat vaginal discharge (Lochia) for women in present study. Besides this record, in Cachar hills district of Assam, India, 5 ml of Elaeagnus caudata fresh root extract diluted in 10 ml of fresh water was also administered orally once a week to prevent miscarriage during pregnancy although there is no scientific study to backup this claim [118]. Apart from present report in Jamaica, Mikania micrantha Kunth. was most popularly used too for wound healing and its extract showed anti-inflammatory and antimicrobial activity against common pathogens, namely Escherichia coli, Staphylococcus aureus and Streptococcus sp. [212]. The decoction of Psidium guajava leaf was effectively used for diarrhoea which already proved to have antidiarrhoeal and protein conservative effects in diarrhoeal rats at a dose of 50 and 100 mg/kg of body weight. It increased the kidney weight and concentration of sodium, potassium and chloride significantly [213]. In the animal study of anti-urolithialic activity of Solanum nigrum, the fruit hydroalcoholic extract elicited potent activity against calcium oxalate urolithiasis effected by ethylene glycol through tumour necrosis factor adiponectin stimulation and alpha inhibition, also maintained the balance between stone promoter and inhibitor such as calcium and magnesium, respectively [214]. Thus, this authenticated the used of S. nigrum for removing kidney stone by the Mizo tribes in India.
Anoectochilus brevilabris Lindl., Begonia inflata C.B. Clark, Dysoxylum excelsum Blume, Embelia vestita Roxb, Ensete glaucum (Roxb.) Cheesman, Gomphogyne cissiformis Griff., Helicia robusta (Roxb.) R. Br. ex Blume, Laurocerasus undulata (Buch- Ham. ex D. Don) M. Roem. and Lobelia angulata G. Forst., Sarcococca pruniformis Lindl. were the plants that did not have biological activity reported previously which means that there is no scientific validation to support their application. Therefore, these plants were especially recommended in carrying out further investigation.
In addition, we compiled the secondary metabolite isolated chemical constituents done by several researchers for all the documented plants in the present study. Further investigation revealed that secondary metabolites from 13 plant species that have neither less nor none chemical compound isolated or identified—Anoectochilus brevilabris Lindl., Begonia inflata C. B. Clark., Castanopsis tribuloides (Sm.) A. DC., Combretum wallichii DC, Elaeagnus caudata Schltdl. ex Momiy., Embelia vestita Roxb., Ensete glaucum (Roxb.) Cheesman, Gomphogyne cissiformis Griff., Helicia robusta (Roxb.) R. Br. ex Blume, Laurocerasus undulata (Buch- Ham. ex D. Don) M. Roem., Lobelia angulata G. Forst., Pandanus odorifer (Forssk.) Kuntze, Sarcococca pruniformis Lindl. (Table 4) which will surely have great potent on ethnopharmacological study.
Discussion
According to our findings, women practitioners (44%) were less than men (56%) which may be explained partly by the low sex ratio of the district; however, it can be assumed that women play lesser role in ethnomedicinal practices [215, 216]. Among self-employed, farmers account for 58.5%, business persons 34.2% and carpenters were 21.4%. Farmers represented the highest percentage as they often lack access to modern healthcare facilities due to various issues ranging from financial, transportation and higher education. These issues forced them to rely on traditional medicines, cultivating and utilising them more regularly than others and somehow playing a big role in conservation too. Through this study, we observed that young informants like students around 18 to 25 years old have little expertise in practicing ethnomedicine and utilised them rarely as compared to elder informants. This may be due to change in mentality brought by education to rely only on prescribed medicines. Further, the results of the usage of plants dominated by the families were followed and confirmed the work done by some researchers stating that greater the plants grew in the study area the more it will be favourably and commonly used [217]. This supports the non-random plant selection hypothesis by Moerman 1979 [218]. Large families such as Asteraceae and Euphorbiaceae were most utilised while Orchidaceae and Poaceae were underutilised (low used report). However, due to non-random selection, small families like Cucurbitaceae and Zingiberaceae became over-represented (high used report). Thus, this implies that medicinal plants are not selected randomly by the inhabitants of Champhai district but are utilised based on their cultural and traditional knowledge [219]. In the present study, we laid out the only accepted botanical names by ‘The Plant List’ and their family, local name, habit, mode of preparation and ailments as illustrated in Table 4.
Out of 93 species, 40 were cultivated species, whereas 53 were found in the wild. There were also 6 invasive alien species most notably Chromolaena odorata and Mikania micrantha which were commonly used to treat wounds topically. This is because wounds are the most common form of injury and these two species can be found almost everywhere [219]. The frequent use of herbaceous plants as medicines among the informants was due to their richness, abundance as well as their ability to grow easily in nature. Meanwhile, many parts of the world have been commonly using herbs as their medicinal ingredients due to their wide range of medicinal properties [220]. Leaves are the most utilised part of the plants due to their ease off collection as compared to their underground part. It is also the active site of photosynthesis accompanied by the production of metabolites [1, 221]. In addition, leaves can be easily prepared and stored. It can be dried quickly under the sun in lesser amount of time than other parts like stem, bark and rhizome.
Similarly, it is also reported that decoction was the most common preparation method for herbal medicine while in some other tribal community [3], preparation of paste was the most common method applied [1, 216, 222]. For decoction the plant part was washed thoroughly and boiled with water administering the juice orally, whereas for paste the materials were crushed or rubbed within palms and applied topically. To make fine powder plant parts were shade dried and ground. Intake of oral administration and external topical formulation were the main mode of administration used in traditional herbal medicines which has also been previously reported [215, 223]. Regarding the duration of consumption of herbal medicine, it depends on the illness whether it was short term or long term. For instance, short-term illness like cold, flu, stomach upset and skin problem, the consumption period did not last more than 1 week. On the contrary, the long-term illness like diabetes, kidney failure and heart diseases, the consumption period of plants (e.g., Flueggea virosa) was much longer and last more than a month and so on.
The inhabitants of the study area extensively exploited medicinal plants to treat various illnesses and other needs which have not been previously reported. For instance, Anoetochilus brevilabris was used for pile treatments, Betula alnoides as toothpaste, Capsicum annuum to soothe and prevent scars from skin burns. Colocasia esculenta to expel lochia, Euphorbia milii as antidiarrhoea, Lablab purpureus as a pain reliever, Mussaenda macrophylla to stop internal bleeding and Parkia timoriana for treating baby umbilical cord. From this study it was clear that among the informants, stomach problems like ulcer, indigestion, diabetes, hypertension and kidney problems were common illness resulting in high user rate of consuming herbal medicines and similar record was reported by Mahwasane et al., [224]. Further, skin problem like dermatitis which was the second highest usage report was the highest ailment in most other tribal communities like Malda district in West Bengal reported by Saha et al. [225].
Generally, majority of the informants did not consume the medicines prescribed by the Doctor’s prescribed medicines along with their herbal medicine and claimed that many plants like Sarcococca pruniformis (tonsil), Psidium guajava (diarrhoea), Mikania micrantha (cut/wound), Flueggea virosa (chicken pox), Elaeagnus caudata (veginal discharge) were really effective and most importantly, none of them reported any adverse effect such as vomiting, headache, nausea, allergic reactions and/or skin rashes. Moreover, regarding the expenditure on buying medicines, 38% of the informants usually purchased their herbal medicines either in raw form (Allium sativum, Allium cepa, Beta vulgaris) or in processed form like juice (Citrus limon, Phyllanthus emblica, Citrus aurantiifolia), fruits (Punica granatum, Phyllanthus emblica, Cucumis sativus), and powder (Curcuma longa). Concerned about the source of their knowledge, all the informants reported that they have heard and learned some of their information from their elders, family and/or acquaintances. Besides these, 30% of the informants have also gathered additional information through social media and 10% through books, magazines and newspapers. This documentation clearly showed that knowledge and cultural practices of herbal medicines had been shared through the indigenous community through word of mouth.
Frequency of citation showed the sociocultural importance of medicinal plants to identify their therapeutic value [16]. The FC value is directly proportional to the use value (UV), the more FC value will increase the used value significantly.
Curcuma longa L. is one of the main commercially grown as seasoning plants in India. In Southeast Asia including India and China, turmeric powder has been used extensively for spice and colouring food material. It had a wide range of medicinal value that curcumin was the main bioactive chemical constituents [226]. C. longa was a mandatory spice that each and every household kept it that’s why the reason used report (UR) for medicinal value and cultural value (CVs) were high among the informants. In case of CVs, the high value was due to a greater number of the used report with lesser-used categories. The informants in present study reported that Flueggea virosa have a prominent effectiveness against diabetes (59 UR) and chickenpox (50 UR). The Mizo tribes extensively used F. virosa and Embelia vestita Roxb. plant to treat chickenpox and measles by bathing once a day with the decoction of leaf mixed with water. Apart from the degree of the used report, this index also attributed to the effectiveness of their use and importance.
Higher in the UV value indicates the more rate of agreeing and sharing their knowledges and practices of the medicinal plants among the informants [216]. Among the Terai forest of western Nepal Curcuma longa L. was also reported as the highest used value [227] similar to this result.
The plants with low UV value were Colocasia esculenta (L.) Schott, Eulophia nuda Lindl. and Ocimum americanum L., Maesa indica (Roxb.) A. DC, Morus macroura Miq, Tectona grandis L.f., Hibiscus sinensis Mill, Elaeis guineensis Jacq, Smilax perfoliata Lour with less than 0.05 UV as shown in Table 4. Tectona grandis L.f. was also described with very low UV value by Ayyanar and Ignacimuthu as relevant to this result [1]. According to Chaudhary et al. 2006, the plants with low used value were in at risk of misrecollecting and passing on to the young generation which might be gradually disappearing [228]. On the other hand, the relevance of knowing the plant used value was for the convenience of pharmacological study and their used reliability [229].
However, Rajakumar and Shivanna had mentioned that the value of Fic depends on the accessibility of the taxa for the treatment of various diseases in the study area. Muscle/Bone problem with 81 UR have the highest Fic value of 0.962 followed by gastro-intestinal disease (GID) with 940 UR and skin care (SC) with 259 UR (Table 5). The lowest Fic value in the present study was the General Health (GH) category (Cold, fever, immunity boost) with 0.887 which was still more than the previous maximum Fic value report in Shimoga district, Karnataka, India i.e. 0.77 in Liver complaints [230]. Most RI value (Phyllanthus emblica) is considered to be versatile on its uses which would also increase the importance of the plant when it is used to treat more illnesses. The high RI values of some species may be attributed to their abundance and availability in the study area [19].
Overall, the quantitative analysis revealed that Curcuma longa was the most relevant species with the highest used value, frequency of citation and cultural value except in relative importance. This is due to the fact that the RI value is independent of the number of informants used report. On the conflict of these report, our study indicated that there was high consistency of the indigenous informant knowledge in the practices of ethnomedicines and utilised the same plants to treat it.
Conclusions
The present study concluded that the native people in the study area have their unique way of utilising medicinal plants to treat different kinds of ailments. We documented 93 valuable medicinal plants belonging to 55 families and 85 genera in which Euphorbiaceae and Asteraceae family were the most widely used in the area. This study supported the non-random selection of medicinal plants hypothesis. Among the plants part, leaves were the most commonly used. No new medicinal taxa were reported, but this study is a first quantitative report of ethnomedicine in this region and no informant had reported an adverse effect of herbal medicines. Their traditional pieces of knowledge had been passed on from their elders mostly through word of mouth. This study also revealed that younger generations between the ages of 18 and 30 have little to no knowledge of preparation of herbal medicines and their use as compared to the older age groups. This is mostly due to the availability of modern clinical drugs in the villages. Therefore, the traditional knowledge and practices of medicinal plants in the study area are somehow at risk of dying. This is why it is important to document the valuable knowledge as well as for conservation of the taxa.
The use of quantitative indices was essential in the field of ethnobotany to determine the most valuable plants along with their role played in a particular culture and to develop conservation initiatives. The plants which have high usage report and frequency of citation were known to possess numerous phytochemical compounds. The calculated informant consensus factor was extremely high, which means that the acquired data can be used as reference and reliable for ethnopharmacological study in the future. Even though the remedial value of many high cited plants has already been verified, there are still some plants that need to be validated. Hence, they are strongly recommended for further studies to develop alternative drugs.
Acknowledgements
The authors were thankful to the department of Horticulture, Aromatic and Medicinal Plant, Mizoram University, for providing the necessary facilities to complete our work. We also offer our heartfelt gratitude to all the local people of Champhai district, Mizoram, who shared their valuable knowledge and precious time for this research.
Abbreviations
- H
Herbs
- Sh
Shurbs
- Cr
Creeper
- T
Tree
- UR
Used reports
- FC
Frequency of citation
- UV
Use value
- Lf
Leaf
- Br
Bark
- Fr
Fruit
- Rh
Rhizome
- St
Stem
- S
Seed
- WP
Whole plants
- YS
Young shoot
Authors' contributions
TBCL and AK carry out ethnobotanical survey, write the manuscript and analyse the data; TBCL, NMT, RZ, LB and AK were study proposer, design the questionnaire and revise the manuscript; NMT and AP design the graphical abstract; RZ and AP were proof reader. All authors read and approved the final manuscript.
Funding
This research did not receive any specific grant from funding agencies in the public, commercial or not-for-profit sectors.
Availability of data and materials
All data generated or analysed during this study are included in this published article.
Declarations
Ethics approval and consent to participate
Not applicable.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Footnotes
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Ayyanara M, Ignacimuthub S. Ethnobotanical survey of medicinal plants commonly used by Kani tribals in Tirunelveli hills of Western Ghats, India. J Ethnopharmacol. 2011;134:851–864. doi: 10.1016/j.jep.2011.01.029. [DOI] [PubMed] [Google Scholar]
- 2.Ghimire BK, Tamang JP, Yu CY, Jung SJ, Chung IM. Antioxidant, antimicrobial activity and inhibition of α-glucosidase activity by Betula alnoides Buch. bark extract and their relationship with polyphenolic compounds concentration. Immunopharmacol Immunotoxicol. 2012;34:824–831. doi: 10.3109/08923973.2012.661739. [DOI] [PubMed] [Google Scholar]
- 3.Simbo DJ. An ethnobotanical survey of medicinal plants in Babungo, Northwest Region, Cameroon. J Ethnobiol Ethnomed. 2010;6:8. doi: 10.1186/1746-4269-6-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Fabricant DS, Farnsworth NR. The value of plants used in traditional medicine for drug discovery. Environ Health Perspect. 2001;109:69–75. doi: 10.1289/ehp.01109s169. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Kadhirvel K, Ramya S, Sudha TS, Ravi AV, Rajasekaran C, Selvi RV, Jayakumararaj R. Ethnomedicinal survey on plants used by tribals in Chitteri Hills. Environ We Int J Sci Tech. 2010;5:35–46. [Google Scholar]
- 6.Rai PK, Lalramnghinglova H. Ethnomedicinal plant resources of Mizoram, India: Implication of traditional knowledge in health care system. Ethnobot Leafl. 2010;3:6. [Google Scholar]
- 7.Tikkanen R, Osborn R, Mossialos E, Djordjevic A, Wharton GA. International Health Care System Profiles, India. The Commonwealth Fund. 2020 https://www.commonwealthfund.org/international-health-policy-enter/countries/india. Accessed 21 June 2021.
- 8.Lalramnghinglova H, Jha LK. Ethnomedicine from Mizoram—North East India. Ethnobotany. 1997;9:105–111. [Google Scholar]
- 9.Lalnundanga, Sahoo UK, Jha LK. Ethnobotanical flora in the humid sub-tropical semi-evergreen forest of Mizoram. In: Proceedings national conference on healthcare and developments of herbal medicines, Raipur. 1997.
- 10.Sharma HK, Chhangte L, Dolui AK. Traditional medicinal plants in Mizoram, India. Fitoterapia. 2001;72(2):146–161. doi: 10.1016/s0367-326x(00)00278-1. [DOI] [PubMed] [Google Scholar]
- 11.Lalramnghinglova H. Ethno-medicinal plants of mizoram. Bishen Singh Mahendra, Pal Singh, Dehradun, India; 2003.
- 12.Singh NP, Singh KP, Singh DK. Flora of Mizoram. Botanical Survey of India. Ministry of Environment and Forest. Government of India, Kolkata; 2002.
- 13.Sawmliana M. The Book of mizoram plants. Zakhuma P, Aizawl, Mizoram; 2003.
- 14.Champion GH, Seth SK. A revised survey of the forest types of India. Dehradun: Natraj Publishers; 1968. [Google Scholar]
- 15.Champhai district. Government of Mizoram, India. 2021. https://champhai.nic.in/about-district/. Accessed 03 Jan 2021.
- 16.Khajuria AK, Manhas RK, Kumar H, Bisht NS. Ethnobotanical study of traditionally used medicinal plants of Pauri District of Uttarakhand, India. J Ethnopharmacol. 2021;276:114204. doi: 10.1016/j.jep.2021.114204. [DOI] [PubMed] [Google Scholar]
- 17.Gazzaneo LRS, Lucena RFP, Albuquerque UP. Knowledge and use of medicinal plants by local specialists in a region of Atlantic Forest in the state of Pernambuco. J Ethnobiol Ethnomed. 2005;1:9. doi: 10.1186/1746-4269-1-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Heinrich M, Ankli A, Frei B, Weimann C, Sticher O. Medicinal plants in Mexico: healers’ consensus and cultural importance. Soc Sci Med. 1998;47:1859–1871. doi: 10.1016/s0277-9536(98)00181-6. [DOI] [PubMed] [Google Scholar]
- 19.Albuquerque UP, Lucena RF, Monteiro JM, Florentino AT, Cecília de Fátima CB. Evaluating two quantitative ethnobotanical techniques. Ethnobot. Res. Appl. 2006;4:051–60. https://ethnobotanyjournal.org/index.php/era/article/view/101.
- 20.Sujarwo W, Caneva G. Using quantitative indices to evaluate the cultural importance of food and nutraceutical plants: comparative data from the Island of Bali (Indonesia) J Cult Herit. 2016;18:342–348. [Google Scholar]
- 21.Kundan SB, Anupam S. Phytoconstituents and therapeutic potential of Allium cepa Linn—a review. Phcog Rev. 2009;3(5):170–180. [Google Scholar]
- 22.Sharquie KE, Al-Obaidi HK. Onion juice (Allium cepa L.), a new topical treatment for alopecia areata. J Dermatol. 2002;29:343–346. doi: 10.1111/j.1346-8138.2002.tb00277.x. [DOI] [PubMed] [Google Scholar]
- 23.Teshika JD, Zakariyyah AM, Zaynab T, Zengin G, Rengasamy KR, Pandian SK, Fawzi MM. Traditional and modern uses of onion bulb (Allium cepa L.): a systematic review. Crit Rev Food Sci Nutr. 2019;59(1):39–70. doi: 10.1080/10408398.2018.1499074. [DOI] [PubMed] [Google Scholar]
- 24.Batiha GES, Beshbishy AM, Elewa Y, Taha A. Chemical constituents and pharmacological activities of garlic (Allium sativum L.): a review. Nutrients. 2020;12:872. doi: 10.3390/nu12030872. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Miron T, Rabinkov A, Mirelman D, Wilchek M, Weiner L. The mode of action of allicin: its ready permeability through phospholipid membranes may contribute to its biological activity. Biochim Biophys Acta. 2000;1463:20–30. doi: 10.1016/s0005-2736(99)00174-1. [DOI] [PubMed] [Google Scholar]
- 26.Harris JC, Cottrell SL, Plummer S, Lloyd D. Antimicrobial properties of Allium sativum (garlic) Appl Microbial Biotechnol. 2001;57:282–286. doi: 10.1007/s002530100722. [DOI] [PubMed] [Google Scholar]
- 27.Ishtiaq M, Hanif W, Khan MA, Ashraf M, Butt AM. An ethnomedicinal survey and documentation of important medicinal folklore food phytonims of Flora of Samahni Valley, (Azad Kashmir) Pakistan. Pakistan J Biol Sci. 2007;10:2241–2256. doi: 10.3923/pjbs.2007.2241.2256. [DOI] [PubMed] [Google Scholar]
- 28.Singh VK, Singh DK. Pharmacological effects of garlic (Allium sativum L.) Annu Rev Biomed Sci. 2008;10:6–26. [Google Scholar]
- 29.Arunkumar S, Muthuselvam M. Analysis of phytochemical constituents and antimicrobial activities of Aloe vera L. against clinical pathogens. World J Agric Sci. 2009;5:572–576. [Google Scholar]
- 30.Christaki E, Florou-Paneri PC. Aloe vera: a plant for many uses. J Food Agric Environ. 2010;8:245–249. [Google Scholar]
- 31.Sahu PK, Giri DD, Singh R, Pandey P, Gupta S, Shrivastava AK, Kumar A, Pandey KD. Therapeutic and medicinal uses of Aloe vera: a review. J Pharm Pharmacol. 2013;4:599–610. [Google Scholar]
- 32.Kalaria P, Gheewala P, Chakraborty M, Kamath J. A phytopharmacological review of Alstonia scholaris: a panoramic herbal medicine. Int J Res Ayurveda Pharm. 2012;3:367–371. [Google Scholar]
- 33.Arulmozhi S, Mazumder PM, Ashok P, Narayanan LS. Pharmacological activities of Alstonia scholaris Linn. (Apocynaceae)—a review. Pharmacogn Rev. 2007;1:163–170. [Google Scholar]
- 34.Baliga MS. Review of the phytochemical, pharmacological and toxicological properties of Alstonia scholaris Linn. R. Br (Saptaparna) Chin J Integr Med. 2012 doi: 10.1007/s11655-011-0947-0. [DOI] [PubMed] [Google Scholar]
- 35.Huang XJ, Chen WH, Ji MH, Guo FY, Shu HM, Zheng CJ. Chemical constituents from leaves of Ananas comosus and their biological activities. Zhong Cao Yao. 2015;46:949–954. [Google Scholar]
- 36.Pavan R, Jain S, Kumar A. Properties and therapeutic application of bromelain: a review. Biotechnol Res Int. 2012;6:976203. doi: 10.1155/2012/976203. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Rathnavelu V, Alitheen NB, Sohila S, Kanagesan S, Ramesh R. Potential role of bromelain in clinical and therapeutic applications. Biomed Rep. 2016;3:283–288. doi: 10.3892/br.2016.720. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Lin TC, Tanaka T, Nonaka G, Nishioka I, Young TJ. Isolation and characterization of novel complex tannins (Flavano-ellagitannins). Anogeissinin and Anogeissusin-B, from Anogeissus acuminata (Roxb ex Dc) Guill et Perr var Lanccolata Wall ex Clarke. Chem Pharm Bull. 1991;39:1144–1147. [Google Scholar]
- 39.Monali PM, Padhy R. Antibacterial activity of green silver nanoparticles synthesized from Anogeissus acuminata against multidrug resistant urinary tract infecting bacteria in vitro and host-toxicity testing. J Appl Biomed. 2018;16:120–125. [Google Scholar]
- 40.Panda SK, Laxmipriya P, Pieter L, Maoxuan L, Johan N, Walter L. Antimicrobial anthelmintic, and antiviral activity of plants traditionally used for treating infectious disease in the Similipal Biosphere Reserve, Odisha, India. Front Pharmacol. 2017;8:658. doi: 10.3389/fphar.2017.00658. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Panda SS, Girgis AS, Prakash A, Khanna L, Khanna P, Shalaby EM, Fawzy NG, Jain SC. Protective effects of Aporosa octandra bark extract against d-galactose induced cognitive impairment and oxidative stress in mice. Heliyon. 2018 doi: 10.1016/j.heliyon.2018.e00951. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Sahu BP, Gouda P, Patnaik C. Aporosa octandra, a Less studied plant species with potential drug activities-I: identification of a new compound from aqueous ethanolic extract of its stem bark. Int J Adv Res Sci Eng Tech. 2016;3:2219–2224. [Google Scholar]
- 43.Vabeiryureilai M, Lalrinzuali K, Rosangkima G, Jagetia GC. Qualitative phytochemical analysis and antioxidant activity of Aporosa octandra (Buch-Ham. ex D. Don) extracts. Int J Pharmacol Res. 2014;6:68–73. [Google Scholar]
- 44.Siddiqui BS, Ali ST, Rasheed M, Kardar MN. Chemical constituents of the flowers of Azadirachta indica. Helv Chim Acta. 2003;86:2787–2796. [Google Scholar]
- 45.Biswas K, Chattopadhyay I, Banerjee RK, Bandyopadhyay U. Biological activities and medicinal properties of neem (Azadirachta indica) Curr Sci. 2002;82:1336–1345. [Google Scholar]
- 46.Doshi GM, Nalawade VV, Mukadam AS, Chaskar PK, Zine SP, Somani RR, Une HD. Structural elucidation of chemical constituents from Benincasa hispida seeds and Carissa congesta roots by gas chromatography: mass spectroscopy. Pharmacogn Res. 2015;7(3):282–293. doi: 10.4103/0974-8490.157179. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Al-Snafi AE. The pharmacological importance of Benincasa hispida. A review. Int J Pharm Sci Res. 2013;4:165–170. [Google Scholar]
- 48.Qadrie ZL, Hawisa NT, Khan MA, Samuel M, Anandan R. Antinociceptive and anti-pyretic activity of Benincasa hispida (Thunb.) cogn. in wistar albino rats. Pak J Pharm Sci. 2009;22:287–290. [PubMed] [Google Scholar]
- 49.El-Hawary SS, Hammouda FM, Tawfik WA, Kassem HA, Abdelshafeek KA, El-Shamy SS. Investigation of some chemical constituents, cytotoxicity and antioxidant activities of Beta vulgaris var. altissima cultivated in Egypt. Rasayan J Chem. 2017;10:1391–1401. [Google Scholar]
- 50.El-Beltagi HS, Mohamed HI, Megahed BHM, Gamal M, Safwat G. Evaluation of some chemical constituents, antioxidant, antibacterial and anticancer activities of Beta vulgaris L. root. Fresenius Environ Bull. 2018;27:6369–6378. [Google Scholar]
- 51.Ninfali P, Angelino D. Nutritional and functional potential of Beta vulgaris cicla and rubra. Fitoterapia. 2013;89:188–199. doi: 10.1016/j.fitote.2013.06.004. [DOI] [PubMed] [Google Scholar]
- 52.Dũng NX, Mõi LD, Leclercq PA. Constituents of the bark oil of Betula alnoides Ham ex. D. Don from Vietnam. J Essent Oil Res. 1995;7:565–566. [Google Scholar]
- 53.Thu NB, Trung TN, Ha DT, Khoi NM, Hung TV, Hien TT, Yim NH, Bae KH. Screening of Vietnamese medicinal plants for cytotoxic activity. Nat Prod Sci. 2010;16:43–49. [Google Scholar]
- 54.Yang DS, Yang YP, Yong-hong Y, Xiao-li L. Chemical constituents of Bischofia javanica. Nat Prod Res Dev. 2013;25:1056–1059. [Google Scholar]
- 55.Khan MR, Kihara M, Domoloso A. Anti-microbial activity of Bidens pilosa, Bischofia javanica, Elmerillia papuana and Sigesbekia orientalis. Fitoterapia. 2001;72:662–665. doi: 10.1016/s0367-326x(01)00261-1. [DOI] [PubMed] [Google Scholar]
- 56.Lingadurai S, Roy S, Joseph RV, Nath LK. Antileukemic activity of the leaf extract of Bischofia javanica blume on human leukemic cell lines. Indian J Pharmacol. 2011;43:143–149. doi: 10.4103/0253-7613.77348. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57.Anadebe VC, Okafor NA, Ezeugo JO, Amanjide IJ, Ogide BC. GC-MS analysis of phytochemical compounds in Cajanus cajan leaf. J Chem Pharm Res. 2017;9:360–363. [Google Scholar]
- 58.Pal D, Mishra P, Sachan N, Ghosh AK. Biological activities and medicinal properties of Cajanus cajan (L) Millsp. J Adv Pharm Technol Res. 2011;2:207–214. doi: 10.4103/2231-4040.90874. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 59.Tu Y, Sun L, Guo M, Chen W. The medicinal uses of Callicarpa L. in traditional Chinese medicine: an ethnopharmacological, phytochemical and pharmacological review. J Ethnopharmacol. 2013;146:465–481. doi: 10.1016/j.jep.2012.12.051. [DOI] [PubMed] [Google Scholar]
- 60.Zhu HB, Li BM, Liu C, Chen RY. Chemical constituents of Camellia sinensis var. assamica. Zhongguo Zhong yao za. 2013;38:1386–1389. [PubMed] [Google Scholar]
- 61.Sarangi AB. Medicinal and therapeutic potentialities of tea (Camellia sinensis L.)—a review. Food Res Int. 2009;42:529–535. [Google Scholar]
- 62.Hamilton-Miller JM. Antimicrobial properties of tea (Camellia sinensis L.) antimicrobe. Agents Chemother. 1995;39:2375–2377. doi: 10.1128/aac.39.11.2375. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63.Grutenherman F, Russo E. Cannabis and cannabinoids, pharmacology, toxicology and therapeutic potential. New York: The Howarth Integrative Healing Press; 2002. [Google Scholar]
- 64.Nuutinen T. Medicinal properties of terpenes found in Cannabis sativa and Humulus lupulus. Eur J Med Chem. 2018;157:198–228. doi: 10.1016/j.ejmech.2018.07.076. [DOI] [PubMed] [Google Scholar]
- 65.Siddiqui BS, Aslam H, Ali ST, Khan S, Begum S. Chemical constituents of Centella asiatica. J Asian Nat Prod Res. 2007;9:407–414. doi: 10.1080/10286020600782454. [DOI] [PubMed] [Google Scholar]
- 66.Kalshetty P, Aswar U, Bodhankar S, Sinnathambi A, Mohan V, Thakurdesai P. Antidepressant effects of standardized extract of Centella asiatica L. in olfactory bulbectomy model. Biomed Aging Pathol. 2012;2:48–53. [Google Scholar]
- 67.Punturee K, Wild CP, Kasinrerk W, Vinitketkumnuen U. Immunomodulatory activities of Centella asiatica and Rhinacanthus nasutus extracts. Asian Pac J Cancer Prev. 2005;6:396–400. [PubMed] [Google Scholar]
- 68.Marin A, Ferreres F, Tomás-Barberán FA, Gil MI. Characterization and quantitation of antioxidant constituents of sweet pepper (Capsicum annuum L.) J Agric Food Chem. 2004;52:3861–3869. doi: 10.1021/jf0497915. [DOI] [PubMed] [Google Scholar]
- 69.Khan FA, Mahmood T, Ali M, Saeed A, Maalik A. Pharmacological importance of an ethnobotanical plant: Capsicum annuum L. Nat Prod Res. 2014;28:1267–1274. doi: 10.1080/14786419.2014.895723. [DOI] [PubMed] [Google Scholar]
- 70.Yogiraj V, Goyal PK, Chauhan CS, Goyal A, Vyas B. Carica papaya Linn: an overview. Int J Herbal Med. 2014;2:1–8. [Google Scholar]
- 71.Adam Y, Nasaruddin AA, Zuraini A, Arifah AK, Zakaria MOFZ, Somchit MN. Diuretic activity of roots from Carica papaya L. and Ananas comosus L. Int J Pharm Sci Rev Res. 2013;23:163–167. [Google Scholar]
- 72.Krishna KL, Paridhavi M, Patel KL. Review on nutritional, medicinal and pharmacological properties of Papaya (Carica papaya Linn.). Nat Prod Radiance. 2008;7:364–73. http://nopr.niscair.res.in/handle/123456789/5695
- 73.Prakash D, Upadhyay G, Gupta C, Pushpangadan P, Singh KK. Antioxidant and free radical scavenging activities of some promising wild edible fruits. Int Food Res J. 2012;19:1109–1116. [Google Scholar]
- 74.Ferreres F, Pereira DM, Valentão P, Andrade PB, Seabra RM, Sottomayor M. New Phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. 2008;56:9967–9974. doi: 10.1021/jf8022723. [DOI] [PubMed] [Google Scholar]
- 75.Aslam J, Khan SH, Siddiqui ZH, Fatima Z, Maqsood M, Bhat MA, Nasim SA, Ilah A, Ahmad IZ, Khan SA, Mujib A. Catharanthus roseus (L.) G. Don. An important drug: it’s applications and production. Pharmacie Globale. 2010;4:1–16. [Google Scholar]
- 76.Gajalakshmi S, Vijayalakshmi SD, Rajeswari V. Pharmacological activities of Catharanthus roseus: a perspective review. Int J Pharm Bio Sci. 2013;4:431–439. [Google Scholar]
- 77.Hassan HM, Eldesoky AM, Al-Rashdi A, Ahmed HM. Green corrosion electrochemistry: Cheilocostus speciosus extract (CSE) investigated electro-analytically as a potential green corrosion inhibitor for copper within acidic solution. Int J Emerg Trends Eng Develop. 2016;7:72–98. [Google Scholar]
- 78.Ayam VS, Gogoi P. Evaluation of antioxidant activity of the selected frequently used traditional wild medicinal plants from Lakhimpur, Assam (India) Pleione. 2018;12:187–192. [Google Scholar]
- 79.Benelli G, Govindarajan M, Rajeswary M, Vaseeharan B, Alyahya SA, Alharbi NS, Kadaikunnan S, Khaled JM, Maggi F. Insecticidal activity of camphene, zerumbone and α-humulene from Cheilocostus speciosus rhizome essential oil against the Old-World bollworm Helicoverpa armigera. Ecotoxicol Environ Saf. 2018;148:781–786. doi: 10.1016/j.ecoenv.2017.11.044. [DOI] [PubMed] [Google Scholar]
- 80.Owolabi MS, Ogundajo A, Yusuf KO, Lajide L, Villanueva HE, Tuten JA, Setzer WN. Chemical composition and bioactivity of the essential oil of Chromolaena odorata from Nigeria. Rec Nat Prod. 2010;4:72–78. [Google Scholar]
- 81.Taiwo OB, Olajide OA, Soyannwo OO, Makinde JM. Anti-inflammatory, antipyretic and antispasmodic properties of Chromolaena Odorata. Pharm Biol. 2000;38:367–370. [Google Scholar]
- 82.Vaisakh MN, Pandey A. The invasive weed with healing properties: a review on Chromolaena odorata. Int J Pharm Sci Res. 2012;3:80–83. [Google Scholar]
- 83.Abyaneh M, Shams-Ghahfarokhi M, Rezaee MB, Jaimand K, Alinezhad S, Saberi R, Yoshinari T. Chemical composition and antiaflatoxigenic activity of Carum carvi L., Thymus vulgaris and Citrus aurantifolia essential oils. Food Control. 2009;20:1018–1024. [Google Scholar]
- 84.Pathan RK, Gali PR, Pathan P, Gowtham T, Pasupuleti S. In vitro antimicrobial activity of Citrus aurantifolia and its phytochemical screening. Asian Pac J Trop Dis. 2012;2:328–331. [Google Scholar]
- 85.Taur DJ, Kulkarni VB, Patil RY, Patil RN. Anthelmintic activity of Ocimum sanctum and Citrus aurantifolia oils. Pharmacologyonline. 2009;3:495–499. [Google Scholar]
- 86.Xu YR, Zhang KF, Xie QJ, Lin JX, Huan KX, Liao Y. Chemical constituents from young fruits of Citrus maxima cv. Shatian. Zhong Yao Cai. 2015;38:1879–1881. [PubMed] [Google Scholar]
- 87.Abirami A, Nagarani G, Siddhuraju P. Antimicrobial activity of crude extract of Citrus hystrix and Citrus maxima. Int J Pharm Sci. 2013;4:1–5. [Google Scholar]
- 88.Shivananda A, Rao DM, Jayaveera KN. Analgesic and anti-inflammatory activities of Citrus maxima (J. Burm) Merr in animal models. Res J Pharm Biol Chem Sci. 2013;4:1800–10. http://rjpbcs.com/pdf/2013_4(2)/
- 89.Kefford JF. The chemical constituents of citrus fruits. Adv Food Res. 1960;2016(9):285–372. [Google Scholar]
- 90.Szczykutowicz MK, Szopa A, Ekiert H. Citrus limon (Lemon) phenomenon—a review of the chemistry, pharmacological properties, applications in the modern pharmaceutical, food, and cosmetics industries, and biotechnological studies. Plants. 2020;9:119. doi: 10.3390/plants9010119. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 91.Jadeja RN, Thounaojam MC, Singh TB, Devkar RV, Ramachandran AV. Traditional uses, phytochemistry and pharmacology of Clerodendron glandulosum Coleb—a review. Asian Pac J Trop Med. 2012;5:1–6. doi: 10.1016/S1995-7645(11)60236-8. [DOI] [PubMed] [Google Scholar]
- 92.Prajapati R, Kalariya M, Umbarkar R, Parmar S, Sheth N. Colocasia esculenta: a potent indigenous plant. Int J Nutr Pharmacol Neurol Dis. 2011;1:90–6. http://www.ijnpnd.com/text.asp?2011/1/2/90/84188
- 93.Agyare C, Boakye YD, Apenteng JA, Dapaah SO, Appiah T, Adow A. Antimicrobial and anti-inflammatory properties of Anchomanes difformis (Bl.) Engl. and Colocasia esculenta (L.) Schott. Biochem Pharmacol. 2016;5:1. 10.4172/2167-0501.1000201.
- 94.Kubde MS, Khadabadi SS, Farooqui IA, Deore SL. In-vitro anthelmintic activity of Colocasia esculenta. Der Pharma Lett. 2010;2:82–85. [Google Scholar]
- 95.Patil BR, Ageely HM. Antihepatotoxic activity of Colocasia esculenta leaf juice. Int J Adv Biotech Res. 2011;2:296–304. [Google Scholar]
- 96.Koné WM, Vargas M, Keiser J. Anthelmintic activity of medicinal plants used in Côte d’Ivoire for treating parasitic diseases. Parasitol Res. 2012;110:2351–2362. doi: 10.1007/s00436-011-2771-z. [DOI] [PubMed] [Google Scholar]
- 97.Joshi RK. Study on essential oil composition of the roots of Crassocephalum crepidioides (Benth.) S. Moore. J Chil Chem Soc. 2014;59:2363–2365. [Google Scholar]
- 98.Tomimori K, Nakama S, Kimura R, Tamaki K, Ishikawa C, Mori N. Antitumor activity and macrophage nitric oxide producing action of medicinal herb Crassocephalum crepidioides. BMC Complement Altern Med. 2012;12:1–11. doi: 10.1186/1472-6882-12-78. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 99.Bahar E, Akter KM, Lee GH, Lee HY, Rashid HO, Choi MK, Bhattarai KR, Hossain MMM, Ara J, Mazumder K, Raihan O. β-Cell protection and antidiabetic activities of Crassocephalum crepidioides (Asteraceae) Benth. S. Moore extract against alloxan-induced oxidative stress via regulation of apoptosis and reactive oxygen species (ROS) BMC Complement Altern Med. 2017;17:179. doi: 10.1186/s12906-017-1697-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 100.Rezig L, Chouaibi M, Msaada K, Hamdi H. Chemical composition and profile characterisation of pumpkin (Cucurbita maxima) seed oil. Ind Crops Prod. 2012;37:82–87. [Google Scholar]
- 101.Md PM, Md TK. Overview on Cucurbita maxima seed. J Dent Med Sci. 2017;16:29–33. [Google Scholar]
- 102.Borah A. Chemical composition, antioxidant, anti-inflammatory, anti-microbial and in-vitro cytotoxic efficacy of essential oil of Curcuma caesia Roxb. leaves: an endangered medicinal plant of North East India. Ind Crops Prod. 2019;129:448–454. [Google Scholar]
- 103.Baghel SS, Baghel RS, Sharma K, Sikarwar I. Pharmacological activities of Curcuma caesia. Int J Green Pharm. 2013;7:1–5. [Google Scholar]
- 104.Lateef EA. Bioactive chemical constituents of Curcuma longa L. rhizomes extract inhibit the growth of human hepatoma cell line (HepG2) Acta Pharm. 2016;66:387–398. doi: 10.1515/acph-2016-0028. [DOI] [PubMed] [Google Scholar]
- 105.Krup V, Prakash LH, Harini A. Pharmacological activities of turmeric (Curcuma longa Linn): a review. J Homeop Ayurv Med. 2013;2:133. [Google Scholar]
- 106.Wu XY, Chao ZM, Wang C, Tan ZG, Sun W. Chemical constituents contained in fatty oil from seeds of Cucumis sativus. Zhongguo Zhong Yao Za Zhi. 2012;37:3252–3255. [PubMed] [Google Scholar]
- 107.Saeedi R, Sultana A, Rahman K. Ethnomedicinal uses and pharmacological activities of different parts of Cucumis sativus Linn: an update. Int J Pharm Sci Res. 2020;11:1549–1556. [Google Scholar]
- 108.Zhu SH, Zhang QJ, Chen Q, Zhou T, Yao RJ. Study on the chemical constituents of Dichrocephala integrifolia. Zhong Yao Cai. 2010;33:53–55. [PubMed] [Google Scholar]
- 109.Emégam NK, Nguepi MSD, Lambou AF, Okomolo FCM, Sotoing GT, Bougolla DP, Pale S, Kameni JSN, Bum EN. Antioxidant properties of Dichrocephala integrifolia (Asteraceae) in a mouse model of monosodium glutamate-induced neurotoxicity. Afr J Tradit Complement Altern Med. 2017;14:147–155. [Google Scholar]
- 110.Kouémou NE, Taiwe GS, Moto FC, Pale S, Ngoupaye GT, Njapdounke JS, Nkantchoua GC, Pahaye DB, Bum EN. Nootropic and neuroprotective effects of Dichrocephala integrifolia on scopolamine mouse model of Alheimer’s disease. Front Pharmacol. 2017 doi: 10.3389/fphar.2017.00847. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 111.Lee CL, Yen MH, Hwang TL, Yang JC, Peng CY, Chen CJ, Chang WY, Wu YC. Anti-inflammatory and cytotoxic component from Dichrocephala integrifolia. Phytochem Lett. 2015;12:237–242. [Google Scholar]
- 112.Gandhi D, Mehta P. Dillenia indica Linn. and Dillenia pentagyna Roxb.: pharmacognostic, phytochemical and therapeutic aspects. J App Pharm Sci. 2013;3:134–142. [Google Scholar]
- 113.Cheng WY, Kuo YH, Huang CJ. Isolation and identification of novel estrogenic compounds in Yam Tuber (Dioscorea alata Cv. Tainung No. 2) J Agric Food Chem. 2007;55:7350–7358. doi: 10.1021/jf0711690. [DOI] [PubMed] [Google Scholar]
- 114.Das A, Chaudhuri D, Chatterjee A. Study of antioxidant and reactive oxygen species scavenging activity of the edible tuber of "Greater Yam" (Dioscorea alata L.) from North-east India. Asian J Pharm Clin Res. 2012;5:74–84. [Google Scholar]
- 115.Maithili V, Dhanabal SP, Mahendran S, Vadivelan R. Antidiabetic activity of ethanolic extract of tubers of Dioscorea alata in alloxan induced diabetic rats. Indian J Pharmacol. 2011;43:455–459. doi: 10.4103/0253-7613.83121. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 116.Nono NR, Nzowa KL, Barboni L, Tapondjou AL. Drymaria cordata (Linn.) willd (caryophyllaceae): ethnobotany, pharmacology and phytochemistry. Adv Biol Chem. 2014;4:160–167. [Google Scholar]
- 117.Liu HB, Zhang CR, Dong SH, Yang SP, Sun Q, Geng MY, Yue JM. Sesquiterpenes from Dysoxylum oliganthum and Dysoxylum excelsum. J Asian Nat Prod Res. 2012;14:224–234. doi: 10.1080/10286020.2011.645810. [DOI] [PubMed] [Google Scholar]
- 118.Jayashree R, Albert S, Minaram N. Medicinal plants of North Cachar Hills district of Assam used by the Dimasa tribe. Indian J Tradit Knowl. 2012;11:520–7. http://nopr.niscair.res.in/handle/123456789/14395.
- 119.Sharma BK, Ramashanker SG, Rahaman L, Nath N, Kaipeng DL. Plant based folk treatments from North East India for jaundice (an overview) J Med Plants Stud. 2016;4:234–247. [Google Scholar]
- 120.Lasekan O, Buettner A, Christlbauer M. Investigation of important odorants of palm wine (Elaeis guineensis) Food Chem. 2007;105:15–23. [Google Scholar]
- 121.Owoyele BV, Owolabi GO. Traditional oil palm (Elaeis guineensis Jacq.) and its medicinal uses: a review. Tang Human Med. 2014 [Google Scholar]
- 122.Yin NGS, Abdullah S, Phin CK. Phytochemical constituents from leaves of Elaeis guineensis and their antioxidant and antimicrobial activities. Int J Pharm Pharm Sci. 2013;5:137–140. [Google Scholar]
- 123.Shivprasad M, Varsha J. GC-MS screening of some bioactive compounds from methanolic extract of medicinally relevant wild edible plant parts. Int J Sci Res Sci Tech. 2018;4:49–56. [Google Scholar]
- 124.Sethiya NK, Brahmbhat K, Chauhan B, Mishra SH. Pharmacognostic and phytochemical investigation of Ensete superbum (Roxb.) Cheesman pseudostem. Indian J Nat Prod Resour. 2016;7:51–8. http://nopr.niscair.res.in/handle/123456789/34105.
- 125.Akter K, Barnes EC, Loa-Kum-Cheung WL, Yin P, Kichu M, Brophy JJ, Barrow RA, Imchen I, Vemulpad SR, Jamie JF. Antimicrobial and antioxidant activity and chemical characterisation of Erythrina stricta Roxb. (Fabaceae) J Ethnopharmacol. 2016;185:171–181. doi: 10.1016/j.jep.2016.03.011. [DOI] [PubMed] [Google Scholar]
- 126.Araújo-Júnior JX, de Oliveira MS, Aquino PG, Alexandre-Moreira MS, Sant’Ana AE. A phytochemical and ethnopharmacological review of the genus Erythrina in Phytochemicals. In: Rao V, editors. A global perspective of their role in nutrition and health. London: InTech; 2012. p. 327–49.
- 127.Subhashini N, Purnima S, Devi JA, Thirupathi AT, Lavanya N. Anti-inflammatory activity of Erythrina stricta Roxb. in albino rats. Int J Pharm Tech Res. 2011;3:1014–1018. [Google Scholar]
- 128.Hada S, Yadav DK, Roat P, Kumari N. Eulophia Nuda: a review of its traditional uses, phytochemistry and pharmacology. Pharm Chem J. 2020;54:40–45. [Google Scholar]
- 129.Jain JB, Kumane SC, Bhattacharya S. Medicinal flora of Madhya Pradesh and Chattisgarh—a review. Indian J Tradit Knowl. 2006;5:237–42. http://nopr.niscair.res.in/handle/123456789/6845.
- 130.Pascal OA, Bertrand AEV, Esaïe T, Sylvie HAM, Eloi AY. A review of the ethnomedical uses, phytochemistry and pharmacology of the Euphorbia genus. J Pharm Innov. 2017;6:34–39. [Google Scholar]
- 131.Rauf A, Muhammad N, Qaisar M, Uddin G, Hussain I. Preliminary antinociceptive studies of methanol extract of Euphorbia milli. Middle-East J Med Plants Res. 2012;1:68–70. [Google Scholar]
- 132.Saleem H, Zengin G, Locatelli M, Mollica A, Ahmad I, Mahomoodally FM, Abidin SAZ, Ahemad N. In vitro biological propensities and chemical profiling of Euphorbia milii Des Moul (Euphorbiaceae): a novel source for bioactive agents. Ind Crops Prod. 2019;130:9–15. [Google Scholar]
- 133.Wang P, Xie C, An L, Yang X, Xi Y, Yuan S, Zhang C, Tuerhong M, Jin DQ, Lee D, Zhang J. Bioactive diterpenoids from the stems of Euphorbia royleana. J Nat Prod. 2019;82:183–193. doi: 10.1021/acs.jnatprod.8b00493. [DOI] [PubMed] [Google Scholar]
- 134.Ashraf A, Sarfraz RA, Rashid MA, Shahi M. Antioxidant, antimicrobial, antitumor, and cytotoxic activities of an important medicinal plant (Euphorbia royleana) from Pakistan. J Food Drug Anal. 2015;23:109–115. doi: 10.1016/j.jfda.2014.05.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 135.Bani S, Kaul A, Jaggi BS, Suri KA, Suri OP, Sharma OP. Anti-inflammatory activity of the hydrosoluble fraction of Euphorbia royleana latex. Fitoterapia. 2000;71:655–662. doi: 10.1016/s0367-326x(00)00225-2. [DOI] [PubMed] [Google Scholar]
- 136.Wang GC, Liang JP, Wang Y, Li Q, Ye WC. Chemical constituents from Flueggea virosa. Chin J Nat Med. 2008;6:251–253. [Google Scholar]
- 137.Chao CH, Cheng JC, Shen DY, Huang HC, Wu YC, Wu TS. Terpenoids from Flueggea virosa and their anti-hepatitis C virus activity. Phytochemistry. 2016;128:60–70. doi: 10.1016/j.phytochem.2016.04.003. [DOI] [PubMed] [Google Scholar]
- 138.Ezeonwumelu JOC, Omar AN, Ajayi AM, Okoruwa AG, Tanayen JK, Kiplagat DM, Okpanachi OA, Abba S, Ezekiel I, Onchweri AN, Okonkwo CO. Phytochemical screening, acute toxicity, anti-inflammatory and anti-pyretic studies of aqueous extract of the root of Flueggea virosa (Roxb. ex Willd.) in rats. Int J Pharm Biomed Sci. 2012;3:128–135. [Google Scholar]
- 139.Wang GC, Li T, Deng FY, Li YL, Ye WC. Five new phenolic glycosides from Hedyotis scandens. Bioorganic Med Chem Lett. 2013;5:1379–1382. doi: 10.1016/j.bmcl.2012.12.077. [DOI] [PubMed] [Google Scholar]
- 140.Rahman MA, Uddin SB, Wilcock CC. Medicinal plants used by Chakma tribe in Hill Tracts districts of Bangladesh. Indian J Tradit Knowl. 2007;6:508–17. http://nopr.niscair.res.in/handle/123456789/991
- 141.Subba B, Basne P. Antimicrobial activity of some medicinal plants from east and central part of Nepal. Int J Appl Sci Biotechnol. 2014;2:88–92. [Google Scholar]
- 142.Jadhav VM, Thorat RM, Kadam VJ, Sathe NS. Hibiscus rosa sinensis Linn – ‘‘Rudrapuspa’’: a review. J Pharm Res. 2009;2:1168–1173. [Google Scholar]
- 143.Mak YM, Chuah LO, Ahmad R, Bhat R. Antioxidant and antibacterial activities of hibiscus (Hibiscus rosa-sinensis L.) and Cassia (Senna bicapsularis L.) flower extracts. J King Saud Univ Sci. 2013;25(4):275–282. [Google Scholar]
- 144.Fu J, Dai L, Lin Z, Lu H. Houttuynia cordata Thunb: a review of phytochemistry and pharmacology and quality control. Chinese Med. 2013;4:101–123. [Google Scholar]
- 145.Mohanraj R, Sivasankar S. Sweet potato (Ipomoea batatas [L.] Lam)—a valuable medicinal food: a review. J Med Food. 2014;17:733–741. doi: 10.1089/jmf.2013.2818. [DOI] [PubMed] [Google Scholar]
- 146.Hossain S, Ahmed R, Bhowmick S, Al Mamun A, Hashimoto M. Proximate composition and fatty acid analysis of Lablab purpureus (L.) legume seed: implicates to both protein and essential fatty acid supplementation. Springer Plus. 2016;5:1899. doi: 10.1186/s40064-016-3587-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 147.Al-Snafi AE. The pharmacology and medical importance of Dolichos lablab (Lablab purpureus)—a review. IOSR J Pharm. 2017;7:22–30. [Google Scholar]
- 148.Wei JC, Wang PC, Zhou XI. The caffeoyl phenylethanoid glycosides from Lindernia ruellioides and their anti-HBV effects. J Asian Nat Prod Res. 2018;20:757–762. doi: 10.1080/10286020.2017.1357549. [DOI] [PubMed] [Google Scholar]
- 149.Das AK, Nongmaithem R. Phytochemical study of selected medicinal plants used by the maring tribe of Chandel district, Manipur. India J Pharmacogn Phytochem. 2019;8:2155–2160. [Google Scholar]
- 150.Kuruvilla GR, Neeraja M, Srikrishna A, Rao SGRS. A new quinone from Maesa indica (Roxb) A DC, (Myrsinaceae) Indian J Chem Sect B. 2010;49:1637–1641. [Google Scholar]
- 151.Patil A, Jadhav V, Arvindekar A, More T. Antidiabetic activity of Maesa indica (Roxb). stem bark in Streptozotoc in induced diabetic rats. American J Phytomed Clin Ther. 2014;2:957–962. [Google Scholar]
- 152.Wei L, Wee W, Siong J, Syamsumir D. Characterization of antimicrobial, antioxidant, anticancer property and chemical composition of Michelia champaca seed and flower extracts. Stamford J Pharm Sci. 2011;4:19–24. [Google Scholar]
- 153.Vimala R, Nagarajan S, Alam M, Susan T, Joy S. Anti-inflammatory and antipyretic activity of Michelia champaca Linn., (White variety), Ixora Brachiata Roxb. and Rhynchosia Cana (Willd.) D.C. flower extract. Indian J Exp Biol. 1997;35:1310–1314. [PubMed] [Google Scholar]
- 154.Dan GD, Yi Z, Wei LE, Tao W, Min HL. Chemical constituents of Mangifera indica leaves (I). Zhong Cao Yao. 2011;42:428–31. http://www.ceps.com.tw/ec/ecJnlIntro.aspx?Jnliid=2790.
- 155.Parvez GMM. Pharmacological activities of mango (Mangifera indica): a review. J Pharmacogn Phytochem. 2016;5:1–7. [Google Scholar]
- 156.Pandey AK, Rai MK, Acharya D. Chemical composition and antimycotic activity of the essential oils of corn mint (Mentha arvensis) and lemon grass (Cymbopogon flexuosus) against human pathogenic fungi. Pharm Biol. 2003;41:421–425. [Google Scholar]
- 157.Thawkar BS, Jawarkar AG, Kalamkar PV, Pawar KP, Kale MK. Phytochemical and pharmacological review of Mentha arvensis. Int J Green Pharm. 2016;10:2. [Google Scholar]
- 158.Chow YL, Quon HH. Chemical constituents of the heartwood of Mesua ferrea. Phytochemistry. 1968;7:1871–1874. [Google Scholar]
- 159.Chahar MK, Sanjaya KDS, Geetha L, Lokesh T, Manohara KP. Mesua ferrea L.: a review of the medical evidence for its phytochemistry and pharmacological actions. Afr J Pharm Pharmacol. 2013;7:211–219. [Google Scholar]
- 160.Shao H, Nan P, Peng S, Zhang C. Study of chemical constituents of essential oil from flowers of Mikania micrantha. Zhong Yao Cai. 2001;24:341–342. [PubMed] [Google Scholar]
- 161.Dev UK, Md Hossain T, Md IZ. Phytochemical investigation, antioxidant activity and antihelmintic activity of Mikania micrantha leaves. World J Pharma Res. 2015;4:121–133. [Google Scholar]
- 162.Lentz DL, Clark AM, Hufford CD, Meurer-Grimes B, Passreiter CM, Cordero J, Ibrahimi O, Okunade AL. Antimicrobial properties of Honduran medicinal plants. J Ethnopharmacol. 1998;63:253–263. doi: 10.1016/s0378-8741(98)00100-7. [DOI] [PubMed] [Google Scholar]
- 163.Yuan K, Lü JL, Yin MW. Chemical constituents of C-glycosylflavones from Mimosa pudica. Yao Xue Xue Bao. 2006;41:435–438. [PubMed] [Google Scholar]
- 164.Joseph B, George J, Mohan J. Pharmacology and traditional uses of Mimosa pudica. Int J Pharma Sci Drug Res. 2013;5:41–44. [Google Scholar]
- 165.Farrag EK, Kassem MES, Bayoumi D, Shaker SE, Afifi MS. Phytochemical study, phenolic profile and antigastric ulcer activity of Morus macroura Miq. fruits extract. J Appl Pharm Sci. 2017;7:152–160. [Google Scholar]
- 166.Sidhu JS, Zafar TA. Bioactive compounds in banana fruits and their health benefits. Food Qual Saf. 2018;2:183–188. [Google Scholar]
- 167.Jyothirmayi N, Rao NM. Banana medicinal uses. J Med Sci Tech. 2015;4:152–160. [Google Scholar]
- 168.Mathew NS, Negi PS. Traditional uses, phytochemistry and pharmacology of wild banana (Musa acuminata Colla): a review. J Ethnopharmacol. 2017;196:124–140. doi: 10.1016/j.jep.2016.12.009. [DOI] [PubMed] [Google Scholar]
- 169.Kim NC, Desjardins AE, Wu CD, Kinghorn AD. Activity of triterpenoid glycosides from the root bark of Mussaenda macrophylla against two oral pathogens. J Nat Prod. 1999;62:1379–1384. doi: 10.1021/np9901579. [DOI] [PubMed] [Google Scholar]
- 170.Chowdhury SR, Akter S, Sharmin T, Islam F, Quadery TM. Antimicrobial activity of five medicinal plants of Bangladesh. J Pharmacogn Phytochem. 2013;2:164–170. [Google Scholar]
- 171.Shadia E, El-Aziz A, Omer EA, Sabra AS. Chemical composition of Ocimum americanum essential oil and its biological effects against, agrotis ipsilon, (Lepidoptera: Noctuidae) Res J Agric Biol Sci. 2007;3:740–747. [Google Scholar]
- 172.Hakkim FL, Arivazhagan G, Boopathy R. Antioxidant property of selected Ocimum species and their secondary metabolite content. J Med Plant Res. 2008;2:250–257. [Google Scholar]
- 173.Thaweboon S, Thaweboon B. In vitro antimicrobial activity of Ocimum americanum L. essential oil against oral microorganisms. Southeast Asian J Trop Med Public Health. 2009;40:1025–1033. [PubMed] [Google Scholar]
- 174.Ahad A, Ganai AA, Sareer O, Najm MZ, Kausar MA, Mujeeb M, Siddiqui WA. Therapeutic potential of oroxylum indicum: a review. J Pharma Res Opinion. 2012;2:163–172. [Google Scholar]
- 175.Singh HV, Chaudhary AK. A review on the taxonomy, ethnobotany, chemistry and pharmacology of Oroxylum indicum Vent. Indian J Pharm Sci. 2011;73:483–490. doi: 10.4103/0250-474X.98981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 176.Hussain A, Oves M, Alajmi MF, Hussain I, Amir S, Ahmed J, Rehman MT, El-Seedi HR, Ali I. Biogenesis of ZnO nanoparticles using Pandanus odorifer leaf extract: anticancer and antimicrobial activities. RSC Adv. 2019;9:15357–15369. doi: 10.1039/c9ra01659g. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 177.Angami T, Bhagawati R, Touthang L, Makdoh B, Bharati KA, Silambarasan R, Ayyanar M. Traditional uses, phytochemistry and biological activities of Parkia timoriana (DC.) Merr., an underutilized multipurpose tree bean: a review. Genet Resour Crop Evol. 2018;65:679–692. [Google Scholar]
- 178.Gaire BP, Subedi L. Phytochemistry, pharmacology and medicinal properties of Phyllanthus emblica Linn. Chin J Integr Med. 2014 doi: 10.1007/s11655-014-1984-2. [DOI] [PubMed] [Google Scholar]
- 179.Lin HY, Yuan CY, Xin WY, Peng LD, Juan CW, Lei LJ, Lai LF. Chemical constituents of Picria fel-terrae. Guangxi Zhiwu Guihaia. 2010;30:887–890. [Google Scholar]
- 180.Kumarasingha R, Karpe AV, Preston S, Yeo TC, Lim DS, Tu CL, Luu J, Simpson KJ, Shaw JM, Gasser RB, Beale DJ. Metabolic profiling and in vitro assessment of anthelmintic fractions of Picria fel-terrae Lour. Int J Parasitol Drugs Drug Resist. 2016;6:171–178. doi: 10.1016/j.ijpddr.2016.08.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 181.Satria D, Silalahi J, Haro G, Ilyas S, Hsb PAZ. Antioxidant and antiproliferative activities of an ethylacetate fraction of Picria fel-terrae Lour. Herbs. Asian Pac J Cancer Prev. 2017;18:399–403. doi: 10.22034/APJCP.2017.18.2.399. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 182.Samuelsen AB. The traditional uses, chemical constituents and biological activities of Plantago major L. a review. J Ethnopharmacol. 2000;71:1–21. doi: 10.1016/S0378-8741(00)00212-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 183.Begum S, Hassan SI, Ali SN, Siddiqui BS. Chemical constituents from the leaves of Psidium guajava. Nat Prod Res. 2004;18:135–140. doi: 10.1080/14786410310001608019. [DOI] [PubMed] [Google Scholar]
- 184.Martha R, Gutiérrez P, Mitchell S, Solis RS. Psidium guajava: a review of its traditional uses, phytochemistry and pharmacology. J Ethnopharmacol. 2008;117:1–27. doi: 10.1016/j.jep.2008.01.025. [DOI] [PubMed] [Google Scholar]
- 185.Tai Z, Zhang F, Cai L, Shi J, Cao Q, Ding Z. Flavonol glycosides of Pseudodrynaria coronans and their antioxidant activity. Chem Nat Compd. 2012;48:221–224. [Google Scholar]
- 186.Jasuja ND, Saxena R, Chandra S, Sharma R. Pharmacological characterization and beneficial uses of Punica granatum. Asain J Plant Sci. 2012;11:251–267. [Google Scholar]
- 187.Djakpo O, Yao W. Rhus chinensis and Galla chinensis—Folklore to modern evidence: review. Phytother Res. 2010;24:1739–1747. doi: 10.1002/ptr.3215. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 188.Rishi P, Bimala S. Extraction and isolation of chemical constituents from Schima wallichii Bark. Int J Eng Sci Res Tech. 2014;3:175–180. [Google Scholar]
- 189.Das S, Ghosh LK. Evaluation of analgesic, antipyretic and anti-inflammatory activity of different fractions of Schima wallichii barks. Pharmacologia. 2013;4:400–403. [Google Scholar]
- 190.Sarbadhikary SB, Bhowmik S, Datta BK, Mandal NC. Antimicrobial and antioxidant activity of leaf extracts of two indigenous angiosperm species of Tripura. Int J Curr Microbiol Appl Sci. 2015;4:643–655. [Google Scholar]
- 191.Wang D, Huang L, Chen S. Senecio scandens Buch-Ham.: a review on its ethnopharmacology, phytochemistry, pharmacology, and toxicity. J Ethnopharmacol. 2013;149:1–23. doi: 10.1016/j.jep.2013.05.048. [DOI] [PubMed] [Google Scholar]
- 192.Hua S, Zhang Y, Liu J, Dong L, Huang J, Lin D, Fu X. Ethnomedicine, phytochemistry and pharmacology of Smilax glabra: an important traditional Chinese medicine. Am J Chin Med. 2018;46:261–297. doi: 10.1142/S0192415X18500143. [DOI] [PubMed] [Google Scholar]
- 193.Biao CY, Ming ZD, Shan YS. Chemical constituents of Smilax perfoliata. Acta Bot Sin. 2004;46:618–620. [Google Scholar]
- 194.Borkataky M. Antimcrobial and antioxidant activity of Smilax perfoliate Lour. Der Pharm Lett. 2014;6:246–250. [Google Scholar]
- 195.Zhao Y, Liu F, Lou HX. Studies on the chemical constituents of Solanum nigrum. Zhong Yao Cai. 2010;33:555–556. [PubMed] [Google Scholar]
- 196.Hameed HI, Calixto CMR, Yahya HM. A review: Solanum nigrum L. antimicrobial, antioxidant properties, hepatoprotective effects and analysis of bioactive natural compounds. Res J Pharm Tech. 2017;10:4063–4068. [Google Scholar]
- 197.Jain RAS, Gupta SSPI, Gabrani R. Solanum nigrum: current perspectives on therapeutic properties. Altern Med Rev. 2011;16:78–85. [PubMed] [Google Scholar]
- 198.Chang FR, Yen CT, El-Shazly M, Yu CY, Yen MH, Cheng YB, Chen SL, Wu YC. Spirostanoids with 1,4-dien-3-one or 3β,7α-diol-5,6-ene moieties from Solanum violaceum. Bioorg Med Chem Lett. 2013;23:2738–2742. doi: 10.1016/j.bmcl.2013.02.060. [DOI] [PubMed] [Google Scholar]
- 199.Karim A, Islam B, Tareq SM, Islam MT. Antinociceptive and antipyretic activities of Solanum violaceum Ortega. Int J Med. 2017;5:90–93. [Google Scholar]
- 200.Mahaldar K, SaifuzMahaldar K, Saifuzzaman M, Irin T, Barman AK, Islam MK, Rahman MM, Islam MA. Analgesic, anthelmintic and toxicity studies of Solanum violaceum Linn. leaves. Orient Pharm Exp Med. 2016;16:147–152. [Google Scholar]
- 201.Bora NS, Kakoti BB, Gogoi B, Goswami AK. Ethno-medicinal claims, phytochemistry and pharmacology of Spondias pinnata: a review. Int J pharm Sci Res. 2014;5:1138–1145. [Google Scholar]
- 202.Goswami DV, Nirmal SA, Patil MJ, Dighe NS, Laware NS, Patta SR. An overview of Tectona grandis: chemistry and pharmacological profile. Phcog Rev. 2009;3:181–185. [Google Scholar]
- 203.Vyas P, Yadav DK, Khandelwal P. Tectona grandis (Teak)—a review on its phytochemical and therapeutic potential. Nat Prod Res. 2019;33:2338–2354. doi: 10.1080/14786419.2018.1440217. [DOI] [PubMed] [Google Scholar]
- 204.El-Ghorab A, El-Massry KF, Shibamoto T. Chemical composition of the volatile extract and antioxidant activities of the volatile and nonvolatile extracts of egyptian corn silk (Zea mays L.) J Agric Food Chem. 2007;55:9124–9127. doi: 10.1021/jf071646e. [DOI] [PubMed] [Google Scholar]
- 205.Mendoza-Díaz S, del Carmen Ortiz-Valerio M, Castaño-Tostado E, de Dios Figueroa-Cardenas J, Reynoso-Camacho R, Ramos-Gómez M, Campos-Vega R, Loarca-Piña G. Antioxidant capacity and antimutagenic activity of anthocyanin and carotenoid extracts from nixtamalized pigmented creole maize races (Zea mays L.) Plant Foods Hum Nutr. 2012;67:442–449. doi: 10.1007/s11130-012-0326-9. [DOI] [PubMed] [Google Scholar]
- 206.Nessa F, Ismail Z, Mohamed N. Antimicrobial activities of extracts and flavonoid glycosides of corn silk (Zea mays L.) Int J Biotechnol Wellness Ind. 2012;1:115–121. [Google Scholar]
- 207.Gupta SK, Sharma A. Medicinal properties of Zingiber officinale Roscoe—a review. IOSR J Pharm Biol Sci. 2011;5:124–129. [Google Scholar]
- 208.Rehman R, Akram M, Akhtar N, Jabeen Q, Shah SA, Ahmed K, Shaheen G, Asif HM. Zingiber officinale Roscoe (Parmacological activity) J Med Plants Res. 2011;5:344–348. [Google Scholar]
- 209.Çakılcıoğlu U, Khatun S, Türkoğlu I, Hayta S. Ethnopharmacological survey of medicinal plants in Maden (Elazığ–Turkey) J Ethnopharmacol. 2011;137:469–486. doi: 10.1016/j.jep.2011.05.046. [DOI] [PubMed] [Google Scholar]
- 210.Akindele AJ, Ibe IF, Adeyemi OO. Analgesic and antipyretic activities of Drymaria cordata (Linn.) Willd (Caryophyllaceae) extract. Afr J Tradit Complement Altern Med. 2012;9:25–35. doi: 10.4314/ajtcam.v9i1.4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 211.Proma JJ, Faruque MO, Rahman S, Bashar ABMA, Rahmatullah M. Analgesic potential and phytochemical screening of Lablab purpureus aerial parts. World J Pharm Pharmaceut Sci. 2014;3:165–173. [Google Scholar]
- 212.Bakir M, Facey PC, Hassan I, Mulder WH, Porter RB. Mikanolide from Jamaican Mikania micrantha. Acta Crystallogr C. 2004;6:11. doi: 10.1107/S0108270104017809. [DOI] [PubMed] [Google Scholar]
- 213.Koriem KM, Arbid MS, Saleh HN. Antidiarrheal and protein conservative activities of Psidium guajava in diarrheal rats. J Integr Med. 2019;17:57–65. doi: 10.1016/j.joim.2018.12.001. [DOI] [PubMed] [Google Scholar]
- 214.Salama AA, El-Kassaby MI, Hassan A. Anti-urolithiatic activity of Solanum nigrum hydroalcoholic extract in ethylene glycol-induced urolithiasis in rats. Egypt Pharmaceut J. 2019;18:311. https://www.epj.eg.net/text.asp?2019/18/4/311/272269.
- 215.Yirga G, Teferi M, Gidey G, Zerabruk S. An ethnoveterinary survey of medicinal plants used to treat livestock diseases in Seharti-Samre district, Northern Ethiopia. Afr J Plant Sci. 2012;6:113–119. [Google Scholar]
- 216.Parthiban R, Vijayakumar S, Prabhu S, Gnanaselvam J, Yabesh EM. Quantitative traditional knowledge of medicinal plants used to treat livestock diseases from Kudavasal taluk of Thiruvarur district, Tamil Nadu, India. Rev Bras Farmacogn. 2016;26:109–121. [Google Scholar]
- 217.Jadid N, Kurniawan E, Himayani CES, Prasetyowati I, Purwani KI, Muslihatin W, Hidayati D, Tjahjaningrum ITD. An ethnobotanical study of medicinal plants used by the Tengger tribe in Ngadisari village, Indonesia. PLoS ONE. 2020;15:7. doi: 10.1371/journal.pone.0235886. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 218.Moerman DE. Symbols and selectivity: a statistical analysis of native American medical ethnobotany. J Ethnopharmacol. 1979;1:111–119. doi: 10.1016/0378-8741(79)90002-3. [DOI] [PubMed] [Google Scholar]
- 219.Kutal DH, Kunwar RM, Uprety Y, Adhikari YP, Bhattarai S, Adhikari B, Kunwar LM, Bhatt MD, Bussmann RW. Selection of medicinal plants for traditional medicines in Nepal. J Eethnobiol Ethnomed. 2021;17(1):1–11. doi: 10.1186/s13002-021-00486-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 220.Addo-Fordjour P, Kofi Anning A, Durosimi Belford EJ, Akonnor D. Diversity and conservation of medicinal plants in the Bomaa community of the Brong Ahafo region, Ghana. J Med Plants Res. 2008;2:226–233. [Google Scholar]
- 221.Ghorbani A. Studies on pharmaceutical ethnobotany in the region of Turkmen Sahra, north of Iran (Part 1): general results. J Ethnopharmacol. 2005;102:58–68. doi: 10.1016/j.jep.2005.05.035. [DOI] [PubMed] [Google Scholar]
- 222.Poonam K, Singh GS. Ethnobotanical study of medicinal plants used by the Taungya community in Terai Arc Landscape, India. J Ethnopharmacol. 2009;123:167–176. doi: 10.1016/j.jep.2009.02.037. [DOI] [PubMed] [Google Scholar]
- 223.Luseba D, Tshisikhawe MP. Medicinal plants used in the treatment of live-stock diseases in Vhembe region, Limpopo province. S Afr J Med Plants Res. 2014;7:593–601. [Google Scholar]
- 224.Mahwasane ST, Middleton L, Boaduo N. An ethnobotanical survey of indigenous knowledge on medicinal plants used by the traditional healers of the Lwamondo area, Limpopo province, South Africa. S Afr J Bot. 2013;88:69–75. [Google Scholar]
- 225.Saha MR, Sarker DD, Sen A. Ethnoveterinary practices among the tribal community of Malda district of West Bengal, India. Indian J Tradit Knowl. 2014;13: 359–67. http://nopr.niscair.res.in/handle/123456789/27931
- 226.Verma RK, Kumari P, Maurya RK, Kumar V, Verma RB, Singh RK. Medicinal properties of turmeric (Curcuma longa L.): a review. Int J Chem Stud. 2018;6(4):1354–1357. [Google Scholar]
- 227.Singh AG, Kumar A, Tewari DD. An ethnobotanical survey of medicinal plants used in Terai forest of western Nepal. J Ethnobiol Ethnomedicine. 2012;8:19. doi: 10.1186/1746-4269-8-19. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 228.Chaudhary MI, He Q, Cheng YY, Xiao PG. Ethnobotany of medicinal plants from Tian Mu Shan biosphere reserve, Zhejiang-Province, China. Asian J Plant Sci. 2006;5:646–653. [Google Scholar]
- 229.Çakılcıoğlu U, Türkoğlu I. An ethnobotanical survey of medicinal plants in Sivrice (Elazığ-Turkey) J Ethnopharmacol. 2010;132:165–175. doi: 10.1016/j.jep.2010.08.017. [DOI] [PubMed] [Google Scholar]
- 230.Rajakumar N, Shivanna MB. Ethnomedicinal application of plants in the eastern region of Shimoga District, Karnataka. India J Ethnopharmacol. 2009;126:64–73. doi: 10.1016/j.jep.2009.08.010. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
All data generated or analysed during this study are included in this published article.

