Abstract
The inhabitants of the floodplain of the Mazagão River in the State of Amapá in the Brazilian Amazon have inherited from indigenous African and Cabocla cultures indications for the use and forms of preparation of medicinal plants to cure diseases of the body and spirit. This study aimed to perform an ethnopharmacological survey of medicinal plants used by the riparian community of the floodplains of the Mazagão River, in the State of Amapá. In this study, we chose semistructured interviews with socioeconomic, ethnopharmacological, and ethnobotanical aims. The collection of medicinal plants occurred during guided tours. The Use Value (UV), Informant Consensus Factor (ICF), Correction Factor (CF), and Fidelity level (FL) were calculated. There were 130 species of medicinal plants, distributed in 116 genera and 57 families; Fabaceae (16), Lamiaceae (14), Euphorbiaceae (7), and Arecaceae (6) include 33.33% of the total species sampled. All 95 native species of floodplain forests were previously described, and 35 are exotic species. The species with the highest UV (≥ 0.5) at the mouth of the Mazagão River were Carapa guianensis (0.91), Pentachlethra macroloba (0.83), Dalbergia subcymosa (0.77), Uncaria tomentosa (0.75), Otacanthus azureus (0.62), Virola surinamensis (0.62), Hura crepitans (0.58), Euterpe oleracea (0.56), and Arrabidaea chica (0.51). These species were also the ones that presented the highest ICF among the informants and 100% in FL for a specific therapeutic use. The study is comprised of 16 categories of therapeutic use, of which the majority of the plants used are related to diseases such as microbial infections (20.67%, 73 species), gastrointestinal disorders (13.31%), and inflammation (11.61%). The results showed that knowledge about the use of medicinal plants along the rivers and streams that form the mouth of the Mazagão River is evenly distributed. Most of the interviewees present diversified knowledge about the medicinal resources because they have a close relationship with the floodplain forest. Native species of this forest predominate among the most commonly used medicinal plants as subsidies for future pharmacological studies.
1. Introduction
The floodplain forest is characterized by flood-prone areas influenced by white water rivers with high nutrient-rich sediment loads of Andean or pre-Andean origin, which occupy approximately 2/3 of the flood-prone areas in the Amazon [1]. These forests are inhabited by riparian people, human populations who live on the flood-prone river banks and who produce their food through vegetable extractivism, logging, fishing, handicrafts, and shrimp trapping [2, 3]. The floodplain has always played a central role in the development of the Amazon region, playing different roles in the food and economic survival of riparian dwellers at each period of their history [4, 5].
The riverside communities of the tropical floodplains coexist with a great diversity of natural resources, and they develop some exploration techniques for their own survival, aiming for the establishment of their own management systems that allows them to achieve their needs with low environmental damage, all of this based on their experiences [6–8].
The use of medicinal plants for the treatment of diseases is related to human evolution itself; its use has been reported in all time periods, in all social strata, and for almost all of humanity. The use of medicinal plants for therapeutical purposes in developing countries such as Brazil can be used as an alternative treatment [9, 10]. Phytotherapy and the use of medicinal plants are traditionally part of popular medicine based on the knowledge of different populations, users, and practitioners. It is an effective form of primary health care for the lower income population. Medicinal plants have strongly contributed to the development of new therapeutic strategies through the isolation and identification of its secondary metabolites. These are known to act directly or indirectly through several molecular and cellular targets [11].
The use of medicinal plant-based medicines and the popular knowledge itself implies the need to implement basic research to clarify and confirm information about the actions of the plants, minimizing side, and toxicological effects so that their use is reliable and safe [12].
Historically, the city of Mazagão was founded in the 16th century in North Africa, then it was transferred in the eighteenth century to Portuguese America. It is located on the banks of the Mutuacá River in the State of Amapá, at the Brazilian Amazon rainforest [13]. The New Village of Mazagão, lost in the banks of the Amazon rainforest, was a point of overlapping of cultures, dualities, and conflicts. The memory of the city of the Moroccan coast was diluted and adapted to the new conditions of Portuguese America, building a new urbanity [14]. At that time, the African Mazagans had to live with the outbreak of malaria, a tropical disease endemic to the region; and in order to survive they used traditional knowledge of the use of medicinal plants of the riverside and indigenous communities [15].
Though cultural aspects such as the religious festivals in praise of St. James were preserved and, to this day in July, the battle waged between the Moors and Christians on the coast of Africa is remembered, new practices also emerged from the cultural synthesis of the Mazans, with indigenous people, slaves, and riparians [16, 17]. In the floodplain forest regions of the Eastern Amazon, medicinal plants represent the main form of disease treatment for most of the riparian populations living in this ecosystem, as they live geographically isolated from the urban centers, which causes barriers between them and the public services, especially health service and basic sanitation [18, 19]. These riverside communities have a very peculiar way of interacting with the environment where they live; in most of the houses, septic tanks are still used, and they overflow periodically when the river floods. This water is collected for consumption, several domestic tasks and even for the preparation of the açaí wine (Euterpe oleracea), which is the main food consumed in the locality, but it does not undergo adequate treatment to be considered potable, making parasites and stomach diseases a recurring problem in the community [18, 20].
The human populations that settled in floodplain regions started to have a very strong connection with the forest, knowing and exploring it, which allowed a greater contact with the vectors of tropical diseases such as malaria, Chagas disease, and tegumentary leishmaniasis, which are endemic diseases of these regions. To treat and control these diseases, they started to use medicinal plants, a knowledge that is acquired through both experience and verbal cultural transmission, which refers to the past knowledge of one generation to another and plays an important historical role as it facilitates human survival through these generations [19]. Therefore, the riverside inhabitants of the floodplain forest possess important collections of plants that are used for therapeutic purposes as they inherited the use and forms of preparation of medicinal plants for the cure of their diseases of the body and spirit from the indigenous African and Cabocla cultures [19]. However, this knowledge is usually restricted and little studied. Undoubtedly, many plants native to floodplains with therapeutic potential remain unknown and will become extinct because logging is reducing forests and decharacterizing traditional communities in the region.
Few ethnobotanical studies have been performed in the area; for instance, Silva [20] surveyed plants used in Carvão District, Mazagão, AP, where 218 different plant species distributed over 69 families were reported. In the riverside communities of Mazagão Velho, Maracá, and Ajurixi Nascimento [21] it has been reported 73 different plant species distributed over 37 families and their medicinal uses. Overall, these ethnobotanical and ethnopharmacological studies indicate an excellent target to pharmacological researches in the north of Brazil [19, 22, 23].
The State of Amapá has rich plant biodiversity, in addition to a great ethnic and cultural diversity, favoring the accumulation of empirical knowledge about medicinal uses of these plants. Considering the importance to rescue this knowledge from traditional communities and systematize it, this study aimed to perform an ethnobotanical and ethnopharmacological survey of medicinal plants used by riverside communities at the mouth of Mazagão River, in the State of Amapá.
2. Materials and Methods
2.1. Study Area
The municipality of Mazagão occupies an area of 13,131 km2, it has a population of 17,032 inhabitants and a population density of 1.30 hab/km2 [24], it is 36 km long from the capital Macapá, and it is located at the right margin of the Vila Nova River, south of the State of Amapá under the geographic coordinates 00° 06′ 54′′ S and -51° 17′ 20′′ W (Figure 1). Data collection occurred at the eastern boundary of the municipality of Mazagão in a riparian community that lives at the mouth of the Mazagão River, which has the Mutuacá Mirim, Espinhel, Grande and Ajudante rivers as tributaries. The community at the mouth lives along the Mazagão River, which is situated to the east of the Amazon River and to the west of the Old Mazagão Village, according to Carim et al. [25], the predominant climate type Ami, based on the Köppen classification, with a minimum temperature of 23°C and a maximum temperature of 33°C (annual average of 27°C), with relative humidity above 80%, high rainfall from 2,000 mm/year to 2,500 mm/year, and the Haplic Gleisol soil with a very clayey texture.
2.2. Research Authorization
At the beginning of the study, a meeting was organized with the community to present the project and its objectives to obtain community consent for the development of the study. Subsequently, according to the Resolutions of the National Commission for Research Ethics involving Humans and the National Health Council/Ministry of Health, the project was submitted to the Ethics Research Committee of the Faculdade Estácio de Macapá. To do so, the project was registered in the Brazil Platform at http://aplicacao.saude.gov.br/plataformabrasil/login.jsf, in which the following was inserted: interview forms (socioeconomic, ethnobotanical and ethnopharmacological), Community Consent Statement, and the terms of Free and Informed Consent, according to Resolution 466/12 of the National Health Council. This study was approved on 04/13/2016 under opinion number 14.94.994.
2.3. Area of Study's Typical Vegetation
Floodplain forests have about 25,000 km2 in the area of the Amazonian estuary; it represents about 4.85% from the State of Amapá area and about 15.46% of the coastal estuarine sector [26]. These forests are the flooded ecosystem with the highest biodiversity in the world and have more than 1,000 different species of trees [27, 28]. The local vegetation is cataloged as Alluvial Dense Ombrophilous Forest [29], and the most representative plant families are Fabaceae, Malvaceae, Meliaceae, and Rubiaceae [30]. There is a significant number of palm trees such as Astrocaryum murumuru Mart., Manicaria saccifera Gaertn., Mauritia flexuosa L. f., Attalea excelsa (Aubl.) Mart., and Euterpe oleracea Mart.; and emerging trees such as Carapa guianensis Alblet, Virola surinamensis (Rol. ex Rottb.) Warb., Mora paraensis (Ducke) Ducke, Calycophyllum spruceanum (Benth.) Hook. f. ex K. Schum., Hevea brasiliensis (Willd. ex A. Juss.) Müll. Arg., Cedrela odorata L., and Pentaclethra macroloba (Willd.) Kuntze [30, 31].
The soil under estuarine floodplain forests of Mazagão, AP is, shallow and continuously subjected to flood. In this area, the soil is cataloged as typical Eutrophic Ta Melanic Gleysol [32].
2.4. Selection of Informants
In the community, there are 128 houses, all of which were visited, but only the families living in the community for at least 10 years were considered in the interviews. In the selected family, the person who everyone agreed was knowledgeable about home remedies (healer) was the one who was always approached because he/she cultivates and holds knowledge about local plants that are medicinal. A total of 93 forms were applied, representing 72.65% of the total families living in the community.
The study area was investigated to get information from local traditional healers having practical knowledge of medicinal plants; they were interviewed in two villages during April 2016 to May 2018. During the course of the study, six field trips were carried out in the study, and a total 30 days were spent with their local traditional healers. Methods of selecting informants depended upon the distribution of local people having sound knowledge.
All participants agreed to sign the terms of Informed Consent. The interviews were conducted with semistructured forms with open and closed questions about the socioeconomic aspects and the identification of respondents (age, ethnicity, schooling, sex, length of time living in the community, religion, food consumption, family income, and participation in any social project of the government) and information about the medicinal plants used (popular name, part used, indications, and preparation) were recorded. In this work, we considered both plants that are used for diseases well known and treatable by traditional medicine and those indicated for cultural diseases such as “panemeira” (a condition in which the individual is unlucky or has bad luck), bewitching, evil eye, or jinx (the individual is haunted by evil spirits). Other conditions included “ferida brava” (Leishmaniosis ulcer), ringworm (individual with itching in the body), bubo (inflammation in the lymph nodes), “úra” or “fly eye” (fly larvae that lodges in the dermis and causes inflammation in the skin), catarrh in the chest (secretion in the lungs), and “nascida” (a tumor that swells in the skin of any part of the body).
2.5. Collection of Botanical Material
The collections were carried out using the guided tour technique [33], which consisted of exploratory walks conducted by the interviewees in the backyard of their residence and in the interior of the forest to identify and collect botanical material from the medicinal plants mentioned during the interview. The referenced species were collected and herborized according to the usual methodology of Fidalgo and Bononi [34]. The plant material was identified by comparison to the Embrapa Eastern Amazon Herbarium; IAN collection; and specialized bibliography [35] and when necessary, via consultations with specialists. Exsiccating of the collected species was included in the IAN of the Embrapa Amazônia Oriental and Herbário Amapaense (HAMAB) of the Institute for Scientific and Technological Research of the State of Amapá. The species mentioned only with the vegetative part were identified, when possible, through specialized literature and using virtual herbarium images for comparison. The spelling and authors of the scientific names were verified in the Missouri Botanical Garden database at www.tropicos.org, and the families were determined according to the classification system proposed by the Angiosperm Phylogenetic Group III [36]. The geographical origin of the species was verified in a specialized bibliography [35, 37].
2.6. Data Analysis
The medicinal plants listed by the informants were organized according to the scientific name, popular name, part used, method of preparation, and indications for medicinal use. The reported diseases and symptoms were grouped into 16 categories of therapeutic use according to the indicated body systems. Data were analyzed statistically and described in percentages using Graphpad Prism software (version 6.0). To analyze the relative importance of a species for its ethnomedicinal use, quantitative data (frequency of use and therapeutic indication) were calculated using the Index of Use Value (UV), Loyalty Level (LL), Informant Consensus Factor (ICF), and Correction Factor (CF), according to the mathematical formulas below.
2.6.1. Use Value (UV)
It is a quantitative index that expresses the therapeutic importance of each species. It is calculated by the following formula: UV = ΣUi/n [38], where UV is equivalent to the Use Value of a species, Ui is the number of therapeutic uses reported for each species of plant, and n is the total number of respondents interviewed [39]. The UV parameter helps determine which plant is most frequently used for specific purposes. UV is high when the plant is mentioned by a large number of informants and low when there are few cited uses [40].
2.6.2. Informant Consensus Factor (ICF)
The proposal by Troter and Logan [41] aims to identify the body systems or categories of diseases that have greater relative importance in the site of the study. The ICF is calculated by obtaining the number of citations of uses in each category (Nur) minus the number of species used (Nt), divided by the number of use citations in each category minus 1. The maximum value a category can achieve is 1, which would indicate that there is a well-defined criterion for selecting medicinal plants in the community and/or that use information is shared among the people.
(1) |
2.6.3. Fidelity Level (FL)
The FL measures the species most frequently used by informants in the study area for a specific therapeutic treatment [42]. FL was calculated using the following formula:
(2) |
where Np is the number of citations for therapeutic use given by an informant indicating a species for the highest therapeutic use and N is the total number of informants who cited the species for some use. FL = 100% means that all informants use the species for a therapeutic application, while values below this value mean that the species is used for different purposes [40].
2.6.4. Correction Factor (CF)
The CF determines the difference in the number of informants who cited uses for each species. The CF is calculated by the following formula: CF = N/ICEMC [43], where N is the total number of informants who cited uses for the species and ICEMC is the number of citations of the most frequent species. To extract the importance values related to the species most cited by the interviewees, the following formula was used: Pcusp = LL x CF [44], where Pcusp is the corrected concordance use index, NF is the loyalty level of use, and CF is the correction factor for each species.
3. Results and Discussion
3.1. Sociocultural Characteristics of Informants
The riverside community at the mouth of the Mazagão River lives on the banks of a floodplain forest; the family income is based on the extractive management of the açaí fruit (Euterpe oleracea) and regional shrimp (Macrobrachium amazonicum) fishery. In this study, 93 residents were interviewed, ranging in age from 18 to 70 years. The oldest informants with ages ranging from 51 to 70 years were responsible for 51% of citations for use of the medicinal plants; informants ranging from 31 and 50 years old for 38.7% of citations; and informants ranging from 18 to 30 years for 10.3%. When comparing the number of plants cited with the age of the interviewees, it can be seen that the oldest female subjects between 55 and 70 years of age presented the highest number of citations for medicinal plant use. Other ethnobotanical studies also point to the fact of older women knowing more about the medicinal use of plant species [6, 45]. The prevalence is likely higher in older women due to the household duties of caring for the children, the house and the yard, and the place around the house where “girais” (wood artifact, a type of raised bed garden that reaches 3 meters from the ground) are built for the planting of medicinal and food plants. Additionally, the riverside inhabitants live on the edge of the forest, which is periodically flooded, and there is a practice of passing on traditional knowledge about the use of medicinal plants to future generations by word of mouth.
With regard to schooling, 20.4% of the older people were never literate, and those with elementary school education until the 5th grade represent 41% of the community; elementary school through the 8th grade, 20%; high school, 8.6%; incomplete high school, 9%; and higher education, 1%. According to Elisabetsky [46], what makes traditional knowledge of interest to science is the verbal communication of the systematic observation of biological phenomena, made by people who are often illiterate but are certainly insightful regarding the observations of the environment where they live. In this study, it is possible to verify that the older interviewees and those with less education in general are able to recognize a greater number of medicinal plants than are the younger interviewees. This pattern is also observed in other studies, such as those by Hanazaki et al. [47], Pinto [6], and Negrelle et al. [48].
3.2. Diversity of Medicinal Plants
A total of 130 medicinal species were identified, which were distributed in 116 genera and 57 families. Fabaceae (16 species), Lamiaceae (14), Euphorbiaceae (7), Arecaceae (6), Asteraceae (4), Rubiaceae (4), Rutaceae (4), Amaranthaceae (4), and Anacardiaceae (4) accounted for the greatest number of species, totaling 48.83% of the sampled species, and 22.5% of the families were represented by only one species. In total, 95 native species of floodplain forest and 35 exotic or introduced species were mentioned (Table 1).
Table 1.
Scientific Name (Family) Voucher n° | Local name | Distribution | Plant part used | Traditional uses | Preparation method and use form | UV |
---|---|---|---|---|---|---|
(1) Acmella oleracea (L.) R.K. Jansen (Asteraceae), IAN 195948 | Jambú | Native | Leaves and inflorescences | Pain, inflammation, Anemia and malaria. | Decoction; 1 cup 3x a day for 7 days | 0,09 |
| ||||||
(2) Acrocomia aculeata (Jacq.) Lodd. ex Mart. (Arecaceae), IAN 195943 | Mucajá | Native | Root and leaves | Catarrh in the chest (secretion in the lung) and cough. | Decoction; 1 spoon 4 x a day for 7 days. | 0,02 |
| ||||||
(3) Adenocalymna alliaceum Miers (Bignoniaceae), IAN 196009 | Cipó d'alho | Native | Leaves and bark | Cold, inflammation of the throat and fever. | Decoction; 1 scoop 2 x daily and inhale 2x steam for 7 days. | 0,17 |
| ||||||
(4) Aeollanthus suaveolens Matt. ex Spreng. (Lamiaceae), IAN 195989 |
Caatinga de mulata | Introduced | Leaves | Irritation of the nerves and strong headache. | Dyeing and infusion; bathe the body 2 x in the day for 10 days. | 0,46 |
| ||||||
(5) Allamanda cathartica L. (Apocynaceae), IAN 196010 |
Buiuçú | Native | Exsudate and leaves | Elimination of lice and antihemintics. | Decoction; 1 spoon 2 x a day for 7 days and soak hair 1 x a day for 10 minutes for 3 days. | 0,01 |
| ||||||
(6) Allium sativum L. (Liliaceae), HAMAB 8938 |
Alho | Introduced | Leaves | Flu, pain in the stomach and antihemintics | Decoction; 1 cup 3 x daily for 7 days. | 0,03 |
| ||||||
(7) Aloe vera (L.) Burm. (Asphodelaceae), IAN 194110 |
Babosa | Native | Leaves | Healing. | Cataplasm; spend 3 x a day until the wound is dry. | 0,10 |
| ||||||
(8) Alstroemeria brasiliensis Spreng. (Alstroemeriaceae), IAN 196011 |
Carajurú, cajuru | Native | Bark and root | Malaria. | Decoction; 1 cup 3 x daily for 7 days. | 0,01 |
| ||||||
(9) Alternanthera brasiliana (L.) Kuntze (Amarathaceae), IAN 194099 |
Perpétua do mato, sempre-viva. | Native | Leaves | Elimination of kidney stone, antitumor, infections of the liver and bladder. | Decoction; leaves of Alternanthera brasiliana, Alternanthera dentata and Alternanthera ficoidea, ingest 1 cup 4 x a day for 20 days. | 0,20 |
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(10) Alternanthera dentata (Moench) Stuchlík ex R.E. Fr. (Amaranthaceae), IAN 195934 | Cibalena | Native | Leaves | Elimination of kidney stone, infections of the liver, stomach pains. | Decoction; leaves of Alternanthera brasiliana, Alternanthera dentata and Alternanthera ficoidea, ingest 1 cup 4 x a day for 20 days. | 0,01 |
| ||||||
(11) Alternanthera ficoidea (L.) Sm. (Amaranthaceae), IAN 195952 | Piriquitinho verde | Native | Leaves | Elimination of kidney stone, inflammation of the uterus and ovary. | Decoction; leaves of Alternanthera brasiliana, Alternanthera dentata and Alternanthera ficoidea, ingest 1 cup 4 x a day for 20 days. | 0,07 |
| ||||||
(12) Anacardium occidentale L. (Anacardiaceae), IAN 195977 | Caju | Native | Leaves | Diarrhea, uterine cramps. | Decoction; 1 cup 3 x daily for 7 days. | 0,16 |
| ||||||
(13) Annona muricata L. (Annonaceae), IAN 195945 |
Graviola | Native | Leaves | Diarrhea and skin sore. | Decoction and infusion; 1 cup 3 x daily for 7 days. | 0,03 |
| ||||||
(14) Arrabidaea chica (Bonpl.) B. Verl. (Bignoniaceae), IAN 194107 |
Pariri | Native | Leaves | Anemia, diarrhea, washing of wounds, yellow skin and swollen body of pregnant woman. | Decoction and maceration; 1 cup 3 x daily for 7 days. | 0,51 |
| ||||||
(15) Astrocaryum murumuru Mart. (Arecaceae), IAN 196007 |
Murumuru | Native | Fruit | Dog eye inflammation and irritation in human eyes. | Decoction and maceration; 1 cup 3 x daily for 7 days. | 0,01 |
| ||||||
(16) Bactris maraja Mart. (Arecaceae), IAN 196006 |
Marajá | Native | Root | Diarrheal, inflammation of the uterus. | Decoction and maceration; 1 cup 3 x daily for 7 days. | 0,02 |
| ||||||
(17) Bauhinia splendens Kunth. (Fabaceae), IAN 196005 |
Escada de jabuti | Native | Bark | Joint pain, rheumatism and syphilis. | Decoction and maceration; 1 cup 3 x daily for 7 days. | 0,03 |
| ||||||
(18) Bixa orellana L. (Bixaceae), IAN 196001 |
Urucum | Native | Fruit | Repellent, burn, diarrhea and asthma. | Syrup and decoction; 1 cup 3 x daily for 7 days. Mix with Carapa guianensis Aubl. oil and pass on the body 1 x a day. | 0,08 |
| ||||||
(19) Brassica oleracea L. (Brassicaceae), IAN 195942 |
Couve manteiga | Introduced | Leaves | Anemia and cholesterol. | Decoction; 1 cup 2 x daily for 7 days. | 0,03 |
| ||||||
(20) Bryophyllum pinnatum (Lam.) Oken (Crassulaceae), IAN 195954 |
Pirarucu | Introduced | Leaves | Irritation of the skin. | Decoction; pass on the skin 2 x in the day for 7 days. | 0,03 |
| ||||||
(21) Libidibia ferrea (Mart. ex Til.) L.P. Queiroz (Fabaceae), IAN 195940 | Jucá | Native | Fruit | Bleeding, inflammation in general, washing of wounds and swelling of the legs. | Decoction and maceration; 1 cup 3 x daily for 7 days. | 0,01 |
| ||||||
(22) Caladium humboldtii Schott (Araceae), IAN 194115 |
Brasileirinho | Native | Leaves | Fever, pain in the uterus and inflammation in general. | Decoction; 1 cup 3 x daily for 7 days. | 0,07 |
| ||||||
(23) Calophyllum brasiliense Cambess. (Clusiaceae), IAN 195937 | Jacareúba | Native | Exsudate and Bark | Joint pain, rheumatism and skin sore. | Exudate; pass on the skin 4 x a day for 7 days. | 0,01 |
| ||||||
(24) Calycophyllum spruceanum (Benth.) Hook. f. ex K. Schum. (Rubiaceae), IAN 195980 |
pau mulato | Native | Bark | Itching, inflammation in general and insect stings. | Decoction; 1 cup 3 x daily for 7 days. | 0,04 |
| ||||||
(25) Carapa guianensis Aubl. (Meliaceae), IAN 194102 |
Andiroba | Native | Seed | Inflammation in general, massage the pregnant belly to put the baby in place. | Oil; ingest 1 teaspoon 4 x daily for 10 days, topical use 2 x daily for 7 days. | 0,91 |
| ||||||
(26) Cecropia pachystachya Trécul (Urticaceae), IAN 195956 |
Embaúba vermelha | Native | Leaves | Skin irritation and verminoses. | Decoction; 1 teaspoon 4x a day for 7 days. | 0,08 |
| ||||||
(27) Cedrela odorata L. (Meliaceae), IAN 195971 |
Cedro | Native | Bark | Verminose, skin irritation, intestinal infections. | Decoction and maceration; 1 cup 4 x daily for 7 days. | 0,08 |
| ||||||
(28) Cereus jamacaru DC. (Cactaceae), IAN 195976 |
Mandacarú. | Native | Branches and root | Pulmonary problems, skin infections, sores and kidney stones. | Decoction; 1 teaspoon 4x a day for 10 days. | 0,01 |
| ||||||
(29) Chenopodium ambrosioides L. (Amaranthaceae), IAN 195978 |
Mastruz | Introduced | Leaves | Pain, inflammation in general and rheumatism. | Decoction; 1 teaspoon 4x a day for 7 days. | 0,11 |
| ||||||
(30) Cichorium intybus L. (Asteraceae), IAN 195979 |
Chicória | Introduced | Leaves and root | Inflammation in general, pain and fever. | Decoction; 1 cup 2 x daily for 7 days. | 0,10 |
| ||||||
(31) Cinnamomum zeylanicum Blume. (Lauraceae), IAN 195982 |
Canela | Introduced | Leaves and bark | Flu, diarrhea, inflammation of the uterus and wounds in the mouth. | Syrup and infusion; 1 cup 2 x daily for 7 days. | 0,02 |
| ||||||
(32) Cissus verticillata (L.) Nicolson & C.E. Jarvis (Vitaceae), IAN 195983 | Cipó-urumucá, cipó-pucá | Native | Leaves | High blood pressure, stroke, anemia, tremors and epileptic seizures. | Decoction; 1 cup 2 x daily for 7 days. | 0,03 |
| ||||||
(33) Citrus aurantium L. (Rutaceae), IAN 195960 |
Laranja da terra | Introduced | Bark | Swelling of a pregnant woman, inflammation in general, and itching of the foot. | Maceration; 1 cup 2 x a day at dawn and dusk for 7 days. | 0,07 |
| ||||||
(34) Citrus limon (L.) Burm. (Rutaceae), IAN 195988 |
Limão galego | Introduced | Fruit | Rheumatism and inflammation of the kidneys. | Decoction; 1 cup 2 x daily for 7 days. | 0,02 |
| ||||||
(35) Citrus limonum L. (Rutaceae), IAN 195989 |
Limão | Introduced | Fruit | Rheumatism and inflammation of the kidneys. | Syrup and infusion; 1 cup 3 x daily and inhale the steam 2 x daily for 7 days. | 0,29 |
| ||||||
(36) Cocos nucifera L. (Arecaceae), IAN 195990 |
Côco | Native | Fruit and root | Hydration of child and verminoses. | Decoction of the root 1 cup 2 x a day for 7 days and fruit water will during the day for 7 days. | 0,02 |
| ||||||
(37) Copaifera sp. (Fabaceae), IAN 195991 |
Copaiba | Native | Bark and oil | Inflammation of the uterus and ovary, and diseases of the stomach. | Decoction; 1 cup 2 x daily for 7 days. | 0,02 |
| ||||||
(38) Costus spicatus (Jacq.) Sw. (Costaceae), IAN 195993 |
Canafiche, canarana | Native | Aerial part | Inflammation of the uterus and ovary, vaginal discharge and syphilis. | Decoction; 1 cup 3 x daily for 7 days. | 0,03 |
| ||||||
(39) Crescentia cujete var. puberula Bureau & K. Schum. (Bignoniaceae), IAN 195959 |
Cuieiro | Native | Leaves and bark | Malaria, fever and rheumatism. | Decoction; 1 cup 3 x daily for 7 days. | 0,05 |
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(40) Croton cajucara Benth. (Euphorbiaceae), IAN 195994 |
Sacaca | Native | Leaves and bark | Diarrhea, diabetes, inflammation of the liver, kidneys and bladder. | Decoction; 1 cup 2 x daily for 7 days. | 0,01 |
| ||||||
(41) Croton urucurana Baill. (Euphorbiaceae), IAN 195996 |
Forsangue | Native | Bark | Hemorrhagic and inflammation of the uterus. | Decoction; 1 cup 3 x daily for 7 days. | 0,18 |
| ||||||
(42) Cucumis anguria L. (Cucurbitaceae), IAN 195998 |
Maxixe | Introduced | Fruit | Eliminate kidney stones, hemorrhoids, inflammation of the kidneys, vomiting. | Decoction; 1 cup 3 x daily for 10 days. | 0,01 |
| ||||||
(43) Cymbopogon citratus (DC.) Stapf (Poaceae), IAN 195953 |
Capim marinho | Introduced | Leaves | Inflammation of the uterus and ovary and abdominal pain. | Decoction; 1 cup 3 x daily for 7 days. | 0,10 |
| ||||||
(44) Dalbergia monetaria L. f. (Fabaceae), IAN 195964 |
Verônica | Native | Bark | Inflammation, diarrhea and intestinal infection. | Decoction and maceration ingest 1 cup 3 x daily for 7 days. | 0,77 |
| ||||||
(45) Dimorphandra gardneriana Tul. (Fabaceae), IAN 195995 |
Faveira | Native | Fruit | High pressure. | Decoction; 1 cup 3 x daily for 7 days. | 0,02 |
| ||||||
(46) Eleutherine bulbosa (Mill.) Urb. (Iridaceae), IAN 195997 |
Marupá, Marupázinho | Introduced | Rhizome | Verminoses, wound healing on the skin. | Decoction; 1 cup 3 x daily for 7 days. | 0,18 |
| ||||||
(47) Erythrina fusca Lour. (Fabaceae), IAN 194108 |
Assacurana | Native | Bark | Pain in body and head, inflammation and verminoses. | Decoction; 1 cup 3 x daily for 7 days. | 0,04 |
| ||||||
(48) Eucalyptus sp. (Myrtaceae), IAN 196000 |
Eucalipto | Introduced | Leaves | Inflammation in general. | Decoction; 1 cup 2 x daily for 7 days. | 0,04 |
| ||||||
(49) Eupatorium triplinerve Vahl. (Asteraceae), IAN 195946 |
Japana | Introduced | Aerial parts | Flu | Syrup and infusion; ingest 1 cup 3 x daily for 7 days. | 0,09 |
| ||||||
(50) Euterpe oleracea Mart. (Arecaceae), HAMAB 10919 |
Açaí | Native | Bark | Diarrhea and intestinal inflammation. | Decoction; 1 cup 3 x daily for 7 days. | 0,56 |
| ||||||
(51) Genipa americana L. (Rubiaceae), IAN 196001 |
Desinflama | Native | Leaves and bark | Diarrhea, sores on the skin, pains and phlegm in the lung. | Decoction; 1 cup 3 x daily for 7 days. | 0,03 |
| ||||||
(52) Gossypium hirsutum L. (Malvaceae), IAN 195690 |
Algodão | Introduced | Leaves | Fever of infections. | Decoction; 1 cup 3 x daily for 7 days. | 0,21 |
| ||||||
(53) Gustavia augusta L. (Lecythidaceae), IAN 196003 |
Geniparana | Native | Bark, leaves and flowers | Brave wound (leishmaniasis). | Poultry, decoction and maceration, ingest 1 x 2 x daily for 10 days. Topical use 2 x in day for 7 days. | 0,04 |
| ||||||
(54) Hevea brasiliensis (Willd. ex A. Juss.) Müll. Arg. (Euphorbiaceae), IAN 196068 | Seringueira | Native | Exsudate | Brave wound (leishmaniasis). | Exudate as poultice, topical use 2 x in day for 7 days. | 0,03 |
| ||||||
(55) Himatanthus sucuuba (Spruce ex Müll. Arg.) Woodson (Apocynaceae), IAN 194107 |
Sucuúba | Native | Bark and exsudate | Verminoses, inflammation and pain in the uterus, malaria and rheumatism. | Cataplasm; topical use 2 x in day for 7 days. | 0,04 |
| ||||||
(56) Hura crepitans L. (Euphorbiaceae), IAN 195981 |
Assacú | Native | Bark | Cancer. | Decoction; 1 cup 2 x daily for 10 days. | 0,58 |
| ||||||
(57) Hymenaea oblongifolia Huber (Fabaceae), IAN 196009 | Jatobá da várzea | Native | Bark and fruit | Diarrhea, pain and inflammation in the body. | Decoction and maceration; 1 cup 2 x daily for 7 days. | 0,17 |
| ||||||
(58) Hypericum perforatum L. (Hyperaceae), IAN 194100 |
Dipirona, hipericão, erva de são João | Introduced | Leaves and casca | Pain, depression, nervous irritation. | Decoction; 1 cup 3 x daily for 10 days. | 0,04 |
| ||||||
(59) Scutellaria agrestis A. St. Hil. ex Benth. (Lamiaceae), IAN 195992 |
Trevo rocho | Native | Leaves and inflorescences | Headache, itchy skin. | Infusion and poultice; topical use 3 x daily for 7 days. | 0,01 |
| ||||||
(60) Jatropha curcas L. (Euphorbiaceae), IAN 195944 |
Pião branco | Introduced | Leaves, seed and bark | Headaches, catarrh in the chest, flu, stroke and scarring. | Dyeing and infusion; 1 cup 2 x daily for 10 days. | 0,38 |
| ||||||
(61) Jatropha gossypiifolia L. (Euphorbiaceae), IAN 195949 |
Pião rocho | Introduced | Leaves | Broken and evil eye. | Infusion; 1 cup 2 x daily for 7 days. | 0,08 |
| ||||||
(62) Centratherum punctatum Cass. (Asteraceae), IAN 195987 | Anador, melhoral | Native | Leaves | Bleeding and inflammation of the kidneys. | Decoction; 1 cup 2 x daily for 10 days. | 0,21 |
| ||||||
(63) Justicia pectoralis Jacq. (Acanthaceae), IAN 194100 |
Anador, melhoral | Native | Leaves | Headache and joint pain. | Decoction; 1 cup 2 x daily for 7 days. | 0,21 |
| ||||||
(64) Lecythis pisonis Cambess. (Lecytidaceae), IAN 196010 |
Sapucaia | Native | Bark, leaves and flowers | Diarrhea and inflammation in general. | Decoction; 1 cup 2 x daily for 10 days. | 0,01 |
| ||||||
(65) Licania macrophylla Benth. (Chrysobalanaceae), IAN 194104 |
Anoerá ou anuerá | Native | Bark | Diarrhea and bleeding. | Decoction and maceration; 1 cup 3 x daily for 7 days. | 0,20 |
| ||||||
(66) Lippiaalba (Mill.) N.E. Br. ex Britton & P. Wilson (Verbenaceae), IAN 194109 | Camelitana, erva cidreira | Native | Leaves and flowers | Pain and catarrh in the chest. | Decoction; 1 cup 3 x daily for 7 days. | 0,01 |
| ||||||
(67) Luffa operculata (L.) Cogn. (Cucurbitaceae), IAN 196013 |
Buchinha ou cabacinha | Native | Leaves, bark and fruit | Flu, abortion and verminosis. | Decoction; 1 cup 3 x daily for 7 days. | 0,02 |
| ||||||
(68) Machaerium lunatum (L.) Ducke (Fabaceae), IAN 195973 |
Aturiá | Native | Leaves | Rheumatism. | Decoction; 1 cup 3 x daily for 7 days. | 0,03 |
| ||||||
(69) Macrolobium acaciifolium (Benth.) Benth. (Fabaceae), IAN 196011 |
Faveira-araparí | Native | Bark | Healing. | Maceration; 1 x 3 x daily and topical use 2 x daily for 7 days. | 0,04 |
| ||||||
(70) Mangifera indica L. (Anacardiaceae), IAN 195965 |
Manga | Introduced | Leaves and bark | Diarrhea and intestinal infections. | Decoction; 1 cup 3 x daily for 7 days. | 0,47 |
| ||||||
(71) Manicaria saccifera Gaerth. (Arecaceae), IAN 195984 |
Bussú | Native | Fruit | Inflammation in the stomach and born in the body (furunculosis). | Maceration; 1 cup 3 x daily for 10 days. | 0,04 |
| ||||||
(72) Maquira calophylla (Poepp. & Endl.) C.C. Berg (Moraceae), IAN 196012 |
Muiratingarana | Native | Bark | Cancer. | Decoction; 1 cup 3 x daily for 20 days. | 0,04 |
| ||||||
(73) Maquira coriacea (H. Karst) C.C. Berg (Moraceae), IAN 196013 | Muiratinga | Native | Bark | Malaria. | Decoction; 1 cup 3 x daily for 7 days. | 0,04 |
| ||||||
(74) Melissa officinalis L. (Lamiaceae), IAN 195947 |
Cidreira, erva-cidreira | Introduced | Leaves and inflorescences | Headaches, digestive problems, anxiety and nervousness. | Infusion; 1 cup 3 x daily for 7 days. | 0,03 |
| ||||||
(75) Mentha × piperita L. (Lamiaceae), IAN 196014 |
Hortelânzinho | Introduced | Leaves | Verminoses and inflammations of the kidney, bladder and liver. | Infusion; 1 cup 3 x daily for 7 days. | 0,26 |
| ||||||
(76) Mentha arvensis L. (Lamiaceae), IAN 196015 |
Vick | Introduced | Leaves | Eliminate phlegm from the chest, headache and flu. | Syrup and infusion; 1 cup 3 x daily and inhale the steam 2 x daily for 7 days. | 0,08 |
| ||||||
(77) Mentha pulegium L. (Lamiaceae), IAN 196016 |
Hortelân grande | Introduced | Leaves | Flu and inflammation of the kidney. | Syrup and infusion; 1 cup 3 x daily and inhale the steam 2 x daily for 7 days. | 0,04 |
| ||||||
(78) Mikania hirsutissima DC. (Asteraceae), IAN 195691 |
Cipó-Sucuriju | Native | Bark | Diarrhea and intestinal infections. | Decoction; 1 cup 3 x daily for 7 days. | 0,03 |
| ||||||
(79) Minquartia guianensis Aubl. (Olacaceae), HAMAB 6910 |
Acapú | Native | Bark | Verminoses. | Decoction and maceration; 1 cup 3 x daily for 7 days. | 0,04 |
| ||||||
(80) Montrichardia linifera (Arruda) Schott (Araceae), IAN 194103 |
Aninga | Native | Leaves and inflorescences | Healing and general inflammation. | Poultry, topical use 2 x daily for 8 days. | 0,09 |
| ||||||
(81) Mora paraensis Ducke (Fabaceae), IAN 195702 |
Pracuúba branca | Native | Bark | Diarrhea, inflammation of the body and irritation of the skin. | Decoction; 1 cup 3 x daily for 7 days. | 0,17 |
| ||||||
(82) Musa balbisiana Colla. (Musaceae), IAN 194111 |
Bananeira | Native | Leaves | Hemorrhage and high blood pressure. | Decoction; 1 cup 3 x daily for 7 days. | 0,06 |
| ||||||
(83) Ocimum basilicum L. (Lamiaceae), IAN 195957 |
Alfavaquinha | Introduced | Leaves | Cough and catarrh in the chest. | Decoction; 1 cup 3 x daily for 7 days. | 0,03 |
| ||||||
(84) Ocimum campechianum Mill. (Lamiaceae), IAN 195974 | Alfavacão | Introduced | Leaves | Cough and catarrh in the chest. | Syrup and infusion; 1 cup 3 x daily and inhale the steam 2 x daily for 7 days. | 0,03 |
| ||||||
(85) Ocimum micranthum Willd. (Lamiaceae), IAN 195969 |
Esturaque | Native | Leaves | Flu, fever and intestinal gas. | Syrup and infusion; 1 cup 3 x daily and inhale the steam 2 x daily for 7 days. | 0,25 |
| ||||||
(86) Ocimum selloi Benth. (Lamiaceae), IAN 196017 |
alfavava cheirosa de anis | Native | Leaves and inflorescences | Intestinal gas, inflammation in the stomach, vomiting, flu and fever. | Decoction; 1 cup 3 x daily for 7 days. | 0,02 |
| ||||||
(87) Ocotea cymbarum Kunth (Lauraceae), IAN 196018 |
louro-mamorim | Native | Bark | Inflammation in the body and muscle pain. | Decoction; 1 cup 3 x daily for 7 days. | 0,04 |
| ||||||
(88) Origanum vulgare L. (Lamiaceae), IAN195970 |
Majerona da angola | Introduced | Leaves and inflorescences | Pains in the body, eliminate phlegm, flu and fever. | Infusion; 1 cup 3 x daily for 8 days. | 0,02 |
| ||||||
(89) Otacanthus azureus (Linden) Ronse (Plantaginaceae), IAN 195972 | Copaibinha | Native | Leaves | Brave wound (leishmaniasis) and inflammation. | Cataplasm, decoction and maceration; 1 cup 2 x daily for 10 days. Topical use 2 x in day for 7 days. | 0,62 |
| ||||||
(90) Ouratea hexasperma (St. Hill.) Benth. (Ochnaceae), IAN 194112 |
Barbatimão | Native | Bark | Rheumatism and inflammation in the stomach. | Decoction; 1 cup 3 x daily for 7 days. | 0,07 |
| ||||||
(91) Parahancornia amapa (Huber) Ducke (Apocynaceae), IAN 196019 |
Leite do amapá | Native | Exsudate | Infections. | Exudate; 1 cup 2 x daily for 7 days. | 0,03 |
| ||||||
(92) Parkia pendula (Willd.) Benth. ex Walp. (Fabaceae), IAN 196010 | Comadre de azeite- visgo | Native | Bark and inflorescences | Skin wounds and bleeding from the skin. | Decoction and maceration; topical use 2 x daily for 7 days. | 0,01 |
| ||||||
(93) Passiflora edulis Sims (Passifloraceae), IAN 195936 |
Maracujá grande | Native | Leaves and bark | Soothing, nervous irritation and inflammation of the stomach. | Decoction; 1 cup 3 x daily for 7 days. | 0,24 |
| ||||||
(94) Passiflora tholozanii Sacco (Passifloraceae), IAN 196004 | Maracujá do mato | Native | Leaves and bark | Brave wound (leishmaniasis), inflammation and soothing. | Decoction; 1 cup 2 x daily for 7 days. | 0,02 |
| ||||||
(95) Pedilanthus tithymaloides Poit. (Euphorbiaceae), IAN 196021 |
Coromina, melhoral | Introduced | Bark | Inflammation in the body and verminoses. | Decoction; 1 cup 2 x daily for 10 days. | 0,04 |
| ||||||
(96) Pentachletra macroloba (Willd.) Kuntze (Fabaceae), IAN 195962 |
Pracaxi | Native | Leaves, inflorescences and bark | Inflammation in the body and verminoses. | Oil; ingest 1 teaspoon 3x a day for 7 days. | 0,83 |
| ||||||
(97) Peperomia pellucida (L.) Kunth (Piperaceae), IAN 195961 | Erva de jaboti | Native | Leaves | Elimination of kidney stones, cough, sore throats and itchy skin. | Decoction; 1 cup 2 x daily for 10 days. | 0,01 |
| ||||||
(98) Petiveria alliaceae L. (Phytolaccaceae), IAN 196022 |
Mucuracaa | Native | Leaves and root | Malaria, pain and phlegm elimination from the chest. | Decoction; 1 cup 2 x daily for 7 days. | 0,36 |
| ||||||
(99) Phyllanthus amarus Schumach. & Thonn. (Phyllanthaceae), IAN 195955 |
Quebra pedra | Native | Aerial parts | Urinary tract pain (Urinary tract infection). | Decoction; 1 cup 2 x daily for 7 days. | 0,03 |
| ||||||
(100) Physalis angulata L. (Solanaceae), IAN 195985 |
Camapú | Native | Root | Anemia and malária. | Decoction; 1 cup 2 x daily for 7 days. | 0,07 |
| ||||||
(101) Platymiscium ulei Harms (Fabaceae), IAN 196023 |
Macacaúba | Native | Bark | Elimination of kidney stones, cough and urinary inflammation. | Decoction; 1 cup 2 x daily for 7 days. | 0,01 |
| ||||||
(102) Plectranthus ornatus Codd. (Lamiaceae), IAN 194114 |
Boldo, boldinho | Introduced | Leaves | Flu, acidity and inflammation of the stomach. | Infusion; 1 cup 2 x daily for 7 days. | 0,26 |
| ||||||
(103) Pogostemon heyneanus Benth. (Lamiaceae), IAN 196024 | Oriza | Introduced | Leaves and inflorescences | Flu, phlegm elimination in the chest and cough. | Syrup and infusion; 1 cup 2 x daily for 10 days. Topical use 2 x in day for 7 days. | 0,01 |
| ||||||
(104) Portulaca pilosa L. (Portulacaceae), IAN 194098 |
Amor crescico | Introduced | Leaves | Pain in urine (urinary tract infection) and verminoses. | Infusion; 1 cup 2 x daily for 7 days. | 0,21 |
| ||||||
(105) Pourouma guianensis Aubl. (Urticaceae), IAN 196025 |
Embaubarana | Native | Bark | Brave wound (leishmaniasis). | Decoction and maceration ingest 1 cup 3 x daily for 7 days Use topic 2 x on day for 7 days. | 0,04 |
| ||||||
(106) Pouteria procera (Mart.) T.D. Penn. (Sapotaceae), IAN 196026 |
Maparajuba | Native | Bark | Verminoses and wounds on the skin. | Decoction ingest 1 cup 2 x daily for 7 days. | 0,04 |
| ||||||
(107) Psidium guajava L. (Myrtaceae), IAN 195950 |
Goiaba | Native | Leaves | Diarrhea, intestinal and renal infections. | Decoction; 1 cup 2 x daily for 7 days. | 0,39 |
| ||||||
(108) Quassia amara L. (Simaroubaceae), IAN 195951 |
Quina | Native | Leaves | Malaria. | Decoction; 1 cup 2 x daily for 7 days. | 0,24 |
| ||||||
(109) Ruta graveolens L. (Rutaceae), IAN 194106 |
Arruda | Introduced | Leaves | Ear pain (ear infection), inflammation in the uterus and skin irritations. | Decoction ingest 1 cup 2 x daily for 7 days. | 0,23 |
| ||||||
(110) Sambucus australis Cham. & Schltdl. (Adoxaceae), IAN 195958 |
Sabugueiro | Native | Leaves and bark | Measles and chicken pox. | Cataplasm and decoction; 1 cup 2 x daily for 7 days. Topical use 2 x a day for 7 days. | 0,02 |
| ||||||
(111) Schinus terebinthifolia Raddi (Anacardiaceae), IAN 194105 | Aroiera branca | Native | Bark | Healing and inflammation. | Decoction; 1 cup 3 x daily for 7 days. Topical use 2 x a day for 7 days. | 0,05 |
| ||||||
(112) Senna reticulata (Willd.) H.S. Irwin & Barneby (Fabaceae), IAN 196027 |
Pacapeá, barajo. | Native | Bark | Elimination of liver stone and rheumatism. | Decoction; 1 cup 3 x daily for 7 days. | 0,18 |
| ||||||
(113) Simaba multiflora A. Juss. (Simaroubaceae), IAN 196028 | Cajurana, Marupaúba. | Native | Bark | Malaria. | Decoction; 1 cup 2 x daily for 7 days. | 0,05 |
| ||||||
(114) Siparuna guianensis Aubl. (Siparunaceae), IAN 195941 | Capitiú | Native | Leaves and bark | Elimination of kidney stones, headache and muscle aches. | Decoction; 1 cup 3 x daily for 7 days. | 0,01 |
| ||||||
(115) Spondias mombin L. (Anacardiaceae), IAN 195999 |
Tapereba | Native | Leaves | Inflammation of the mouth and throat and local massages. | Decoction; 1 cup 2 x daily for 7 days. | 0,44 |
| ||||||
(116) Stryphnodendron adstringens Mart. (Fabaceae), IAN 194113 |
Barbatimão | Native | Bark | Urinary Tract Pain (Kidney Infections). | Decoction and maceration; 1 cup 3 x daily for 7 days. | 0,06 |
| ||||||
(117) Symphonia globulifera L. f (Clusiaceae), IAN 194101 |
Anani | Native | Bark | Anemia and malaria. | Decoction; 1 cup 3 x daily for 7 days. | 0,11 |
| ||||||
(118) Syzygium cumini (L.) Skeels (Myrtaceae), IAN 194097 |
Ameixa | Introduced | Bark | Diarrhea and bleeding. | Decoction; 1 cup 3 x daily for 7 days. | 0,07 |
| ||||||
(119) Terminalia catappa L. (Combretaceae), IAN 195975 |
Castanhola | Introduced | Bark | Malaria. | Decoction; 1 cup 3 x daily for 7 days. | 0,04 |
| ||||||
(120) Theobroma cacau L. (Malvaceae), IAN 195967 |
Cacau | Native | Leaves and seed | Cleaning of body wounds and verminoses. | Decoction and maceration; 1 cup 2 x daily for 7 days. | 0,06 |
| ||||||
(121) Theobroma grandiflorum (Willd. ex Spreng.) K. Schum. (Malvaceae), IAN 195966 |
Cupuaçú | Native | Bark and fruit | High and fortifying body pressure. | Decoction; 1 cup 3 x daily for 7 days. | 0,03 |
| ||||||
(122) Triplaris surinamensis Cham. (Polygonaceae), IAN 195939 | Tachí da várzea | Native | Bark | Rheumatism. | Decoction; 1 cup 3 x daily for 7 days. | 0,04 |
| ||||||
(123) Uncaria guianensis (Aubl.) J.F. Gmel. (Rubiaceae), IAN 196011 | Jupindá vermelho | Native | Leaves and bark | Diarrhea, hemorrhage and cancer. | Decoction; 1 cup 3 x daily for 7 days. | 0,01 |
| ||||||
(124) Uncaria tomentosa (Willd.) DC. (Rubiaceae), IAN 195935 | Jupindá | Native | Leaves and bark | Diarrhea, hemorrhage and cancer. | Decoction; 1 cup 3 x daily for 7 days. | 0,75 |
| ||||||
(125) Unonopsis floribunda Diels (Annonaceae) IAN 195938 | Envira-sangue | Native | Bark | Rheumatism and hemorrhage. | Decoction; 1 cup 3 x daily for 7 days. | 0,04 |
| ||||||
(126) Vatairea guianensis Aubl. (Fabaceae), IAN 196002 |
Fava de bolacha | Native | Bark and seed | Irritation of the skin. | Decoction; 1 cup 3 x daily for 7 days. | 0,05 |
| ||||||
(127) Virola surinamensis (Rol.) Warb. (Myristicaceae), IAN 195963 | Virola | Native | Bark and fruit | Born in the body (furunculosis) and intestinal infections. | Decoction and exudate as poultice; topical use 2 x a day for 7 days. | 0,62 |
| ||||||
(128) Vismia macrophylla Kunth (Clusiaceae), IAN 195986 |
Lacre da folha grande | Native | Bark | Brave wound (leishmaniasis) and skin irritation. | Decoction; 1 cup 2 x daily for 10 days. | 0,04 |
| ||||||
(129) Vitex agnus-castus L. (Lamiaceae), IAN 195968 |
Alecrim de angola, Pau de angola | Introduced | Leaves | Cough and phlegm elimination from the chest. | Syrup; 1 teaspoon 3 times a day for 10 days. | 0,04 |
| ||||||
(130) Zingiber officinale Roscoe (Zingiberaceae), HAMAB 10286 | Gengibre | Introduced | Rhizome | Sore throat (inflammation of the throat) and inflammation in the joints. | Decoction; 1 cup 2 x daily for 7 days. | 0,01 |
Native Species: plant that is natural, own of the region of forest of low várzea.
Species Introduced: a species that is established beyond its natural range, after being transported and introduced intentionally or accidentally by man.
Inventories in Amazonian floodplain forests have shown that Fabaceae has the greatest diversity of species [1, 5, 25, 49, 50]. This fact is demonstrated in this study and is corroborated by Guarado Neto and Moraes [51], who state that when human populations use the native forest for medicinal purposes, the family that has the largest number of species used is the most representative family of the forest.
A study performed by Vásquez et al. [52] at riverside communities of Manacapuru, in the state of Amazonas, reported that 82.7% of the plants used were cultivated, and the family Lamiaceae was the most representative, while in our study the most representative plant family regarding the frequency of citations was Fabaceae. Of the plants cited, 73.07% of them were taken from the forest while 26.93% were cultivated, showing that the people from this community enter the forest to search for the plants.
The “Use” criterion of a species is in the versatility of being mentioned for several therapeutic indications in the community [53, 54]. According to Alexiades [55], the most reliable medicinal uses are those already used by informants, relatives or acquaintances. The species with the highest levels of use agreement and frequency were Carapa guianensis, Pentaclethra macroloba, Dalbergia monetaria, Uncaria tomentosa, Otacanthus azureus, Virola surinamensis, Hura crepitans and Euterpe oleracea. In other studies, carried out in the Brazilian Amazon, the species Carapa guianensis, Pentaclethra macroloba, Uncaria tomentosa, and Virola surinamensis were also the most cited in terms of therapeutic use, demonstrating their regional value and the certainty that these plants may become targets in pharmacological research in the region [56, 57].
3.3. Used Plant Parts
A total of 170 therapeutic preparations were mentioned, and bark, aerial parts, latex, rhizome, leaf, seed, root, flower, inflorescence, and fruit were the parts of the plant used in the preparations. The most used parts were leaf (40%), bark (32.95%), fruits (7.64%), root (4.7%), and inflorescence (4.7%). In the community, parts of the same plant may be used for distinct indications, such as in Carapa guianensis, Pentaclethra macroloba, and Virola surinamensis, whose oil extracted from the seed is used topically in the case of inflammatory processes of the skin, as a repellent and for the healing of wounds, and the leaves and barks are used in oral preparations by decoction for inflammation of the digestive, urinary, and reproductive systems.
The leaves are vegetative structures that stand out in the methods of ethnomedicinal preparations by decoction, maceration, and infusion in traditional communities in Brazil [50, 58, 59] and in other regions of the world [39, 60–63]. One of the reasons is the ease of collection [64] and the production of secondary metabolites present mainly in the leaves [65]. Phytochemical studies with leaves contained flavonoids, tannins, saponins, steroids, and triterpenoids [66, 67]. According to Matos and Matos [68], flavonoids have direct action on capillaries and potentiate ascorbic acid, whose hemorrhagic action and anti-inflammatory action are similar to cortisone. Tannins are used in the treatment of burns, in the recomposition of exposed tissue proteins and in the formation of slightly antiseptic coating [66]. Steroids have important therapeutic properties (cardiotonic, anabolic, contraceptive, and anti-inflammatory) [69]. According to Robbers et al. [70], the triterpenoids have antimicrobial and antitumor action, but some are very toxic to the human body.
3.4. Forms of Ethnomedicinal Preparations
The preparation forms were classified as decoction, infusion, syrup, maceration, oil, hydration water, latex, tincture, and poultice (Table 1). Decoction was the most used form of preparation (59.4%), followed by maceration (11.5%) and infusion (9.7%), and the other six forms of preparation combined corresponded to 19.4%. According to Amorozo and Gély [71] and Lisboa [72], decoction is the most common way of administration home remedies in Amazonian communities. Decoction is performed so that the home remedy is stored in a refrigerator and has more use lifetime. Teas obtained by decoction or infusion are consumed orally and can be used in baths for various types of diseases, including the cultural diseases reported in this work such as “nascida”, “panemeira”, bewitching, evil eye, “úra”, and bubo.
In the community, women collect the fruits of Carapa guianensis (andiroba) and Pentaclethra macroloba (pracaxi), which are dispersed in the water, for the production of medicinal oil, a common management practice to commercialized them in the city of Macapá.
Maceration is a preparation that uses barks, leaves, branches and roots that are immersed in water and/or alcohol, are indicated for inflammation, diarrhea and other intestinal disorders, and are consumed by mouth. In the community, the latex that flows from the trunk of medicinal tree species is applied to wounds, and in this study, it is also collected in medicinal bottles for oral use. According to Viega and Scudeller [73], the use of bark, root, and latex in the preparation of home remedies is known as medicinal bottle, and it is a preparation that is widely disseminated throughout the Amazon and other areas of the world.
3.5. Therapeutic Indications
The riverside residents reported 2103 phytotherapeutic uses for medicinal plants, which were grouped into 16 categories of therapeutic use. For this, the type of body system involved was related to the disease and symptoms, as well as the medicinal species used in the community. It was observed that most of the plants used are related to diseases such as microbial infections (20.67%, 73 species), gastrointestinal disorders (13.31%, 47 species) and inflammations (11.61%, 41 species), emphasizing that 1 specie can be cited for several diseases (Table 2). Studies carried out in traditional communities in Brazil often point to several plant species for problems of the gastrointestinal system, including parasitic diseases and infections caused by microbial agents [57, 74, 75]. These results corroborate studies carried out in communities that do not have basic sanitation in developing countries alongside Latin America [38, 57, 76–79], and this ranking may therefore be related to economic conditions and regional habits as the riparian region studied does not present basic sanitation, and the community uses septic tanks and collects water directly from the river for their essential needs.
Table 2.
Category of therapeutic use | Number of plants used | Cited uses | ICF |
---|---|---|---|
Microbial Infections | 73 | 532 | 0,86 |
| |||
Gastrointestinal disorders | 47 | 412 | 0,89 |
| |||
Inflammatory disorders | 41 | 321 | 0,88 |
| |||
Pain, fever, cold | 25 | 167 | 0,86 |
| |||
Malaria | 25 | 90 | 0,73 |
| |||
Cardiovascular disorders | 24 | 79 | 0,71 |
| |||
Parasites | 23 | 66 | 0,66 |
| |||
Respiratory Infections | 23 | 111 | 0,86 |
| |||
Rheumatism | 23 | 49 | 0,54 |
| |||
Disorders of the Nervous System | 11 | 45 | 0,77 |
| |||
Renal, hepatic and biliary disorders | 9 | 30 | 0,72 |
| |||
Healing | 8 | 41 | 0,83 |
| |||
Leishmaniasis | 8 | 74 | 0,9 |
| |||
Cancer | 5 | 58 | 0,93 |
| |||
Gynecological disorders | 5 | 12 | 0,64 |
| |||
Metabolic Diseases | 3 | 16 | 0,87 |
Leão et al. [80] performed an ethnobotanical survey in Santa Barbara, state of Pará. Similarly to this study, the authors observed that the major diseases and symptoms treated by the community were gastrointestinal disorders, microbial infections, and inflammations. This was also reported in other study by Amorozo [58].
In this study, the species Carapa guianensis (100%), Pentaclethra macroloba (90-92%), Dalbergia monetaria (78-85%), Uncaria tomentosa (80-82%), Virola surinamensis (43-68%), Otacanthus azureus (66%), Hura crepitans (41-64%), and Euterpe oleracea (41-56%) (Figure 2) are widely used by the riverside community to treat microbial infections, gastrointestinal disorders, inflammatory conditions, leishmaniasis, and cancer, as seen by the use agreement index (Table 3). According to Vendruscolo and Mentz [53], this index indicates the most promising species to perform pharmacological researches according to their use.
Table 3.
Category of therapeutic use | Scientific Name | NF | FC | Pcusp |
---|---|---|---|---|
Microbial Infections | Carapa guianensis | 100 | 1 | 100 |
Hura crepitans | 100 | 0,64 | 64 | |
Otacanthus azureus | 96,7 | 0,68 | 66 | |
Uncaria tomentosa | 97,2 | 0,82 | 80 | |
Pentaclethra macroloba | 100 | 0,92 | 92 | |
Copaifera sp. | 100 | 1 | 100 | |
Dalbergia monetaria | 92,3 | 0,85 | 78 | |
| ||||
Gastrointestinal disorders | Euterpe oleracea | 89,8 | 0,62 | 56 |
Carapa guianensis | 100 | 1 | 100 | |
Uncaria tomentosa | 100 | 0,82 | 82 | |
Spondias mombin | 100 | 0,48 | 48 | |
Dalbergia monetaria | 100 | 0,85 | 85 | |
Virola surinamensis | 100 | 0,68 | 68 | |
| ||||
Inflammatories disorders | Carapa guianensis Aubl. | 100 | 1 | 100 |
Uncaria tomentosa | 92,1 | 0,82 | 76 | |
Pentachletra macroloba | 97,5 | 0,92 | 90 | |
Dalbergia monetaria | 100 | 0,85 | 85 | |
Virola surinamensis | 79,3 | 0,54 | 43 | |
Copaifera sp. | 100 | 1 | 100 | |
| ||||
Pain, Fever, Cold | Plectranthus ornatus | 92,1 | 0,82 | 76 |
Eleutherine bulbosa | 97,5 | 0,92 | 90 | |
Origanum vulgare | 100 | 0,85 | 85 | |
Petiveria alliacea | 79,3 | 0,54 | 43 | |
Jatropha curcas | 92,1 | 0,82 | 76 | |
| ||||
Malaria | Symphonia globulifera | 100 | 0,85 | 85 |
Parkia pendula | 97,5 | 0,92 | 90 | |
Petiveria alliacea | 100 | 0,68 | 68 | |
Maquira coriacea | 92,1 | 0,82 | 76 | |
Arrabidaea chica | 100 | 0,85 | 85 | |
Quassia amara | 100 | 0,68 | 68 | |
Sambucus australis | 92,1 | 0,82 | 76 | |
| ||||
Cardiovascular disorders | Minquartia guianensis | 92,1 | 0,82 | 76 |
Licania macrophylla | 97,5 | 0,92 | 90 | |
Croton urucurana | 100 | 0,85 | 85 | |
Arrabidaea chica | 79,3 | 0,54 | 43 | |
Jatropha curcas | 92,1 | 0,82 | 76 | |
| ||||
Parasites | Portulaca pilosa | 92,1 | 0,82 | 76 |
Symphonia globulifera | 97,5 | 0,92 | 90 | |
Cedrela odorata | 100 | 0,85 | 85 | |
Eleutherine bulbosa | 79,3 | 0,54 | 43 | |
Arrabidaea chica | 77,1 | 0,44 | 34 | |
| ||||
Respiratory Infections | Gossypium hirsutum | 92,1 | 0,82 | 76 |
Adenocalymna alliaceum | 97,5 | 0,92 | 90 | |
Mentha pulegium | 100 | 0,85 | 85 | |
Eupatorium triplinerve | 79,3 | 0,54 | 43 | |
Citrus limonum | 96,4 | 0,32 | 31 | |
Ocimum campechianum | 92,3 | 0,28 | 26 | |
Chenopodium ambrosioides | 78,6 | 0,13 | 10 | |
| ||||
Rheumatism | Justicia pectoralis | 60 | 0,14 | 8 |
Carapa guianensis | 100 | 1 | 100 | |
Siparuna guianensis | 92,1 | 0,82 | 76 | |
Ocotea cymbarum | 97,5 | 0,92 | 90 | |
Petiveria alliacea | 100 | 0,85 | 85 | |
Copaifera sp. | 100 | 1 | 100 | |
| ||||
Disorders of the Nervous System | Aeollanthus suaveolens | 92,1 | 0,82 | 76 |
Genipa americana | 97,5 | 0,92 | 90 | |
Hypericum perforatum | 100 | 0,85 | 85 | |
Cítrus aurantium | 79,3 | 0,54 | 43 | |
Passiflora tholozanii | 100 | 0,02 | 2 | |
Passiflora edulis | 95,8 | 0,27 | 26 | |
Eleutherine bulbosa | 70,6 | 0,14 | 10 | |
| ||||
Renal, hepatic and biliary disorders | Alternanthera brasiliana | 92,1 | 0,82 | 76 |
Senna reticulata | 97,5 | 0,92 | 90 | |
Arrabidaea chica | 100 | 0,85 | 85 | |
Phyllanthus amarus | 79,3 | 0,54 | 43 | |
Croton cajucara | 33,3 | 0,01 | 0 | |
| ||||
Healing | Portulaca pilosa | 92,1 | 0,82 | 76 |
Montrichardia linifera | 97,5 | 0,92 | 90 | |
Macrolobium acaciifolium | 100 | 0,85 | 85 | |
Eleutherine bulbosa | 79,3 | 0,54 | 43 | |
Jatropha curcas | 16,7 | 0,07 | 1 | |
| ||||
Leishmaniasis | Hura crepitans | 79,6 | 0,51 | 41 |
Otacanthus azureus | 96,7 | 0,68 | 66 | |
Pourouma guianensis | 92,1 | 0,82 | 76 | |
Gustavia augusta | 97,5 | 0,92 | 90 | |
Vismia macrophylla | 100 | 0,85 | 85 | |
Passiflora tholozanii | 79,3 | 0,54 | 43 | |
Eleutherine bulbosa | 70,6 | 0,14 | 10 | |
| ||||
Cancer | Alternanthera brasiliana | 52,6 | 0,12 | 6 |
Hura crepitans | 94,7 | 0,64 | 61 | |
Uncaria tomentosa | 97,1 | 0,8 | 78 | |
Uncaria guianensis | 92,1 | 0,82 | 76 | |
Maquira coriacea | 97,5 | 0,92 | 90 | |
Passiflora tholozanii | 100 | 0,85 | 85 | |
| ||||
Gynecological disorders | Hura crepitans | 79,3 | 0,54 | 43 |
Copaifera sp. | 100 | 1 | 100 | |
Uncaria tomentosa | 97,1 | 0,8 | 78 | |
Uncaria guianensis | 50 | 0,01 | 1 | |
Carapa guianensis | 100 | 1 | 100 | |
Pentachletra macroloba | 97,5 | 0,92 | 90 | |
Dalbergia monetaria | 100 | 0,85 | 85 | |
| ||||
Metabolic Diseases | Euterpe oleracea | 81,1 | 0,51 | 41 |
Arrabidaea chica | 100 | 0,85 | 85 | |
Croton cajucara | 79,3 | 0,54 | 43 |
Ethnopharmacological studies performed with the species C. guianensis, P. macroloba, D. monetaria, and U. tomentosa show that species are popularly used to treat abscesses, asthma, skin diseases, infectious diseases, deep wounds, gastritis, inflammations, gastric ulcer [16, 23, 44, 80]. Currently, this is being confirmed experimentally in studies with the oil from the seeds of C. guianensis that show its anti-inflammatory activity [35, 80], antiallergic activity [81–83], and wound-healing activity [84, 85]. Also, phytochemical studies attribute anti-inflammatory and antiallergic activity to the tetranortriterpenoids, main molecules of C. guianensis oil [86]. The same occurs with U. tomentosa, whose extract is reported to have antimicrobial, anti-inflammatory and anticancer activity in vitro and in vivo [87]; this is due to the presence of alkaloids, triterpenic heterosides, and polyphenols, mainly tannins [88–90].
The species P. macroloba has some medicinal application against snakebites. Triterpenic saponins isolated from its fruit were reported to be effective against snake venom [91]. Also, the essential oil of O. azureus has bactericidal, antioxidant [92], antifungal [93], and leishmanicidal activity [94]. However, the species D. monetaria, V. surinamensis, O. azureus, H. crepitans, and E. oleracea still need further in vitro and in vivo pharmacological research to corroborate their use in folk medicine.
Of the informants, 100% believe in the efficacy of medicinal plants in common diseases such as fever, diarrhea, and infections and prefer to use them because they understand that there are no side effects and because it is a therapeutic resource free of cost and easily obtainable in the community; however, when serious complications result from malaria and heart disease, they prefer drugs from the pharmacy because they works faster.
3.6. Comparison of the Different Indices
In this study, UVs between 0.91 and 0.56 were from native medicinal plants that are frequently used as an ethnomedicinal resource by the riparians: Carapa guianensis (0.91), Pentachletra macroloba (0.83), Dalbergia monetaria (0.77), Uncaria tomentosa (0.75), Otacanthus azureus (0.62), Virola surinamensis (0.62), Hura crepitans (0.58), and Euterpe oleracea (0.56). These species were the most versatile in the therapeutic preparations and obtained a use index ranging from 100% to 56%; they also were the most frequent in the study area, with a loyalty index of 100% for a specific therapeutic use (Table 1). The most important species for a community are those that have the highest Use Value, and they should be prioritized for conservation [95].
The species Carapa guianensis and Uncaria tomentosa have been among the most phytochemically studied species in recent years. Studies show that C. guianensis (andiroba) oil has anti-inflammatory [35, 95], antiparasitic [96], antispasmodic [97], repellent, antiallergic, antirheumatic and healing properties [98]. Pharmacological tests performed in vitro and in vivo with U. tomentosa (jupindá) showed antioxidant [99], anticancer [100], anti-inflammatory [101], antimicrobial [102], antiherpetic [103] and antidiabetic [104] activities. In turn, Pentaclethra macroloba, Virola surinamensis, Dalbergia monetaria, Otacanthus azureus, Virola surinamensis, Hura crepitans, and Euterpe oleracea are little known pharmacologically.
Eight floodland forest native species are mentioned for the first time in an ethnobotanical study in the region, and no pharmacological studies have been found for Allamanda cathartica (0.01), which is used for the treatment of intestinal parasites; Astrocaryum murumuru (0.01), used for the treatment of eye infections of dogs and skin irritations of other animals; Calophyllum brasiliense (0.01), used for joint inflammations and skin ulcers; Passiflora tholozanii (0.02), used for leishmaniasis ulcers, cancer, depression and soothing; Manicaria saccifera (0.04), used for gastritis; Pourouma guianensis (0.04), used for leishmaniasis joint inflammation and ulcers; Triplaris surinamensis (0.04), used for the treatment of joint inflammation; and Unonopsis floribunda (0.04), used for joint and stomach inflammation. Although many species are reported for the treatment of the diseases mentioned, these species deserve attention because the region is going through a rural exodus, and people with this knowledge are decreasing in number and have no successors of that knowledge, which is traditionally passed by word of mouth.
The Informant Consensus Factor (ICF) was calculated for 16 categories of therapeutic uses (Table 2). Leishmaniasis is endemic in the riverside area and recorded an ICF value of 0.9, followed by cancer (0.93), gastrointestinal disorders such as diarrhea, vomiting, and gastritis (0.89), inflammation in the uterus and burns (0.88), diabetes and albumin (0.87), and microbial, respiratory infections and pain, fever and cold symptoms (0.86); these include diseases such as itching, uterine infections, body aches, insect bites, flu, catarrh in the chest and cough. Nervous system disorders such as epilepsy, convulsions and depression had ICF values of 0.77; malaria, 0.73; renal and bile calculi, 0.72; infarction, bleeding, and high blood pressure, 0.71; followed by verminoses, 0.66; gynecological problems after childbirth, 0.64; and joint inflammation, 0.54.
High ICF values clearly showed that the community uses medicinal plants for their health problems and that there are well-defined choice criteria, which are shared orally [48, 105]. A total of 73 medicinal plants were used for microbial infections, followed by 47 that are referred for the gastrointestinal system and 41 for general inflammation in the body. According to the interviewees, the therapeutic use of plants in the community is the first alternative for the treatment of health problems, and in many cases, it constitutes the only immediate resource for this purpose, as there are difficulties in accessing allopathic medicines because they live far from urban centers, have small boats as transportation means, which are called “rabetas”, and do not have public health units for simple clinical care for diarrhea, headaches and infections. According to Lima et al. [106], the rich traditional knowledge of communities living in isolation in the Amazon arises from the need to have an alternative therapeutic treatment, caused by the limited access to the public health network and the great cultural influence of these peoples.
In the study, the floodland forest native species with the highest values of relative importance, for the treatment of the most frequent diseases in the community, are as follows (Table 3): Carapa guianensis, Hura crepitans, Otacanthus azureus Uncaria tomentosa, Uncaria guianensis, Pentaclethra macroloba, Copaifera sp., Dalbergia monetaria, Spondias mombin, Virola surinamensis, Symphonia globulifera, Parkia pendula, Maquira coriacea, Croton urucurana, Quassia amara, Genipa americana, Vismia macrophylla, Gustavia augusta, and Passiflora tholozanii. They are the most versatile because they can be used in various therapeutic treatments.
4. Conclusion
This is a pioneer study of the riparian community in flooded areas of Mazagão, and it shows that knowledge about plants and their medicinal uses is diverse and widespread in the community, likely because of the high incidence of tropical diseases such as malaria and leishmaniasis as well as the difficulty in accessing medicines distributed by the government and easy access to local plants. The riparians listed 130 ethnospecies, of which 95 are mostly native trees of lowland forest. In the study, the residents showed that they use conservation practices such as not annealing the individuals when collecting bark/bast; in addition, after extracting medicinal oil from the copaiba trunk, they always allow one year for the plant to recover, and if needed, they search for another trunk so as to not to exhaust the resource. They also collect Carapa guianensis (andiroba) and Pentachletra macroloba (pracaxi) fruits, which are dispersed in the water, for extraction of the medicinal oil, which is marketed in urban areas. Residents report that they have a potential consumer market for these medicinal oils and that organization is lacking to make the production of this oil profitable. Therefore, native medicinal species should be prioritized for conservation, as riparians depend on the collection of these plants as the main drugs for the region's endemic and cultural diseases; furthermore, these plants may be used for future pharmacological studies. Studies of this nature reinforce the importance of the relationship between the community and biodiversity, valuing, and bringing visibility to the ethnobotanical and ethnopharmacological knowledge they possess. The systematization of knowledge about these resources rescues popular knowledge, contributing not only to the conservation of diversity but also to the preservation of a rich and important cultural heritage.
Acknowledgments
The authors would like to thank CAPES (no. 3292/2013 AUXPE) and CNPq Proc. 407768/2013-0 (RAPBioFar) for the financial support.
Data Availability
All data generated and analyzed to support this study are included in this published article. The project was submitted to the Ethics Research Committee of the Faculdade Estácio de Macapá (http://aplicacao.saude.gov.br/plataformabrasil/login.jsf, under the opinion no. 14.94.994). And the complete information of the individual interviews could be requested from the corresponding authors.
Conflicts of Interest
The authors declare that there are no conflicts of interest regarding the publication of this paper.
References
- 1.Wittmann F., Schongart J., Brito J. M., et al. Manual of Trees from Central Amazonian Várzea Floodplains: Taxonomy, Ecology and Use. INPA; 2010. [Google Scholar]
- 2.Almeida S. S., Amaral D. D., Silva A. S. Análise florística e estrutura de florestas de várzea no estuário amazônico. Acta Amazonica. 2004;34(4):513–524. doi: 10.1590/S0044-59672004000400005. [DOI] [Google Scholar]
- 3.Queiroz J. A. L., Mochiutti S. Cultivo de açaizeiros e manejo de açaizais para a produção de frutos. Embrapa Amapá. 2001 [Google Scholar]
- 4.Martins A. G., Rosário D. L., Barros M. N., Jardim M. A. G. Levantamento etnobotânico de plantas medicinais, alimentares e tóxicas da ilha do Combu, município de Belém, estado do Pará, Brasil. Revista Brasileira de Farmácia. 2005;86(1):21–30. [Google Scholar]
- 5.Rodrigues L. M. B., Lira A. U. S., Santos F. A., Jardim M. A. G. Composição florística e uso das espécies vegetais em dois ambientes de florestas de várzea. Revista Brasileira de Farmácia. 2006;87(2):45–48. [Google Scholar]
- 6.Pinto E. P. P., Amorozo M. C. M., Furlan A. Conhecimento popular sobre plantas medicinais em comunidades rurais de mata atlântica - Itacaré, BA, Brasil. Acta Botanica Brasilica. 2006;20(4):751–762. doi: 10.1590/S0102-33062006000400001. [DOI] [Google Scholar]
- 7.Albuquerque U. P., Andrade L. D. H. C. Conhecimento botânico tradicional e conservação em uma área de caatinga no estado de Pernambuco, Nordeste do Brasil. Acta Botanica Brasilica. 2002;16(3):273–285. doi: 10.1590/s0102-33062002000300004. [DOI] [Google Scholar]
- 8.Ribeiro A. S., Palha M. d., Tourinho M. M., Whiteman C., Silva A. d. Utilização dos recursos naturais por comunidades humanas do Parque Ecoturístico do Guamá, Belém, Pará. Acta Amazonica. 2007;37(2):235–240. doi: 10.1590/S0044-59672007000200009. [DOI] [Google Scholar]
- 9.Oliveira F. G. S., Lehn C. R. Riscos e perspectivas na utilização de fitoterápicos no Brasil. Opará: Etnicidades, Movimentos Sociais e Educação, Paulo Afonso. 2015;3(4):35–44. [Google Scholar]
- 10.Pinto L. N., Flor A. S. O., Barbosa W. L. R. Fitoterapia popular na Amazônia Paraense: uma abordagem no município de Igarapé-Mirí, estado do Pará nos anos de 2000 e 2008. Revista Ciências Farmacêuticas Básica Aplicada. 2011;35(2):305–311. [Google Scholar]
- 11.Calixto J. B. Twenty-five years of research on medicinal plants in Latin America: a personal view. Journal of Ethnopharmacology. 2005;100(1-2):131–134. doi: 10.1016/j.jep.2005.06.004. [DOI] [PubMed] [Google Scholar]
- 12.Firmo W. D. C., Menezes V. A. M., Passos C. E. D. C., et al. Contexto histórico, uso popular e concepção científica sobre plantas medicinais. Caderno de Pesquisa. 2011;18(especial):90–95. [Google Scholar]
- 13.Véronique B. Passado Português, presente negro e indizibilidade ameríndia: o caso de MazagãoVelho, Amapá. Religião & Sociedade. 2008;28(2):11–29. doi: 10.1590/S0100-85872008000200002. [DOI] [Google Scholar]
- 14.de Assunção P. Revista eletrônica de Arquitetura e Urbanismo. Vol. 1. São Paulo, Brazil: Universidade São Judas Tadeu; 2009. Mazagão: cidades em dois continentes; pp. 22–55. [Google Scholar]
- 15.Silva A. C. D., Custódio E. S., Foster E. D. L. S. Intangible cultural heritage and religiosity: Celebrations in the Mazagão Velho, in the state of Amapá. Estudos Teológicos. 2015;55(2):388–403. [Google Scholar]
- 16.Laurent V. Mazagão a cidade que atravessou o Atlântico: do Marrocos à Amazônia, (1769-1783) São Paulo, Brazil: Martins Fontes; 2008. [Google Scholar]
- 17.Sant’Ana D. A. C. O Mito Moderno da Natureza Intocada. São Paulo, Brazil: Hucitec NAPUB USP; 2008. [Google Scholar]
- 18.Lomba R. M. Modos de vida ribeirinho na comunidade Foz do Rio Mazagão – Mazagão (AP/Brasil) Ateliê Geográfico. 2017;11(1):257–276. doi: 10.5216/ag.v11i1.35381. [DOI] [Google Scholar]
- 19.de Mendonça M. S., de Souza M. A. D., Cassino M. F., et al. Plantas medicinais usadas por comunidades ribeirinhas do médio Rio Solimões, Amazonas: identificação, etnofarmacologia e caracterização estrutural. Universidade Federal do Amazonas; 2014. [Google Scholar]
- 20.Silva R. B. L. Diversidade, uso e manejo de quintais agroflorestais no Distrito do Carvão, Mazagão-AP, Brasil [PhD thesis] Belém, Brazil: Universidade Federal do Pará; 2010. [Google Scholar]
- 21.Nascimento E. S. Levantamento dos conhecimentos etnobotânicos de comunidades ribeirinhas do estuário amapaense. Macapá, Brasil: Universidade Federal do Amapá; 2011. [Google Scholar]
- 22.dos Santos-Silva J. P. G., de Oliveira P. C. Ethnobotany of Medicinal Plants in the Low Land Community Igarapé do Costa, SantarémPará, Brazil. Ambiente y Sostenibilidad. 2016;2016(6):136–151. [Google Scholar]
- 23.Vásques S. P. F., Mendonça M. S., Noda S. N., Vásques S. P. F., Mendonça M. S. Etnobotânica de plantas medicinais em comunidades ribeirinhas do Município de Manacapuru, Amazonas, Brasil. Acta Amazônica. 2014;44(4):457–472. doi: 10.1590/1809-4392201400423. [DOI] [Google Scholar]
- 24.IBGE. Instituto Brasileiro de Geografia e Estatística. censo populacional; 2010. http://www.ibge.gov.br. [Google Scholar]
- 25.Carim M. J. V. C., Jardim M. A. G., Medeiros T. D. S. Composição florística e estrutura da floresta de várzea no município de Mazagão, Estado do Amapá, Brasil. Scientia Forestalis. 2008;36(79):191–201. [Google Scholar]
- 26.Pinto A. C., Simas A. P. S. C., Tardin A. T., et al. Instituto de Pesquisas Científicas e Tecnológicas do Estado do Amapá. Brasil: Macapá; 2002. Macrodiagnóstico do Estado do Amapá: Primeira aproximação do zoneamento econômico ecológico. [Google Scholar]
- 27.Wittmann F., Schöngart J., Montero J. C., et al. Tree species composition and diversity gradients in white-water forests across the Amazon Basin. Journal of Biogeography. 2006;33(8):1334–1347. doi: 10.1111/j.1365-2699.2006.01495.x. [DOI] [Google Scholar]
- 28.Wittmann F., Schöngart J., Junk W. J. Phytogeography, species diversity, community structure and dynamics of Central Amazonian floodplain forests. Amazonian Floodplain Fororest. 2010;210:61–102. doi: 10.1007/978-90-481-8725-6_4. [DOI] [Google Scholar]
- 29.IBGE. Manual técnico da vegetação brasileira. Rio de janeiro, Brazil: IBGE; 2012. Instituto Brasileiro de Geografia e Estatística. [Google Scholar]
- 30.Carim J. V. M., Wittmann M. F. K., Piedade M. T. F., Guimarães J. R. S., Tostes L. C. L. Composition, diversity, and structure of tidal "Várzea" and "Igapó" floodplain forests in eastern Amazonia, Brazil. Brazilian Journal of Botany. 2017;40(1):115–124. doi: 10.1007/s40415-016-0315-6. [DOI] [Google Scholar]
- 31.Rabelo B. V. Mazagão: Realidades Que Devem Ser Conhecidas. Macapá, Brasil: IEPA; 2005. [Google Scholar]
- 32.Pinto E. R. Solos, hidrologia e estrutura populacional de pracuubeiras em florestas de várzea do estuário amazônico. Macapá, Brazil: Universidade Federal do Amapá; 2014. [Google Scholar]
- 33.Albuquerque U. P., Lucena R. F. P. Livro Rápido/Núcleo de Publicações em Ecologia e Etnobotânica Aplicada. Recife, Brazil: Pernambuco; 2004. Methods and techniques in the etnobotany research. [Google Scholar]
- 34.Fidalgo O., Bononi L. R. Técnica de coleta, preservação e herborização de material botânico. São Paulo, Brasil: Instituto de Botânica; 1989. [Google Scholar]
- 35.Lorenzi H., Matos F. J. A. Plantas Medicinais no Brasil: nativas e exóticas cultivadas. Nova Odessa, Brasil: Instituto Plantarum; 2008. [Google Scholar]
- 36.Angiosperm Phylogeny Group (APG) An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV. Botanical Journal of the Linnean Society. 2016;181:1–20. [Google Scholar]
- 37.Carneiro A. M., Irgang B. E. Origem e distribuição geográfica das espécies ruderais da Vila de Santo Amaro, General Câmara, Rio Grande do Sul. Iheringia, Série Botânica. 2005;60(2):175–188. [Google Scholar]
- 38.Phillips O., Gentry A. H. The useful plants of Tambopata, Peru: I. Statistical hypotheses tests with a new quantitative technique. Economic Botany. 1993;47(1):15–32. doi: 10.1007/BF02862203. [DOI] [Google Scholar]
- 39.Morvin Yabesh J. E., Prabhu S., Vijayakumar S. An ethnobotanical study of medicinal plants used by traditional healers in silent valley of Kerala, India. Journal of Ethnopharmacology. 2014;154(3):774–789. doi: 10.1016/j.jep.2014.05.004. [DOI] [PubMed] [Google Scholar]
- 40.Kichu M., Malewska T., Akter K., et al. An ethnobotanical study of medicinal plants of Chungtia village, Nagaland, India. Journal of Ethnopharmacology. 2015;166:5–17. doi: 10.1016/j.jep.2015.02.053. [DOI] [PubMed] [Google Scholar]
- 41.Troter R. T., Logan M. H. Informant consensus: a new approach for identifying potentially effective medicinal plants. In: Etkin N. L., editor. Plants in Indigenous Medicine and Diet. New York, NY, USA: Redgrave Publishing Company; 1986. pp. 91–112. [Google Scholar]
- 42.Friedman J., Yaniv Z., Dafni A., Palewitch D. A preliminary classification of the healing potential of medicinal plants, based on a rational analysis of an ethnopharmacological field survey among Bedouins in the Negev Desert, Israel. Journal of Ethnopharmacology. 1986;16(2-3):275–287. doi: 10.1016/0378-8741(86)90094-2. [DOI] [PubMed] [Google Scholar]
- 43.Da Silva V. A., Andrade L. D., De Albuquerque U. P. Revising the Cultural Significance Index: The case of the Fulnio in Northeastem Brazil. Field Methods. 2016;18(1):98–108. doi: 10.1177/1525822X05278025. [DOI] [Google Scholar]
- 44.Pasa M. C., Ávila G. d. Ribeirinhos e recursos vegetais: a etnobotânica em Rondonópolis, Mato Grosso, Brasil. Interações (Campo Grande) 2010;11(2):195–204. doi: 10.1590/S1518-70122010000200008. [DOI] [Google Scholar]
- 45.Brasileiro B. G., Pizziolo V. R., Matos D. S., Germano A. M., Jamal C. M. Plantas medicinais utilizadas pela população atendida no "Programa de Saúde da Família", Governador Valadares, MG, Brasil. Revista Brasileira de Ciências Farmacêuticas. 2008;44(4):629–636. doi: 10.1590/S1516-93322008000400009. [DOI] [Google Scholar]
- 46.Elisabetsky E. Etnofarmacologia. Ciência e Cultura. Campinas. 2003;55(3):35–36. [Google Scholar]
- 47.Hanazaki N., Tamashiro J. Y., Leitão-Filho H. F., Begossi A. Diversity of plant use in two caiçara communities from the Atlantic Forest coast, Brazil. Biodiversity and Conservation. 2000;9(5):597–615. doi: 10.1023/a:1008920301824. [DOI] [Google Scholar]
- 48.Negrelle R. R. B., Fornazzari K. R. C. Estudo etnobotânico em duas comunidades rurais (Limeira e Ribeirão Grande) de Guaratuba (Paraná, Brasil) Revista Brasileira de Plantas Medicinais. 2007;9(2):36–54. [Google Scholar]
- 49.Queiroz J. A. L., Mochiutti S., Machado A. S., Galvão F. Composição florística e estrutura de floresta em várzea alta estuarina amazônica. Revista Floresta. 2005;35(1):41–56. doi: 10.5380/rf.v35i1.2430. [DOI] [Google Scholar]
- 50.Ming L. C., Amaral J. A. Aspectos etnobotânicos de plantas medicinais na reserva extrativista "Chico Mendes". The New York Botanical Garden. 2015 http://www.nybg.org/bsci/acre/www1/medicinal.html. [Google Scholar]
- 51.Guarim Neto G., Morais R. G. Recursos medicinais de espécies do Cerrado de Mato Grosso: um estudo bibliográfico. Acta Botanica Brasilica. 2003;17(4):561–584. doi: 10.1590/S0102-33062003000400009. [DOI] [Google Scholar]
- 52.Vásquez S. P., Mendonça M. S., Noda S. d. Etnobotânica de plantas medicinais em comunidades ribeirinhas do Município de Manacapuru, Amazonas, Brasil. Acta Amazonica. 2014;44(4):457–472. doi: 10.1590/1809-4392201400423. [DOI] [Google Scholar]
- 53.Vendruscolo G. S., Mentz L. A. Estudo da concordância das citações de uso e importância das espécies e famílias utilizadas como medicinais pela comunidade do bairro Ponta Grossa, Porto Alegre, RS, Brasil. Acta Botanica Brasilica. 2006;20(2):367–382. doi: 10.1590/S0102-33062006000200012. [DOI] [Google Scholar]
- 54.Santos-Silva J. P. G., Oliveira P. C. Ethnobotany of Medicinal Plants in the Low Land Community Igarapé do Costa, Santarém–Pará, Brazil. Revista del Doctorado Interinstitucional en Ciencias Ambientales: Ambiente y Sostenibilidad. 2016;6:136–151. doi: 10.25100/ays.v0i0.4295. [DOI] [Google Scholar]
- 55.Alexiades M. N., Sheldon J. W. Selected Guidelines for Ethnobotanical Research: A Field Manual. Bronx, NY, USA: Institute of Economic Botany, The New York Botanical Garden; 1996. [Google Scholar]
- 56.Miranda E. M., Sousa J. A., Pereira R. C. A. Caracterização e avaliação de populações nativas de unha-de-gato [Uncaria tomentosa (Willd.) D.C. e Uncaria guianensis (Aubl.) Gmel.] no vale do rio Juruá-AC. Revista Brasileira de Plantas Medicinais. 2003;5(2):41–46. [Google Scholar]
- 57.Filocreão A. S., Galindo A. G., Dos Santos T. D. Fitoterapia na Amazônia: a experiência do estado do Amapá-Brasil. Desenvolvimento e Meio Ambiente. 2017;40 doi: 10.5380/dma.v40i0.43655. [DOI] [Google Scholar]
- 58.Amorozo M. C. Uso e diversidade de plantas medicinais em Santo Antonio do Leverger, MT, Brasil. Acta Botanica Brasilica. 2002;16(2):189–203. doi: 10.1590/S0102-33062002000200006. [DOI] [Google Scholar]
- 59.Guarim Neto G., Morais R. G. Recursos medicinais de espécies do Cerrado de Mato Grosso: Um estudo Bibliografico. Acta Botanica Brasilica. 2003;17(4):561–584. doi: 10.1590/S0102-33062003000400009. [DOI] [Google Scholar]
- 60.Sadat-Hosseini M., Farajpour M., Boroomand N., Solaimani-Sardou F. Ethnopharmacological studies of indigenous medicinal plants in the south of Kerman, Iran. Journal of Ethnopharmacology. 2017;199:194–204. doi: 10.1016/j.jep.2017.02.006. [DOI] [PubMed] [Google Scholar]
- 61.Ayyanar M., Ignacimuthu S. Ethnobotanical survey of medicinal plants commonly used by Kani tribals in Tirunelveli hills of Western Ghats, India. Journal of Ethnopharmacology. 2011;134(3):851–864. doi: 10.1016/j.jep.2011.01.029. [DOI] [PubMed] [Google Scholar]
- 62.Amri E., Kisangau D. P. Ethnomedicinal study of plants used in villages around Kimboza forest reserve in Morogoro, Tanzania. Journal of Ethnobiology and Ethnomedicine. 2012;8(1) doi: 10.1186/1746-4269-8-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63.Gidey Y., Mekonen T., Mezgebe K. Survey of medicinal plants used to treat human ailments in Hawzen district, Northern Ethiopia. International Journal of Biodiversity and Conservation. 2011;3(13):709–714. [Google Scholar]
- 64.Giday M., Asfaw Z., Woldu Z. Medicinal plants of the Meinit ethnic group of Ethiopia: an ethnobotanical study. Journal of Ethnopharmacology. 2009;124(3):513–521. doi: 10.1016/j.jep.2009.05.009. [DOI] [PubMed] [Google Scholar]
- 65.Ghorbani A. Studies on pharmaceutical ethnobotany in the region of Turkmen Sahra, north of Iran (part 1): general results. Journal of Ethnopharmacology. 2005;102(1):58–68. doi: 10.1016/j.jep.2005.05.035. [DOI] [PubMed] [Google Scholar]
- 66.Braca A., Sortino C., Politi M., Morelli I., Mendez J. Antioxidant activity of flavonoids from Licania licaniaeflora. Journal of Ethnopharmacology. 2002;79(3):379–381. doi: 10.1016/S0378-8741(01)00413-5. [DOI] [PubMed] [Google Scholar]
- 67.de Carvalho M. G., de Oliveira Cândido L. F., Da Costa P. M., Rumjanek V. M. Chromones from Licania arianeae (Chrysobalanaceae) Natural Product Research (Formerly Natural Product Letters) 2005;19(1):7–12. doi: 10.1080/14786410410001730265. [DOI] [PubMed] [Google Scholar]
- 68.Matos J. M. D., Matos M. E. O. Farmacognosia Curso teórico-prático. Fortaleza, Brazil: UFC, Edições; 1989. [Google Scholar]
- 69.Mendes B., VenΓncio C. M. N., Jardim M. A. G., da Silva J. C., Venâncio C. M. N. Informações fitoterápicas e composição química de Mikania lindleyana DC. (Asteraceae) Revista Brasileira de Farmácia. 2002;83(1):27–29. [Google Scholar]
- 70.Robbers J. E., Speedie M. K., Tyler V. E. Farmacognosia Biotecnologia. Editorial Premier. São Paulo. 1997 [Google Scholar]
- 71.Amorozo M. C. M., Gély A. L. Uso de plantas medicinais por caboclos do baixo Amazonas, Barcarena, PA, Brasil. Boletim do Museu Paraense Emílio Goeldi. Nova Série Botânica. 1998;4(1):47–131. [Google Scholar]
- 72.Lisboa P. L. B. Caxiuanã: Populações Tradicionais, Meio Físico e Diversidade Biológica. Belém, PA, Brazil: Museu Paraense Emílio Goeldi; 2002. [Google Scholar]
- 73.Veiga J., Scudeller V. Revista Brasileira de Plantas Medicinais. Vol. 17. Campinas; 2015. Etnobotânica e medicina popular no tratamento de malária e males associados na comunidade ribeirinha Julião – baixo Rio Negro (Amazônia Central) pp. 737–747. [DOI] [Google Scholar]
- 74.Medeiros M. F., Fonseca V. S., Andreata R. H. Plantas medicinais e seus usos pelos sitiantes da Reserva Rio das Pedras, Mangaratiba, RJ, Brasil. Acta Botanica Brasilica. 2004;18(2):391–399. doi: 10.1590/S0102-33062004000200019. [DOI] [Google Scholar]
- 75.Bueno N. R., Castilho R. O., da Costa R. B., et al. Medicinal plants used by the kaiowá and guarani indigenous populations in the caarapó reserve, Mato Grosso do Sul, Brazil. Acta Botanica Brasilica. 2005;19(1):39–44. doi: 10.1590/S0102-33062005000100005. [DOI] [Google Scholar]
- 76.Silva-Almeida M. F., Amorozo M. C. M. Medicina popular no Distrito de Ferraz, Município de Rio Claro, Estado de São Paulo. Brazilian Journal of Ecology. 1998;2:36–46. [Google Scholar]
- 77.Heinrich M., Ankli A., Frei B., Weimann C., Sticher O. Medicinal plants in Mexico: healers' consensus and cultural importance. Social Science & Medicine. 1998;47(11):1859–1871. doi: 10.1016/S0277-9536(98)00181-6. [DOI] [PubMed] [Google Scholar]
- 78.Bennett B. C., Prance G. T. Introduced plants in the indigenous pharmacopoeia of northern South America. Economic Botany. 2000;54(1):90–102. doi: 10.1007/BF02866603. [DOI] [Google Scholar]
- 79.Fernandez E. C., Sandi Y. E., Kokoska L. Ethnobotanical inventory of medicinal plants used in the bustillo province of the potosi department. Bolivia1. 2003;4:35–72. doi: 10.1016/S0367-326X(03)00053-4. [DOI] [PubMed] [Google Scholar]
- 80.Leão R. B. A., Coelho-ferreira M. R., Jardim M. A. G., Leão R. B. A. Levantamento de plantas de uso terapêutico no município de Santa Bárbara do Pará, Estado do Pará, Brasil. Revista Brasileira de Farmácia. 2007;88(1):21–25. [Google Scholar]
- 81.Penido C., Conte F. P., Chagas M. S. S., Rodrigues C. A. B., Pereira J. F. G., Henriques M. G. M. O. Anti-allergic effects of natural tetranortriterpenoids isolated from Carapa guianensis Aublet on allergen-induced vascular permeability and hyperalgesia. Inflammation Research. 2005;54(7):295–303. doi: 10.1007/s00011-005-1357-6. [DOI] [PubMed] [Google Scholar]
- 82.Ferraris F. K., Moret K. H., Figueiredo A. B. C., Penido C., das Graças Henriques M. O. Gedunin, a natural tetranortriterpenoid, modulates T lymphocyte responses and ameliorates allergic inflammation. International Immunopharmacology. 2012;14(1):82–93. doi: 10.1016/j.intimp.2012.06.002. [DOI] [PubMed] [Google Scholar]
- 83.Penido C., Costa K. A., Costa M. F. D. S., Pereira J. D. F. G., Siani A. C., Henriques M. D. G. M. D. O. Inhibition of allergen-induced eosinophil recruitment by natural tetranortriterpenoids is mediated by the suppression of IL-5, CCL11/eotaxin and NFκB activation. International Immunopharmacology. 2006;6(2):109–121. doi: 10.1016/j.intimp.2005.07.011. [DOI] [PubMed] [Google Scholar]
- 84.Nayak B. S., Kanhai J., Milne D. M., et al. Investigation of the wound healing activity of Carapa guianensis L. (Meliaceae) bark extract in rats using excision, incision, and dead space wound models. Journal of Medicinal Food. 2010;13(5):1141–1146. doi: 10.1089/jmf.2009.0214. [DOI] [PubMed] [Google Scholar]
- 85.Nayak B. S., Kanhai J., Milne D. M., Pereira L. P., Swanston W. H. Experimental evaluation of ethanolic extract of carapa guianensis L. leaf for its wound healing activity using three wound models. Evidence-Based Complementary and Alternative Medicine. 2011;2011 doi: 10.1093/ecam/nep160.419612 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 86.Ferraris F. K., Rodrigues R., Da Silva V. P., Figueiredo R., Penido C., Henriques M. D. G. M. O. Modulation of T lymphocyte and eosinophil functions in vitro by natural tetranortriterpenoids isolated from Carapa guianensis Aublet. International Immunopharmacology. 2011;11(1):1–11. doi: 10.1016/j.intimp.2010.09.010. [DOI] [PubMed] [Google Scholar]
- 87.Zhang Q., Zhao J. J., Xu J., Feng F., Qu W. Medicinal uses, phytochemistry and pharmacology of the genus Uncaria. Journal of Ethnopharmacology. 2015;173:48–80. doi: 10.1016/j.jep.2015.06.011. [DOI] [PubMed] [Google Scholar]
- 88.Pavei C., Kaiser S., Borré G. L., Ortega G. G. Validation of a LC method for polyphenols assay in cat's claw (Uncaria tomentosa) Journal of Liquid Chromatography & Related Technologies. 2010;33(17):1551–1561. doi: 10.1080/10826076.2010.503753. [DOI] [Google Scholar]
- 89.Pavei C., Kaiser S., Verza S. G., Borre G. L., Ortega G. G. HPLC-PDA method for quinovic acid glycosides assay in Cat's claw (Uncaria tomentosa) associated with UPLC/Q-TOF-MS analysis. Journal of Pharmaceutical and Biomedical Analysis. 2012;62:250–257. doi: 10.1016/j.jpba.2011.12.031. [DOI] [PubMed] [Google Scholar]
- 90.Sheng Y., Åkesson C., Holmgren K., Bryngelsson C., Giamapa V., Pero R. W. An active ingredient of Cat's Claw water extracts: Identification and efficacy of quinic acid. Journal of Ethnopharmacology. 2005;96(3):577–584. doi: 10.1016/j.jep.2004.10.002. [DOI] [PubMed] [Google Scholar]
- 91.da Silva J. O., Fernandes R. S., Ticli F. K., et al. Triterpenoid saponins, new metalloprotease snake venom inhibitors isolated from Pentaclethra macroloba. Toxicon. 2007;50(2):283–291. doi: 10.1016/j.toxicon.2007.03.024. [DOI] [PubMed] [Google Scholar]
- 92.Reddy L. J., Beena J., Spandana G., Reshma D. J. Evaluation of antibacterial and antioxidant activities of the leaf essential oil and leaf extracts of Otacanthus caerulus (Linden) Ronse. International Journal of Pharmacy and Pharmaceutical Science Research. 2012;2:20–25. [Google Scholar]
- 93.Houël E., Rodrigues A. M. S., Jahn-Oyac A., et al. In vitro antidermatophytic activity of Otacanthus azureus (Linden) Ronse essential oil alone and in combination with azoles. Journal of Applied Microbiology. 2014;116(2):288–294. doi: 10.1111/jam.12377. [DOI] [PubMed] [Google Scholar]
- 94.Houël E., Gonzalez G., Bessière J.-M., et al. Therapeutic switching: From antidermatophytic essential oils to new leishmanicidal products. Memórias do Instituto Oswaldo Cruz. 2015;110(1):106–113. doi: 10.1590/0074-02760140332. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 95.Shanley P., Rosa N. A. Conhecimento em erosão: um inventário etnobotânico na fronteira de exploração da Amazônia Oriental. Boletim do Museu Paraense Emílio Goeldi. 2005;1:147–171. [Google Scholar]
- 96.Costa-Silva J. H., Lima C. R., Silva E. J. R., et al. Acute and subacute toxicity of the Carapa guianensis Aublet (Meliaceae) seed oil. Journal of Ethnopharmacology. 2008;116(3):495–500. doi: 10.1016/j.jep.2007.12.016. [DOI] [PubMed] [Google Scholar]
- 97.Prophiro J. S., da Silva M. A. N., Kanis L. A., da Silva B. M., Duque-Luna J. E., da Silva O. S. Evaluation of time toxicity, residual effect, and growth-inhibiting property of Carapa guianensis and Copaifera sp. in Aedes aegypti. Parasitology Research. 2012;110(2):713–719. doi: 10.1007/s00436-011-2547-5. [DOI] [PubMed] [Google Scholar]
- 98.Santos O. J. D., Malafaia O., Ribas-Filho J. M., Czeczko N. G., Santos R. H. P., Santos R. A. P. Efeito de Schinus terebinthifolius Raddi (aroeira) e Carapa guianensis Aublet (andiroba) na cicatrização de gastrorrafias. Arquivos Brasileiros de Cirurgia Digestiva. 2013;26(2):84–91. doi: 10.1590/s0102-67202013000200003. [DOI] [PubMed] [Google Scholar]
- 99.Dreifuss A. A., Bastos-Pereira A. L., Fabossi I. A. Uncaria tomentosa exerts extensive anti-neoplastic effects against the walker-256 tumour by modulating oxidative stress and not by alkaloid activity. PLos One. 2013;8(2):1–14. doi: 10.1371/journal.pone.0054618.e54618 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 100.Pilarski R., Filip B., Wietrzyk J., Kuraś M., Gulewicz K. Anticancer activity of the Uncaria tomentosa (Willd.) DC. preparations with different oxindole alkaloid composition. Phytomedicine. 2010;17(14):1133–1139. doi: 10.1016/j.phymed.2010.04.013. [DOI] [PubMed] [Google Scholar]
- 101.Rojas-Duran R., González-Aspajo G., Ruiz-Martel C., et al. Anti-inflammatory activity of mitraphylline isolated from Uncaria tomentosa bark. Journal of Ethnopharmacology. 2012;143(3):801–804. doi: 10.1016/j.jep.2012.07.015. [DOI] [PubMed] [Google Scholar]
- 102.Ccahuana-Vasquez R. A., Ferreira dos Santos S. S., Koga-Ito C. Y., Cardoso Jorge A. O. Antimicrobial activity of Uncaria tomentosa against oral human pathogens. Brazilian Oral Research. 2007;21(1):46–50. doi: 10.1590/S1806-83242007000100008. [DOI] [PubMed] [Google Scholar]
- 103.Caon T., Kaiser S., Feltrin C., et al. Antimutagenic and antiherpetic activities of different preparations from Uncaria tomentosa (cat's claw) Food and Chemical Toxicology. 2014;66:30–35. doi: 10.1016/j.fct.2014.01.013. [DOI] [PubMed] [Google Scholar]
- 104.Domingues A., Sartori A., Golim M. A., et al. Prevention of experimental diabetes by Uncaria tomentosa extract: Th2 polarization, regulatory T cell preservation or both? Journal of Ethnopharmacology. 2011;137(1):635–642. doi: 10.1016/j.jep.2011.06.021. [DOI] [PubMed] [Google Scholar]
- 105.Baydoun S., Chalak L., Dalleh H., Arnold N. Ethnopharmacological survey of medicinal plants used in traditional medicine by the communities of Mount Hermon, Lebanon. Journal of Ethnopharmacology. 2015;173:139–156. doi: 10.1016/j.jep.2015.06.052. [DOI] [PubMed] [Google Scholar]
- 106.Lima R. A., Magalhães A. S., Santos M. R. A. Levantamento etnobotânico de plantas medicinais utilizadas na cidade de Vilhena , Rondônia. Revista Pesquisa & Criação. 2011;10(2):165–179. [Google Scholar]
Associated Data
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Data Availability Statement
All data generated and analyzed to support this study are included in this published article. The project was submitted to the Ethics Research Committee of the Faculdade Estácio de Macapá (http://aplicacao.saude.gov.br/plataformabrasil/login.jsf, under the opinion no. 14.94.994). And the complete information of the individual interviews could be requested from the corresponding authors.