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Evidence-based Complementary and Alternative Medicine : eCAM logoLink to Evidence-based Complementary and Alternative Medicine : eCAM
. 2019 Sep 15;2019:3057180. doi: 10.1155/2019/3057180

Exploring Antimalarial Herbal Plants across Communities in Uganda Based on Electronic Data

Denis Okello 1,2,3, Youngmin Kang 1,3,
PMCID: PMC6766105  PMID: 31636682

Abstract

Malaria is one of the most rampant diseases today not only in Uganda but also throughout Africa. Hence, it needs very close attention as it can be severe, causing many deaths, especially due to the rising prevalence of pathogenic resistance to current antimalarial drugs. The majority of the Ugandan population relies on traditional herbal medicines for various health issues. Thus, herein, we review various plant resources used to treat malaria across communities in Uganda so as to provide comprehensive and valuable ethnobotanical data about these plants. Approximately 182 plant species from 63 different plant families are used for malaria treatment across several communities in Uganda, of which 112 plant species have been investigated for antimalarial activities and 96% of the plant species showing positive results. Some plants showed very strong antimalarial activities and could be investigated further for the identification and validation of potentially therapeutic antimalarial compounds. There is no record of an investigation of antimalarial activity for approximately 39% of the plant species used for malaria treatment, yet these plants could be potential sources for potent antimalarial remedies. Thus, the review provides guidance for areas of further research on potential plant resources that could be sources of compounds with therapeutic properties for the treatment of malaria. Some of the plants were investigated for antimalarial activities, and their efficacy, toxicity, and safety aspects still need to be studied.

1. Introduction

Malaria, a dangerous and life-threatening disease caused by Plasmodium parasites is spread to humans through bites of infected female Anopheles mosquitoes [1]. It is one of the most widespread diseases today not only in Uganda but also throughout Africa. Hence, careful monitoring of malaria is required as the disease can be severe and can cause many deaths, especially due to the increasing prevalence of resistance to current antimalarial drugs. Among the five parasitic species that cause malaria to humans, Plasmodium falciparum and Plasmodium vivax are the deadliest [2, 3]. P. falciparum and P. vivax being the most prevalent malaria parasites in sub-Saharan Africa and regions of the Americas, respectively, were responsible for about 99.7% and 74.1% of malaria cases in 2017 [4]. In Southeast Asia, Plasmodium knowlesi is the most common cause of malaria, accounting for up to 70% of malaria cases, although it has been known to infect Old-World monkeys more [5]. Two other species of Plasmodium, Plasmodium malariae and Plasmodium ovale, generally cause mild fevers. Approximately 216 million malaria cases were registered in 2016, with a death toll of up to 445,000 [1]. According to the World Health Organization [6], the incidence of malaria in Uganda, at 47.8%, was the highest worldwide in 2005. According to Njoroge and Bussman [7], malaria is responsible for one to two million deaths annually in Africa. Typical symptoms of malaria include high fever, fatigue, headache, muscle ache, nausea, abdominal discomfort, and profuse sweating. However, in extreme cases and cases of prolonged illness without treatment, brain tissue injury, pulmonary edema, kidney failure, severe anemia, yellow discoloration of the skin, and low blood sugar may be noted (Figure 1) [1, 2]. In Uganda, malaria is one of the major causes of illness and death [7]. Statistically, it accounts for 46% of children's sicknesses, almost 40% of outpatient visits to hospitals and clinics, 25% of hospital admissions, 14% of inpatient deaths, and approximately 23% of infant mortalities [7].

Figure 1.

Figure 1

Illustration of some common symptoms of malaria.

In different parts of the world, the use of herbs and herbal extracts in the management and treatment of malaria is very common since herbs are cheap and readily available besides being effective. In fact, the use of herbal medicine for treatment worldwide is on the rise. Over 80% of the Ugandan population relies directly on herbal plants for their health care primarily [8]. A great majority of the population uses traditional herbal medicines because of their confirmed therapeutic value [8]. The increase in preference for herbal remedies coupled with resistance exhibited by pathogenic strains, including Plasmodium species, to the modern drugs available is the driving force behind researchers' interest in herbal plants for possible alternatives for more effective antimalarial drugs [9, 10].

This review was aimed at providing comprehensive ethnobotanical information about various plant resources with antimalarial properties that are primarily used to manage and treat malaria across communities in Uganda, based on which further evaluation of these plants such as those of their efficacy and safety for the treatment of malaria may be based.

2. Methods and Materials

In the review, the data search processes employed by Komakech et al. [11] were modified to gather information on herbal plants for malaria treatment in Uganda from peer-reviewed articles in English published in scientific journals and other verifiable databases, with a focus on plant species and families, plant parts used, antimalarial activities of the extracts from herbal plants, and mechanisms of action of novel antimalarial phytochemicals and derivatives. Electronic literature databases such as PubMed, Medline, Scopus, SciFinder, Google Scholar, and Science Direct were carefully searched for suitable information. The following words were used as key search terms: (“Herbal medicine in Uganda” OR “Herbs in Uganda” OR “Traditional remedies in Uganda” OR “Natural remedies in Uganda” OR “Anti-malarial herbs in Uganda” OR “Anti-malarial plants in Uganda” OR “Ugandan herbs” OR “Ugandan ethno-medicine” OR “Ugandan phyto-medicine”), AND (“anti-plasmodial activities” OR “anti-malarial activities” OR “anti-plasmodial effects” OR “anti-malarial effects” OR “malaria treatment” OR “malaria management”) OR (“Malaria in Uganda” AND “prevalence” OR “occurrence” OR “distribution” OR “herbal treatment” OR “herbal remedies” OR “phyto-medicine” OR “phyto remedy” OR “plant parts used for treatment”) OR (Phytochemicals for malaria treatment OR Artemisinins OR Quinine OR Noble anti-malarial compounds OR Plant derived anti-malarial compounds AND mechanisms of action OR modes of action) OR (“Malaria herbal medicine in Uganda” OR “Herbal medicine in Uganda” OR “Herbal malaria remedy in Uganda” OR “Natural malaria medicine in Uganda” OR “Traditional malaria herbal medicine” OR “Malaria herbal recipe” AND “dosage” OR “dose” OR “dose given” OR “mode of administration” OR “means of traditional extraction” OR “traditional extraction” OR “Toxicity” OR “Safety and toxicity” OR “Policy framework” OR “other ethno-pharmacological uses” OR “other ethno-pharmacological utilizations” OR “other ethno-medicinal uses”). The information gathered was verified separately for its reliability; any discrepancies discovered were resolved by discussions between the authors. Thereafter, these data were summarized and analyzed, and comparisons were made to draw conclusions.

3. Prevalence of Malaria

Malaria in Uganda is highly endemic because the climate is favorable for its consistently stable and year-round transmission in about 99% of the country, with the country's entire population being at risk for contraction [12]. The most vulnerable groups of people at great risk for malaria are expectant mothers and young children under the age of 5 years [12]. The malarial parasite, P. falciparum, is most commonly the cause of malaria throughout Uganda, accounting for over 90% of malaria cases. However, Betson et al. [13] have warned of the potential for the emergence of infections due to P. malariae and P. ovale spp. as well, since there is much focus on countering P. falciparum infections. In 2016, Larocca et al. [14] indicated that Uganda was one of the leading countries in the world with malaria incidence rate as high as 478 cases per 1,000 population per year. Specifically, overall registered death cases caused by malaria in children were between 70,000 and 100,000 annually in Uganda [14]. Tremendous effort has been made to control malaria in Uganda by the government-headed Uganda Malaria Reduction Strategic Plan and Mass Action Against Malaria. These efforts have greatly reduced the malaria burden and incidence from 272 cases per 1000 population in 2016/17 to 191 cases per 1000 population in 2017/18 [12]. Although there has been a general reduction in the incidence of malaria, studies indicate that malaria prevalence along lakes, for example, Lake Victoria, and in remote areas of the country (villages) as well as areas closer to forests are much higher, with over 450 malaria cases per 1000 population (Figure 2) [12, 13, 15]. Communities around lakeshores in Uganda have always had high prevalence of malaria among children and especially the young ones despite routine treatments [12, 16]. Through the government initiative to control malaria, the prevalence in some districts remained as low as 4.3% in 2018 [12]. Malaria control strategies including indoor residual spraying along with house to house distribution of mosquito nets treated with insecticides resulted in a remarkable reduction in malaria burdens in many parts of the country [17]. Raouf et al. [18] observed that significant reductions in the levels of malaria in Uganda cannot be sustained if the current control measures are terminated.

Figure 2.

Figure 2

Malaria prevalence in Uganda (modified from [12]).

4. Mechanisms of Actions of Novel Phytochemicals in Malaria Treatment

Herbal plants are extremely rich in phytochemicals that are highly efficacious in the treatment of malaria, such as sesquiterpenes and sesquiterpene lactones, fluoroquinolones, chalcones, flavanones, phenolics, quinones, coumarins, and alkaloids (Table 1) [35, 36]. The herbal plants that are used as prophylactic measures to prevent malaria as well contain some of these compounds (Table 2). From these groups of compounds, active metabolites including quinine and artemisinin have been derived and the most successful antimalarial drugs to date have been obtained. Artemisinins from Artemisia annua a plant belonging to the family Asteraceae have actually been an integral part of the fight against malaria, with artemisinin-based combination therapy contributing enormously to modern day treatments [36]. They have been effective against all strains of P. falciparum including multi-drug-resistant ones [36, 37].

Table 1.

Herbs used in the treatment of malaria in Uganda.

Plant family Scientific name Local name Part used Growth form Mode of preparation Dose and mode of administration for malaria Status of antimalarial/antiplasmodial activity investigation Other ailments treated Reference(s)
Acanthaceae Justicia betonica L. Nalongo/quinine Leaves/whole plant Herb Decoction About 120 ml every 8 hours for a week Investigated Diabetes, yellow fever, diarrhea [10, 19]
Justicia anselliana (Nees) T. Anderson Kwiniini omuganda Leaves/twig Herb Decoction Orally taken, dose not specified No record [20]
Monechma subsessile C. B. Clarke Erazi Leaves Decoction Orally taken, dose not specified No record Abdominal pain [19]
Thunbergia alata Sims Kasaamusaamu/ntudde buleku Leaves/whole plant Climber Decoction About 120 ml every 8 hours for a week No record False teeth [8, 10]
Alliaceae Allium cepa L. Katungulu Bulb Herb No record [21]
Aloeaceae Aloe dawei A. Berger (wild/cultivated) Kigagi Leaves Herb Decoction A glassful once a day for 7 days Investigated Candida [10]
Aloe kedongensis (wild) Kigagi Leaves Herb Decoction Orally taken, dose not specified Investigated [19, 22]
Aloe volkensii (cultivated) Kigagi Leaves Herb Decoction/infusion Orally taken, dose not specified No record [19]
Aloe ferox Mill Kigagi Leaves Herb Decoction Orally taken, dose not specified Investigated Wounds, digestive disorders, rheumatic arthritis [18, 19]
Aloe lateritia (wild) Kigagi Leaves/root Herb Decoction Orally taken, dose not specified No record [19]
Amaranthaceae Amaranthus hybridus L. Bbuga Leaves Herb Decoction Half a glass every 24 hours for 7 days No record [10]
Anacardiaceae Mangifera indica L. Muyembe gwakona Leaves/bark Tree Decoction 4 and 3 teaspoons after every 8 hours for adults and children, respectively, for a week Investigated Diarrhea, dysentery, body pain, venereal diseases, cough, syphilis [10, 23]
Rhus natalensis Bernh. Ex Krauss Omesheshe Leaves Shrub Decoction Orally taken, dose not specified Investigated [24]
Rhus vulgaris Meikle Kakwasokwaso/tebudda Leaves Shrub Decoction Half a glass every 8 hours for 7 days No record Skin rush, erectile dysfunction [10]
Apiaceae Heteromorpha trifoliata Eckl. & Zeyh. Omumemena Leaves/roots Herb Decoction Orally taken, dose not specified No record [19]
Centella asiatica (L.) Urb. Kabo Kabakyala/mbutamu Leaves/whole plant Herb Decoction 4 teaspoons thrice a day for 4 days Investigated [10]
Apocynaceae Alstonia boonei De Wild. Mubajangalabi Bark Tree Decoction Orally taken, dose not specified Investigated [8]
Carissa edulis (Forssk.) Vahl Muyunza, ekamuriei Roots Herb Decoction Orally taken, dose not specified Investigated Epilepsy, fever, cough, syphilis, measles, dysentery [21, 23]
Carissa spinarum Lodd. ex A. DC. Omuyonza Roots Decoction Orally taken, dose not specified Investigated [19]
Catharanthus roseus G. Don Sekagya Leaves Herb Decoction About 120 ml every 8 hours for a week Investigated [10]
Araceae Culcasia faleifolia Engl. Ntangawuzi yomukibira Roots Herb Decoction About 120 ml once a day for a week No record [10]
Aristolochiaceae Aristolochia elegans Mast. Musuja welaba/nakasero Seeds/sap Vine Steeped in water and drunk A glassful once a day Investigated Abdominal pain, East coast fever [8, 19]
Aristolochia tomentosa Sims. Kankapu Stem Climber Infusion Oral, dose not specified No record Wounds, skin diseases, snake bites [23]
Asclepiadaceae Gomphocarpus physocarpus E. Mey. Kafumbo Leaves Herb Decoction Half a glass daily for a week No record [10]
Asphodelaceae Aloe vera (L.) Burm. f. Kigagi/alovera Leaves Herb Decoction 1 teaspoon and 1 tablespoon 3 times a day for children and adults, respectively, for a week Investigated Stomach ache [8, 25]
Asteraceae Ageratum conyzoides L. Namirembe Whole plant/leaves Herb Decoction A glassful thrice a day for 7 days Investigated Worms, weakness in pregnancy [8, 10]
Artemisia annua L. Sweet anne Leaves Herb Decoction Oral, dose not specified Investigated Fever [19]
Artemisia afra Jacq. ex Willd Pasile Leaves Herb Infusion Oral, dose not specified Investigated Fever [10]
Aspilia africana (Pers.) C. D. Adams Makayi, ekarwe Whole plant/leaves/roots Herb Decoction 8 teaspoons 3 times a day for a week Investigated Abdominal aches, measles, diarrhea, wounds, induction of appetite [10, 19]
Baccharoides adoensis (Sch. Bip. ex Walp.) H. Rob. Okellokello Leaves Shrub Decoction 1 teaspoon and 1 tablespoon 3 times a day for children and adults, respectively, for a week; bath-leaves squeezed and added to bathing water Investigated Flu, skin rush, ear infections [25, 26]
Bidens grantii Sherff Ehongwa Leaves, flower Herb Decoction Oral, dose not specified No record Pregnancy disorders, prehepatic jaundice [19]
Bidens pilosa L. Sere/labika Whole plant/leaves Herb Decoction/fresh leaf extract 4 teaspoons thrice a day for 4 days Investigated Diarrhea, wounds [10, 23]
Bothriocline longipes N. E. Br. Ekyogayanja Leaves Decoction Oral, dose not specified Investigated Fever, ague, paludism [19, 24]
Conyza bonariensis (L.) Ndasha Leaves Decoction Oral, dose not specified No record Stomach ache, body pain, anemia, respiratory problems [19]
Conyza floribunda H. B. K. Kafumbe Leaves Herb Decoction About 120 ml once a day for a week No record Headache [10]
Conyza sumatrensis (Retz.) E. H. Walker Kati kati Leaves Herb No record Wounds, sore throat, ringworms [21, 27]
Crassocephalum vitellinum Kitonto Leaves Herb Honey added to decoction 2 teaspoons thrice a day for 7 days Investigated [10, 19]
Emilia javanica (Burm. F.) C. B. Rob. Nakate Whole plant Herb Decoction Half a glass once a day for a week No record [10]
Guizotia scabra Chiov. Ekiterankuba Leaves Decoction Oral, dose not specified Investigated Stomach ache, HIV/AIDS opportunistic infections [19]
Gynura scandens O. Hoffm. Ekizimya-muriro Leaves Decoction Oral, dose not specified No record Febrile convulsions [19]
Melanthera scandens (Schumach. & Thonn.) Roberty Makaayi Leaves Herb Decoction Oral, dose not specified Investigated Stomach ache, body odour, yellow fever [8]
Pluchea ovalis DC. Omuneera Leaves Decoction Oral, dose not specified No record [19]
Microglossa pyrifolia (Lam.)O. Ktze Kafugankande Whole plant/leaves/roots Herb Decoction Half a glass thrice a day for a week Investigated Cough, abdominal disorders, chest pain [10, 19, 28]
Schkuhria pinnata (Lam.) Apunait Leaves Herb Infusion 1 teaspoon and 1 tablespoon 3 times a day for children and adults, respectively, for a week Investigated Wounds, skin diseases, diabetes, ear infections, wounds [23, 25]
Sigesbeckia orientalis L. Kyaryaho Roots Decoction Oral, dose not specified No record Wounds, stomach ache [19]
Solanecio mannii (Hook. f.) C. Jeffrey Omusununu Leaves Decoction Oral, dose not specified Investigated Fever, indigestion [19]
Sonchus oleraceus L. Entahutara Leaves Decoction Oral, dose not specified No record Stomach ache, scars, anemia, diarrhea [8, 19]
Tagetes minuta L. Kawunyira Whole plant/leaves Herb Decoction Half a glass thrice a day for a week Investigated Flu, headache, convulsions [10]
Tithonia diversifolia A. Gray Kimyula Leaves Herb Decoction Half a glass thrice a day for a week Investigated Diabetes, abdominal pain [10, 19, 25]
Vernonia adoensis Sch. Bip. ex Walp. Nyakajuma Leaves/flowers Decoction Oral, dose not specified Investigated Diarrhea, dizziness [19]
Vernonia amygdalina Delile Mululuza/labwori Whole plant/roots Shrub Decoction Half a glass 2 times a day for 5 days Investigated Headache, stomach ache, burns, baths [8, 10, 19, 20]
Vernonia cinerea (L.) Less. Kayayana Bark Tree Decoction Half a glass thrice a day for a week Investigated Fever, vomiting, inflammation [10]
Vernonia lasiopus O. Hoffm. Kaluluza kasajja Roots/leaves Shrub Fresh leaf extract/root decoction 2 teaspoons thrice a day for 7 days Investigated Abdominal pain, cough, migraine headache, delayed delivery [8, 10, 19, 20]
Bignoniaceae Markhamia lutea (Benth.) K. Schum. Musambya/muzanganda Roots Tree Decoction A glassful once a day for 7 days Investigated Cough, diarrhea [8, 10, 19]
Spathodea campanulata Buch. -Harm. ex DC. Kifabakazi Bark Tree Decoction Half a glass 3 times a day for 5 days Investigated Increased vaginal fluid, skin infection, infertility, hernia [8, 10]
Caesalpiniaceae Cassia didymobotrya Fres. Mukyula Leaves Shrub Decoction About 120 ml every 8 hours for a week Investigated [10]
Chamaecrista nigricans Greene Epeduru lo didi Leaves Herb Infusion Oral, dose not specified No record Labour induction, hypertension, retained placenta [23]
Erythrophleum pyrifolia Omurama Leaves/roots Investigated [24]
Senna spectabilis (DC.) H. S. Irwin & Barneby Gasiya Leaves Tree Decoction Half a glass twice a day for 5 days Investigated [10]
Caesalpinioideae Cassia hirsuta Kasagalansansi Roots Herb Infusion Investigated Stomach pains [23]
Canelliaceae Warbugia ugandensis Sprague Omukuzanume Bark/leaves Tree Decoction/powder swallowed with banana Half a glass once a day for a week Investigated Toothache, flu, skin diseases, asthma, stomach ache, body and muscle pain [10, 20, 27]
Caricaceae Carica papaya L. Paapali essajja Leaves Tree Decoction Half a glass twice a day for 3 days Investigated Snake bite, sterility, cough, cancer, body pain, induces labour [10, 19, 23, 25]
Celastraceae Maytenus senegalensis Echomai Roots Tree Decoction Oral, dose not specified Investigated Toothache, skin diseases, chest pain, wound, fever [23]
Chenopodiaceae Chenopodium ambrosioides L. Kawuna wuna Leaves Investigated Headache, epilepsy [21]
Chenopodium opulifolium Koch & Ziz Namuvu Leaves No record Oral wounds, skin rush, toothache [8, 21]
Combretaceae Combretum molle G. Don Ndagi Bark Tree Decoction Half a glass once a day for 3 days Investigated Cough, [10, 21]
Crassulaceae Kalanchoë densiflora Rolfe Kisanasana Leaves Herb No record [21]
Cucurbitaceae Cucurbita maxima Lam. Kasuunsa Leaves Herb Decoction Half a glass once a day for 7 days Investigated Abdominal pain [10, 25, 27]
Momordica foetida Schumach. Orwihura Leaves Decoction Oral, dose not specified Investigated Vomiting, baths, cough, flue, worms [19, 26, 28]
Dracaenaceae Dracaena steudneri Engl. Kajjolyenjovu Leaves Herb Decoction Half a glass thrice a day for a week No record Scars, cough, syphilis, kidney stones, snake bites [8, 10]
Ebenaceae Euclea latideus Staff Emusi Roots Shrub Decoction Oral, dose not specified Investigated Ringworms, swollen legs [23]
Euphorbiaceae Alchornea cordifolia (Schumach.) Mull. Arg. Luzibaziba Leaves Herb Decoction Half a glass once a day for 7 days Investigated Shaking body [8, 10]
Bridelia micrantha Baill. Katazamiti Bark Tree Decoction Half a glass thrice a day for a week Investigated [10]
Clutia abyssinica Jaub. & Spach Omubarama Leaves Decoction Oral, dose not specified Investigated Fever, diarrhea [19]
Croton macrostachyus Olive. Ookota Roots/bark Tree Decoction Oral, dose not specified Investigated Tuberculosis, stomach ache, cough, fever, asthma [23]
Fluegea virosa (Roxb. ExWillb.)Voigt Lukandwa/mukandula Leaves Shrub Decoction Half a glass 3 times a day for a week Investigated Miscarriage, chest pains, infertility in women [8, 10, 21, 23]
Jatropha curcas L. Kirowa Leaves Shrub Investigated Tooth decay, headache, weakness in pregnancy [21]
Macaranga schweinfurthii Pax Kyeganza Bark Tree Decoction Half a glass 3 times a day for a 5 days No record [10]
Phyllanthus (pseudo) niruri Mull. Arg. Nakitembe Leaves Shrub Decoction Half a glass 3 times a day for a 7 days Investigated [10]
Shirakiopsis elliptica (Hochst.) H.–J. Esser Musasa Back Tree Decoction Oral, dose not specified No record [20]
Tetrorchidium didymostemon (Baill.) Pax & K. Hoffm. Ekiziranfu Bark Decoction Used as enema No record Jaundice, measles, gastrointestinal disorders, enema [8, 19]
Fabaceae Arachis hypogea (NC) Ebinyobwa Leaves Fresh extract Oral, dose not specified No record [19]
Cajanus cajan (L.) Druse Entondaigwa Leaves Shrub Fresh extract 100 ml once a day for a week Investigated Diarrhea, body pain [27]
Crotalaria agatiflora Schweinf. Kijjebejebbe Whole shoot Shrub Fresh extract Daily bath No record High blood pressure [10]
Crotalaria ochroleuca G. Don Alayo Leaves Herb Fresh extract 1 teaspoon and 1 tablespoon 3 times a day for children and adults, respectively, for a week No record Stomach ache [28]
Entada abyssinica Steud. ex A. Rich. Mwolola Leaves Tree Decoction Investigated Oral wounds, body weakness, wounds, skin infections [8, 20, 26]
Entada africana Guill. & Perr. Mwolola Bark Tree Decoction 4 and 3 teaspoons after every 8 hours for adults and children, respectively, for a week Investigated [10]
Erythrina abyssinica Lam. Girikiti/lacoro Bark Tree Decoction Half a glass 3 times a day for a 5 days Investigated Fever, leprosy, burns, tuberculosis, toothache, syphilis [10, 23]
Erythrina excelsa Bak. Bajjangala Bark Tree Decoction Half a glass 3 times a day for a week No record Wounds, candida [10]
Indigofera arrecta Hochst. Ex A. Rich Omushoroza Roots/bark No record Abdominal pain [19]
Indigofera congesta Baker Namasumi Twig Herb Infusion Oral, dose not specified No record [8, 20]
Indigofera emerginella Steud. ex A. Rich Omunyazabashumba Leaves/roots Shrub Decoction Oral, dose not specified Investigated Cough [19]
Macrotyloma axillare Verdc. Akihabukuru Leaves No record Impotence, dizziness [19]
Pseudarthria hookeri Wight & Arn Omukongorani/kikakala Leaves/whole plant Herb Decoction One teaspoon thrice a day for 4 days No record Fever [19, 20, 25, 29]
Rhynchosia viscosa DC Omutegansi Flower No record Labour induction [19]
Senna absus (L.) Roxb. Mucuula Shrub Leaves Fresh extract Oral, dose not specified No record Prolonged embryo in uterus [8]
Senna didymobotrya (Fresen.) H. S. Irwin & Barneby Omugabagaba/kivumuzi Herb Leaves, twig Decoction Oral, dose not specified Investigated Change of sex of child [8, 19, 20, 29]
Senna siamea (Lam.) H. S. Irwin & Barneby Garcia Roots Tree Fresh extract A cupful (500 ml) once a day for 3 days Investigated Abdominal pain, sore throat [25, 27]
Tamarindus indica L. Cwaa/nkoge Bark Tree Decoction Oral, dose not specified Investigated Convulsions, fever [8, 21]
Flacourtiaceae Ocoba spinosa Forssk Ekalepulepu Roots Herb Decoction Oral, dose not specified No record Syphilis, skin problems, wounds, headache, impotence, stomach ache [23]
Trimeria bakeri Gilg. Omwatanshare Leaves Shrub Decoction Oral, dose not specified Investigated [24]
Hypericaceae Harungana madagascariensis Lam. Mukaabiransiko/mulirira Bark Tree Decoction 2 tablespoons thrice a day for 3 days Investigated Yellow fever [8, 10]
Labiatae Hyptis pectinata Poir. Bongoloza Whole plant Herb Decoction Oral, dose not specified No record [20, 29]
Lamiaceae Aeolanthus repens Oliv. Ntulagi Leaves Herb Decoction Quarter a glass thrice a day for 3 days No record [10]
Ajuga remota Benth. Kitinwa Leaves Herb Decoction Half a glass once a day for a week Investigated Stomach ache [10]
Clerodendrum myricoides R. Br. Kikonge Leaves Shrub Decoction Half a glass daily for a week Investigated Syphilis, intestinal problems, induction of labour [10, 28]
Clerodendrum rotundifolium Oliv. Kisekeseke Roots/leaves Shrub Fresh leaf extract/root decoction Half a glass daily for a 5 days Investigated Diabetes [10]
Hoslundia opposita Vahl. Kamunye Leaves Herb Decoction Half a glass 3 times a day for a week; bath Investigated Ulcers [8, 10, 25]
Leonotis nepetifolia Schimp. exBenth Kifumufumu Whole plant Herb Decoction A glassful thrice a day for 3 days Investigated Headache [10, 21]
Ocimum basilicum Emopim Leaves Herb Infusion Half a glass 3 times a day for a week Investigated Fever, eye cataract [23, 27]
Ocimum gratissimum Willd. Mujaaja Leaves Herb Decoction Half a glass 3 times a day for 5 days Investigated Wounds, ear infections, chest pain [10, 21]
Ocimum lamiifolium Hochst. Omwenyi Leaves Decoction Half a glass 3 times a day for a week Investigated Abdominal pain [19]
Plectranthus barbatus Ebiriri omutano Whole plant/leaves, roots/stem Herb Infusion Oral, dose not specified Investigated Fever, heart disease, snake bite [10, 23]
Plectranthus caninus Roth Kibwankulata Leaves Herb Decoction 4 and 2 teaspoons thrice a day for adults and children, respectively, for a week No record [10]
Plectranthus cf. forskohlii Ekizera Leaves Decoction Oral, dose not specified No record [19]
Rosmarinus officinalis L. Rosemary Leaves Herb Decoction Half a glass twice a day for 5 days Investigated Chest pain [10]
Tetradenia riparia (Hochst.) Codd Kyewamala Leaves Herb Decoction One teaspoon twice a day for a week Investigated [10]
Lauranceae Persea americana Mill. Ovakedo Leaves Tree Decoction Oral, dose not specified Investigated Fungal and bacterial infection, high blood pressure, intestinal worms and parasites [23]
Loranthaceae Tapinanthus constrictiflorus (Engl.) Danser Enzirugaze Leaves Herb Decoction A glass daily for 7 days No record [10]
Malvaceae Hibiscus surattensis L. Nantayitwako musota Leaves Shrub Decoction Half a glass thrice a day for 7 days No record High blood pressure [10]
Meliaceae Azadirachta indica A. Juss. Neem Leaves Tree Decoction About 120 ml once a day for 7 days Investigated Dental decay/ache, yellow fever, cough, skin diseases, diabetes, nausea [10, 19, 23, 25]
Carapa grandiflora Sprague Omukeete Leaves/bark Tree Decoction Half a glass twice a day for 7 days No record [10]
Melia azedarach Elira Leaves Tree Decoction Oral, dose not specified Investigated Fever, skin disease, itching wounds, parasitic worms [23]
Menispermaceae Cissampelos mucronata A. Rich. Kavawala Leaves/whole plant Herb Decoction Half a glass twice a day for 5 days Investigated [10]
Mimosaceae Acacia hockii De willd Ekisim Roots Tree Decoction Oral, dose not specified No record Diarrhea, syphilis, dysentery [23, 30]
Acacia nilotica Investigated [31]
Acacia sieberiana Etiriri Roots Tree Decoction Oral, dose not specified No record Dysentery, epilepsy, cough [21, 23]
Albizia coriaria Welw. Lugavu Bark Tree Decoction 1 and 3 teaspoons thrice a day for children and adults, respectively, for a week. Investigated Skin diseases, diarrhea [10]
Albizia grandibracteata Taube Nongo Bark Tree Decoction Half a glass once a day for a week Investigated Yellow fever, anemia, fungal infections of scalp [8, 10, 32]
Albizia zygia (DC.) Macbr. Mulongo Bark Tree Investigated [21]
Newtonia buchananii (Baker) Gilb. & Perr. Mpewere Bark Tree Dried, powdered, added to boiling water Half a glass once a day for a week No record [10]
Moraceae Antiaris toxicaria Lesch. Kirundu Bark Tree Decoction Half a glass once a day for a week Investigated Weakness in pregnancy, headache [8, 10]
Ficus natalensis Hochst Tree Investigated Gonorrhea [8, 33]
Ficus saussureana DC. Muwo Bark Tree Decoction Half a glass thrice a day for 7 days No record [10]
Milicia excels (Welw.) C. C. Berg. Mivule Bark Tree Decoction Half a glass thrice a day for 7 days Investigated Burns, fresh cuts, skin rush [8, 10]
Moringaceae Moringa oleifera Lam Moringa Leaves/roots Tree Decoction/chewed raw A glassful thrice a day for 7 days; a handful of fresh leaves chewed 3 times for 4 days Investigated Joint pains [21, 25]
Musaceae Musa paradisiaca (NC) Kabalagala Leaves Herb Decoction Oral, dose not specified Investigated Jaundice, prolonged embryo in uterus [19]
Myricaceae Myrica kandtiana Engl. (NC) Omujeeje Leaves Decoction Oral, dose not specified No record Vomiting, diarrhea [19]
Myristicaceae Pycnanthus angolensis (Welw.)Warb. Lunaba Leaves Tree Decoction Half a glass a day Investigated [10]
Myrsinaceae Maesa lanceolata Forssk. Kiwondowondo Leaves Shrub Decoction Half a glass thrice a day for 7 days Investigated Febrile convulsions [10, 19, 24]
Myrtaceae Eucalyptus grandis Maiden. Kalitunsi Leaves Tree Decoction Half a glass a day No record Cough [8, 10]
Psidium guajava L. Mupeera Leaves Tree Decoction Half a glass thrice a day for a week Investigated Bloody diarrhea, typhoid, wounds, cough [10, 23]
Syzygium cordatum Hochst. Mugeege Bark Tree Decoction Oral, dose not specified Investigated Dry cough, skin rush, wounds [8, 10, 20, 29]
Syzygium cumini (L.) Skeels Jambula Leaves Tree Decoction Half a glass thrice a day for a week Investigated Cough [32]
Syzygium guineense (Willd.) DC. Kalunginsanvu Bark Tree Decoction Oral, dose not specified Investigated [20]
Papillionaceae Butyrospermuum paradoxum Ekunguri Roots Tree Decoction Oral, dose not specified No record Labour pains, headaches [23]
Ormocarpum trachycarpum Ederut Roots Shrub Decoction Oral, dose not specified No record Pneumonia, snake bite [23]
Passifloraceae Passiflora edulis Sims Akatunda Leaves Herb Fresh extract Oral, dose not specified No record Diarrhea, cough [19]
Pittosporaceae Pittosporum brachcalya Not defined Not defined Shrub No record [34]
Pittosporum mannii Hook. f. Subsp. ripicola (J. Leon)Cuf. Mubajjankon Leaves Shrub Infusion/decoction Half a glass a day for a week No record [10]
Poaceae Cymbopogon citratus Stapf. Kisubi Leaves Grass Decoction 120 ml every after 8 hours for a week Investigated Dental caries, influenza, cough, cancer, indigestion, fever [10, 19, 23]
Digitaria scalarum Chiov. Lumbugu Leaves Grass Decoction 120 ml every after 8 hours for a week No record [10]
Imperata cylindrical (L.) Beauv. var. africana (Anderss.) C. E. Hubbard Lusenke Roots Grass Dried, powdered, added boiling water/decoction 120 ml once a day for a week No record Abdominal pain [10]
Zea mays L. Luyange lwakasoli Flowers/husks Cereal grass Decoction 120 ml every after 8 hours for a week Investigated Boosts immunity [10]
Polygalaceae Securidaca longipedunculata Fresen. Eliloi Roots Shrub Decoction Oral, dose not specified Investigated Skin diseases, measles, cough, hernia, diarrhea [23]
Maesopsis eminii Engl. Musizi Bark Tree Decoction Half a glass thrice a day for a week No record [10]
Portulacaceae Talinum portulacifolium (Forssk.) Asch. ex Schweinf. Mpozia Leaves Herb Oral, dose not specified No record [21]
Rosaceae Prunus africana (Hook. f.) Kalkman Ntaseesa or Ngwabuzito Bark Tree Decoction 2 and 3 teaspoons thrice a day for children and adults, respectively, for a week Investigated Fainting, cancer [8, 10]
Rubus steudneri schweinf. Nkenene Leaves Herb Decoction Half a glass once a day for a week No record [10]
Rubiaceae Coffea canephora Froehner Mwanyi Leaves Shrub Decoction Oral, dose not specified No record [21]
Hallea rubrostipulata (K. Schum.) J.-F. Leroy Muziku Bark Tree Decoction Oral, dose not specified Investigated [20]
Pentas longiflora Oliv. Ishagara Leaves Decoction Oral, dose not specified Investigated Fever [19]
Vangueria apiculata K. Schum. Matugunda Bark Shrub Decoction 2 and 3 teaspoons thrice a day for children and adults, respectively, for a week No record [10]
Rutaceae Citrus reticulata Omuqugwa Roots Tree Decoction Oral, dose not specified Investigated Weight loss induction, cancer, skin diseases [23]
Citrus sinensis Omucungwa/cungwa Roots Tree Decoction Oral, dose not specified Investigated Vomiting, cough, diabetes [21, 23, 25]
Teclea nobilis Delile Omuzo Aerial parts Decoction Oral, dose not specified Investigated Body cleanser [32]
Toddalia asiatica Baill. Kawule Roots Climber Decoction Half a glass thrice a day for a week Investigated Cough, abdominal pain [10, 19, 24]
Zanthoxylum chalybeum Engl. Ntale ya ddungu Roots Tree Decoction Oral, dose not specified Investigated Body swellings, stomach ache, cough, fever, chest pain [10, 23, 28]
Zanthoxyllum leprieurii Guill. & Perr. Mutatembwa/munyenye Bark Tree Decoction drunk Half a glass thrice a day for a week No record [10]
Salicaceae Trimeria grandifolia ssp. tropica (Hochst.) Warb. Omwatanshare Leaves Decoction Oral, dose not specified Investigated [19]
Sapindaceae Blighia unijugata Baker Nkuzanyana Bark Tree Decoction drunk Half a glass twice a day for a week Investigated Wounds, vomiting, skin diseases, fibroids, cervical cancer [8, 10]
Sapotaceae Manilkara obovata (Sabine & G. Don) Nkunya Bark Tree Decoction Oral, dose not specified No record [20]
Scrophulariaceae Sopubia ramosa (Hochst.) Hochst. Kakulunkanyi Whole plant Herb Decoction Oral, dose not specified No record [20]
Simaroubaceae Harrisonia abyssinica Olive. Ekeroi Roots/leaves Shrub Decoction Oral, dose not specified Investigated Fever, wounds, syphilis, snake bite, abdominal pain [23]
Solanaceae Datura stramonium Thunb. Amadudu Leaves Herb Decoction drunk Half a glass thrice a day for a week No record Ulcers, stomach ache, chest pain [10]
Physalis peruviana L. Ntuntunu Leaves Herb Decoction drunk Half a glass 3 times a day for a week No record Vomiting, febrile convulsions, fainting [8, 10, 19]
Solanum nigrum L. Nsugga Leaves Herb Decoction drunk Half a glass 3 times a day for a week Investigated Ear infection, headache, epilepsy, STI, diarrhea [8, 10]
Tiliaceae Trumfetta rhomboidea Jacq. Musombankoko Roots Shrub Decoction drunk Half a glass once a day for a week No record [10]
Ulmaceae Celtis africana L. Akasisa Leaves Tree Decoction drunk Half a glass a day for a week Investigated [10]
Umbelliferae Steganotania araliacea Hoeshst Ematule Roots/leaves Tree Decoction Oral, dose not specified No record Measles, body swelling [23]
Verbenaceae Lantana camara Kanpanga Leaves Shrub Decoction Oral, dose not specified Investigated Wounds, measles, tuberculosis, pneumonia, snake bite, chest pain [23]
Lantana trifolia L. Omuhukye Leaves Decoction Orally taken, dose not specified Investigated Yellow fever, ringworms, muscle pain, prolapsed rectum [8, 19]
Zingiberaceae Curcuma longa L. Binjali Rhizome Herb Fresh extract 30 ml thrice a day for 3 days Investigated [28]

Table 2.

Some herbs used in malaria prevention amongst communities in Uganda.

Plant family Plant species Local name Plant form Mode of use to prevent malaria Reference(s)
Cleomaceae Cleome gynandra L. Akeyo Herb Leaves are cooked and eaten as a prophylactic measure [25]
Cucurbitaceae Cucurbita maxima Duchesne Acuga Scrambler Leaves cooked and pasted with groundnut then eaten [25]
Euphorbiaceae Manihot esculenta Crantz Gwana Herb Tuber peelings are dried then burnt in house so that smoke repels mosquitoes [25]
Fabaceae Crotalaria ochroleuca G. Don Alayo Herb Leaves are cooked and eaten as a prophylactic measure [25]
Lamiaceae Ocimum forsskaolii Benth. Yat cola Herb Leaves dried and burnt so that smoke chases away mosquitoes; bath infusion to repel mosquito [25]
Rosmarinus officinalis L. Rosemary Herb Leaves are cooked and eaten as a prophylactic measure; planted around the house to repel mosquitoes [10]
Malvaceae Gossypium hirsutum L. Pama Shrub Cotton lint is dried and burnt so that smoke keeps away mosquitoes [25]
Musaceae Musa sp. Labolo kwon Shrub Fruit peeling are dried and burnt in the house to produce smoke that keeps away mosquitoes [25]
Myrtaceae Eucalptus grandis Maiden. Kalitunsi Tree Leave and branches are burnt to repel mosquitoes [25]
Poaceae Cymbopogon citratus Stapf. Kisubi Grass Planted around the house to repel mosquitoes; taken in tea as a prophylactic measure [19, 23]
Solanaceae Solanum americanum Mill. Ocuga Herb Leaves are cooked and eaten as a prophylactic measure [25]

The mechanism of action of artemisinin is widely debated but the most accepted theory is that of activation of the molecule by heme, which enables it to produce free radicals that then destroy the proteins needed for parasite survival [36]. The presence of an uncommon chemical peroxide linkage bridge in artemisinin, a sesquiterpene lactone, is the most probable reason for its antimalarial effects. Cleavage of the peroxide linkage bridge in the presence of iron (II) ions (from heme) forms very reactive free radicals that undergo rapid rearrangement to form more stable carbon-centered radicals, which chemically modify the parasite and inhibit various processes within the parasite molecules, resulting in its death [36]. Artemisinin acts on primarily the trophozoite parasitic phase and prevents disease progression. It kills circulating ring-stage parasites, thus increasing the therapeutic response [37]. Mok et al. [38] suggested that artemisinin is linked to the upregulation of unfolded protein response pathways, which leads to decreased parasitic growth and development. Shandilya et al. [39] suggested that artemisinin is activated by iron, which then functionally inhibits PfATP6, a calcium pump, by terminating phosphorylation, nucleotide binding, and actuator domains, eventually leading to a functional loss of PfATP6 of the Plasmodium parasite and its death. A study by Mbengue et al. [40] indicated that artemisinin strongly inhibits phosphoinositide-3-kinase (PfPI3K), an enzyme important in cellular activities including growth, multiplication, differentiation, and survival in P. falciparum.

Cinchona tree bark, from which quinine was isolated, has been used to treat malaria since 1632 [41]. The World Health Organization listed quinine as one of the important medicines needed in a health system [42]. It is however only used to treat malaria caused by chloroquine-resistant strain of P. falciparum in the absence of artemisinins [43]. A popular hypothesis about the mechanism of action of quinine is based on chloroquine, another quinoline drug which is closely linked to quinine and has been comprehensively studied. Quinine inhibits the pathway of biocrystallization of hemozoin, resulting in the accumulation of the free cytotoxic heme which eventually kills the parasite [44].

Most of the plants used in the treatment of malaria in Uganda contain alkaloids greatly implicated in antiplasmodial activity (Table 3). A number of alkaloids target apicoplast, an organelle in the Plasmodium parasite, while others such as benzylisoquinoline alkaloids in Cissampelos mucronata, a plant belonging to the family Menispermaceae inhibits protein synthesis in the parasite [99].

Table 3.

Antiplasmodial/antimalarial activities of investigated plants used for malaria treatment in Uganda and their active chemical constituents.

Plant family Scientific name Part used Extracting solvent Means of traditional extraction Report on antiplasmodial, IC50 (μg/ml)/antimalarial activity (Plasmodium strain) Active chemical constituents Reference(s)
Acanthaceae Justicia betonica L. Shoot Methanol Hot water 69.6 (chloroquine sensitive, K39) Justetonin (indole(3,2-b) quinoline alkaloid glycoside) [20]
Water >100 (chloroquine sensitive, K39)
Aloeaceae Aloe dawei A. Berger (wild/cultivated) Leaves Ether Cold water; mashing; hot water Extract had anti-P. falciparum activity value of 7.97 (95% CI: 3.56 to 17.85) μg/ml with 50% schizonts suppression per 200 WBC (EC50) Anthraquinones, aloin, lectins, [19, 45]
Aloe kedongensis (wild) Leaves Methanol Hot water 87.7 (chloroquine sensitive, D6); 67.8 (chloroquine resistant, W2) Anthrone, C-glucoside homonataloin, anthraquinones, aloin, lectins [19, 46]
Aloe ferox Mill Leaves Dichloromethane Water 21 (chloroquine sensitive, D10) Mannans, polymannans, anthraquinones, aloin, lectins, anthrones [19, 31, 47]
Water >100 (chloroquine sensitive, D10)
Anacardiaceae Mangifera indica L. Leaves Chloroform:Methanol (1 : 1) Hot water Inhibited growth of P. falciparum by 50.4% at 20 μg/ml Phenolics [48, 49]
Stem bark Ethanol >50 (chloroquine resistant, FcB1)
Rhus natalensis Bernh. Ex Krauss Leaves Ethanol Hot water 6.6 (P. falciparum) Triterpenoids [24]
Apiaceae Centella asiatica (L.) Urb. Whole plant Water Water 58.6 (chloroquine sensitive, D6); not detected (chloroquine resistant, W2) Phenolics and flavonoids [50]
Apocynaceae Alstonia boonei De Wild. Stem bark Water Hot water 80.97% suppressive activity at 200 mg/kg (P. berghei) in combination with other two local herbs. Alkaloids, triterpenoids [51]
Carissa edulis (Forssk.) Vahl Stem bark Dichloromethane Mashing; hot water 33 (chloroquine sensitive, D10) Lignan, nortrachelogenin [52]
Carissa spinarum Lodd. ex A. DC. Root bark Methanol Hot water 14.5 (chloroquine sensitive, D6) Saponins, sesquiterpenes [53]
Catharanthus roseus G. Don Leaves Methanol Hot water 4.6 (chloroquine sensitive, D6); 5.3 (chloroquine resistant, W2) Alkaloids, terpenoids, flavonoids, esquiterpenes [54]
Aristolochiaceae Aristolochia elegans Mast. Seeds Methanol Water >50 (chloroquine sensitive, 3D7); undetectable (chloroquine resistant, W2) Sesquiterpenoids, diterpenoids, monoterpenoids, alkaloids [19, 55]
Asphodelaceae Aloe vera (L.) Burm. f. Leaves Water Cold water; mashing; hot water Antiplasmodial activity in terms of EC50 values 0.289 to 1.056 μg/ml (chloroquine sensitive) Aloin, anthraquinones, aloe-emodin [56]
Asteraceae Ageratum conyzoides L. Whole plant Methanol Hot water 11.5 (chloroquine sensitive, D6); 12.1 (chloroquine resistant, W2) Flavonoids [54]
Artemisia annua L. Leaves Water Hot water 1.1 (chloroquine sensitive, D10); 0.9 (chloroquine resistant, W2) Sesquiterpenes and sesquiterpene lactones including artemisinin, flavonoids such as chrysoplenol-D, eupatorin, chyrsoplenetin [19, 57]
Artemisia afra Jacq. Ex Willd Leaves Methanol Hot water 9.1 (chloroquine sensitive, D6); 3.9 (chloroquine resistant, W2) Acacetin, genkwanin, 7-methoxyacacetin [54]
Aspilia africana (Pers.) C. D. Adams Leaves Ethanol Hot water Significant chemo suppressive effect of 92.23% (400 mg/kg) on P. berghei Saponins, terpenoids, alkaloids, resins, tannins, flavonoids, sterols [19, 58]
Baccharoides adoensis (Sch. Bip. ex Walp.) H. Rob. Leaves Petroleum ether Hot water 4.6 (chloroquine resistant, K1) Flavonoids [26]
Aspilia africana L. Leaves Dichloromethane Hot water; mashing 8.5 (chloroquine sensitive, D10) Flavonoids including quercetin 3,3′-dimethyl ether 7-0-α-L-rhamnopyranosyl-(1 ⟶ 6)-β-D-glucopyranose and quercetin 3,3′-dimethyl ether 7-0-β-D-glucopyranose [52]
Bothriocline longipes N. E. Br. Leaves Chloroform Hot water 3.7 (P. falciparum) 5-alkylcoumarins, [19, 24]
Ethanol 50 (P. falciparum)
Crassocephalum vitellinum Leaves Ethyl acetate Hot water 40.6% inhibition of P. falciparum at 10 μg/ml Flavonoids [32]
Guizotia scabra Chiov. Whole plant Crude ethanol Hot water 49.09% growth inhibition at 100 μg/ml (chloroquine resistant, Dd2) Lactones, eudesmanoline [59]
Melanthera scandens (Schumach. & Thonn.) Roberty Leaves Chloroform Hot water 68.83% chemo suppression activity (P. berghei) Triterpenoid saponins [60]
Microglossa pyrifolia (Lam.)O. Ktze Leaves Hot water <5 (both chloroquine sensitive, NF54 and resistant, FCR3) E-phytol; 6e-geranylgeraniol-19-oic acid [2, 28]
Schkuhria pinnata (lam.) Whole plant Water Hot water 22.5 (chloroquine sensitive, D6); 51.8 (chloroquine resistant, W2) Schkuhrin I and schkuhrin II [54]
Methanol 1.3 (chloroquine sensitive, D6); 6.8 (chloroquine resistant, W2)
Solanecio mannii (Hook. f.) C. Jeffrey Leaves Methanol Water 21.6 (chloroquine sensitive, 3D7); 26.2 (chloroquine resistant, W2) Phytosterols, n-alkanes and N-hexacosanol, [19, 55]
Tagetes minuta L. Leaves Ethyl acetate Water 61.0% inhibition of P. falciparum at 10 μg/ml [32]
Tithonia diversifolia A. Gray Leaves Methanol Water 1.2 (chloroquine sensitive, 3D7); 1.5 (chloroquine resistant, W2) Tagitinin C, sesquiterpene lactones [55]
Vernonia adoensis Sch. Bip. ex Walp. Leaves Methanol Hot water 83.4% inhibition of parasitaemia, at 600 mg/kg (P. berghei) Glycocides, glaucolides [19, 61]
Vernonia amygdalina Delile Leaves Methanol/dichloromethane Hot water; cold water 2.7 (chloroquine resistant, K1) Coumarin, sesquiterpene lactones including vernolepin, vernolin, vernolide, vernodalin and hydroxyvernodalin, steroid glucosides [19, 26]
Vernonia cinerea (L.) Less. Whole plant Water Hot water >50 (chloroquine sensitive, 3D7); 37.2 (chloroquine resistant, K1) Sesquiterpene lactone [62]
Vernonia lasiopus O. Hoffm. Leaves Methanol Mashing; hot water 44.3 (chloroquine sensitive, D6); 52.4 (chloroquine resistant, W2) Sesquiterpene lactones, polysaccarides [19, 54]
Bignoniaceae Markhamia lutea (Benth.) K. Schum. Leaves Ethyl acetate Hot water 71% inhibition of P. falciparum at 10 μg/ml Phenylpropanoid glycosides, cycloartane triterpenoids [32]
Spathodea campanulata Buch.-Harm. ex DC. Stem bark Ethyl acetate Water 28.9% inhibition of P. falciparum at 10 μg/ml Quinone (lapachol) [32]
Caesalpiniaceae Cassia didymobotrya Fres. Leaves Methanol Hot water 23.4 (chloroquine sensitive, D6); undetectable (chloroquine resistant, W2) Alkaloids [54]
Erythrophleum pyrifolia Leaves Ethanol Hot water >50 (P. falciparum) [24]
Senna spectabilis (DC.) H. S. Irwin & Barneby Leaves Ethanol Water 59.29% growth inhibition at 100 mg/kg body weight dose (P. berghei) Piperidine alkaloids [63]
Caesalpinioideae Cassia hirsuta Root back Methanol Water 32.0 (chloroquine sensitive 3D7) [64]
Canelliaceae Warbugia ugandensis Sprague Stem back Methanol Hot water 6.4 (chloroquine sensitive, D6); 6.9 (chloroquine resistant, W2) Sesquiterpenes e.g. muzigadiolide [27, 54]
Water 12.9 (chloroquine sensitive, D6); 15.6 (chloroquine resistant, W2)
Caricaceae Carica papaya L. Leaves Ethyl acetate Hot water 2.96 (chloroquine sensitive, D10); 3.98 (chloroquine resistant, DD2) Alkaloids, saponins, tannins, glycosides [65]
Methanol 10.8 (chloroquine sensitive, D10)
Celastraceae Maytenus senegalensis Roots Hot water 1.9 (chloroquine sensitive, D6); 2.4 (chloroquine resistant, W2) Terpenoids, pentacyclic triterpenes e.g. pristimerin [66]
Chenopodiaceae Chenopodium ambrosioides L. Leaves Crude hydroalcoholic extract Hot water Inhibited the P. falciparum growth, exhibiting an IC50 of 25.4 μg/ml Sesquiterpenes, monoterpenes [67]
Combretaceae Combretum molle G. Don Stem back Acetone Water 8.2 (chloroquine sensitive 3D7) Phenolics, punicalagin [68]
Cucurbitaceae Cucurbita maxima Lam. Seeds Crude ethanol Hot water 50% reduction of parasitaemia levels in P. berghei infected mice at 500 mg/kg. Phenols, terpenoids, alkaloids, tannins [69]
Momordica foetida Schumach. Shoot Water Hot water 6.16 (chloroquine sensitive, NF54); 0.35 (chloroquine resistant, FCR3) Saponins, alkaloid, cardiac glycosides [28]
Ebenaceae Euclea latideus Staff Root back Hexane Water 38.2 (chloroquine sensitive, 3D7); 38.9 (chloroquine resistant, Dd2) Triterpenoids lupeol, betulin, 3β-(5-hydroxyferuloyl)lup-20(30)-ene [23]
Euphorbiaceae Alchornea cordifolia (Schumach.) Mull. Arg. Leaves Water Hot water 4.8 (chloroquine resistant, K1) Phenolics including ellagic acid [70]
Bridelia micrantha Baill. Stem bark Methanol Hot water 19.4 (chloroquine sensitive, D6); 14.2 (chloroquine resistant, W2) [50]
Clutia abyssinica Jaub. & Spach Leaves Methanol Water 7.8 (chloroquine sensitive, D6); 11.3 (chloroquine resistant, W2) Diterpenes [54]
Croton macrostachyus Olive. Leaves Chloroform Hot water Chemotherapeutic effect of 66–82% in malaria mouse model Triterpenoids including lupeol [71]
Fluegea virosa (Roxb. ExWillb.)Voigt Leaves Water/methanol Hot water 2 (chloroquine resistant, W2) Bergenin [72]
Jatropha curcas L. Leaves Ethyl acetate Hot water 5.1 (chloroquine sensitive, NF54); 2.4 (chloroquine resistant, K1) Alkaloids, saponnins, glycosides, tannins [73]
Phyllanthus (pseudo) niruri Mull. Arg. Water Hot water Ranged from 2.9 to 4.1 (both chloroquine sensitive, 3D7 and resistant, Dd2) Coumarins including 1-O-galloyl-6-O-luteoyl-a-D-glucose [74]
Fabaceae Cajanus cajan (L.) Druse Leaves Crude ethanol Mashing 29.0 (P. falciparum) Cajachalcone; [75]
Entada abyssinica Steud. ex A. Rich. Seeds Methanol Hot water >5 (chloroquine resistant, K1) Flavonoids, terpenoids [26, 32]
Entada africana Guill. & Perr. Leaves Ethanol Hot water 26.4 (chloroquine sensitive, HB3); 28.9 (chloroquine resistant, FcM29) Phenolics [76]
Erythrina abyssinica Lam. Stem bark Ethyl acetate Hot water 83.6% inhibition of P. falciparum at 10 μg/ml Chalcones (5-prenylbutein, homobutein), flavanones including 5-deoxyabyssinin II, abyssinin III and abyssinone IV [32]
Indigofera emerginella Steud. ex A. Rich Leaves Ethanol Hot water 5.8 (P. falciparum) [24]
Senna didymobotrya (Fresen.) H. S. Irwin & Barneby Leaves Methanol Hot water >100 (chloroquine sensitive, K39) Quinones [20, 29]
Senna siamea (Lam.) H. S. Irwin & Barneby Leaves Ethanol Mashing; hot water 28.8 (chloroquine sensitive, 3D7); 48.3 (chloroquine resistant, W2) Phenolic derivative, chrobisiamone a, anhydrobarakol [77]
Tamarindus indica L. Stem bark Water Hot water 25.1% chemo suppressive activity at 10 mg/kg (P. berghei) Saponins (leaves), tannins (fruits) [78]
Flacourtiaceae Trimeria bakeri Gilg. Leaves Petroleum ether Hot water 3.9 (P. falciparum) Triterpenoids [24]
Hypericaceae Harungana madagascariensis Lam. Stem bark Water Hot water 9.64 (chloroquine resistant, K1) Quinones including bazouanthrone, feruginin a, harunganin, harunganol a [70]
Lamiaceae Ajuga remota Benth. Whole plant Ethanol Hot water 55 (chloroquine sensitive, FCA/GHA); 57 (chloroquine resistant, W2) Ajugarin-1, ergosterol-5,8-endoperoxide, 8-O-acetylharpagide, steroids [79]
Clerodendrum myricoides R. Br. Root bark Methanol Hot water 4.7 (chloroquine sensitive, D6); 8.3 (chloroquine resistant, W2) [50, 80]
Clerodendrum rotundifolium Oliv. Leaves Methanol Mashing; hot water <5 (both chloroquine sensitive, NF54 and resistant, FCR3) Saponins, tannins [28]
Hoslundia opposita Vahl. Leaves Ethyl acetate Hot water 66.2% inhibition of P. falciparum at 10 μg/ml Quinones, saponins, abietane diterpenes (3-O-benzoylhosloppone) [32]
Leonotis nepetifolia Schimp. exBenth Leaves Ethyl acetate Water 27.0% inhibition of P. falciparum at 10 μg/ml [32]
Ocimum basilicum Leaves Ethanol Hot water 68.14 (chloroquine sensitive, CQ-s); 67.27 (chloroquine resistant, CQ-r) [50, 80]
Ocimum gratissimum Willd. Leaves/twigs Dichloromethane Hot water 8.6 (chloroquine resistant, W2) Flavonoids [47, 49]
Ocimum lamiifolium Hochst. Leaves Water Water Significantly suppressed parasitaemia, 22.2%, 26.8% and 35.5% at dose of 200, 400 and 600 mg·kg, respectively (P. berghei) [81]
Plectranthus barbatus Leaves/stem Dichloromethane Hot water No activity [23, 47]
Rosmarinus officinalis L. Hot water Essential oil at a concentration 15867 ng/ml had no antimalarial activity [82]
Tetradenia riparia (Hochst.) Codd Root Hot water 13.2 (chloroquine-sensitive, NF54) [83]
Lauranceae Persea americana Mill. Leaves Ethanol Hot water 10.15 (chloroquine sensitive, 3D7); 44.94 (chloroquine resistant, W2) Phenolics [84]
Meliaceae Azadirachta indica A. Juss. Leaves Hot water 17.9 (chloroquine sensitive, D6); 43.7 (chloroquine resistant, W2) Terpenoids, isoprenoids, gedunin [49, 66]
Melia azedarach Leaves Methanol Hot water 55.1 (chloroquine sensitive, 3D7); 19.1 (chloroquine resistant, W2) [85]
Menispermaceae Cissampelos mucronata A. Rich. Root bark Methanol Hot water 8.8 (chloroquine sensitive, D6); 9.2 (chloroquine resistant, W2) Benzylisoquinoline alkaloids [80]
Mimosaceae Acacia nilotica Stem bark Methanol Hot water Dose of 100 mg/kg b/w produced parasitic (P. berghei) inhibition 77.7% Tannins, flavonoids, terpenes [86]
Albizia coriaria Welw. Stem bark Methanol Hot water 15.2 (chloroquine sensitive, D6); 16.8 (chloroquine resistant, W2) Triterpenoids, lupeol, lupenone [54]
Albizia grandibracteata Taube Leaves Ethyl acetate Hot water 22.0% inhibition of P. falciparum at 10 μg/ml [32]
Albizia zygia (DC.) Macbr. Stem bark Methanol Water 1.0 (chloroquine resistant, K1) Flavonoids mainly 3′,4′,7-trihydroxyflavone [87]
Moraceae Antiaris toxicaria Lesch. Stem bark Ethyl acetate Hot water 36.4% inhibition of P. falciparum at 10 μg/ml [32]
Ficus natalensis Hochst Leaves Hexane Hot water 6.7 (P. falciparum) [88]
Milicia excels (Welw.) C. C. Berg. Leaves Ethanol Hot water 76.7% chemo suppressive activity at 250 mg/kg/day (P. berghei) [89]
Moringaceae Moringa oleifera Lam Leaves Methanol Mashing; hot water 9.8 (chloroquine sensitive, D6); not detected (chloroquine resistant, W2) Flavonols [49, 80]
Musaceae Musa paradisiaca (NC) Leaves Ethyl acetate Hot water 75 (chloroquine sensitive, 3D7); 100 (chloroquine resistant, Dd2) Flavonoids [49, 90]
Myristicaceae Pycnanthus angolensis (Welw.)Warb. Leaves 50% ethanol Hot water >1000 (chloroquine sensitive, 3D7) Talaumidin [91]
Myrsinaceae Maesa lanceolata Forssk. Twig Dichloromethane:Methanol (1 : 1) Hot water 5.9 (chloroquine sensitive, D10) Lanciaquinones, 2,5, dihydroxy-3-(nonadec-14-enyl)-1,4-benzoquinone [24, 52, 55]
Myrtaceae Psidium guajava L. Stem back Water Hot water 10–20 (chloroquine sensitive, D10) Phenols, flavonoids, carotenoids, terpenoids [49, 92]
Syzygium cordatum Hochst. Twig Dichloromethane:Methanol (1 : 1) Hot water 14.7 (chloroquine sensitive, D10) [55]
Syzygium cumini (L.) Skeels Stem back Hot water 0.25 to 27.1 (chloroquine-resistant strains) [93]
Syzygium guineense (Willd.) DC. Leaves Crude ethanol Hot water 49.09% chemo suppression at 400 mg/kg (P. berghei) [94]
Poaceae Cymbopogon citratus Stapf. Whole plant Hot water 99.89% suppression of parasitaemia at 1600 mg/kg Flavonoids [20, 49, 95]
Zea mays L. Husks Ethyl acetate Hot water 9.3 (chloroquine sensitive, 3D7); 3.7 (chloroquine resistant, INDO) Alkaloids, flavonoids and triterpenoids [96]
Polygalaceae Securidaca longipedunculata Fresen. Leaves Dichloromethane Hot water 6.9 (chloroquine sensitive, D10) Saponins, flavonoids, alkaloids, steroids [92]
Rosaceae Prunus africana (Hook. f.) Kalkman Stem bark Methanol Hot water 17.3 (chloroquine sensitive, D6); not detected (chloroquine resistant, W2) Terpenoids [54]
Rubiaceae Hallea rubrostipulata (K. Schum.) J.-F. Leroy Root Ethanol Water 100 μg/ml extract had 65.54% growth inhibition (chloroquine resistant, Dd2) Alkaloids [59]
Pentas longiflora Oliv. Root Methanol Hot water 0.99 (chloroquine sensitive, D6); 0.93 (chloroquine resistant, W2) Pyranonaphthoquinones, pentalongin (1) and psychorubrin (2), naphthalene derivative mollugin (3) [97]
Rutaceae Citrus reticulata Seeds (isolimonexic acid methyl ether) Hot water <4.76 (both chloroquine sensitive, D6 and resistant, W2) Limonin, isolimonexic acid methyl ether, ichangin, deacetylnomilin, obacunone [98]
Citrus sinensis 70% ethanol Hot water 53.27% suppression of parasitaemia at 700 mg/kg Tannins, alkaloids, saponins, flavonoids [20, 24, 99]
Teclea nobilis Delile Bark Ethyl acetate Water 54.7% inhibition of P. falciparum at 10 μg/ml Quinonline alkaloids [32]
Toddalia asiatica Baill. Root bark Methanol Water 6.8 (chloroquine sensitive, D6); 13.9 (chloroquine resistant, W2) Furoquinolines (nitidine, 5,6-dihydronitidine), coumarins [80]
Zanthoxylum chalybeum Engl. Stem bark Water Hot water 4.3 (chloroquine sensitive, NF54); 25.1 (chloroquine resistant, FCR3) Chelerythine, nitidine, methyl canadine [28]
Salicaceae Trimeria grandifolia ssp. tropica (Hochst.) Warb. Leaves Methanol Hot water >50 (chloroquine sensitive, 3D7) [55]
Sapindaceae Blighia unijugata Baker Leaves Ethyl acetate Hot water 2.3% inhibition of P. falciparum at 10 μg/ml [32]
Simaroubaceae Harrisonia abyssinica Olive. Roots Hot water 4.4 (chloroquine sensitive, D6); 10.25 (chloroquine resistant, W2) Limonoids, steroids [66]
Solanaceae Solanum nigrum L. Fruit Methanol Hot water 10.3 (chloroquine sensitive, 3D7); 18.7 (chloroquine resistant, K1) Steroidal alkaloids, flavonoids [100]
Ulmaceae Celtis africana L. Stem bark Ethyl acetate Hot water 37.5% inhibition of P. falciparum at 10 μg/ml [32]
Verbenaceae Lantana camara Leaves Dichloromethane Hot water 8.7 (chloroquine sensitive, 3D7); 5.7 (chloroquine resistant, W2) Sesquiterpenes, triterpenes, flavonoids [30]
Lantana trifolia L. Arial parts Petroleum ether Hot water 13.2 (P. falciparum) Steroids, terpenoids, alkaloids, saponins [24]
Ethanol >50 (P. falciparum)
Zingiberaceae Curcuma longa L. Hot water; mashing 5 mg/kg had a significantly high chemo suppressive activity of 56.8% (P. berghei) Polyphenolic curcumin [101]

Flavonoids in a vast number of plants used for malaria treatment in Uganda are common to plants in the family Asteraceae such as B. longipes, A. conyzoides, and A. africana although other herbal plants from different families including C. roseus in Apocynaceae and A. zygia and A. nilotica in Mimosaceae also have them as active antiplasmodial constituents (Table 3). Flavonoids exhibit great antiplasmodial activity against different strains of the malaria parasite although the mechanism of antimalarial action is not clear [99]. Some studies suggest that flavonoids impede the influx of myoinositol and L-glutamine in erythrocytes that are infected [99]. Some flavonoids increase the level of oxidation of erythrocytes and inhibit protein synthesis in malaria parasites [99]. Furthermore, flavonoids are believed to inhibit fatty acid biosynthesis (FAS II) in Plasmodium [102].

Artemisinin resistance in P. falciparum has been reported in Vietnam, Cambodia, Muang Lao, and Thailand. A report published in 2018 showed over 30 separate cases in Southeast Asia of artemisinin resistance [36]. In case of resistance, parasitic clearance is slowed down and gametocytemia increases, resulting in greater selective pressure on other partner drugs to which resistance increases, thereby posing a great health threat. Thus, it is very important that the discovery of other drugs with novel mechanisms of action be prioritized by extensive exploration of the huge medicinal plant resources in Africa, which have been used by locals for effective malaria treatment yet have never been scientifically investigated for their antimalarial potential. Amoa Onguéné et al. [35] emphasized that it was indeed Africa's turn to offer a new antimalarial drug to humanity since artemisinin was discovered in Asia and quinine in Latin America.

5. Herbs and Plant Parts Used to Manage and Treat Malaria across Communities in Uganda

About 182 plant species from about 63 different plant families are used to treat malaria across several communities in Uganda (Table 1). Of the 63 plant families, species within the family Asteraceae are most widely used in the country to treat malaria, constituting up to 15% of all plant species used (Figure 3(a)). This is followed by species from Fabaceae (9%), Lamiaceae (8%), Euphorbiaceae (6%), and Mimosaceae (4%) families, with Myrtaceae, Aloeaceae, and Rutaceae families each contributing approximately 3% to the total number of species used for malaria treatment in Uganda (Figure 3(a)). The remaining families contribute only 49% of the total plant species used for malaria treatment (Figure 3(a)).

Figure 3.

Figure 3

(a) Composition of plant species in each family used to treat malaria. (b) Percentage use of plant parts for treatment of malaria.

The plant parts greatly used to treat malaria are leaves (54.4%) followed by roots (17.4%) and bark (16%); whole plants and other plant parts are used less commonly (Figure 3(b)). A particular herbal plant is commonly used singly though some times in combination with other herbs. The most common way of use is by boiling the medicinal plant part in water and then drinking the decoction; ingestion of fresh extracts and powdered forms of the herbs is also practiced (Table 1).

Different herbal remedies are used in different communities in different parts of the country depending on the geographical distribution of the medicinal plant species, for example, Warburgia ugandensis is particularly used in the eastern part of Uganda. However, herbal plant species such as Bidens pilosa L. are spread throughout the country and thus well known for malaria treatment across the country. In a study conducted by Ssegawa and Kasenene [20], no tree species in the forests of southern Uganda were more useful than Hallea rubrostipulata and Warburgia ugandensis in the treatment of malaria. These medicinal plants are known by different local names in different parts of the country as Uganda has diverse ethnic groups, including the Luo, Baganda, Itesots, and Banyankole/Bakiga.

Among all communities in Uganda, some measures are taken to control malaria, including draining of stagnant water, clearing and burning bushes, sleeping under insecticide-treated mosquito nets, and house spraying with insecticides.

6. Mode of Preparation and Use of Herbs in Treatment of Malaria in Uganda

The mode of preparation and use of herbs among different communities vary depending on the nature of the herb and plant parts used for malaria treatment [10]. Most commonly, the herbal medicines are prepared as water extracts in the form of decoction and infusion or as steam baths (Table 1) [19, 23]. The herbal plant water extract is made mostly by boiling a handful of the medicinal plant parts such as leaves in a litre of water and then given to the patient to take orally (Table 1) [23]. The dose of the extract given is dependent on the age of the patient and the “strength” of the herbal medicine although occasionally the weight of the patient [19, 23]. The quantity of extract given ranges from 100 to 500 ml, 100 to 250 ml, and 1 to 3 tea or tablespoons for adults, older children, and young children below 5 years of age, respectively, between 1 and 3 times a day for about a week or until when patient has recovered [19, 25]. The extracts are mostly prepared from single herbal plants or from combination of two herbal plants, for example, a decoction of Tamarindus indica and Mangifera indica is common [25].

In some cases, the medicinal plant parts are dried then pulverized to powder and 2–5 tablespoons of the power added to water and boiled to make a decoction. Some medicinal plant parts such as bark of M. indica stem and roots of V. lasiopus and their powders are boiled for long until the water is half the initial amount [25]. The herbal plant powder can also be added to cold or hot water and stirred and then drunk as recommended [10].

Medicine for malaria treatment from a herb such as B. pilosa can be made by squeezing a handful of its freshly picked leaves and drinking 1–3 teaspoons of the extract a day (Table 1) [23]. Occasionally, malaria herbal medicines can be obtained by preparing different plant parts in combination, for example, an infusion can be made from fresh leaves and pounded fresh roots of V. amygdalina [25]. This is then taken orally in a recommended dose. A handful of medicinal plant parts such as leaves can be squeezed and mixed with cold or warm water for bath, for example, leaves of B. adoensis [25]. Some common herbs are also eaten as vegetables as a prophylactic measure against malaria while others are planted in pots around houses or burnt to drive away mosquitoes (Table 2).

7. Antimalarial Activities and Toxicity of Herbs Used in Uganda for Malaria Treatment

Some studies have been performed on antiplasmodial/antimalarial activities of some of the herbal plants used in Uganda to treat malaria by using various strains of malarial parasites to confirm effectiveness as malaria treatment [26, 28]. Furthermore, a broad range of phytochemicals responsible for biological activities in some of the antimalarial herbs have been isolated and identified [23]. Of the 182 plant species used in Uganda for the treatment of malaria, 112 plant species (64%) have been investigated for antimalarial activities, of which 108 plants showed positive results and only four plant species did not give positive results when tested for antimalarial activities (Table 1). For about 70 plant species (39%) that are used among different communities in Uganda for the treatment of malaria, there was no record of investigation for antimalarial activities (Table 1).

The antimalarial activity of herbal plants is due to the presence of a number of metabolically active compounds [23]. These compounds may occur in the form of alkaloids, sesquiterpenes, quinones, triterpenoids, flavonoids, quassinoids, limonoids, terpenes, chalcones, coumarins, or other miscellaneous forms [85]. The solvent of extraction largely determines the concentrations of the active metabolites in the extract. For example, methanolic extracts of the herbal plants are in general more active in vitro than water extracts probably due to the presence of higher amounts of more active lipophilic compounds (Table 3) [54].

The levels of activity of the antimalarial plant extracts depend on the concentration of the active antimalarial secondary metabolites [54]. For example, gedunin, a very active compound against Plasmodium present in leaves of A. indica had an IC50 of 0.02 μg/ml against P. falciparum, but its concentration in the plant is in very low and thus moderate activity of its extract (Table 3) [23, 54].

The synergistic effect of the interaction of the different active secondary metabolites is a main contributing factor to the high levels of antiplasmodial activity of some of the herbal plant extracts, for example, in A. afra, none of the isolated flavonoids and sesquiterpenes had a high activity, yet the plant extract had an IC50 of 3.9 μg/ml against P. falciparum suggesting a synergistic effect of the compounds in the extract [54]. The presence of particular active compounds in the herbal plant extracts is key in enhancing its antimalarial property. The compound 6E-geranylgeraniol-19-oic-acid a diterpene isolated from M. pyrifolia aqueous extract was considered responsible for its antiplasmodial activity; nitidine isolated from Z. chalybeum had an IC50 as low as 0.17 μg/ml against P. falciparum 3D7 [10]; and pristimerin with an IC50 0.5 mg/ml against P. falciparum was the main active ingredient in M. senegalensis extract, making it have a very high antiplasmodial activity [54]. The presence of a moderate amount of a minimum of two secondary metabolites in the extract could explain the efficacy of the herbal extracts for malaria treatment [10]. The pathogenic strains used may be different for different in vitro studies; thus, resistance of the parasite to the active metabolites could cause a variation in the level of antimalarial activity of the extracts [10]. Herbal plants with no antiplasmodial activity suggest the absence of the metabolically active compounds against the Plasmodium parasites in their extracts [23]. Table 4 indicates a list of herbal plants used for malaria treatment in Uganda with high antiplasmodial activities (IC50<5 μg/ml in one of its solvent extracts or high percentage inhibition of plasmodia) that could be potentially investigated further.

Table 4.

Top 17 herbal plants used locally in Uganda for malaria treatment with highest antimalarial/antiplasmodial activities (arranged alphabetically).

Plant family Plant species Plant part Extracting solvent Report on antiplasmodial, IC50 (μg/ml)/antimalarial activity (Plasmodium strain) Active chemical constituents Toxicity/safety information Reference(s)
Asteraceae Artemisia afra Jacq. Ex Willd Leaves Methanol 3.9 (chloroquine resistant, W2) Acacetin, genkwanin, 7-methoxyacacetin Cytotoxicity was observed in Vero cells [54, 103]
Artemisia annua L. Leaves Water 0.9 (chloroquine resistant, W2); 1.1 (chloroquine sensitive, D10) Sesquiterpenes and sesquiterpene lactones including artemisinin Generally safe and effective; nausea may occur on drinking herbal extract; artemisinin, an active compound in the extract is safe for pregnant women at least during second and third trimesters [19, 57, 104]
Aspilia africana (Pers.) C. D. Adams Leaves Ethanol Significant chemo suppressive effect of 92.23% (400 mg/kg) on P. berghei Saponins, terpenoids, alkaloids, resins, tannins, flavonoids, sterols No signs of toxicity in mice even at a dose as high as 5000 mg/kg [19, 58]
Jatropha curcas L. Leaves Ethyl acetate 2.4 (chloroquine resistant, K1) Alkaloids, saponnins, glycosides, tannins Moderate toxicity on thrombocyte line and a protective effect on cardiovascular system; no signs of toxicity in mice following oral administration of 5000 mg/kg body weight (bw) dose [73, 105]
Microglossa pyrifolia (Lam.)O. Ktze Leaves Dichloromethane 1.5 (chloroquine sensitive, 3D7; 2.4 chloroquin resistant, W2) E-phytol; 6e-geranylgeraniol-19-oic acid Relatively high cytotoxicity against cells from the human foetal lung fibroblast cell line [2, 28, 55]
Schkuhria pinnata (lam.) Whole plant Methanol 1.3 (chloroquine sensitive, D6) Schkuhrin I and schkuhrin II Methanol extract: low cytotoxicity against human cells; aqueous extracts: no observed toxicity observed in mice [32, 54]
Tithonia diversifolia A. Gray Leaves Methanol 1.2 (chloroquine sensitive, 3D7); 1.5 (chloroquine resistant, W2) Tagitinin C, sesquiterpene lactones Aerial parts are cytotoxic against cells from the human foetal lung fibroblast cell line [55]
Vernonia amygdalina delile Leaves Methanol/dichloromethane 2.7 (chloroquine resistant, K1) Coumarin, sesquiterpene lactones including vernolepin, vernolin, vernolide, vernodalin and hydroxyvernodalin, steroid glucosides Petroleum ether extract shows strong cytotoxicity [19, 26, 32]
Caricaceae Carica papaya L. Leaves Ethyl acetate 2.96 (chloroquine sensitive, D10); 3.98 (chloroquine resistant, DD2) Alkaloids, saponins, tannins, glycosides No serious toxicity reported, carpaine, an active compound against P. falciparum had high selectivity and was nontoxic to normal RBCs [65, 106]
Celastraceae Maytenus senegalensis Roots 1.9 (chloroquine sensitive, D6); 2.4 (chloroquine resistant, W2) Terpenoids, pentacyclic triterpenes, e.g., pristimerin No toxicity observed in ethanol extract [66, 107]
Cucurbitaceae Momordica foetida Schumach. Shoot Water 0.35 (chloroquine resistant, FCR3); 6.16 (chloroquine sensitive, NF54) Saponins, alkaloid, phenolic glycosides including 5,7,4′-Trihydroxyflavanone and kaempferol No pronounced toxicity against human hepatocellular (HepG2) and human urinary bladder carcinoma (ECV-304, derivative of T-24) cells [26, 28, 108]
Euphorbiaceae Alchornea cordifolia (Schumach.) Mull. Arg. Leaves Water 4.8 (chloroquine resistant, K1) Phenolics including ellagic acid No mortality in mice in acute toxicity test [70, 109]
Fluegea virosa (Roxb. ExWillb.)Voigt Leaves Water/methanol 2 (chloroquine resistant, W2) Bergenin Nontoxic, extracts exposed to murine macrophages did not slow or inhibit growth of cells [72, 110]
Phyllanthus (pseudo) niruri Mull. Arg. Water Ranged from 2.9 to 4.1 (both chloroquine sensitive, 3D7 and resistant, Dd2) Coumarins including 1-O-galloyl-6-O-luteoyl-a-D-glucose No toxicity was observed; thus, LD50 of the aqueous extract is >5000 mg/kg. b.w. [74, 111]
Lamiaceae Clerodendrum rotundifolium Oliv. Leaves Methanol 0.02 (chloroquine sensitive, CQS); 1.56 (chloroquine resistant, CQR) Iridoid glycosides such as serratoside A, serratoside B and monomelittoside, diterpenoids including uncinatone, clerodin, and sugiol Not explored [28, 33]
Mimosaceae Albizia zygia (DC.) Macbr. Stem bark Methanol 1.0 (chloroquine resistant, K1) Flavonoids, mainly 3′,4′,7-trihydroxyflavone The aqueous extract is relatively safe on subacute exposure [87, 112]
Rubiaceae Pentas longiflora Oliv. Root Methanol 0.99 (chloroquine sensitive, D6); 0.93 (chloroquine resistant, W2) Pyranonaphthoquinones, pentalongin (1) and psychorubrin (2), naphthalene derivative mollugin (3) Low cytotoxicity [97]
Rutaceae Citrus reticulata Seeds (isolimonexic acid methyl ether) <4.76 (both chloroquine sensitive, D6 and resistant, W2) Limonin, isolimonexic acid methyl ether, ichangin, deacetylnomilin, obacunone Dermal 50% lethal dose (LD50) of undiluted leaf oil is >2 g/kg in rabbits; seed extract causes respiratory distress and strong spleen contraction [34, 113]

Although herbs are generally considered safer when used for treatment compared to conventional drugs, some of the herbs used traditionally to treat malaria in Uganda may be efficacious, but there is a need to have them used with caution as some may be toxic (Table 4). There is a variation in degree of toxicity depending on the sensitivity of animals, tissue or cells used, type of extract, nature of the test substance, dose, and mode of administration [114]. According to Lacroix et al. [32] one third of the herbs for malaria treatment in Uganda they investigated had significant antiplasmodial activity with low toxicity. Some of the plant parts with good antiplasmodial/antimalarial activities with no or low toxicity include leaves of A. annua, leaves of A. africana, S. pinnata whole plant, leaves of C. papaya, and leaves of F. virosa amongst others (Table 4). There are however extracts of some plants used for malaria treatment with very good activity against Plasmodium but with high toxicity; such plant extracts include petroleum ether leaf extract of V. amygdalina and dichloromethane leaf extract of M. pyrifolia (Table 4) [32, 55]. Clerodendrum rotundifolium is on those plants that have very good antimalarial/antiplasmodial activities but have not been investigated for their toxicity (Table 4) [33].

8. Traditional Health Care Practice and Policy Framework in Uganda

The health care system of Uganda consists of the public, private-profit oriented, and private-nonprofit oriented sectors. There is quite a large sector of informal health care including traditional medicine practitioners, drug shops, medicine vendors, and complementary and alternative practitioners. The contribution of traditional health practitioners to Uganda's health care system was not valued until lately [115]. The negative perspective could be traced back to the colonial times when culture including use of traditional medicine such as herbs for treatment was considered primitive and so discouraged [115]. Efforts are now being made to promote the use of traditional medicine since the government has realized that traditional health practitioners are key contributors to its primary health care system [115]. The Ministry of Health created a public-private partnership with the traditional health practitioners following a recommendation that they be brought into the mainstream health system [115, 116].

A policy on Traditional and Complementary Medicine was created to regulate traditional medicine practice focusing on research and development while emphasizing the propagation, protection, and sustainable use of medicinal plant resources [115, 116]. For collaboration between the mainstream health care sector and traditional health practitioners, the Ministry of Health submitted a bill for the creation of the National Council of Indigenous and Complementary Medicine Practitioners, a semiautonomous body that shall as well protect their intellectual property rights [115, 116].

The National Drug Authority (NDA) is a body that ensures quality control of all medical products including herbal medicines in Uganda under the government statute and policy of 1993 [117]. In Uganda, there is no special regulatory measure for herbal medicines in that the same laws and policies for conventional pharmaceuticals also apply to the herbal medicinal products. A policy was introduced in 2002 to have herbal medicines registered, but so far, no registration of any herbal medicine has been made [117].

Herbal medicines though vastly used in Uganda are not sufficiently regulated. A system to license and track traditional health practitioners or their products is still lacking in the country, and the efforts to have the TCM integrated in the mainstream health care system is still a long way from being realized.

9. Conclusion

Uganda is rich in indigenous plant resources that are used by its people to treat malaria. Communities in different regions of the country use different herbs within their geographical range, though a few common herbs are used by different communities across the country. Many herbs used for malaria treatment among several communities have not been investigated for their efficacy, and yet they could be potential sources for antimalarial remedies including drugs. Few studies have been conducted to document herbs for malaria treatment in the country, especially in the northern region. Some of the plants investigated for antimalarial/antiplasmodial activities have been found to lack efficacy, toxicity, and safety study aspects. Some plants used in the local communities had very strong antimalarial activities and could be investigated further for the identification and validation of the potential therapeutic antimalarial compounds. This review is critical in that it clearly highlights herbal plants documented in Uganda for malaria treatment but have never been investigated for their antimalarial potential, thus providing guidance for further research on potential natural plant resources that could be sources of novel compounds with therapeutic properties for the treatment of malaria.

Acknowledgments

This study was supported under the framework of International Cooperation Program (Korea-South Africa Cooperative Research Project for Excavation of Candidate Resources of Complementary and Alternative Medicine) managed by National Research Foundation of Korea (grant nos. 2017093655 and KIOM:D17470). Additionally, this study was equally supported by grants from Development of Foundational Techniques for the Domestic Production of Herbal Medicines (K18405) and Applicational Development of Standardized Herbal Resources (KSN1911420), from the Korea Institute of Oriental Medicine (KIOM), through the Ministry of Science and ICT, Republic of Korea.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors' Contributions

Denis Okello carried out the data search and was the main contributor in writing the manuscript. Youngmin Kang technically designed and helped in writing the manuscript. Both authors read and approved the final manuscript.

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