ORIGINAL RESEARCH article

Front. Pharmacol., 25 February 2026

Sec. Ethnopharmacology

Volume 16 - 2025 | https://doi.org/10.3389/fphar.2025.1702353

An ethnopharmacological assessment of medicinal plants in Malanje Municipality, Angola

  • 1. Instituto Politécnico, Universidade Rainha Njinga A Mbande, Malanje, Angola

  • 2. Universidade Rainha Njinga a Mbande, Malanje, Angola

  • 3. Departamento de Farmacia, Facultad de Química y Farmacia, Universidad Central “Marta Abreu” de Las Villas, Santa Clara, Villa Clara, Cuba

  • 4. Departamento de Biologia, Faculdade de Ciências Naturais da Universidade Agostinho Neto, Luanda, Angola

Abstract

Background:

Malanje Municipality in north-central Angola harbors exceptional botanical and cultural diversity, yet remains poorly documented for traditional medicinal plant knowledge; this study provides the first systematic ethnopharmacological baseline to guide pharmacological prioritization, conservation, and policy-relevant integration of traditional medicine.

Methods:

Between 2018 and 2023, we conducted semi-structured interviews (n = 20 traditional healers), participatory observation, in situ photographic documentation, and GPS mapping. Voucher specimens were taxonomically verified against herbarium material and online resources. Quantitative indices included frequency measures and rank order priority (ROP); therapeutic indications were grouped using ICD-11 categories.

Results:

Informants reported 272 ethnospecies, of which 78 taxa (39 families) were identified to species level. Fabaceae (9%), Asteraceae (6.4%), and Euphorbiaceae, Poaceae, and Zingiberaceae (each 5.1%) were most represented families. Leaves (53.8%) and roots (42.3%) were the principal parts used; decoction (60%) and maceration (31%) were the most common preparations. ROP prioritized Terminalia brachystemma (81.8), Securidaca longepedunculata (54.4), and Mondia whitei (52.2) for follow-up study. Treated conditions clustered in gastrointestinal disorders (43.6%) and infectious/parasitic diseases (29.5%). Healers reported several contraindications and observable adverse effects.

Conclusion:

This work provides the first comprehensive ethnopharmacological register for Malanje Municipality, highlighting high-priority species for phytochemical, pharmacological, and toxicological evaluation and identifying conservation and sustainable-use concerns (notably root harvest). Limitations include a modest sample of informants and incomplete taxonomic resolution for many ethnospecies.

Recommendations:

Expand sampling across the province, complete voucher identification, perform contamination and toxicity screening, and develop community-led cultivation and stewardship plans that align with Angola’s National Policy for Traditional and Complementary Medicine.

Introduction

Medicinal plants have been central to human progress, forming the backbone of traditional therapies and contributing significantly to modern pharmaceuticals (). Angola, blessed with rich botanical diversity, boasts approximately 6850 native plants, including 997 endemic species (). Despite their profound economic, commercial, and health benefits, ethnobotanical research remains sparse. Encouragingly, recent studies are beginning to uncover how the Angolan populace traditionally uses these medicinal plants (; ; ; ; Urso et al., 2016). These investigations, conducted mainly in the northern and southern regions, underscore both the richness of Angola’s ethnobotanical heritage and the urgent need to expand research to underrepresented areas, such as Malanje.

Herbs and medicinal plants occupy a vital place in the cultural and traditional practices of African societies. In Angola, this legacy is reflected in a vast repertoire of culinary, ritual, and healing traditions developed to manage a wide range of ailments. Knowledge of these natural resources is predominantly transmitted orally through storytelling, apprenticeship, and communal experience (; ; Tchamba, 2019). However, the oral nature of this knowledge has contributed to a scarcity of written records, limiting the documentation and scientific validation of species diversity, their pharmacological roles, and their cultural importance. Preserving and studying these natural resources is therefore essential not only for safeguarding indigenous knowledge systems but also for promoting their transformation into standardized natural products that can strengthen healthcare systems and stimulate bioeconomic development (Mendonça et al., 2015).

Across Africa, many nations have adopted World Health Organization (WHO) guidelines encouraging the integration of traditional medicine into formal health systems (WHO, 2013). Angola took an important step in this direction on October 2, 2020, by approving the National Policy for Traditional and Complementary Medicine through Presidential Decree No. 253/20. : this landmark policy promotes the coexistence of evidence-based traditional practices and modern medicine, encouraging scientific research to evaluate their safety, efficacy, and socio-economic impact. Ethnopharmacological research is thus recognized as a key instrument for effectively implementing this policy ().

Historical accounts, such as those documented by Tchamba et al. (2024), highlight the pivotal role of 19th-century Christian missionaries in cataloging the medicinal flora of Angola, thereby laying the early foundations for ethnopharmacological inquiry in the region. These early records attest to the longstanding integration of plant-based remedies into local healing systems, a tradition that remains vibrant and culturally embedded.

In recent years, scientific investigations have further illuminated the pharmacological potential of key Angolan species. For example, Samba et al. (2025) conducted an in-depth phytochemical and pharmacological evaluation of Cochlospermum angolense, demonstrating notable antioxidant activity and reinforcing the therapeutic prospects suggested by traditional use. Such findings underscore the importance of bridging ancestral knowledge with contemporary analytical approaches to validate, strengthen, and sustainably harness indigenous plant resources.

Studies from surrounding provinces provide additional methodological and contextual grounding. In Uíge, surveys by and documented a rich repertoire of medicinal species used by Bakongo communities, particularly in disturbed savannah ecosystems where ecological pressure intersects with cultural resilience. Similarly, and examined the economic and medicinal relevance of native flora in Cuanza Norte, emphasizing the dual role these plants play in both primary healthcare and household livelihoods.

Further south, Urso et al. (2016) investigated Mopane woodland communities, revealing extensive knowledge of wild plants used for medicinal and nutritional purposes. In Bié Province, Novotna et al. (2020) described the practices of root doctors, traditional healers whose treatments draw on deep ethnomedical expertise and an intimate understanding of local biodiversity. Collectively, these regional studies attest to the remarkable diversity and depth of Angola’s ethnobotanical landscape, highlighting its scientific relevance, cultural significance, and the need for continued, systematic documentation.

Despite these advances, Malanje remains conspicuously understudied, leaving a significant gap in understanding regional patterns of medicinal plant use. The province occupies a transitional ecological zone between Guineo-Congolian forest influences and central-eastern savannah ecosystems, suggesting high potential for botanical and cultural diversity. The main objective of this study is to contribute to filling that gap by documenting and analyzing the ethnopharmacological knowledge of traditional healers in Malanje Municipality.

Beyond increasing Angola’s ethnopharmacological baseline, it aims to identify species with potential pharmacological and socio-economic importance, help the preservation of indigenous knowledge, and support sustainable biodiversity management; ultimately, this research provides a vital foundation for future surveys, pharmacological validation, bioprospecting efforts, and policy initiatives aimed at integrating traditional medicine into national healthcare and biodiversity conservation strategies.

Materials and methods

The research was carried out through several stages: conducting a bibliographic study to select the appropriate methodology, selecting and contacting informants, performing interviews, engaging in participatory observation to identify the reported ethnospecies, and organizing, processing, and analyzing the collected data.

Local of study

The study was conducted in the Municipality of Malanje, located in Malanje Province, north-central Angola. The municipality covers an area of approximately 2,422 km2 and lies at an average elevation of 1,122 m above sea level, between coordinates 9°32′24.54″S and 16°20′27.46″E, as show the Figure 1 (). It has an estimated population of approximately 221,275 inhabitants. In the Köppen classification, the study area has a tropical rainforest climate, characterized by a well-defined rainy season lasting 6–7 months (from October to April), with precipitation between 900 and 1,200 mm, and a dry season of 5–6 months (from May to September). Average annual temperatures range from 20 °C to 25 °C, and relative humidity varies between 65% and 75%. Soil types in Malanje vary regionally: the northern areas are dominated by Ferralsols and Acrisols, while the central and southern zones are characterized by Luvisols, with transitional areas showing intergrades with Cambisols (; Pereira, 2023).

FIGURE 1

The municipality borders Kiwaba Nzogi to the north, Mucari to the east, the municipalities of Cangandala and Mussende (Cuanza Sul Province) to the south, and Cacuso and Calandula to the west. Malanje Province is predominantly inhabited by members of the Kimbundu ethnolinguistic group, whose language, Kimbundu, is widely spoken across both rural and urban contexts. Despite this demographic predominance, the province exhibits considerable ethnolinguistic heterogeneity, with minority populations such as the Bakongo, Chokwe, and Umbundu also present.

Population: A total of twenty (20) traditional healers participated in the survey, selected through convenience sampling. With the assistance of the local Association of Traditional Healers of Malanje, participants were identified and contacted. The healers practiced in diverse settings, with some based in local markets and others operating from dedicated herbalist shops, reflecting the typical contexts of traditional healing in the region.

Ethical procedures

The Ethics Committee of the University Rainha Njinga a Mbande approved the project (0017/2018). Additional authorization from the local authorities was also obtained. The Code of Ethics of the International Society of Ethnobiology () was followed during the fieldwork.

Registration of ethnobotanical information

The data were gathered through interviews and participatory observation (as evidenced in the attached survey form) to collect detailed information on the common and scientific names of plants, the parts used, processing methods, and the primary ailments treated. Additional data were collected on traditional healers practicing natural medicine with medicinal plants. With the assistance of healers familiar with the habitats of each species, in vivo photographs were taken, and GPS coordinates were recorded. A botanical specialist, Dr. Amândio Gomes, a coauthor, subsequently performed taxonomic identification by comparison with authenticated herbarium material, using dichotomous keys and specialized references (e.g., Conspectus Florae Angolensis and Flora Zambesiaca), and verified updated scientific names through online databases such as https://www.worldfloraonline.org and https://powo.science.kew.org) and by direct observation. Throughout the study, special emphasis was placed on conserving medicinal plant resources and preserving indigenous ethnobotanical knowledge. Community participation was encouraged to ensure that traditional healers and residents remain active custodians of both biological and cultural heritage, promoting sustainable use and intergenerational transmission of local knowledge. The conservation status of the collected plants was checked using the IUCN Red List of Threatened Species ().

Data analysis

Plant species are categorized by their family, scientific name, common name, parts utilized, preparation methods, and therapeutic applications in order of significance. The ethnopharmacological data collected were quantitatively evaluated using the rank order priority (ROP) metric to gauge their healing potential.

The healing potential of a plant can be established by ROP and was calculated using the following formula (Siddique et al., 2021):

Here, FL is the level of fidelity, and RP is the relative popularity of the species in question.

The fidelity level (FL) is, in turn, determined using the following expression (Siddique et al., 2021).

Here, Ip is the number of informants who mentioned the species for the same principal purpose, and Iu is the total number of informants who mentioned the plant for any use.

The formula used for calculating relative popularity (RP) is

where Iu is the number of informants who suggested a particular plant species and Imc is the number of informants who cited the most frequently cited plant species. RP takes values between 0 and 1. The most popular species have an RP value closer to 1, while the unpopular, or less known, have an RP value closer to 0.

According to Formulas 1, 2, the ROP can also be expressed as shown in Equations 4, 5 presented below:

Simplifying terms, it could be expressed as follows:

Although the FL allows for estimating the healing potential of a species concerning its most cited use, it also makes it difficult to compare the relative importance with other medicinal plants with similar FL. For this reason, the ROP is a more appropriate parameter for assigning an order of curative potential in an ethnobotanical study. According to Equation 5, the ROP does not depend on the number of informants who cite the plant for any use, but on the number of times it is cited for the most frequent use and the number of times the most cited species is mentioned.

Botanical species with high ROP values have great curative potential. They are candidates for further studies, such as pharmacognosic, phytochemical, and biological assays, to evaluate their biological activity, therapeutic effectiveness, and toxicity.

The International Classification of Diseases (ICD-11) was used to group plants into different categories for medicinal purposes (WHO, 2019).

Results and discussion

Sociodemographic characteristics of the informants

The study involved 20 participants, 10 men and 10 women, who worked predominantly in the Cangambo market (13), with a smaller number working in traditional medicine stalls (5) and in the Ritondo neighborhoods (2). The predominance of healers operating in the Cangambo market, followed by those in the traditional medicine stalls and the Ritondo neighborhoods, highlights the central role of marketplaces as hubs for the circulation of knowledge, medicinal products, and therapeutic practices. Recent ethnobotanical research underscores that these spaces serve as strategic environments for the preservation and transmission of traditional knowledge, functioning as dynamic interfaces where healers and community members interact and exchange experiences (; ).

These healers were on average 51 years old, ranging from a young 26-year-old to a seasoned 75-year-old, with an impressive average of 25 years of experience in the field. Studies carried out in Uíge (; ) and southern Angola (Urso et al., 2016) indicate that knowledge of medicinal plants is cumulative and strongly shaped by lived experience. Educational attainment varied significantly: 55% were illiterate, 40% had completed primary education, and only 5% had secondary education. These educational levels are consistent with previous research in Angola (Urso et al., 2016) and highlight a trend within the community of traditional healers.

Gender representation among practitioners was balanced, with equal numbers of men and women involved. Women demonstrated greater familiarity with plants located near homes and villages, particularly those used for treating mild illnesses, preparing food, and caring for children (Torres‐Avilez et al., 2026). Men, in contrast, were more engaged with species cultivated on farms or collected in remote wilderness areas (). As and emphasize, gender functions as an organizing principle rather than a limiting factor: both men and women hold significant mastery, and their distinct specializations together reinforce the resilience and breadth of traditional medicinal knowledge.

The present study did not aim to examine how informants’ characteristics influence traditional knowledge. However, a survey carried out in communities in southern Angola did not show notable differences in this aspect (Urso et al., 2016).

Age and duration of experience working with medicinal plants lend greater expertise to traditional healers in using natural remedies to address health issues. In our study, 95% of the respondents were over 30 years old, suggesting a gradual replacement of individuals knowledgeable in traditional medicine. This highlights the urgent need for scientific research to document and preserve the wealth of information on medicinal plants in Malanje.

The high occurrence of illiteracy among participants indicates that oral transmission of knowledge plays a crucial role in traditional medicine in Malanje. This underscores the importance of documenting and preserving the wisdom held by these healers.

Botanical identification, floristic richness, and relative popularity level

From the 20 interviews conducted in Malanje, an array of 272 ethnospecies of medicinal plants were cataloged (see Supplementary Material), all renowned for their healing properties. These plants are known by local names in Kimbundu, making botanical identification and cross-referencing with external sources challenging. Ethnobotanical wisdom varied widely among individuals; many plants were mentioned by only a handful of informants, highlighting a potential threat to preserving this traditional knowledge. A study in Bié province, Angola (Novotna et al., 2020), uncovered that 34 ethnospecies used in traditional medicine were mentioned by only a single informant. Comparable findings emerged from ethnobotanical research in Bibala Municipality, Namibe Province (Urso et al., 2016), where most plants were noted by just one or two individuals. Similarly, in the Cuanza Sul Province (), out of the 94 ethnospecies documented, 33 (34.74%) were noted by only one informant, while 26 (27.37%) were cited by two others. These instances might arise because herbalists and traditional healers view their wisdom as a sacred or economic secret, which they choose not to share with others in their field. A similar pattern emerged in a study conducted in Zimbabwe (Ngarivhume et al., 2015). These parallel findings suggest a common approach to the distribution of knowledge among practitioners, healers, and therapists of traditional medicine across various regions of Angola. This underscores the necessity of pursuing further ethnopharmacological research to document and preserve the rich knowledge held by different communities.

The multitude of documented plant species reveals that traditional medicinal practices leveraging natural products remain a prevalent choice for residents of this area. Through participatory observation, macroscopic analysis, and sample comparison with existing literature, 78 ethnospecies (28.7%) were successfully identified (Table 1). This highlights local expertise in therapeutic uses and underscores the necessity for botanical research to classify these plants taxonomically and thoroughly document the region’s botanical wealth.

TABLE 1

No.FamilyScientific nameHabitusCommon nameDistribution data for each speciesCollecting placeROP
1.CombretaceaeTerminalia brachystemma Welw. ex HiernTree/shrubMueia (Kimb.)NativeShrubland savanna81.8
2.PolygalaceaeSecuridaca longepedunculata Fresen.ShrubMutungo (Kimb.)NativeShrubland savanna54.4
3.ApocynaceaeMondia whitei (Hook.f.) SkeelsClimbingMundondo (Kimb.)NativeCropland/forest gallery52.2
4.CochlospermaceaeCochlospermum angolense Welw. ex Oliv.ShrubMbrututo (Kimb.)NativeShrubland savanna34
5.RubiaceaeMussaenda arcuata Poir.ShrubKabolebole (Kimb.)NativeShrubland savanna31.7
6.FabaceaeSenna occidentalis (L.) LinkShrubMudia-nhoca (Kimb.)NativeDisturbed places29.4
7.ZingiberaceaeAframomum alboviolaceum (Ridl.) K.Schum.Annual herbGinguenga (Kimb.)NativeShrubland savanna27.2
8.AnnonaceaeMonodora myristica (Gaertn.) DunalTreeJipepe (Kimb.)NativeForest gallery27.1
9.AnacardiaceaeLannea welwitschii (Hiern) Engl.TreeMucumbi (Kimb.)NativeForest gallery22.7
10.AnnonaceaeXylopia aethiopica (Dunal) A.Rich.TreeMissae (Kimb.)NativeForest gallery18.7
11.FabaceaeVachellia sieberiana (DC.) Kyal. & Boatwr.TreeMusonge (Kimb.)NativeWooded savanna18.1
12.BurseraceaeCanarium schweinfurthii Engl.TreeMubafo (Kimb.)NativeForest gallery18.1
13.MoringaceaeMoringa oleifera Lam.ShrubMoringa (port.)NaturalizedFallows/cropland15.8
14.EuphorbiaceaeRicinus communis L.ShrubJimono (Kimb.)NaturalizedDisturbed places15.8
15.RubiaceaeCrossopteryx febrifuga Benth.ShrubMussesse (Kimb.)NativeShrubland savanna15.4
16.PoaceaeCymbopogon densiflorus StapfGrassSaco-saco (Kimb.)NaturalizedCropland13.5
17.MyrtaceaeEucalyptus globulus Labill.TreeEucalipto (Port.)CultivatedFallows11.3
18.FabaceaeBauhinia forficata LinkShrubPata de vaca (Port.)IntroducedDisturbed places11.3
19.AmaranthaceaeDysphania ambrosioides (L.) Mosyakin & ClemantsAnnual herbSanta Maria (Port.)NaturalizedDisturbed places11.3
20.FabaceaeEriosema psoraleoides (Lam.) G.DonShrubKidiambuiz (Kimb.)NativeDisturbed places11.3
21.CelastraceaeGymnosporia senegalensis Loes.ShrubMussambela (Kimb.)NativeShrubland savanna11
22.AsparagaceaeAsparagus sp.Annual herbKanhanga (Kimb.)NativeShrubland savanna11
23.AmaranthaceaeBeta vulgaris L.Annual herbBeterraba (Port.)IntroducedCropland6.8
24.EuphorbiaceaeEuphorbia pulcherrima
Willd. ex Klotzsch
ShrubBico de Papagaio (Port.)NativeArid savanna6.8
25.ZingiberaceaeAframomum melegueta K. Schum.Annual herbNdungo à congo (Kimb.)NativeForest gallery6.7
26.ZingiberaceaeZingiber officinale Rosc.Annual herbGingibre (Port.)CultivatedCropland6.7
27.AmaryllidaceaeAllium cepa L.Annual herbCebola (Port.)CultivatedCropland6.7
28.SolanaceaeNicotiana tabacum L.Annual herbTabaqueiro (Port.)CultivatedCropland4.5
29.SolanaceaeSolanum lycopersicum L.Annual herbTomateiro (Port.)CultivatedCropland4.5
30.RutaceaeCitrus limon (L.) Burm. F.ShrubLimoeiro (Port.)CultivatedCropland4.5
31.PhyllanthaceaePhyllanthus niruri L.ShrubQuebra-pedra (Port.)NativeShrubland savanna4.5
32.MyrtaceaePsidium guajava L.ShrubGoiabeira (Port.)CultivatedCropland4.5
33.MeliaceaeAzadirachta indica A.Juss.TreeNeem (Port.)IntroducedDisturbed places4.5
34.LauraceaePersea americana Mill.TreeAbacateiro (Port.)CultivatedCropland4.5
35.PhyllanthaceaeHymenocardia acida Tul.ShrubMupexi (Kimb.)NativeShrubland savanna/miombo4.5
36.CostaceaeCostus spiralis (Jacq.) RoscoeAnnual herbMuengueya samba (Kimb.)NativeShrubland savanna4.5
37.CaricaceaeCarica papaya L.Tree/herbMamoeiro (Port.)CultivatedCropland4.5
38.AsteraceaeTithonia diversifolia (Hemsl.) A.GrayShrubCura-tudo (port.)IntroducedDisturbed places4.5
39.ArecaceaeElaeis guineensis (Jacq.)Tree palmPalmeira (Port.)NaturalizedCropland4.5
40.ApocynaceaePicralima nítida (Stapf) T.Durand & H.DurandTreeKikongo (Kimb.)IntroducedForest gallery4.5
41.XanthorrhoeaceaeAloe ferox Mill.Herb succulentXandala (Kimb.)IntroducedCropland4.5
42.AmaryllidaceaeAllium sativum L.HerbAlho (Port.)CultivatedCropland4.5
43.PoaceaeSaccharum officinarum L.GrassCana de açúcar (Port.)CultivatedCropland4.5
44.AmaranthaceaeSpinacia oleracea L.HerbEspinafre (Port)CultivatedCropland4.5
45.AsteraceaeArtemisia absinthium L.ShrubLosna (Port.)NativeShrubland savanna4.5
46.EuphorbiaceaeManihot esculenta CrantzShrubMandioqueira (Port.)CultivatedCropland4.5
47.EuphorbiaceaeAlchornea cordifolia (Schumach. & Thonn.) Müll.ArgShrubMbunze (Kimb.)NativeForest gallery4.5
48.SolanaceaeCapsicum annuum L.HerbGindungo (Port.)CultivatedCropland2.2
49.PoaceaeCymbopogon citratus (DC.) StapfGrassCaxinde (Kimb.)CultivatedCropland2.2
50.MyrtaceaeEugenia uniflora L.ShrubPitangueira (Port.)IntroducedCropland2.2
51.MalvaceaeAbelmoschus esculentus (L.) Moench.ShrubQuiabo (Port.)CultivatedCropland2.2
52.ClusiaceaeGarcinia mannii Oliv.ShrubNgadiadia (Kimb.)NativeForest gallery2.2
53.AsteraceaeAcanthospermum hispidum DC.HerbKauenha (Kimb.)IntroducedDisturbed places2.2
54.AnacardiaceaeMangifera indica L.TreeMangueira (Port.)CultivatedCropland2.2
55.MoraceaeFicus thonningii BlumeTreeLemba-lemba (Kimb.)NativeForest gallery2.2
56.AsteraceaeVernonia spHerbKidiassute (Kimb.)IntroducedDisturbed places2.2
57.ZingiberaceaeAlpinia zerumbet (Pers.) B.L. Burtt & R.M.Sm.HerbColónia (Port.)IntroducedornamentalNc
58.MalvaceaeCola acuminata (P. Beauv.) Schott & Endl.TreeDikazo (Kimb.)NativeForest galleryNc
59.RubiaceaeCoffea canephora Pierre ex A.FroehnerShrubCafeeiro (Port.)CultivatedCroplandNc
60.PoaceaeZea mays L.GrassMilheiro (Port.)CultivatedCroplandNc
61.NyctaginaceaeBoerhavia diffusa L.HerbMutumbata (Kimb.)NaturalizedDisturbed placesNc
62.MusaceaeMusa paradisiaca L.HerbBananeira (Port.)CultivatedCroplandNc
63.LauraceaeCinnamomum verum J.Presl.ShrubCanela (Port.)IntroducedCroplandNc
64.LamiaceaeOcimum gratissimum L.HerbAlfa vaca (Port.)IntroducedCroplandNc
65.LamiaceaeMentha arvensis L.HerbHortelã (Port.)IntroducedCroplandNc
66.CannabaceaeCannabis sativa L.HerbLiamba (Port.)IntroducedCroplandNc
67.AsteraceaeAgeratum conyzoides L.HerbCabuabuata (Kimb.)NativeDisturbed placesNc
68.ApiaceaeFoeniculum vulgare Mill.HerbFuncho (Port.)CultivatedCroplandNc
69.AnacardiaceaeSpondias mombin L.TreeGajajeira (Port.)IntroducedCroplandNc
70.ViburnaceaeSambucus nigra L.ShrubSabugueiro (Port.)IntroducedCroplandNc
71.FabaceaePericopsis angolensis (Baker) MeeuwenTreeNgambo (Kimb.)NativeMiombo/savannaNc
72.ArecaceaeCocos nucifera L.Tree palmCoqueiro (Port)IntroducedCroplandNc
73.RosaceaeFragaria sp.HerbMorangueiro (Port.)IntroducedCroplandNc
74.LamiaceaeRosmarinus officinalis L.HerbAlecrim (Port.)IntroducedCroplandNc
75.FabaceaeArachis hypogaea L.HerbGinguba (Port.)CultivatedCroplandNc
76.MalvaceaeSterculia dawei SpragueTreeMulende (Kimb.)NativeForest galleryNc
77.FabaceaeSenna spectabilis (DC.) H.S.Irwin & BarnebyTreeAcacia (port.)IntroducedDisturbed placesNc
78.PicrodendraceaeOldfieldia dactylophylla (Welw. ex Oliv.) J.LéonardTreeMubatangombe (Kimb.)NativeShrubland savanna/miomboNc

Plant identification and ethnopharmacological assessment (ROP).

Abbreviations: Port, Portuguese; Kimb, Kimbundu.

Accurate recording of forest biodiversity offers a clearer picture of the conservation status of the most significant and frequently utilized species, thereby preventing agroforestry methods that could jeopardize ecosystem stability. In light of this, research () has pointed out the disappearance of medicinal plants from their natural habitats in parts of Cuanza Sul, adjacent to Malanje. This loss stems from improper farming techniques, unregulated resource exploitation, and frequent fires, emphasizing the crucial need to safeguard these environments.

The study identified 78 species across 39 families (see Table 2), averaging approximately 2 species per family, which underscores a rich tapestry of botanical diversity in medicinal plants. Interestingly, twenty-one of these families (53.8%) are each represented by just one species. Additionally, three of the medicinal plants (1.1%) could only be classified down to the genus level. The family Fabaceae leads the list as the most frequently cited at 9%, followed by Asteraceae at 6.4%, and then Euphorbiaceae, Poaceae, and Zingiberaceae, each contributing 5.1%.

TABLE 2

No.FamilyNumber of speciesPercent (%)
1.Fabaceae79
2.Asteraceae56.4
3.Euphorbiaceae45.1
4.Poaceae45.1
5.Zingiberaceae45.1
6.Amaranthaceae33.8
7.Anacardiaceae33.8
8.Lamiaceae33.8
9.Malvaceae33.8
10.Myrtaceae33.8
11.Rubiaceae33.8
12.Solanaceae33.8
13.Amaryllidaceae22.6
14.Annonaceae22.6
15.Apocynaceae22.6
16.Arecaceae22.6
17.Lauraceae22.6
18.Phyllanthaceae22.6
19.Viburnaceae11.3
20.Apiaceae11.3
21.Asparagaceae11.3
22.Burseraceae11.3
23.Cannabaceae11.3
24.Caricaceae11.3
25.Celastraceae11.3
26.Clusiaceae11.3
27.Cochlospermaceae11.3
28.Combretaceae11.3
29.Costaceae11.3
30.Meliaceae11.3
31.Moraceae11.3
32.Moringaceae11.3
33.Musaceae11.3
34.Nyctaginaceae11.3
35.Picrodendraceae11.3
36.Polygalaceae11.3
37.Rosaceae11.3
38.Rutaceae11.3
39.Xanthorrhoeaceae11.3

Species distribution categorized based on family.

Ethnobotanical studies in Angola and elsewhere (; ; ; ; ; Novotna et al., 2020) have identified Fabaceae as a commonly used plant family. Plants with the highest ROP include Terminalia brachystemma (81.8), Securidaca longepedunculata (54.4), Mondia whitei (52.2), Cochlospermum angolense (34), Mussaenda arcuata (31.7), Senna occidentalis (29.4), Aframomum alboviolaceum (27.2), and Monodora myristica (27.1) (Table 1). Additionally, 22 plants were noted by only one informant each and lacked ROP calculations.

Drawing on the ethnopharmacological insights of our informants (see Table 3), we found that 17 plants are used to address a single ailment. Numerous plants integral to traditional medicine in Malanje exhibit diverse therapeutic applications. Particularly noteworthy are the seven plants with the highest ROP values, which have multiple medicinal purposes, including treatments for gastrointestinal issues and parasitic infections. Similar patterns were documented in Uíge (; ), where plants with highly specific applications are firmly embedded in cultural practice and valued for their perceived efficacy. Among the 78 botanically identified plants, an intriguing revelation is that 19 lack recorded medicinal uses in the existing literature, as highlighted in Table 3.

TABLE 3

No.Scientific nameTraditional usePlant parts usedMethod of preparationApplicationRecorded literature usesReference
1.Terminalia brachystemma Welw. ex HiernOpen cervix, paludism, and stomachacheRoot and leafMacerationOral, rectal, and vaginalAntifungal (in vitro), Masoko et al. (2005)
2.Securidaca longepedunculata Fresen.Inflammation, constipation, and stomachacheRootMacerationTopicalAnticonvulsants (in vivo)
3.Mondia whitei (Hook.f.) SkeelsStomachache, colic, and sexual impotenceRootMacerationOral and inhalationAntimalarials (in vivo)Olanlokun et al. (2021)
4.Cochlospermum angolense Welw. ex Oliv.Hepatitis and paludismRootMacerationOral and topicalAnti-oxidant (in vitro)Samba et al. (2025)
5.Mussaenda arcuata Poir.Bone pain, thrombosis, and labor painLeafMacerationTopicalNot reported​
6.Senna occidentalis (L.) LinkStomachache, paludism, snake bite, and herniaRoot and leafDecoctionOralAntidiabetic (in vitro)Mishra et al. (2022)
Nde et al. (2022)
7.Monodora myristica (Gaertn.) DunalStomachache, kyphosis, open cervix, and inflammationSeedDecoctionOral and topicalAntidepressants (in vivo)
8.Aframomum alboviolaceum (Ridl.) K.Schum.Abortion prevention and kyphosisRootDecoctionOralNot reported​
9.Lannea welwitschii (Hiern) Engl.Fractures, toothache, and thrombosisStemCataplasmOral, topical, and rectalAnti-proliferative (in vitro)Saraux et al. (2023)
10.Xylopia aethiopica (Dunal) A. Rich.Stomachache, kyphosis, and open cervixSeedDecoctionOralAnti-cancer (in vitro)
11.Vachellia sieberiana (DC.) Kyal. & Boatwr.Inflammation, infertility, and backpainRootMacerationOral and topicalNot reported​
12.Canarium schweinfurthii Engl.Stomachache, open cervix, typhoid fever, and herniaStemDecoctionOralTermiticide (in vivo)Nagawa et al. (2015)
13.Moringa oleífera Lam.StomachacheRoot, leaf, and seedDecoctionOralAnti-inflammatory (in vivo)Sulaiman et al. (2008)
14.Ricinus communis L.Headache, constipation, and thrombosisLeaf and fruitDecoctionOral and topicalPhytoremediation (in vitro)Yao et al. (2023)
15.Crossopteryx febrifuga (Afzel. Ex G.Don) Benth.Toothache and anemiaLeaf and rootDecoctionOral and inhalationAlzheimer (in vitro)Tamfu et al. (2022)
16.Cymbopogon densiflorus StapfKyphosis, hernia, and stomachacheFlowerDecoctionOralAsthma (in vitro)Takaisi-Kikuni et al. (2000)
17.Eucalyptus globulus Labill.Asthma, tuberculosis, paludism, and coughLeafDecoctionInhalation, oral, and topicalRepellent (in vitro)Pan et al. (2020)
18.Bauhinia forficata LinkSexual impotence and hepatitisRootDecoctionOralAnti-diabetes (in vivo)Tonelli et al. (2022)
19.Dysphania ambrosioides (L.) Mosyakin & ClemantsStomachache, fever, epilepsy, hernia, and infertilityLeafDecoctionOral, rectal, vaginal, and inhalationalAnti-inflammatory (in vivo)
20.Eriosema psoraleoides (Lam.) G. DonSexual impotence, menstrual disorders, and intestinal infectionsRootMacerationOral and topicalNot reported​
21.Gymnosporia senegalensis Loes.CancerRootMacerationOralAnti-inflammatory (in vitro)
22.Asparagus sp.Stomachache and infertilityRoot and leafMacerationOralCancer (in vitro)
23.Beta vulgaris L.AnemiaRootDecoctionOralTesticular oxidative damage (in vitro)Ojo et al. (2023)
24.Euphorbia pulcherrima
Willd. ex Klotzsch
Typhoid feverRootDecoctionOralCancer (in vitro)Moustak et al. (2018)
25.Aframomum melegueta K. Schum.HemorrhoidsSeedMacerationOral and topicalNot reported​
26.Zingiber officinale Rosc.Sexual impotence, paludism, yellow fever, and thrombosisRootDecoctionOralAnti-inflammatory (in vitro)Murugesan et al. (2020)
27.Allium cepa L.Inflammation, diabetes, injuries, flu, and herniaRootInfusionOralAnti-inflammatory (in vitro)
28.Nicotiana tabacum L.Hemorrhoids, asthma, and anginaLeafDecoctionOral, topical, and sublingualAnti-Alzheimer (in vivo)Rawat et al. (2013)
29.Solanum lycopersicum L.Hemorrhage and headacheLeafInfusionOral and nasalAnti-cancerogenic (invitro)
30.Citrus limon (L.) Burm. F.Typhoid fever and paludismFruitDecoctionOral and topicalAnti-tumor (in vitro)Zhou et al. (2021)
31.Phyllanthus niruri L.Kidney failure and kidney stonesLeafDecoctionOralAnti-inflammatory (in vivo)
32.Psidium guajava L.Diarrhea and stomachacheLeafDecoctionOral and inhalationHypertension (in vivo)
33.Azadirachta indica A. Juss.Paludism and typhoid feverLeafDecoctionOral, inhalation, rectal, and topicalHypertension (in vitro)
34.Persea americana Mill.Hypertension, diarrhea, headache, and herniaLeaf, fruit, and seedDecoctionOral, topical, and inhalationAnti-tumor (in vitro)
35.Hymenocardia acida Tul.Diarrhea, hemorrhoids, and psychosisRootDecoctionOralHypertension (in vivo)
36.Costus spiralis (Jacq.) RoscoeUrinary infection and sexual impotenceStemDecoctionOral, vaginal, and topical (cataplasm)Hypertension (in vivo)
37.Carica papaya L.Constipation, headache, and facilitates childbirthRoot, leaf, and fruitDecoctionOral and inhalationDengue fever (in vivo)Subenthiran et al. (2013)
38.Entada abyssinica Steud.Paludism, spinal pain, and sexual impotenceLeafDecoctionOralNot reported​
39.Elaeis guineensis Jacq.Headache, burns, antidote, and prevents abortionFruit, flower, and stemMacerationOral and inhalationHealing activity (in vivo)Rajoo et al. (2021)
40.Picralima nítida (Stapf) T. Durand & H. DurandInflammation and bone painStemMacerationOral and topical (bath)Not reported​
41.Aloe ferox Mill.Typhoid fever, stomachache, and alopeciaLeafMacerationOral and topicalAntidiabetic (in vitro)Mhaladi et al. (2016)
42.Allium sativum L.Inflammation, stomachache, and coughRootMacerationOralColon cancer (in vitro)
43.Saccharum officinarum L.Heart failure and anemiaLeafDecoctionOralHypertension (in vitro)
44.Spinacia oleracea L.AnemiaLeafDecoctionOralNot reported​
45.Artemisia absinthium L.Respiratory diseasesLeafDecoctionOral and topical (bath)Focal cerebral ischemia (in vitro)
46.Manihot esculenta CrantzMeaslesLeafMacerationOralNot reported​
47.Alchornea cordifolia (Schumach. & Thonn.) Müll.ArgFeverRootDecoctionTopical, oral, and sublingualNot reported​
48.Capsicum annuum L.Epilepsy and labor painRoot and leafMacerationOralAnti-fungal (in vitro)
49.Cymbopogon citratus (DC.) StapfCough, bladder pain, kidney obstruction, stomachache, and prevents abortionLeafDecoctionOralGastroprotective activity (in vivo)Manvitha and Bidya (2014)
50.Eugenia uniflora L.Bloody diarrheaLeafDecoctionOralDiuretic (in vitro)
51.Abelmoschus esculentus (L.) Moench.Glaucoma, conjunctivitis, and sexual impotenceLeaf and fruitInfusionOralType 2 diabetes (in vitro)
52.Garcinia mannii Oliv.Paludism and colicSeedDecoctionOralNot reported​
53.Acanthospermum hispidum DC.Vaginal bleeding, paludism, diabetes, hepatitis, and antidoteLeafDecoctionOral and topicalAntiviral (in vitro)
54.Mangifera indica L.Abscess, hemorrhoids, and paludismLeaf and StemDecoctionOral and topicalAnti-inflammatory (in vivo)Saviano et al. (2022)
55.Ficus thonningii BlumeHypertensionLeafMacerationOralDiarrhea (in vitro)
56.Vernonia spStomachache and herniaRootDecoctionOral and inhalationDiabetes (in vitro)
57.Alpinia zerumbet (Pers.) B.L. Burtt & R.M.Sm.Stomachache and bladder painRootInfusionOralNot reported​
58.Cola acuminata (P.Beauv.) Schott & Endl.Nausea and vomitingFruitMacerationOralAlzheimer’s (in vivo)
59.Coffea canephora Pierre ex A.FroehnerDiarrhea, wounds, and burnsFruitInfusionOral and topicalNot reported​
60.Zea mays L.Abortion preventionStigmasDecoctionOral and topicalNot reported​
61.Boerhavia diffusa L.Labor painLeafMacerationOralAnti-inflammatory (in vitro)Mathias et al. (2020)
62.Musa paradisiaca L.Prevention of abortion, hemorrhoids, and stimulation of laborLeafMacerationOralAnti-tumor (in vivo)
63.Cinnamomum verum J.Presl.Stomachache and coughLeafDecoctionOral and topicalAnti-diabetic (in vivo)
64.Ocimum gratissimum L.Internal fever, hiccups, and coughLeafDecoctionOral, inhalation, topical, and sublingualAnti-inflammatory (in vivo)Shittu et al. (2016)
65.Mentha arvensis L.Stomachache and epilepsyRoot and leafDecoctionOralAnalgesic (in vivo)
66.Cannabis sativa L.Psychosis, asthma, cough, bronchitis, nausea, vomiting, measles, and tuberculosisLeafDecoctionOral, rectal, and sublingualAnti-fungal (in vitro)
67.Ageratum conyzoides L.InfertilityLeafMacerationOral, inhalation, and topicalSleeping sickness (in vitro)Nour et al. (2010)
68.Foeniculum vulgare Mill.Intestinal gas, flu, colic, kidney failure, and whooping coughRoot, stem, leaf, and flowerDecoctionOral and topicalGastroprotective (invitro)
69.Spondias mombin L.Stomachache and hypotensionRoot and fruitMacerationOral and topicalAnti-inflammatory
70.Sambucus nigra L.Measles and epilepsyLeaf and flowerDecoctionOral and topicalAnti-inflammatory (in vitro)Skowrońska et al. (2022)
71.Pericopsis angolensis (Baker) MeeuwenThrombosis and bone fractureLeaf and RootDecoctionOralNot reported​
72.Cocos nucifera L.Typhoid feverRootDecoctionOralAntifungal (in vitro)
73.Fragaria sp.EpilepsyRootMacerationOral and topicalNot reported​
74.Rosmarinus officinalis L.ObesityLeafDecoctionOral, inhalation, and topicalAntifungal (in vitro)
75.Arachis hypogaea L.HeadacheSeedCataplasmTopicalNot reported​
76.Sterculia dawei SpragueKyphosisRootMacerationOralNot reported​
77.Senna spectabilis (DC.) H.S. Irwin & BarnebyDiabetes, paludism, colic, diarrhea, and typhoid feverRoot and leafDecoctionOral, inhalation, and topicalTrypanocidal activity (in vitro)
78.Oldfieldia dactylophylla (Welw. ex Oliv.) J.LéonardTyphoid fever and open cervixRoot, stem, and leafDecoctionOralNot reported​

Traditional knowledge of medicinal plants in Malanje.

Local informants consider most plants harmless, although a few come with noted side effects. For example, Coffea canephora might keep you up at night, Cocos nucifera can lead to constipation, Nicotiana tabacum could cause nausea and vomiting, and Ricinus communis is known for inducing diarrhea. Conversely, traditional healers point out that certain species, such as Senna occidentalis, Terminalia brachystemma, Citrus limon, Phyllanthus niruri, Allium sativum, Solanum lycopersicum, Nicotiana tabacum, Securidaca longepedunculata, and Azadirachta indica, have contraindications. Unfortunately, many people think that medicinal plants and natural remedies are harmless simply because they are “natural,” but this assumption is not accurate (). Traditional practitioners mainly rely on culturally inferred undesirable effects, with adverse reactions often linked to sensory perceptions, particularly among newborns and pregnant women, who react to the strong odor and bitter taste as signs of toxicity. Ethnobotanical research among Brazilian communities has shown that local residents often have limited knowledge of the harmful potential of various plant species (Oler et al., 2019).

However, for this study, the recognition of contraindications by healers in Malanje suggests a meaningful level of empirical knowledge within local therapeutic practices. Their awareness of potential risks indicates a nuanced understanding of medicinal species, which is consistent with observations reported in other African ethnopharmacological studies. For example, Senna occidentalis has been associated with hepatotoxic effects when used over long periods (Adebayo et al., 2016), and Securidaca longepedunculata may become toxic when taken in excessive doses (Iwu 1997). These correspondences do not imply complete alignment but rather point to areas where local experience and scientific evidence converge, highlighting the potential value of integrating traditional knowledge into broader health and conservation discussions.

It is important to emphasize that, beyond the secondary metabolites that may render a species toxic, another crucial factor in assessing the safety of plant products is the contamination of forested regions, predominantly from heavy metals that medicinal plants can absorb (; Sarma et al., 2012). Recent research has identified levels of heavy metals and organic pesticides in natural products exceeding regulatory limits (; ; ; ; Wang et al., 2019), underscoring the need for stringent quality controls on medicinal plant raw materials. Furthermore, mycotoxin contamination can compromise the quality and safety of these plant-based medicines, mainly when storage and preservation practices are inadequate ().

Therefore, assessing the efficacy and safety of these plants is crucial for their use in humans (Saad et al., 2017). The World Health Organization has emphasized the necessity of quality control for herbal medicines, especially regarding their safety (WHO, 2011; WHO, 2013). Recent ethnobotanical research highlights the toxic potential of traditional medicinal plants in Morocco ().

In this vein, the Polytechnic Institute at Rainha Njinga a Mbande University is conducting pharmacognosic and phytochemical studies on the most commonly used traditional medicine plants in Malanje to address these concerns.

Plant parts used in traditional medicine

Figure 2 reveals that leaves and roots are the most commonly utilized plant parts. Of the 78 plants identified, leaves take the lead, being used in 42 instances (53.8%). Roots, on the other hand, were mentioned in 33 cases (42.3%).

FIGURE 2

This preference likely stems not only from the medicinal properties of these plant parts but also from their year-round availability and ease of collection, unlike flowers or fruits, which are seasonal. Ethnobotanical studies frequently highlight this trend, showcasing leaves as a primary raw material (; ; ; ; ; Varela et al., 2022). Moreover, research indicates the prominent use of roots in traditional medicine practices in regions such as Bibala, Namibe Province (Urso et al., 2016), and Kuito and Cuemba, Bié Province (Novotna et al., 2020).

The preference for using underground parts stems, in part, from the age-old belief passed down among medicinal practitioners that roots hold the richest concentration of healing substances and the most potent therapeutic qualities. However, overharvesting parts of medicinal plants that are crucial to their survival, such as roots, stems, and bark, constitutes destructive ethnopharmacological practice and significantly harms the floral reserves in regions plagued by overexploitation or poor management (). Although the conservation status of the recorded species indicated no immediate threats, comprehensive Red List assessments of Angolan flora remain limited. Therefore, it is crucial to raise awareness and provide training for traditional healers on sustainable harvesting practices, including substituting roots with less destructive plant parts, to preserve plant populations and sustain the continuity of traditional medicinal knowledge. Interestingly, many of these species offer alternative parts such as leaves and flowers, which might possess equally potent medicinal properties (). In this vein, the historical documentation of Antunes and Dekindt, as reported by Tchamba et al. (2024), highlights their role in preserving traditional knowledge of medicinal plants in Angola and reveals a reduced dependence on roots among the population.

The current research (Figure 3) revealed that decoction (60%) and maceration (31%) are the primary techniques for processing and extraction, similar to other ethnobotanical studies conducted in Angola (Novotna et al., 2020). These age-old methods predominantly use water as the solvent, with temperature being the key differentiator between them. Given this, extracts mostly capture high-polarity metabolites, which, unfortunately, restricts the therapeutic potential of the obtained extracts.

FIGURE 3

Classification of treated pathologies (ICD-11)

The traditional medicine of Malanje often addresses three major conditions (Table 4): gastrointestinal issues at 43.6%, infectious or parasitic diseases at 29.5%, and a mix of symptoms—such as inflammation and fever—either tied to other illnesses or standing alone, making up 20.5%. Furthermore, 14.1% of the drug applications are geared toward treating conditions related to the genitourinary system, pregnancy, childbirth, and postnatal care. Interestingly, the medicinal plants identified in this research do not cater to disorders linked to the immune system, sleep problems, ear or mastoid issues, or neonatal conditions.

TABLE 4

Treated pathologya# Of plants based on ROP classesTotal%
Nc0–2425–4950–100
Infectious or parasitic diseases515212329.5
Neoplasms-1--11.3
Diseases of the blood or blood-forming organs-4--45.1
Endocrine, nutritional, or metabolic diseases32--56.4
Mental, behavioral, or neurodevelopmental disorders11--22.6
Diseases of the nervous system47--1114.1
Diseases of the visual system-1--11.3
Diseases of the circulatory system26--810.3
Diseases of the respiratory system45--911.5
Diseases of the digestive system821233443.6
Diseases of the skin-1--11.3
Diseases of the musculoskeletal system or connective tissue232-79.0
Diseases of the genitourinary system38--1114.1
Conditions related to sexual health-6-179.0
Pregnancy, childbirth, or the puerperium44211114.1
Injury, poisoning, or certain other consequences of external causes-31-45.1
Symptoms, signs, or clinical findings not elsewhere classified310211620.5

Distribution of the diseases addressed by the medicinal plants mentioned, categorized according to ROP classes.

Nc, ROP not calculated.

a

International Classification of Diseases. Adapted from “ICD-11: International Classification of Diseases (11th revision),” World Health Organization (WHO, 2019). Retrieved from https://icd.who.int/browse11/l-m/en.

These findings likely reflect the real-world prevalence of certain ailments, such as malaria and typhoid fever, which have high rates not just in Malanje but across Angola in general (WHO, 2018).

Comparative analysis of ethnopharmacological and pharmacological evidence

The ethnopharmacological register compiled in Malanje brings to light plant species of notable cultural and therapeutic relevance. Among those most consistently prioritized by local healers are Terminalia brachystemma, Securidaca longepedunculata, Mondia whitei, Cochlospermum angolense, Aframomum alboviolaceum, and Monodora myristica. A comparative reading alongside pharmacological literature reveals compelling convergence while exposing evidence gaps that merit systematic investigation.

Terminalia brachystemma (Mueia), widely employed for gastrointestinal complaints, aligns with findings on related Terminalia species demonstrating antimicrobial, antioxidant, and hepatoprotective activity, as reported by . Nonetheless, document cytotoxicity at high concentrations, pointing to the need for careful dose–response and safety evaluations. Similarly, Securidaca longepedunculata (Mutungo), highly valued for managing fever and pain, is supported by evidence of analgesic, anti-inflammatory, antimalarial, and antimicrobial effects summarized by Abubakar et al. (2019). Yet, concerns regarding neurotoxicity and high-dose toxicity in root–bark extracts, highlighted by Mongalo et al. (2015), remain insufficiently addressed in community practice.

In the case of Mondia whitei (Mundondo), healers describe its use as a tonic and digestive aid. Scientific studies expand this profile: and document aphrodisiac, antioxidant, antimicrobial, and anti-stress activities, indicating promising therapeutic breadth, although systematic toxicity assessments and clinical studies remain limited. Cochlospermum angolense (Mbrututo), traditionally used for hepatic disorders and malaria prophylaxis, has been supported by recent analyses reporting strong antioxidant and hepatoprotective effects, including works by Samba et al. (2025) and . However, as with many medicinal species, rigorous toxicity evaluations and clinical-outcome research remain scarce.

Aframomum alboviolaceum (Ginguenga), prescribed for digestive and infectious conditions, is distinguished by its essential-oil richness. Literature reviews by and highlight anti-sickling, antimicrobial, antimalarial, and anti-inflammatory properties, although variability in traditional preparation methods continues to complicate alignment with pharmacological findings. Finally, Monodora myristica (Jipepe), employed for gastrointestinal and infectious disorders, exhibits antioxidant, antihypertensive, hepatoprotective, antibacterial, antifungal, and neuroprotective effects, as demonstrated by and . Although seed and bark extracts appear safe at typical traditional doses, reports suggest that high concentrations may influence lipid metabolism.

Taken together, these observations illustrate that traditional knowledge in Malanje frequently converges with pharmacological evidence, particularly for the management of gastrointestinal and infectious disease while highlighting persistent gaps concerning toxicity, dosage standardization, and clinically validated outcomes. The register, therefore, serves not only as culturally grounded documentation of local therapeutic practices but also as a strategic shortlist of priority species for future pharmacological, toxicological, and clinical research. Integrating ethnographic insights with biomedical inquiry can support preservation, rigorous evaluation, and potential incorporation of traditional remedies in ways that strengthen both community healthcare practice and national health strategies.

Relevance in the context of Malanje municipality

Despite the ecological potential, the Malanje region has remained largely absent from ethnopharmacological surveys, leaving a critical gap in Angola’s national knowledge base. From a sociocultural perspective, Malanje is predominantly inhabited by the Kimbundu ethnolinguistic group, whose oral traditions serve as the primary vehicle for transmitting medicinal knowledge. Marketplaces such as Cangambo function as hubs for the circulation of remedies and therapeutic practices, underscoring the importance of documenting this knowledge before it is eroded by urbanization, generational shifts, and high levels of illiteracy among healers. Recording local names, practices, and preparation methods not only preserves cultural identity but also strengthens intergenerational transmission of knowledge.

Healthcare relevance

The ethnopharmacological register compiled in Malanje Municipality offers significant potential to strengthen healthcare delivery at both community and institutional levels. By documenting 272 ethnospecies and identifying 78 botanical species across 39 families, the study provides a structured baseline of traditional practices that directly address the most prevalent local health concerns. The predominance of remedies for gastrointestinal disorders and infectious or parasitic diseases reflects the burden of disease in the region, underscoring the relevance of this knowledge to primary care. High-priority species such as Terminalia brachystemma, Securidaca longepedunculata, and Mondia whitei emerge as candidates for pharmacological validation, conservation, and possible integration into standardized phytomedicines. Moreover, the register supports Angola’s National Policy for Traditional and Complementary Medicine by providing evidence to guide the safe, culturally sensitive incorporation of traditional practices into formal health systems.

Validity of the information

The validity of this information lies primarily in its ethnographic and cultural dimensions. Systematic interviews, participatory observation, and taxonomic verification ensure that the register accurately reflects community knowledge and therapeutic priorities. The use of ROP adds quantitative weight, highlighting species most valued by healers. However, the register’s validity as clinical evidence remains limited. ROP measures popularity and fidelity of use rather than proven efficacy, and the absence of standardized dosage, toxicity profiles, and clinical outcome data prevents direct translation into biomedical practice. Thus, while the register is reliable as a cultural and ethnobotanical baseline, it must be regarded as exploratory evidence requiring further pharmacological and clinical validation before therapeutic claims can be generalized.

Limitations and future directions

Several limitations must be acknowledged. The sample size was relatively small (20 healers) and concentrated in specific markets and neighborhoods, potentially underrepresenting the diversity of practices across rural and peri-urban areas. Although 272 ethnospecies were recorded, only 78 were identified to the species level, leaving a substantial proportion of the local pharmacopoeia taxonomically unresolved. Furthermore, preparation methods varied among healers, and no standardized dosages or toxicity data were collected, constraining the ability to assess risks and benefits. Although this study provides an initial register of medicinal plants in Malanje, much remains to be done. Future research could broaden sampling to include healers from other municipalities across the province, thereby offering a more representative picture of local practices. Completing taxonomic identification and undertaking pharmacognosic and phytochemical analyses of high-ROP species, such as Terminalia brachystemma, Securidaca longepedunculata, and Mondia whitei, would help clarify their bioactive constituents and therapeutic potential. Careful safety assessments, including toxicity assays and contaminant screening, are also needed to better understand risk thresholds and ensure community wellbeing. Conservation strategies, including the possible cultivation of high-demand species, may help reduce pressure on wild populations. In addition, policy-oriented research could explore ways of aligning ethnopharmacological findings with Angola’s National Policy for Traditional and Complementary Medicine while ensuring that traditional knowledge holders are respected and benefit fairly from any future bioprospecting or product development.

As part of the medicinal plants initiative at the Polytechnic Institute of Rainha Njinga a Mbande University, steps are being taken toward the creation of a herbarium for specimen storage. Although this stage has not yet been reached, our team has worked alongside local healers to encourage sustainable plant collection practices and fire-prevention techniques. We have also established communication with local authorities to share information on the municipality’s biodiversity potential and discuss collective strategies to preserve its ecological diversity. GPS coordinates for each species have been carefully recorded, providing a resource for future monitoring and conservation efforts. These are modest beginnings, but they represent important steps toward safeguarding both biological and cultural heritage in Malanje.

Statements

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving humans were approved by the local ethics committee (Polytechnic Institute, University Rainha Njinga a Mbande) (0017/2018). The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.

Author contributions

AB: Conceptualization, Investigation, Methodology, Visualization, Writing – review and editing. AAM: Investigation, Visualization, Writing – review and editing, Data curation, Formal analysis. AM: Investigation, Visualization, Writing – review and editing, Methodology. PK: Investigation, Writing – review and editing, Visualization, Writing – original draft. MJ: Data curation, Investigation, Visualization, Writing – original draft, Writing – review and editing. MG: Data curation, Methodology, Investigation, Visualization, Writing – original draft, Writing – review and editing. MS: Investigation, Visualization, Writing – review and editing. BC: Investigation, Methodology, Writing – review and editing, Data curation, Formal analysis, Validation. YH: Visualization, Writing – original draft, Writing – review and editing, Conceptualization, Data curation, Formal analysis, Methodology, Supervision, Validation. DM: Investigation, Methodology, Visualization, Writing – review and editing, Conceptualization, Data curation, Formal analysis, Resources, Supervision, Validation. VR: Data curation, Formal analysis, Methodology, Validation, Visualization, Writing – review and editing, Investigation, Project administration, AG: Formal analysis, Investigation, Methodology, Validation, Visualization, Writing – review and editing, Data curation. EB: Conceptualization, Formal analysis, Investigation, Methodology, Supervision, Validation, Visualization, Writing – review and editing, Data curation, Project administration, Resources, Writing – original draft. EV: Conceptualization, Formal analysis, Investigation, Methodology, Project administration, Resources, Supervision, Validation, Visualization, Writing – review and editing, Data curation, Funding acquisition, Writing – original draft.

Funding

The author(s) declared that financial support was received for this work and/or its publication. The study was founded by the National Plan for Development of Science and Technology, Ministry of Science Technology and Innovation (PDCT, MESCTI), Angola grant number 0015/2018.

Conflict of interest

The author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The author(s) declared that generative AI was used in the creation of this manuscript. During the preparation of this work, the authors used ChatGPT (OpenAI, San Francisco, CA, United States) to improve the language and readability of the manuscript. After using this tool, the authors reviewed and edited the content as needed and take full responsibility for the integrity and accuracy of the manuscript. No generative AI tools were used to generate, analyze, or interpret data, or to draw scientific conclusions.

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Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphar.2025.1702353/full#supplementary-material

References

  • 1

    AbubakarU. S.DanmalamU. H.IbrahimH.MaihaB. B. (2019). A review on African violet tree (Securidaca longipedunculata): a traditional drug with multiple medicinal uses. J. Chem.4 (03), 7–14. Available online at: https://sciarena.com/article/a-review-on-africanviolet-tree-securidaca-longipedunculata-fresen-a-traditional-drug-with-multiplemedicinal-uses

  • 2

    AdebayoS. A.AmooS. O. (2019). South African botanical resources: a gold mine of natural pro-inflammatory enzyme inhibitors?. S. Afr. J. Bot.123, 214–227. 10.1016/j.sajb.2019.03.020

  • 3

    AdeyemiO. O.AkindeleA. J.YemitanO. K.AigbeF. R.FagboF. I. (2010). Anticonvulsant, anxiolytic and sedative activities of the aqueous root extract of Securidaca longepedunculata Fresen. J. Ethnopharmacol.130 (2), 191–195. 10.1016/j.jep.2010.04.028

  • 4

    AgirigaA. N.SiwelaM. (2017). Monodora myristica (Gaertn.) dunal: a plant with multiple food, health and medicinal applications: a review. Am. J. Food Technol.12 (4), 271–284. 10.3923/ajft.2017.271.284

  • 5

    AkissiZ. L. E.Yao-KouassiA. P.MagidA. A.KoffiJ. K.Voutquenne-NazabadiokoL. (2023). Chemical constituents and antioxidant capacities of Asparagus africanus Lam. Phytochem. Lett.53, 22–30. 10.1016/j.phytol.2022.11.004

  • 6

    AłtynI.TwarużekM. (2020). Mycotoxin contamination concerns herbs and medicinal plants. Toxins12 (3), 182. 10.3390/toxins12030182

  • 7

    AmorimA. C. L.LimaC. K. F.HovellA. M. C.MirandaA. L. P.RezendeC. M. (2009). Antinociceptive and Hypothermic Evaluation of the Leaf Essential Oil and Isolated Terpenoids From Eugenia Uniflora L.(Brazilian Pitanga). Phytomedicine.

  • 8

    AmorozoM. C. d. M.GélyA. (1988). Uso de plantas medicinais por caboclos do baixo Amazonas. Barcarena, Pa, Brasil. Bol. Mus. Para. Emílio Goeldi, Sér. Bot.4 (1). Available online at: https://repositorio.museu-goeldi.br/server/api/core/bitstreams/0f76cd85-f29e-4fe8-842e-518d5a966804/content (Accessed Feburary 01, 2018)

  • 9

    Angola (2025). Presidential decree no. 285/20 of 2 October. the national policy for traditional and alternative medicine. 1st Ser. Official Gazette N°155. Available online at: https://faolex.fao.org/docs/pdf/ang198704.pdf. (Accessed January 22, 2021)

  • 10

    AnnazH.AbdelaalS.MandourD. A.MahdiI.MahmoudM. F.SobehM. (2023). Mexican tea (Dysphania ambrosioides (L.) Mosyakin and Clemants) seeds attenuate tourniquet-induced hind limb ischemia–reperfusion injury by modulating ROS and NLRP3 inflammasome pathways. J. Funct. Foods108, 105712. 10.1016/j.jff.2023.105712

  • 11

    AroraH.SharmaA.SharmaS. (2023). Thyme essential oil fostering the efficacy of aqueous extract of licorice against fungal phytopathogens of Capsicum annuum L. J. Biosci. Bioeng.135 (6), 466–473. 10.1016/j.jbiosc.2023.03.003

  • 12

    AsiminiceseiD.-M.VasilachiI. C.GavrilescuM. (2020). Heavy metal contamination of medicinal plants and potential implications on human health. Rev. Chim.71 (7), 16–36. 10.37358/RC.20.7.8222

  • 13

    AthaydesB. R.TostaC.CarminatiR. Z.KusterR. M.KitagawaR. R.GonçalvesR. D. C. R. (2022). Avocado (Persea americana Mill.) seeds compounds affect Helicobacter pylori infection and gastric adenocarcinoma cells growth. J. Funct. Foods99, 105352. 10.1016/j.jff.2022.105352

  • 14

    BerardoM. E. V.MendietaJ. R.VillamonteM. D.ColmanS. L.NercessianD. (2024). Antifungal and antibacterial activities of Cannabis sativa L. resins. J. Ethnopharmacol.318, 116839. 10.1016/j.jep.2023.116839

  • 15

    BiswasN. N.SahaS.AliM. K. (2014). Antioxidant, antimicrobial, cytotoxic and analgesic activities of ethanolic extract of Mentha arvensis L. Asian Pac. J. Trop. Biomed.4 (10), 792–797. 10.12980/apjtb.4.2014c1298

  • 16

    BoraK. S.SharmaA. (2010). Neuroprotective effect of Artemisia absinthium L. on focal ischemia and reperfusion-induced cerebral injury. J. Ethnopharmacology129 (3), 403–409. 10.1016/j.jep.2010.04.030

  • 17

    CabralB.SiqueiraE.BitencourtM. A.LimaM. C.LimaA. K.OrtmannC. F. (2016). Estudo fitoquímico e potencial antiinflamatório e antioxidante das folhas de cajazeira Spondias. Rev. Bras. Farmacogn.26, 304–311. 10.52076/eacad-v3i2.192

  • 18

    Cantero-GonzálezG.AlvarengaN.Florentín-PavíaM. M.Gonzalez-MaldonadoP.SoteloP. H. (2023). Antiviral activity of two Acanthospermum species against herpes simplex virus 1. J. Ethnopharmacol.303, 115958. 10.1016/j.jep.2022.115958

  • 19

    ChengY.YuY.WangC.ZhuZ. e.HuangM. (2021). Efeito inibitório do extrato de melaço de cana-de-açúcar (Saccharum officinarum L.) na formação de aminas heterocíclicas em asas de frango fritas. Controle Aliment.119, 107490. 10.1016/j.foodcont.2020.107490

  • 20

    CockI. E.van VuurenS. F. (2020). The traditional use of southern African medicinal plants for the treatment of bacterial respiratory diseases: a review of the ethnobotany and scientific evaluations. J. Ethnopharmacol.263, 113204. 10.1016/j.jep.2020.113204

  • 21

    CoutoA. G.KassuyaC. A.CalixtoJ. B.PetrovickP. R. (2013). Anti-inflammatory, antiallodynic effects and quantitative analysis of gallic acid in spray dried powders from Phyllanthus niruri leaves, stems, roots and whole plant. Rev. Bras. Farmacogn.23 (1), 124–131. 10.1590/s0102-695x2013000100017

  • 22

    DangarembiziR.ErlwangerK. H.MoyoD.ChivandiE. (2013). Phytochemistry, pharmacology and ethnomedicinal uses of Ficus thonningii (Blume Moraceae): a review. African Journal of Traditional. Complementary Altern. Med.10 (2), 203–212. 10.4314/ajtcam.v10i2.4

  • 23

    DarR. A.ShahnawazM.QaziP. H. (2017). General overview of medicinal plants: a review. J. Phytopharm.6 (6), 349–351. 10.31254/phyto.2017.6608

  • 24

    DasS.BhattacharjeeS.DeyS.Gutiérrez-GrijalvaE. P.HerediaJ. B.NissapatornV.et al (2020). Plants of the genus Terminalia: an insight on its biological potentials, pre-clinical and clinical studies. Front. Pharmacol.11, 561248. 10.3389/fphar.2020.561248

  • 25

    de Assis BragaD. C.GomesP. M.BatistaM. A. C.de SouzaJ. A.BastosJ. C. S. A.Rodrigues-das-DôresR. G.et al (2022). Effects of Psidium guajava L. leaves extract on blood pressure control and IL-10 production in salt-dependent hypertensive rats. Biomed. and Pharmacother.155, 113796. 10.1016/j.biopha.2022.113796

  • 26

    de Farias SilvaD.BezerraP. H. S.de Sousa RibeiroL. L.VianaM. D. M.de LimaA. A.da Silva NetoG. J.et al (2021). Costus spiralis (Jacq.) roscoe leaves fractions have potential to reduce effects of inflammatory diseases. J. Ethnopharmacology268, 113607. 10.1016/j.jep.2020.113607

  • 27

    DeehP. B. D.SathiyaseelanA.Vishven NaveenK.WangM.-H. (2024). Phytochemical analysis and antioxidant potential of Mondia whitei and Guibourtia tessmannii against H2O2-induced cytotoxicity in PC3 cells. J. Biomol. Struct. Dyn.43, 9790–9804. 10.1080/07391102.2024.2335299

  • 28

    DograN. K.KumarS.KumarD. (2020). Vernonia anthelmintica (L.) Willd.: an ethnomedicinal, phytochemical, pharmacological and toxicological review. J. Ethnopharmacology256, 112777. 10.1016/j.jep.2020.112777

  • 29

    EkeanyanwuR. C.NkwochaC. C.EkeanyanwuC. L. (2021). Behavioural and biochemical indications of the antidepressant activities of essential oils from monodora myristica (Gaertn) seed and Xylopia aethiopica (Dunal) fruit in rats. IBRO Neurosci. Rep.10, 66–74. 10.1016/j.ibneur.2021.01.001

  • 30

    ElkhalifaA. E. O.AlshammariE.AdnanM.AlcantaraJ. C.Mahgoub AwadelkareemA.EltoumN. E.et al (2021). Okra (Abelmoschus Esculentus) as a potential dietary medicine with nutraceutical importance for sustainable health applications. Molecules26 (3), 696. 10.3390/molecules26030696

  • 31

    FançonyA. P. (2021). Etnobotânica sobre plantas medicinais na localidade do Jombe I - Conda, Cuanza Sul - Angola. Rev. Fitos15 (2), 242–256. 10.32712/2446-4775.2021.1066

  • 32

    FelixC.LucenaR. F. P.FelixL. P.CordeiroJ. M. P.FerreiraE. da C.BonifácioK. M. (2019). Etnobotânica da Serra do Jatobá: usos locais e conservação. FLOVET1 (11), 39–65. Available online at: https://periodicoscientificos.ufmt.br/ojs/index.php/flovet/article/view/10380

  • 33

    GerszbergA.Hnatuszko-KonkaK.KowalczykT.KononowiczA. K. (2015). Tomato (Solanum lycopersicum L.) in the service of biotechnology. Plant Cell, Tissue Organ Cult. (PCTOC)120, 881–902. 10.1007/s11240-014-0664-4

  • 34

    GhavamM. (2022). GC-MS analysis and antimicrobial activities of a rosmarinus officinalis L. essential oil from Kashan Region (Iran). Biochem. Syst. Ecol.105, 104507. 10.1016/j.bse.2022.104507

  • 35

    GöhreA.Toto-NienguesseÁ. B.FuturoM.NeinhuisC.LautenschlägerT. (2016). Plants from disturbed savannah vegetation and their usage by Bakongo tribes in Uíge, Northern Angola. J. Ethnobiol. Ethnomedicine12 (42). 10.1186/s13002-016-0116-9

  • 36

    GonçalvesF. M. P.TchambaJ. E.LagesF. M. O. P.AlexandreJ. L. M. (2019). Conhecimento etnobotânico da província da Huíla (Angola): um contributo baseado nos registos de campo do colector José Maria Daniel. Rev. Int. Em Língua Port.35, 83–102. 10.31492/2184-2043.RILP2018.35/pp.83-102

  • 37

    GoyderD. J.GonçalvesF. M. P. (2019). “The flora of Angola: collectors, richness, and endemism,” in Biodiversity of Angola (Springer International Publishing), 79–96. 10.1007/978-3-030-03083-4_5

  • 38

    HagariR. W.NgutaJ. M. (2025). Ethnopharmacology, toxicology and phytochemical composition of Mondia whitei (Hook. f.) Skeels (Apocynaceae). Afr. J. Pharm. Pharmacol.19 (5), 52–61. 10.5897/ajpp2025.5434

  • 39

    HaqI. (2004). Safety of medicinal plants. Pak J. Med. Res.43 (4), 203–210. Available online at: PakMediNet ‐ View Abstract.

  • 40

    HeinzeC.DitschB.CongoM. F.JoséI. J.NeinhuisC.LautenschlaegerT. (2017). First ethnobotanical analysis of useful plants in Cuanza Norte, north Angola. Res. and Rev. J. Botanical Sci.6 (2), 44–53. 10.1186/s13002-016-0116-9

  • 41

    HeinzeC.DundãoM. D. F.NeinhuisC.LautenschlägerT. (2019). The economicc potential of selected native plants from Cuanza Norte, northern Angola. Econ. Bot.73 (73), 96–111. 10.1007/s12231-018-9439-x

  • 42

    Hernández-FloresE. J.Blancas-BenitezF. J.Montaño-LeyvaB.González-EstradaR. R. (2023). Antifungal potential of aqueous extracts of coconut (Cocos nucifera L.) by-products against blue mold disease on Persian lime during storage. Food Control.148, 109632. 10.1016/j.foodcont.2023.109632

  • 43

    HossiH. (2017). Estudo da bioatividade de compostos fitoquímicos de plantas medicinais africanas: cochlospermum angolensis. Master’s thesis, Porto, Portugal: Instituto Politécnico do Porto.

  • 44

    HuntleyB.J. (2023). “Soil, water and nutrients,” in Ecology of Angola (Cham: Springer). 10.1007/978-3-031-18923-4_6

  • 45

    InkotoC. L.NgboluaK.-T.-N.KilembeJ. T.AshandeC. M.LukokiF. L.TshilandaD. D.et al (2021). A mini review on the phytochemistry and pharmacology of Aframomum alboviolaceum (Zingiberaceae). South Asian Res. J. Nat. Prod.4 (3), 24–35. Available online at: https://journalsarjnp.com/index.php/SARJNP/article/view/85

  • 46

    International Society of Ethnobiology (2006). International society of Ethnobiology code of ethics (with 2008 additions). Available online at: http://ethnobiology.net/code-of-ethics/. (Accessed February 24, 2018)

  • 47

    IsholaI. O.IkuomolaB. O.AdeyemiO. O. (2018). Protective role of Spondias mombin leaf and Cola acuminata seed extracts against scopolamineinduced cognitive dysfunction. Alexandria Journal Medicine54 (1), 27–39. 10.1016/j.ajme.2016.08.001

  • 48

    IsioguguO. N.EzikeA. C.PeterI. E.OnwukaA. M.ObiB. C.AbonyiU. C. (2018). “Effects of monodora Myristica root bark on acute and chronic inflammation,” in Proceedings of the West African Network for Natural Products Research Conference.

  • 49

    IUCN (2018). The IUCN red list of threatened species. Version 2018-2. Available online at: http://www.iucnredlist.org (Accessed October 30, 2018).

  • 50

    IwuM. M. (1997). African ethnobotany: poisons and drugs: chemistry, pharmacology, toxicology. J. Nat. Prod.60 (08), 864–865. 10.1021/np960638h

  • 51

    IwuanyanwuV. U.BanjoO. W.BabalolaK. T.OlajideO. A. (2023). Neuroprotection by Alstonia boonei De Wild., Anacardium occidentale L., Azadirachta indica A. Juss. and Mangifera indica L. J. Ethnopharmacol.310, 116390. 10.1016/j.jep.2023.116390

  • 52

    JadidN.WidodoA. F.ErmavitaliniD.Sa'adahN. N.GunawanS.NisaC. (2023). The medicinal Umbelliferae plant Fennel (Foeniculum vulgare Mill.): cultivation, traditional uses, phytopharmacological properties, and application in animal husbandry. Arabian J. Chem.16, 104541. 10.1016/j.arabjc.2023.104541

  • 53

    JenaA. K.KaranM.VasishtK. (2017). Plant parts substitution-based approach as a viable conservation strategy for medicinal plants: a case study of Premna latifolia Roxb. J. Ayurveda Integr. Med.8 (2), 68–72. 10.1016/j.jaim.2016.11.003

  • 54

    JoujehR.JoujehD. (2023). Traditional uses, chemical composition and pharmacological activities of the genus terminalia. Int. J. Sci. Res. Biol. Sci.10 (4), 19–31. Available online at: https://ijsrbs.isroset.org/index.php/j/article/view/598

  • 55

    KarahanF.OzyigitI. I.SaracogluI. A.YalcinI. E.OzyigitA. H.IlcimA. (2020). Heavy metal levels and mineral nutrient status in different parts of various medicinal plants collected from eastern mediterranean region of Turkey. Biol. Trace Elem. Res.197 (1), 316–329. 10.1007/s12011-019-01974-2

  • 56

    KharchoufaL.BouhrimM.BencheikhN.AddiM.HanoC.MechchateH.et al (2021). Potential toxicity of medicinal plants inventoried in northeastern Morocco: an ethnobotanical approach. Plants10 (6), 1108. 10.3390/plants10061108

  • 57

    KohzadiS.ShahmoradiB.GhaderiE.LoqmaniH.MalekiA. (2019). Concentration, source, and potential human health risk of heavy metals in the commonly consumed medicinal plants. Biol. Trace Elem. Res.187 (1), 41–50. 10.1007/s12011-018-1357-3

  • 58

    KueteV.SandjoL. P.MbavengA. T.ZeinoM.EfferthT. (2015). Cytotoxicity of compounds from Xylopia aethiopica towards multi-factorial drug-resistant cancer cells. Phytomedicine22 (14), 1247–1254. 10.1016/j.phymed.2015.10.008

  • 59

    KumarN.KulsoomM.ShuklaV.KumarD.KumarS.TiwariJ.et al (2018). Profiling of heavy metal and pesticide residues in medicinal plants. Environ. Sci. Pollut. Res.25 (29), 29505–29510. 10.1007/s11356-018-2993-z

  • 60

    KwonK. B.KimE. K.JeongE. S.LeeY. H.LeeY. R.ParkJ. W.et al (2006). Cortex cinnamomi extract prevents streptozotocin- and cytokine-induced β-cell damage by inhibiting NF-κB. World J. Gastroenterol.12 (27), 4331–4337. 10.3748/wjg.v12.i27.4331

  • 61

    LautenschlägerT.MoniziM.PedroM.MandombeJ. L.BránquimaM. F.HeinzeC.et al (2018). First large-scale ethnobotanical survey in the province of Uíge, northern Angola. J. Ethnobiol. Ethnomedicine14 (1), 51. 10.1186/s13002-018-0238-3

  • 62

    LavudiK.HemalathaS.KokkantiR. R.HarikaG. V. S.PatnaikS.PenchalaneniJ. (2022). Anti-tumour efficacy of Musa paradisiaca flower extracts on DMBA induced mammary carcinogenesis in female wistar rats. South Afr. J. Bot.151, 200–207. 10.1016/j.sajb.2022.09.037

  • 63

    LeeH. S.KwonY. J.SeoE. B.KimS. K.LeeH.LeeJ. T.et al (2023). Anti-inflammatory effects of Allium cepa L. peel extracts via inhibition of JAK-STAT pathway in LPS-stimulated RAW264. 7 cells. J. Ethnopharmacol.317, 116851. 10.1016/j.jep.2023.116851

  • 64

    LimK. T.AmanahA.ChearN. J. Y.ZahariZ.ZainuddinZ.AdenanM. I. (2018). Inhibitory effects of (+)-spectaline and iso-6-spectaline from Senna spectabilis on the growth and ultrastructure of human-infective species Trypanosoma brucei rhodesiense bloodstream form. Exp. Parasitology184, 57–66. 10.1016/j.exppara.2017.11.007

  • 65

    LiuM.KaterereD. R.GrayA. I.SeidelV. (2009). Phytochemical and antifungal studies on Terminalia mollis and Terminalia brachystemma. Fitoterapia80 (6), 369–373. 10.1016/j.fitote.2009.05.006

  • 66

    LiuQ.WuF.ChenY.AlrashoodS. T.AlharbiS. A. (2021). Anti-human colon cancer properties of a novel chemotherapeutic supplement formulated by gold nanoparticles containing Allium sativum L. leaf aqueous extract and investigation of its cytotoxicity and antioxidant activities. Arabian J. Chem.14 (4), 103039. 10.1016/j.arabjc.2021.103039

  • 67

    LuoL.WangB.JiangJ.FitzgeraldM.HuangQ.YuZ.et al (2021). Heavy metal contaminations in herbal medicines: determination, comprehensive risk assessments, and solutions. Front. Pharmacol.11, 595335. 10.3389/fphar.2020.595335

  • 68

    MaY.XuH.SunY.FanH.LiY.SongX.et al (2025). Botanical, phytochemistry, pharmacology and applications of genus Aframomum: a review. Rec. Nat. Prod.19 (2), 118–149. 10.25135/rnp.508.2502.3429

  • 69

    MaigaA.MalterudK. E.DialloD.PaulsenB. S. (2006). Antioxidant and 15-lipoxygenase inhibitory activities of the Malian medicinal plants Diospyros abyssinica (Hiern) F. White (Ebenaceae), Lannea velutina A. Rich (Anacardiaceae) and Crossopteryx febrifuga (Afzel) Benth. (Rubiaceae). J. Ethnopharmacology104 (1-2), 132–137. 10.1016/j.jep.2005.08.063

  • 70

    MakgathoM. E.NxumaloW.RaphokoL. A. (2018). Anti-mycobacterial,-oxidative,-proliferative and-inflammatory activities of dichloromethane leaf extracts of Gymnosporia senegalensis (Lam.) loes. South Afr. J. Bot.114, 217–222. 10.1016/j.sajb.2017.11.002

  • 71

    MalikK.AhmadM.ZhangG.RashidN.ZafarM.SultanaS.et al (2018). Traditional plant-based medicines used to treat musculoskeletal disorders in Northern Pakistan. Eur. J. Integr. Med.19, 17–64. 10.1016/j.eujim.2018.02.003

  • 72

    MangaF. N.El KhattabiC.FontaineJ.BerkenboomG.DuezP.NoyonC.et al (2013). Vasorelaxant and antihypertensive effects of methanolic extracts from Hymenocardia acida Tul. J. Ethnopharmacology146 (2), 623–631. 10.1016/j.jep.2013.02.002

  • 73

    ManvithaK.BidyaB. (2014). Review on pharmacological activity of Cymbopogon citratus. Int. J. Herb. Med.Available online at: https://www.florajournal.com/vol1issue6/feb2014/C3.1.pdf?

  • 74

    MasokoP.PicardJ.EloffJ. N. (2005). Antifungal activities of six south African Terminalia species (Combretaceae). J. Ethnopharmacol.99 (2), 301–308. 10.1016/j.jep.2005.01.061

  • 75

    MathiasG. P.PanigrahiT.ShanbaghS.SadhanaV.BabuP.RasikalaK.et al (2020). Combination of aqueous extracts of Phyllanthus niruri, Boerhavia diffusa, and Picrorhiza kurroaor Zingiber officinalealone inhibit intracellular inflammatory signaling Cascade. J. Herb. Med.23, 100378. 10.1016/j.hermed.2020.100378

  • 76

    MendonçaD. I. M. D.MataR. C. S.SebastiãoN. N.BorgesC. M. P. (2015). Um breve olhar sobre algumas plantas medicinais angolanas. Bol. Soc. Port. Quím.39 (138), 23–30. 10.52590/M3.P670.A30001988

  • 77

    MhaladiR.Madamombe-MandunaI. T.MasheleS. S. (2016). Antidiabetic and cytotoxic activities of Aloe ferox Mill. South Afr. J. Bot.100 (103), 332. 10.1016/j.sajb.2016.02.107

  • 78

    MishraA. K.ChahalP.SinghH.KumarA.MishraA. (2022). Exploration of hepatoprotective and antidiabetic potential of Senna occidentalis L. and isolation of a bioactive compound by column chromatography. South Afr. J. Bot.148, 144–153. 10.1016/j.sajb.2022.04.024

  • 79

    MongaloN. I.McGawL. J.FinnieJ.Van StadenJ. (2015). Securidaca longipedunculata Fresen (Polygalaceae): a review of its ethnomedicinal uses, phytochemistry, pharmacological properties and toxicology. J. Ethnopharmacol.165, 215–226. 10.1016/j.jep.2015.02.041

  • 80

    MoustakaJ.PanterisE.AdamakisI. D. S.TanouG.GiannakoulaA.EleftheriouE. P.et al (2018). High anthocyanin accumulation in poinsettia leaves is accompanied by thylakoid membrane unstacking, acting as a photoprotective mechanism, to prevent ROS formation. Environ. Exp. Bot.154, 44–55. 10.1016/j.envexpbot.2018.01.006

  • 81

    MurugesanS.VenkateswaranM. R.JayabalS.PeriyasamyS. (2020). Evaluation of the antioxidant and anti-arthritic potential of Zingiber officinale Rosc. by in vitro and in silico analysis. South Afr. J. Bot.130, 45–53. 10.1016/j.sajb.2019.12.019

  • 82

    NagawaC.BöhmdorferS.RosenauT. (2015). Chemical composition and anti-termitic activity of essential oil from Canarium schweinfurthii Engl. Industrial Crops Prod.71, 75–79. 10.1016/j.indcrop.2015.03.078

  • 83

    NdeA. L.ChukwumaC. I.ErukainureO. L.ChukwumaM. S.MatsabisaM. G. (2022). Ethnobotanical, phytochemical, toxicology and anti-diabetic potential of Senna occidentalis (L.) link; A review. J. Ethnopharmacol.283, 114663. 10.1016/j.jep.2021.114663

  • 84

    NgarivhumeT.van't KloosterC. I. E. A.de JongJ. T. V. M.van der WesthuizenJ. H. (2015). Medicinal plants used by traditional healers for the treatment of malaria in the Chipinge district in Zimbabwe. J. Ethnopharmacol.159, 224–237. 10.1016/j.jep.2014.11.011

  • 85

    NourA. M.KhalidS. A.KaiserM.BrunR.Wai’lE. A.SchmidtT. J. (2010). The antiprotozoal activity of methylated flavonoids from Ageratum conyzoides L. J. Ethnopharmacology129 (1), 127–130. 10.1016/j.jep.2010.02.015

  • 86

    NovotnaB.PolesnyZ.Pinto-BastoM. F.van DammeP.PudilP.MazancovaJ.et al (2020). Medicinal plants used by 'root doctors', local traditional healers in Bié province, Angola. J. Ethnopharmacol.260, 112662. 10.1016/j.jep.2020.112662

  • 87

    OjoO. A.AgboolaA. O.OgunroO. B.IyobhebheM.ElebiyoT. C.RotimiD. E.et al (2023). Beet leaf (beta vulgaris L.) extract attenuates iron-induced testicular toxicity: experimental and computational approach. Heliyon9 (7), e17700. 10.1016/j.heliyon.2023.e17700

  • 88

    OlanlokunJ. O.BodedeO.PrinslooG.OlorunsogoO. O. (2021). Comparative antimalarial, toxicity and mito-protective effects of Diospyros mespiliformis Hochst. ex A. DC. and Mondia whitei (Hook. f.) Skeels on Plasmodium berghei infection in mice. J. Ethnopharmacol.268, 113585. 10.1016/j.jep.2020.113585

  • 89

    OlerJ. R. L.AmorozoM. C. de M.MonteiroR.Butturi-GomesD. (2019). Etnobotânica de plantas tóxicas como subsídio para campanhas de prevenção de acidentes: um estudo de caso em Cananéia, São Paulo, Brasil. Sci. Plena15 (11). 10.14808/sci.plena.2019.111201

  • 90

    PanM.LeiQ.ZhangH. (2020). Prediction and confirmation of active ingredients in Eucalyptus globulus labill leaves. Industrial Crops Prod.154, 112631. 10.1016/j.indcrop.2020.112631

  • 91

    PereiraG. (2023). Ethnographic map of Malanje [unpublished internal document, kindly provided]. Luanda, Angola: Faculdade de Ciências Naturais da Universidade Agostinho Neto.

  • 92

    RajooA.RamanathanS.MansorS. M.SasidharanS. (2021). Formulation and evaluation of wound healing activity of Elaeis guineensis Jacq leaves in a Staphylococcus aureus infected Sprague Dawley rat model. J. Ethnopharmacol.266, 113414. 10.1016/j.jep.2020.113414

  • 93

    RawatA.MaliR. R.SainiA. K.ChauhanP. K.SinghV.SharmaP. (2013). Phytochemical properties and pharmcological activities of Nicotiana tabacum: a review. Indian J. Pharm. Biol. Res.1, 74–82. 10.30750/ijpbr.1.2.9

  • 94

    SaadB.ZaidH.ShanakS.KadanS. (2017). “Introduction to medicinal plant safety and efficacy,” in Anti-Diabetes and Anti-Obesity Medicinal Plants and Phytochemicals (Springer International Publishing), 21–55. 10.1007/978-3-319-54102-0_2

  • 95

    SambaN.BarriosA. M.De LeónE. G.RaposoC.LahlouR. A.CurtoJ.et al (2025). Cochlospermum angolense Welw ex oliv: phytochemical profile, antioxidant activity, and therapeutic prospects. Molecules30 (13), 2768. 10.3390/molecules30132768

  • 96

    SarauxN.BrunaL.EbrahimiS. N.KarimouS.ChristenP.CuendetM. (2023). Antiproliferative activity of compounds isolated from the root bark of Lannea acida in multiple myeloma cell lines. Phytochemistry209, 113641. 10.1016/j.phytochem.2023.113641

  • 97

    SarmaH.DekaS.DekaH.SaikiaR. R. (2012). Accumulation of heavy metals in selected medicinal plants. Rev. Environ. Contam. Toxicol.214, 63–86. 10.1007/978-1-4614-0668-6_4

  • 98

    SavianoA.RaucciF.CasilloG. M.MansourA. A.PiccoloV.MontesanoC.et al (2022). Anti-inflammatory and immunomodulatory activity of Mangifera indica L. reveals the modulation of COX-2/mPGES-1 axis and Th17/Treg ratio. Pharmacol. Res.182, 106283. 10.1016/j.phrs.2022.106283

  • 99

    ShanleyP.GaiaG. (2013). Conservation from Brazilian Amazonian women's perspectives. Ethnobot. Res. and Appl.11, 29–40.

  • 100

    ShittuS.-T. T.OyeyemiW. A.LasisiT. J.ShittuS.A.-S.LawalT. T.OlujobiS. T. (2016). Aqueous leaf extract of Ocimum gratissimum improves hematological parameters in alloxan-induced diabetic rats via its antioxidant properties. Int. J. Appl. Basic Med. Res.6(2):p 96–100. 10.4103/2229-516X.179016

  • 101

    SiddiqueH.PendryB.RashidM. A.RahmanM. M. (2021). Medicinal plants used to treat infectious diseases in the central part and a northern district of Bangladesh – an ethnopharmacological perception. J. Herb. Med.29, 100484. 10.1016/j.hermed.2021.100484

  • 102

    SkowrońskaW.GranicaS.CzerwińskaM. E.OsińskaE.BazylkoA. (2022). Sambucus nigra L. leaves inhibit TNF-α secretion by LPS-stimulated human neutrophils and strongly scavenge reactive oxygen species. J. Ethnopharmacol.290, 115116. 10.1016/j.jep.2022.115116

  • 103

    SubenthiranS.ChoonT. C.CheongK. C.ThayanR.TeckM. B.MuniandyP. K.et al (2013). Carica papaya leaves juice significantly accelerates the rate of increase in platelet count among patients with dengue fever and dengue haemorrhagic fever. Evidence‐Based Complementary Altern. Med.2013 (1), 616737. 10.1155/2013/616737

  • 104

    SulaimanM. R.ZakariaZ. A.BujariminA. S.SomchitM. N.IsrafD. A.MoinS. (2008). Evaluation of Moringa oleifera aqueous extract for antinociceptive and anti-inflammatory activities in animal models. Pharm. Biology46 (12), 838–845. 10.1080/13880200802366710

  • 105

    Takaisi-KikuniN. B.TshilandaD.BabadyB. (2000). Antibacterial activity of the essential oil of Cymbopogon densiflorus. Fitoterapia71 (1), 69–71. 10.1016/s0367-326x(99)00097-0

  • 106

    TamfuA. N.RolandN.MfifenA. M.KucukaydinS.GayeM.BotezatuA. V.et al (2022). Phenolic composition, antioxidant and enzyme inhibitory activities of Parkia biglobosa (Jacq.) Benth., Tithonia diversifolia (Hemsl) A. Gray, and Crossopteryx febrifuga (Afzel.) Benth. Arabian J. Chem.15 (4), 103675. 10.1016/j.arabjc.2021.103675

  • 107

    TchambaJ. J. (2019). As plantas - usos e costumes dos povos da província da Huíla, um estudo exploratório com Securidaca longipedunculata e Uapaca kirkiana. Rev. TransVersos15, 417–432. 10.12957/transversos.2019.41864

  • 108

    TchambaJ. J.CatarinoS.DuarteM. C.SilvaJ. M. N.RomeirasM. M.CatarinoL. (2024). Ethnobotany in Angola: the contribution of late 19th century Christian missionaries to the knowledge of medicinal wild plants. J. Ethnopharmacol.334, 118511. 10.1016/j.jep.2024.118511

  • 109

    TonelliC. A.de OliveiraS. Q.da Silva VieiraA. A.BiavattiM. W.RitterC.ReginattoF. H.et al (2022). Clinical efficacy of capsules containing standardized extract of Bauhinia forficata link (pata-de-vaca) as adjuvant treatment in type 2 diabetes patients: a randomized, double blind clinical trial. J. Ethnopharmacol.282, 114616. 10.1016/j.jep.2021.114616

  • 110

    Torres-AvilezW.de MedeirosP. M.AlbuquerqueU. P. (2016). Effect of gender on the knowledge of medicinal plants: systematic review and meta-analysis. Evid. Based Complement Alterna. Med.6592363. 10.1155/2016/6592363

  • 111

    UrsoV.SignoriniM. A.ToniniM.BruschiP. (2016). Wild medicinal and food plants used by communities living in Mopane woodlands of southern Angola: results of an ethnobotanical field investigation. J. Ethnopharmacol.177, 126–139. 10.1016/j.jep.2015.11.041

  • 112

    VarelaE. P.AssunçãoV. K.MingL. C.ZanetteV. C. (2022). Semeando saberes: a etnobotânica e o quintal na valorização do conhecimento da mulher agricultora. Rev. Etnobiología20 (2), 213235. Available online at: https://revistaetnobiologia.mx/index.php/etno/article/view/494?

  • 113

    WangZ.WangH.WangH.LiQ.LiY. (2019). Heavy metal pollution and potential health risks of commercially available Chinese herbal medicines. Sci. Total Environ.653, 748–757. 10.1016/j.scitotenv.2018.10.388

  • 114

    WHO (2011). Quality control methods for herbal materials. Geneva, ,Switzerland: World Health Organization. Available online at: https://www.who.int/publications/i/item/9789241500739.

  • 115

    WHO (2013). WHO Traditional Medicine Strategy: 2014-2023. Geneva, ,Switzerland: World Health Organization. Available online at: https://www.who.int/publications/i/item/9789241506096. (Accessed 22 January, 2018)

  • 116

    WHO (2018). WHO Country Cooperation Strategy at a Glance: Angola. Angola: World Health Organization. Available online at: https://apps.who.int/iris/bitstream/handle/10665/136994/ccsbrief_ago_en.pdf?sequence=1&isAllowed=y. (Accessed January 22, 2019)

  • 117

    WHO (2019). International Classification of Diseases 11th Revision (ICD-11). Geneva, Switzerland: World Health Organization. Available online at: https://icd.who.int/browse11/l-m/en. (Accessed June 20, 2020)

  • 118

    YaoH.ShiW.WangX.LiJ.ChenM.LiJ.et al (2023). The root-associated Fusarium isolated based on fungal community analysis improves phytoremediation efficiency of Ricinus communis L. in multi metal-contaminated soils. Chemosphere324, 138377. 10.1016/j.chemosphere.2023.138377

  • 119

    ZhouL.SongZ.ZhangS.LiY.XuJ.GuoY. (2021). Construction and antitumor activity of selenium nanoparticles decorated with the polysaccharide extracted from Citrus limon (L.) Burm. f. (Rutaceae). Int. J. Biol. Macromol.188, 904–913. 10.1016/j.ijbiomac.2021.07.142

Summary

Keywords

indigenous knowledge, traditional healers, biodiversity conservation, rank order priority, Terminalia

Citation

Barroso AA, Martins AA, Morais A, Katenda PCF, Jamba MF, Gonçalves MFA, Sebastião MA, Chimbuco BN, Hernández YS, Mota DS, Ribalta VR, Gomes A, Barreto EH and Ekundi-Valentim E (2026) An ethnopharmacological assessment of medicinal plants in Malanje Municipality, Angola. Front. Pharmacol. 16:1702353. doi: 10.3389/fphar.2025.1702353

Received

09 September 2025

Revised

23 November 2025

Accepted

01 December 2025

Published

25 February 2026

Volume

16 - 2025

Edited by

Muhammad Nabeel Ghayur, University of Pikeville, United States

Reviewed by

Klaus Peter Latté, Independent Researcher, Berlin, Germany

Luis Catarino, University of Lisbon, Portugal

Updates

Copyright

*Correspondence: Eduardo Ekundi-Valentim,

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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