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. | Family | Scientific name | Habitus | Common name | Distribution data for each species | Collecting place | ROP |
|---|---|---|---|---|---|---|---|
| 1. | Combretaceae | Terminalia brachystemma Welw. ex Hiern | Tree/shrub | Mueia (Kimb.) | Native | Shrubland savanna | 81.8 |
| 2. | Polygalaceae | Securidaca longepedunculata Fresen. | Shrub | Mutungo (Kimb.) | Native | Shrubland savanna | 54.4 |
| 3. | Apocynaceae | Mondia whitei (Hook.f.) Skeels | Climbing | Mundondo (Kimb.) | Native | Cropland/forest gallery | 52.2 |
| 4. | Cochlospermaceae | Cochlospermum angolense Welw. ex Oliv. | Shrub | Mbrututo (Kimb.) | Native | Shrubland savanna | 34 |
| 5. | Rubiaceae | Mussaenda arcuata Poir. | Shrub | Kabolebole (Kimb.) | Native | Shrubland savanna | 31.7 |
| 6. | Fabaceae | Senna occidentalis (L.) Link | Shrub | Mudia-nhoca (Kimb.) | Native | Disturbed places | 29.4 |
| 7. | Zingiberaceae | Aframomum alboviolaceum (Ridl.) K.Schum. | Annual herb | Ginguenga (Kimb.) | Native | Shrubland savanna | 27.2 |
| 8. | Annonaceae | Monodora myristica (Gaertn.) Dunal | Tree | Jipepe (Kimb.) | Native | Forest gallery | 27.1 |
| 9. | Anacardiaceae | Lannea welwitschii (Hiern) Engl. | Tree | Mucumbi (Kimb.) | Native | Forest gallery | 22.7 |
| 10. | Annonaceae | Xylopia aethiopica (Dunal) A.Rich. | Tree | Missae (Kimb.) | Native | Forest gallery | 18.7 |
| 11. | Fabaceae | Vachellia sieberiana (DC.) Kyal. & Boatwr. | Tree | Musonge (Kimb.) | Native | Wooded savanna | 18.1 |
| 12. | Burseraceae | Canarium schweinfurthii Engl. | Tree | Mubafo (Kimb.) | Native | Forest gallery | 18.1 |
| 13. | Moringaceae | Moringa oleifera Lam. | Shrub | Moringa (port.) | Naturalized | Fallows/cropland | 15.8 |
| 14. | Euphorbiaceae | Ricinus communis L. | Shrub | Jimono (Kimb.) | Naturalized | Disturbed places | 15.8 |
| 15. | Rubiaceae | Crossopteryx febrifuga Benth. | Shrub | Mussesse (Kimb.) | Native | Shrubland savanna | 15.4 |
| 16. | Poaceae | Cymbopogon densiflorus Stapf | Grass | Saco-saco (Kimb.) | Naturalized | Cropland | 13.5 |
| 17. | Myrtaceae | Eucalyptus globulus Labill. | Tree | Eucalipto (Port.) | Cultivated | Fallows | 11.3 |
| 18. | Fabaceae | Bauhinia forficata Link | Shrub | Pata de vaca (Port.) | Introduced | Disturbed places | 11.3 |
| 19. | Amaranthaceae | Dysphania ambrosioides (L.) Mosyakin & Clemants | Annual herb | Santa Maria (Port.) | Naturalized | Disturbed places | 11.3 |
| 20. | Fabaceae | Eriosema psoraleoides (Lam.) G.Don | Shrub | Kidiambuiz (Kimb.) | Native | Disturbed places | 11.3 |
| 21. | Celastraceae | Gymnosporia senegalensis Loes. | Shrub | Mussambela (Kimb.) | Native | Shrubland savanna | 11 |
| 22. | Asparagaceae | Asparagus sp. | Annual herb | Kanhanga (Kimb.) | Native | Shrubland savanna | 11 |
| 23. | Amaranthaceae | Beta vulgaris L. | Annual herb | Beterraba (Port.) | Introduced | Cropland | 6.8 |
| 24. | Euphorbiaceae | Euphorbia pulcherrima Willd. ex Klotzsch | Shrub | Bico de Papagaio (Port.) | Native | Arid savanna | 6.8 |
| 25. | Zingiberaceae | Aframomum melegueta K. Schum. | Annual herb | Ndungo à congo (Kimb.) | Native | Forest gallery | 6.7 |
| 26. | Zingiberaceae | Zingiber officinale Rosc. | Annual herb | Gingibre (Port.) | Cultivated | Cropland | 6.7 |
| 27. | Amaryllidaceae | Allium cepa L. | Annual herb | Cebola (Port.) | Cultivated | Cropland | 6.7 |
| 28. | Solanaceae | Nicotiana tabacum L. | Annual herb | Tabaqueiro (Port.) | Cultivated | Cropland | 4.5 |
| 29. | Solanaceae | Solanum lycopersicum L. | Annual herb | Tomateiro (Port.) | Cultivated | Cropland | 4.5 |
| 30. | Rutaceae | Citrus limon (L.) Burm. F. | Shrub | Limoeiro (Port.) | Cultivated | Cropland | 4.5 |
| 31. | Phyllanthaceae | Phyllanthus niruri L. | Shrub | Quebra-pedra (Port.) | Native | Shrubland savanna | 4.5 |
| 32. | Myrtaceae | Psidium guajava L. | Shrub | Goiabeira (Port.) | Cultivated | Cropland | 4.5 |
| 33. | Meliaceae | Azadirachta indica A.Juss. | Tree | Neem (Port.) | Introduced | Disturbed places | 4.5 |
| 34. | Lauraceae | Persea americana Mill. | Tree | Abacateiro (Port.) | Cultivated | Cropland | 4.5 |
| 35. | Phyllanthaceae | Hymenocardia acida Tul. | Shrub | Mupexi (Kimb.) | Native | Shrubland savanna/miombo | 4.5 |
| 36. | Costaceae | Costus spiralis (Jacq.) Roscoe | Annual herb | Muengueya samba (Kimb.) | Native | Shrubland savanna | 4.5 |
| 37. | Caricaceae | Carica papaya L. | Tree/herb | Mamoeiro (Port.) | Cultivated | Cropland | 4.5 |
| 38. | Asteraceae | Tithonia diversifolia (Hemsl.) A.Gray | Shrub | Cura-tudo (port.) | Introduced | Disturbed places | 4.5 |
| 39. | Arecaceae | Elaeis guineensis (Jacq.) | Tree palm | Palmeira (Port.) | Naturalized | Cropland | 4.5 |
| 40. | Apocynaceae | Picralima nítida (Stapf) T.Durand & H.Durand | Tree | Kikongo (Kimb.) | Introduced | Forest gallery | 4.5 |
| 41. | Xanthorrhoeaceae | Aloe ferox Mill. | Herb succulent | Xandala (Kimb.) | Introduced | Cropland | 4.5 |
| 42. | Amaryllidaceae | Allium sativum L. | Herb | Alho (Port.) | Cultivated | Cropland | 4.5 |
| 43. | Poaceae | Saccharum officinarum L. | Grass | Cana de açúcar (Port.) | Cultivated | Cropland | 4.5 |
| 44. | Amaranthaceae | Spinacia oleracea L. | Herb | Espinafre (Port) | Cultivated | Cropland | 4.5 |
| 45. | Asteraceae | Artemisia absinthium L. | Shrub | Losna (Port.) | Native | Shrubland savanna | 4.5 |
| 46. | Euphorbiaceae | Manihot esculenta Crantz | Shrub | Mandioqueira (Port.) | Cultivated | Cropland | 4.5 |
| 47. | Euphorbiaceae | Alchornea cordifolia (Schumach. & Thonn.) Müll.Arg | Shrub | Mbunze (Kimb.) | Native | Forest gallery | 4.5 |
| 48. | Solanaceae | Capsicum annuum L. | Herb | Gindungo (Port.) | Cultivated | Cropland | 2.2 |
| 49. | Poaceae | Cymbopogon citratus (DC.) Stapf | Grass | Caxinde (Kimb.) | Cultivated | Cropland | 2.2 |
| 50. | Myrtaceae | Eugenia uniflora L. | Shrub | Pitangueira (Port.) | Introduced | Cropland | 2.2 |
| 51. | Malvaceae | Abelmoschus esculentus (L.) Moench. | Shrub | Quiabo (Port.) | Cultivated | Cropland | 2.2 |
| 52. | Clusiaceae | Garcinia mannii Oliv. | Shrub | Ngadiadia (Kimb.) | Native | Forest gallery | 2.2 |
| 53. | Asteraceae | Acanthospermum hispidum DC. | Herb | Kauenha (Kimb.) | Introduced | Disturbed places | 2.2 |
| 54. | Anacardiaceae | Mangifera indica L. | Tree | Mangueira (Port.) | Cultivated | Cropland | 2.2 |
| 55. | Moraceae | Ficus thonningii Blume | Tree | Lemba-lemba (Kimb.) | Native | Forest gallery | 2.2 |
| 56. | Asteraceae | Vernonia sp | Herb | Kidiassute (Kimb.) | Introduced | Disturbed places | 2.2 |
| 57. | Zingiberaceae | Alpinia zerumbet (Pers.) B.L. Burtt & R.M.Sm. | Herb | Colónia (Port.) | Introduced | ornamental | Nc |
| 58. | Malvaceae | Cola acuminata (P. Beauv.) Schott & Endl. | Tree | Dikazo (Kimb.) | Native | Forest gallery | Nc |
| 59. | Rubiaceae | Coffea canephora Pierre ex A.Froehner | Shrub | Cafeeiro (Port.) | Cultivated | Cropland | Nc |
| 60. | Poaceae | Zea mays L. | Grass | Milheiro (Port.) | Cultivated | Cropland | Nc |
| 61. | Nyctaginaceae | Boerhavia diffusa L. | Herb | Mutumbata (Kimb.) | Naturalized | Disturbed places | Nc |
| 62. | Musaceae | Musa paradisiaca L. | Herb | Bananeira (Port.) | Cultivated | Cropland | Nc |
| 63. | Lauraceae | Cinnamomum verum J.Presl. | Shrub | Canela (Port.) | Introduced | Cropland | Nc |
| 64. | Lamiaceae | Ocimum gratissimum L. | Herb | Alfa vaca (Port.) | Introduced | Cropland | Nc |
| 65. | Lamiaceae | Mentha arvensis L. | Herb | Hortelã (Port.) | Introduced | Cropland | Nc |
| 66. | Cannabaceae | Cannabis sativa L. | Herb | Liamba (Port.) | Introduced | Cropland | Nc |
| 67. | Asteraceae | Ageratum conyzoides L. | Herb | Cabuabuata (Kimb.) | Native | Disturbed places | Nc |
| 68. | Apiaceae | Foeniculum vulgare Mill. | Herb | Funcho (Port.) | Cultivated | Cropland | Nc |
| 69. | Anacardiaceae | Spondias mombin L. | Tree | Gajajeira (Port.) | Introduced | Cropland | Nc |
| 70. | Viburnaceae | Sambucus nigra L. | Shrub | Sabugueiro (Port.) | Introduced | Cropland | Nc |
| 71. | Fabaceae | Pericopsis angolensis (Baker) Meeuwen | Tree | Ngambo (Kimb.) | Native | Miombo/savanna | Nc |
| 72. | Arecaceae | Cocos nucifera L. | Tree palm | Coqueiro (Port) | Introduced | Cropland | Nc |
| 73. | Rosaceae | Fragaria sp. | Herb | Morangueiro (Port.) | Introduced | Cropland | Nc |
| 74. | Lamiaceae | Rosmarinus officinalis L. | Herb | Alecrim (Port.) | Introduced | Cropland | Nc |
| 75. | Fabaceae | Arachis hypogaea L. | Herb | Ginguba (Port.) | Cultivated | Cropland | Nc |
| 76. | Malvaceae | Sterculia dawei Sprague | Tree | Mulende (Kimb.) | Native | Forest gallery | Nc |
| 77. | Fabaceae | Senna spectabilis (DC.) H.S.Irwin & Barneby | Tree | Acacia (port.) | Introduced | Disturbed places | Nc |
| 78. | Picrodendraceae | Oldfieldia dactylophylla (Welw. ex Oliv.) J.Léonard | Tree | Mubatangombe (Kimb.) | Native | Shrubland savanna/miombo | Nc |
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. | Family | Number of species | Percent (%) |
|---|---|---|---|
| 1. | Fabaceae | 7 | 9 |
| 2. | Asteraceae | 5 | 6.4 |
| 3. | Euphorbiaceae | 4 | 5.1 |
| 4. | Poaceae | 4 | 5.1 |
| 5. | Zingiberaceae | 4 | 5.1 |
| 6. | Amaranthaceae | 3 | 3.8 |
| 7. | Anacardiaceae | 3 | 3.8 |
| 8. | Lamiaceae | 3 | 3.8 |
| 9. | Malvaceae | 3 | 3.8 |
| 10. | Myrtaceae | 3 | 3.8 |
| 11. | Rubiaceae | 3 | 3.8 |
| 12. | Solanaceae | 3 | 3.8 |
| 13. | Amaryllidaceae | 2 | 2.6 |
| 14. | Annonaceae | 2 | 2.6 |
| 15. | Apocynaceae | 2 | 2.6 |
| 16. | Arecaceae | 2 | 2.6 |
| 17. | Lauraceae | 2 | 2.6 |
| 18. | Phyllanthaceae | 2 | 2.6 |
| 19. | Viburnaceae | 1 | 1.3 |
| 20. | Apiaceae | 1 | 1.3 |
| 21. | Asparagaceae | 1 | 1.3 |
| 22. | Burseraceae | 1 | 1.3 |
| 23. | Cannabaceae | 1 | 1.3 |
| 24. | Caricaceae | 1 | 1.3 |
| 25. | Celastraceae | 1 | 1.3 |
| 26. | Clusiaceae | 1 | 1.3 |
| 27. | Cochlospermaceae | 1 | 1.3 |
| 28. | Combretaceae | 1 | 1.3 |
| 29. | Costaceae | 1 | 1.3 |
| 30. | Meliaceae | 1 | 1.3 |
| 31. | Moraceae | 1 | 1.3 |
| 32. | Moringaceae | 1 | 1.3 |
| 33. | Musaceae | 1 | 1.3 |
| 34. | Nyctaginaceae | 1 | 1.3 |
| 35. | Picrodendraceae | 1 | 1.3 |
| 36. | Polygalaceae | 1 | 1.3 |
| 37. | Rosaceae | 1 | 1.3 |
| 38. | Rutaceae | 1 | 1.3 |
| 39. | Xanthorrhoeaceae | 1 | 1.3 |
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 name | Traditional use | Plant parts used | Method of preparation | Application | Recorded literature uses | Reference |
|---|---|---|---|---|---|---|---|
| 1. | Terminalia brachystemma Welw. ex Hiern | Open cervix, paludism, and stomachache | Root and leaf | Maceration | Oral, rectal, and vaginal | Antifungal (in vitro) | , Masoko et al. (2005) |
| 2. | Securidaca longepedunculata Fresen. | Inflammation, constipation, and stomachache | Root | Maceration | Topical | Anticonvulsants (in vivo) | |
| 3. | Mondia whitei (Hook.f.) Skeels | Stomachache, colic, and sexual impotence | Root | Maceration | Oral and inhalation | Antimalarials (in vivo) | Olanlokun et al. (2021) |
| 4. | Cochlospermum angolense Welw. ex Oliv. | Hepatitis and paludism | Root | Maceration | Oral and topical | Anti-oxidant (in vitro) | Samba et al. (2025) |
| 5. | Mussaenda arcuata Poir. | Bone pain, thrombosis, and labor pain | Leaf | Maceration | Topical | Not reported | |
| 6. | Senna occidentalis (L.) Link | Stomachache, paludism, snake bite, and hernia | Root and leaf | Decoction | Oral | Antidiabetic (in vitro) | Mishra et al. (2022) Nde et al. (2022) |
| 7. | Monodora myristica (Gaertn.) Dunal | Stomachache, kyphosis, open cervix, and inflammation | Seed | Decoction | Oral and topical | Antidepressants (in vivo) | |
| 8. | Aframomum alboviolaceum (Ridl.) K.Schum. | Abortion prevention and kyphosis | Root | Decoction | Oral | Not reported | |
| 9. | Lannea welwitschii (Hiern) Engl. | Fractures, toothache, and thrombosis | Stem | Cataplasm | Oral, topical, and rectal | Anti-proliferative (in vitro) | Saraux et al. (2023) |
| 10. | Xylopia aethiopica (Dunal) A. Rich. | Stomachache, kyphosis, and open cervix | Seed | Decoction | Oral | Anti-cancer (in vitro) | |
| 11. | Vachellia sieberiana (DC.) Kyal. & Boatwr. | Inflammation, infertility, and backpain | Root | Maceration | Oral and topical | Not reported | |
| 12. | Canarium schweinfurthii Engl. | Stomachache, open cervix, typhoid fever, and hernia | Stem | Decoction | Oral | Termiticide (in vivo) | Nagawa et al. (2015) |
| 13. | Moringa oleífera Lam. | Stomachache | Root, leaf, and seed | Decoction | Oral | Anti-inflammatory (in vivo) | Sulaiman et al. (2008) |
| 14. | Ricinus communis L. | Headache, constipation, and thrombosis | Leaf and fruit | Decoction | Oral and topical | Phytoremediation (in vitro) | Yao et al. (2023) |
| 15. | Crossopteryx febrifuga (Afzel. Ex G.Don) Benth. | Toothache and anemia | Leaf and root | Decoction | Oral and inhalation | Alzheimer (in vitro) | Tamfu et al. (2022) |
| 16. | Cymbopogon densiflorus Stapf | Kyphosis, hernia, and stomachache | Flower | Decoction | Oral | Asthma (in vitro) | Takaisi-Kikuni et al. (2000) |
| 17. | Eucalyptus globulus Labill. | Asthma, tuberculosis, paludism, and cough | Leaf | Decoction | Inhalation, oral, and topical | Repellent (in vitro) | Pan et al. (2020) |
| 18. | Bauhinia forficata Link | Sexual impotence and hepatitis | Root | Decoction | Oral | Anti-diabetes (in vivo) | Tonelli et al. (2022) |
| 19. | Dysphania ambrosioides (L.) Mosyakin & Clemants | Stomachache, fever, epilepsy, hernia, and infertility | Leaf | Decoction | Oral, rectal, vaginal, and inhalational | Anti-inflammatory (in vivo) | |
| 20. | Eriosema psoraleoides (Lam.) G. Don | Sexual impotence, menstrual disorders, and intestinal infections | Root | Maceration | Oral and topical | Not reported | |
| 21. | Gymnosporia senegalensis Loes. | Cancer | Root | Maceration | Oral | Anti-inflammatory (in vitro) | |
| 22. | Asparagus sp. | Stomachache and infertility | Root and leaf | Maceration | Oral | Cancer (in vitro) | |
| 23. | Beta vulgaris L. | Anemia | Root | Decoction | Oral | Testicular oxidative damage (in vitro) | Ojo et al. (2023) |
| 24. | Euphorbia pulcherrima Willd. ex Klotzsch | Typhoid fever | Root | Decoction | Oral | Cancer (in vitro) | Moustak et al. (2018) |
| 25. | Aframomum melegueta K. Schum. | Hemorrhoids | Seed | Maceration | Oral and topical | Not reported | |
| 26. | Zingiber officinale Rosc. | Sexual impotence, paludism, yellow fever, and thrombosis | Root | Decoction | Oral | Anti-inflammatory (in vitro) | Murugesan et al. (2020) |
| 27. | Allium cepa L. | Inflammation, diabetes, injuries, flu, and hernia | Root | Infusion | Oral | Anti-inflammatory (in vitro) | |
| 28. | Nicotiana tabacum L. | Hemorrhoids, asthma, and angina | Leaf | Decoction | Oral, topical, and sublingual | Anti-Alzheimer (in vivo) | Rawat et al. (2013) |
| 29. | Solanum lycopersicum L. | Hemorrhage and headache | Leaf | Infusion | Oral and nasal | Anti-cancerogenic (invitro) | |
| 30. | Citrus limon (L.) Burm. F. | Typhoid fever and paludism | Fruit | Decoction | Oral and topical | Anti-tumor (in vitro) | Zhou et al. (2021) |
| 31. | Phyllanthus niruri L. | Kidney failure and kidney stones | Leaf | Decoction | Oral | Anti-inflammatory (in vivo) | |
| 32. | Psidium guajava L. | Diarrhea and stomachache | Leaf | Decoction | Oral and inhalation | Hypertension (in vivo) | |
| 33. | Azadirachta indica A. Juss. | Paludism and typhoid fever | Leaf | Decoction | Oral, inhalation, rectal, and topical | Hypertension (in vitro) | |
| 34. | Persea americana Mill. | Hypertension, diarrhea, headache, and hernia | Leaf, fruit, and seed | Decoction | Oral, topical, and inhalation | Anti-tumor (in vitro) | |
| 35. | Hymenocardia acida Tul. | Diarrhea, hemorrhoids, and psychosis | Root | Decoction | Oral | Hypertension (in vivo) | |
| 36. | Costus spiralis (Jacq.) Roscoe | Urinary infection and sexual impotence | Stem | Decoction | Oral, vaginal, and topical (cataplasm) | Hypertension (in vivo) | |
| 37. | Carica papaya L. | Constipation, headache, and facilitates childbirth | Root, leaf, and fruit | Decoction | Oral and inhalation | Dengue fever (in vivo) | Subenthiran et al. (2013) |
| 38. | Entada abyssinica Steud. | Paludism, spinal pain, and sexual impotence | Leaf | Decoction | Oral | Not reported | |
| 39. | Elaeis guineensis Jacq. | Headache, burns, antidote, and prevents abortion | Fruit, flower, and stem | Maceration | Oral and inhalation | Healing activity (in vivo) | Rajoo et al. (2021) |
| 40. | Picralima nítida (Stapf) T. Durand & H. Durand | Inflammation and bone pain | Stem | Maceration | Oral and topical (bath) | Not reported | |
| 41. | Aloe ferox Mill. | Typhoid fever, stomachache, and alopecia | Leaf | Maceration | Oral and topical | Antidiabetic (in vitro) | Mhaladi et al. (2016) |
| 42. | Allium sativum L. | Inflammation, stomachache, and cough | Root | Maceration | Oral | Colon cancer (in vitro) | |
| 43. | Saccharum officinarum L. | Heart failure and anemia | Leaf | Decoction | Oral | Hypertension (in vitro) | |
| 44. | Spinacia oleracea L. | Anemia | Leaf | Decoction | Oral | Not reported | |
| 45. | Artemisia absinthium L. | Respiratory diseases | Leaf | Decoction | Oral and topical (bath) | Focal cerebral ischemia (in vitro) | |
| 46. | Manihot esculenta Crantz | Measles | Leaf | Maceration | Oral | Not reported | |
| 47. | Alchornea cordifolia (Schumach. & Thonn.) Müll.Arg | Fever | Root | Decoction | Topical, oral, and sublingual | Not reported | |
| 48. | Capsicum annuum L. | Epilepsy and labor pain | Root and leaf | Maceration | Oral | Anti-fungal (in vitro) | |
| 49. | Cymbopogon citratus (DC.) Stapf | Cough, bladder pain, kidney obstruction, stomachache, and prevents abortion | Leaf | Decoction | Oral | Gastroprotective activity (in vivo) | Manvitha and Bidya (2014) |
| 50. | Eugenia uniflora L. | Bloody diarrhea | Leaf | Decoction | Oral | Diuretic (in vitro) | |
| 51. | Abelmoschus esculentus (L.) Moench. | Glaucoma, conjunctivitis, and sexual impotence | Leaf and fruit | Infusion | Oral | Type 2 diabetes (in vitro) | |
| 52. | Garcinia mannii Oliv. | Paludism and colic | Seed | Decoction | Oral | Not reported | |
| 53. | Acanthospermum hispidum DC. | Vaginal bleeding, paludism, diabetes, hepatitis, and antidote | Leaf | Decoction | Oral and topical | Antiviral (in vitro) | |
| 54. | Mangifera indica L. | Abscess, hemorrhoids, and paludism | Leaf and Stem | Decoction | Oral and topical | Anti-inflammatory (in vivo) | Saviano et al. (2022) |
| 55. | Ficus thonningii Blume | Hypertension | Leaf | Maceration | Oral | Diarrhea (in vitro) | |
| 56. | Vernonia sp | Stomachache and hernia | Root | Decoction | Oral and inhalation | Diabetes (in vitro) | |
| 57. | Alpinia zerumbet (Pers.) B.L. Burtt & R.M.Sm. | Stomachache and bladder pain | Root | Infusion | Oral | Not reported | |
| 58. | Cola acuminata (P.Beauv.) Schott & Endl. | Nausea and vomiting | Fruit | Maceration | Oral | Alzheimer’s (in vivo) | |
| 59. | Coffea canephora Pierre ex A.Froehner | Diarrhea, wounds, and burns | Fruit | Infusion | Oral and topical | Not reported | |
| 60. | Zea mays L. | Abortion prevention | Stigmas | Decoction | Oral and topical | Not reported | |
| 61. | Boerhavia diffusa L. | Labor pain | Leaf | Maceration | Oral | Anti-inflammatory (in vitro) | Mathias et al. (2020) |
| 62. | Musa paradisiaca L. | Prevention of abortion, hemorrhoids, and stimulation of labor | Leaf | Maceration | Oral | Anti-tumor (in vivo) | |
| 63. | Cinnamomum verum J.Presl. | Stomachache and cough | Leaf | Decoction | Oral and topical | Anti-diabetic (in vivo) | |
| 64. | Ocimum gratissimum L. | Internal fever, hiccups, and cough | Leaf | Decoction | Oral, inhalation, topical, and sublingual | Anti-inflammatory (in vivo) | Shittu et al. (2016) |
| 65. | Mentha arvensis L. | Stomachache and epilepsy | Root and leaf | Decoction | Oral | Analgesic (in vivo) | |
| 66. | Cannabis sativa L. | Psychosis, asthma, cough, bronchitis, nausea, vomiting, measles, and tuberculosis | Leaf | Decoction | Oral, rectal, and sublingual | Anti-fungal (in vitro) | |
| 67. | Ageratum conyzoides L. | Infertility | Leaf | Maceration | Oral, inhalation, and topical | Sleeping sickness (in vitro) | Nour et al. (2010) |
| 68. | Foeniculum vulgare Mill. | Intestinal gas, flu, colic, kidney failure, and whooping cough | Root, stem, leaf, and flower | Decoction | Oral and topical | Gastroprotective (invitro) | |
| 69. | Spondias mombin L. | Stomachache and hypotension | Root and fruit | Maceration | Oral and topical | Anti-inflammatory | |
| 70. | Sambucus nigra L. | Measles and epilepsy | Leaf and flower | Decoction | Oral and topical | Anti-inflammatory (in vitro) | Skowrońska et al. (2022) |
| 71. | Pericopsis angolensis (Baker) Meeuwen | Thrombosis and bone fracture | Leaf and Root | Decoction | Oral | Not reported | |
| 72. | Cocos nucifera L. | Typhoid fever | Root | Decoction | Oral | Antifungal (in vitro) | |
| 73. | Fragaria sp. | Epilepsy | Root | Maceration | Oral and topical | Not reported | |
| 74. | Rosmarinus officinalis L. | Obesity | Leaf | Decoction | Oral, inhalation, and topical | Antifungal (in vitro) | |
| 75. | Arachis hypogaea L. | Headache | Seed | Cataplasm | Topical | Not reported | |
| 76. | Sterculia dawei Sprague | Kyphosis | Root | Maceration | Oral | Not reported | |
| 77. | Senna spectabilis (DC.) H.S. Irwin & Barneby | Diabetes, paludism, colic, diarrhea, and typhoid fever | Root and leaf | Decoction | Oral, inhalation, and topical | Trypanocidal activity (in vitro) | |
| 78. | Oldfieldia dactylophylla (Welw. ex Oliv.) J.Léonard | Typhoid fever and open cervix | Root, stem, and leaf | Decoction | Oral | Not 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 classes | Total | % | |||
|---|---|---|---|---|---|---|
| Nc | 0–24 | 25–49 | 50–100 | |||
| Infectious or parasitic diseases | 5 | 15 | 2 | 1 | 23 | 29.5 |
| Neoplasms | - | 1 | - | - | 1 | 1.3 |
| Diseases of the blood or blood-forming organs | - | 4 | - | - | 4 | 5.1 |
| Endocrine, nutritional, or metabolic diseases | 3 | 2 | - | - | 5 | 6.4 |
| Mental, behavioral, or neurodevelopmental disorders | 1 | 1 | - | - | 2 | 2.6 |
| Diseases of the nervous system | 4 | 7 | - | - | 11 | 14.1 |
| Diseases of the visual system | - | 1 | - | - | 1 | 1.3 |
| Diseases of the circulatory system | 2 | 6 | - | - | 8 | 10.3 |
| Diseases of the respiratory system | 4 | 5 | - | - | 9 | 11.5 |
| Diseases of the digestive system | 8 | 21 | 2 | 3 | 34 | 43.6 |
| Diseases of the skin | - | 1 | - | - | 1 | 1.3 |
| Diseases of the musculoskeletal system or connective tissue | 2 | 3 | 2 | - | 7 | 9.0 |
| Diseases of the genitourinary system | 3 | 8 | - | - | 11 | 14.1 |
| Conditions related to sexual health | - | 6 | - | 1 | 7 | 9.0 |
| Pregnancy, childbirth, or the puerperium | 4 | 4 | 2 | 1 | 11 | 14.1 |
| Injury, poisoning, or certain other consequences of external causes | - | 3 | 1 | - | 4 | 5.1 |
| Symptoms, signs, or clinical findings not elsewhere classified | 3 | 10 | 2 | 1 | 16 | 20.5 |
Distribution of the diseases addressed by the medicinal plants mentioned, categorized according to ROP classes.
Nc, ROP not calculated.
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.
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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
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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
© 2026 Barroso, Martins, Morais, Katenda, Jamba, Gonçalves, Sebastião, Chimbuco, Hernández, Mota, Ribalta, Gomes, Barreto and Ekundi-Valentim.
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*Correspondence: Eduardo Ekundi-Valentim, eduardoekundi@urnm.edu.ao
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