Heliyon 9 (2023) e22977 Available online 29 November 2023 2405-8440/© 2023 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). Medicinal plants used for management of diabetes and hypertension in Ghana Tonny Asafo-Agyei a, Yaw Appau a,*, Kofi Bobi Barimah a, Alex Asase b a Centre for Plant Medicine Research, Department of Plant Development, P. O. Box 73 Akuapem-Mampong, Ghana b University of Ghana, Department of Plant and Environmental Biology, P. O. Box LG 55, Legon, Ghana A R T I C L E I N F O Keywords: Diabetes Hypertension Ethnobotany Herbalist Ghana A B S T R A C T Diabetes and hypertension have been declared as a global health menace of the 21st Century. Thus, the search for potential therapeutic agents from medicinal plants for the management of diabetes and hypertension is important. This study was undertaken to investigate medicinal plants being used in the management of diabetes and hypertension by herbalists in Ghana. Data were obtained from 36 herbalists through questionnaire interviews and conversations. Botanical specimens were collected, processed and identified following standard ethnobotanical methods. Data were analyzed using Fidelity Level (FL) and Informant Consensus Factor (ICF). A total of 39 species of plants belonging to 31 families were reported being used for management of diabetes and hypertension. Eighteen of these plants are used for the treatment of hypertension, 12 species for diabetes, and 9 species for management of both diseases. Informant consensus factor was highest for plants used to treat both diseases (IFC = 0.82) followed by hypertension (ICF = 0.31) and then diabetes (IFC = 0.24). FL values were high for Carica papaya L. Moringa oleifera Lam. and Khaya senegalensis A. Juss. for the management of both diabetes and hypertension. Of the 14 species used for hypertension, Tetrapleura tetraptera (Schum. ex. Thonn.) recorded the highest FL value whiles Momordica charantia L. recorded the highest FL value for antidiabetic plants. Baphia nitida G. Lodd, Luffa aegyptiaca Mill. and Tapinanthus banguwensis (Engl. & k. Krause) Dancing are being mentioned for the first time in the management of hypertension. Herbal medicines for treatments of both diabetes and hypertension were usually prepared from multiple plant pre- scriptions by boiling the plant parts, and the decoctions drunk for treatments. The results show that there is substantial preclinical evidence to support the usefulness of some of these herbs as an important choice for patients with diabetes and hypertension. However, clinical studies are important to confirm the efficacy and safety of the herbal medicines prescribed by herbalists. 1. Introduction Since time immemorial medicinal plants have, and continue to play a key role in the healthcare delivery system in the world, particularly in developing countries. It is reported that about 80 % of the population in developing countries depend on traditional medicine, largely herbal medicine, for their primary health care and socio-economic needs [1,2]. In Africa, many areas lack hospitals and even where they are available, they are far from most of the populace. For instance, Torres-León et al. [3] reported that local * Corresponding author. E-mail address: yappau@cpmr.org.gh (Y. Appau). Contents lists available at ScienceDirect Heliyon journal homepage: www.cell.com/heliyon https://doi.org/10.1016/j.heliyon.2023.e22977 Received 28 February 2023; Received in revised form 26 July 2023; Accepted 23 November 2023 mailto:yappau@cpmr.org.gh www.sciencedirect.com/science/journal/24058440 https://www.cell.com/heliyon https://doi.org/10.1016/j.heliyon.2023.e22977 https://doi.org/10.1016/j.heliyon.2023.e22977 http://crossmark.crossref.org/dialog/?doi=10.1016/j.heliyon.2023.e22977&domain=pdf https://doi.org/10.1016/j.heliyon.2023.e22977 http://creativecommons.org/licenses/by-nc-nd/4.0/ Heliyon 9 (2023) e22977 2 people have to walk for at least 53 km to access the conventional healthcare system, and thus resorted to plant medicine for their healthcare needs. Medicinal plants have been reported as being used in the treatment and management of many diseases such as malaria [4,5], tuberculosis [6,7], hepatitis B [8] and typhoid fever [9] in both developing and developed countries of the world. As a result, the World Health Organization has recommended its adoption into the mainstream health system including some herbal products on the essential medicine list [10]. Efforts to improve and consolidate herbal medicine have been enormous with the availability of scientific evidence supporting the efficacy of herbal medicine [11–13]. Studies have explored the importance of medicinal plants in the management of diabetes [14], and hypertension [15] in other jurisdictions. However, in Ghana there is inadequate knowledge about medicinal plants being used by herbalists in different areas in the management of diabetes and hypertension declared as a global health menace of the 21st Century [16,17]. Diabetes mellitus is a chronic endocrine disorder that adversely alters the metabolism of carbohydrates, proteins, fat, electrolytes and water, predominantly due to a derangement in insulin production and/or action [18]. Diabetes is associated with long-term complications such as heart disease, stroke, kidney failure, blindness, nerve damage and neuropathy, atherosclerosis, chronic in- fections, immune deficiency and peripheral vascular disease that may lead to ulcers, gangrene and amputation [19,20]. Studies have reported on two main types of diabetes mellitus, namely, Type 1 and Type 2 [21,22]. Type 1 diabetes is mostly attributed to inadequate secretion of insulin resulting in chronic hyperglycemia [21]. Type 2 diabetes mellitus is reported to be more prevalent than all types of diabetes and affects about 90 % of the global population [23], which is caused by inefficient metabolic processes or organ damage or malfunction. Bahrami and Gerstein [24] noted that type 2 diabetes mellitus is a serious public health menace as 50 % of people living with it are undiagnosed. It has been estimated that about 7 % of the world’s population has diabetes [25,26], and 80 % of such cases are reported in developing countries. The eighth edition of the International Diabetes Federation (IDF) Atlas report noted that Sub-Saharan Africa accounts for 77 % of all diabetes-related deaths in people under 60 years worldwide. Likewise, IDF projected prevalence rate of diabetes in Africa is 156 % by the year 2045 [27]. According to [28] the incidence rate of diabetes in Ghana is 4.1 % and it is expected to rise to 5.0 % by 2030. Similarly, available statistics indicate that of all disease conditions reported in the various hospital across Ghana, diabetes-related complications accounts for about 6 % between 2002 and 2017 [29]. Hypertension is the most common risk factor for acute myocardial infarction, stroke, and peripheral vascular disease, and is the major known factor for cardiovascular disease and its mortality [30,31]. The major causes of hypertension include excessive alcohol intake, obesity, stress, too much salt intake, oral contraceptive drugs, renal failure, tobacco use, lack of exercise and hereditary-related [32,33]. It is reported that about 40 % of the world’s adult population (25 years and above) have been identified with hypertension, out of this; Africa leads with 46 % [21,34]. Hypertension has been classified broadly into two main types; primary and secondary hypertension. Primary hypertension results in high Blood Pressure for which no medical reason has been confirmed and constitutes about 90–95 % of all reported cases [35]. While, secondary hypertension is induced by conditions that affect the heart, kidney, arteries Fig. 1. A map of Ghana showing location regions of respondents. T. Asafo-Agyei et al. Heliyon 9 (2023) e22977 3 or the endocrine system [36]. Diabetes and hypertension are pathophysiologically related diseases. Epidemiological studies have indicated the co-existence of diabetes and hypertension in some patients, and both diseases share common risk factors [37]. There are several commercial drugs available for the treatment or management of diabetes and hypertension. These drugs include Glibenclamide and metformin for the management of diabetes and Amlodipine and Lisinopril for the management of hypertension. However, the intensive and vigorous management regimes associated with the use of orthodox medicine for the management of both diabetes and hypertension coupled with drug resistance, related side effects, and high treatment cost has necessitated a paradigm shift towards plant medicine regime [38, 39]. Studies have shown that medicinal plants due to their active ingredients, medicinal and antioxidant compounds have beneficial effects on human health and have a therapeutic effect on various organs of the body and various diseases [4,40,41]. Therefore, it is imperative to explore potential therapeutic agents with minimal side effects from medicinal plants, which may be useful in the management of diseases. As yet, there is a scarcity of studies on medicinal plants being used by herbalists in the management of diabetes and hypertension in Ghana. Thus, this present study aimed to investigate the pharmacotherapeutic potential of medicinal plants that are being used by herbalists in the management of diabetes and hypertension in Ghana. Specifically, the study addresses the following questions: (1) What species of medicinal plants are used in the management of diabetes and hypertension in Ghana? (2) How are the medicinal plants being prepared and used in the management of the diseases; (3) What are the common symptoms for the diagnosis of diabetes and hypertension by herbalists? 2. Materials and methods 2.1. Study area The present study was conducted at the Centre for Plant Medicine Research (CPMR) in Ghana. The Centre for Plant Medicine Research (CPMR) is one of the leading research institutions in Ghana. It was established by the Government of Ghana in 1975 as an Agency of the Ministry of Health mandated to undertake research into plant medicine. This makes the Centre a unique research institution in Sub-Saharan Africa and beyond. The CPMR is located on Latitude 5◦55′04.7″N and Longitude 0◦08′ 03.2″ W in the peri- urban town of Akuapem-Mampong in the Eastern Region of Ghana. Ghana is situated in West Africa bounded by Burkina Faso on the north, Togo on the eastern border, Côte d’ivoire on the west, and the Gulf of Guinea on the south (Fig. 1). The country has a total surface area of 238,540 km2. Total annual rainfall ranges from 780 mm in the dry eastern coastal belt to 2200 mm in the wet southwest corner of the country. Traditional medicine is a major component of the health care delivery system in the country [42]. Thus traditional healers in Ghana such as herbal practitioners, fetish priests, divine healers, psychic practitioners and traditional medicine practitioners are well-organized under an umbrella organization Ghana Federation of Traditional Medicine Healers Association (GHAFTRAM). 2.2. Selection of herbalists and ethnobotanical interviews A total of 36 registered herbalists belonging to GHAFTRAM were involved in this study. The 36 herbalists represented 64 % of the 56 herbalists that participated in a training workshop organized by CPMR in September 2022. Herbalists who participated in this study were located in the Western (44 %), Greater Accra (22 %), Eastern (19 %) and Ashanti (14 %) regions of Ghana. Ethnobotanical data were acquired from the herbalists through conversation and interviews using a semi-structured questionnaire with predetermined open-ended and direct questions. Pretesting of the questionnaire was undertaken with 20 randomly selected herbalists within the study area and improvements were made to the questionnaire before its use. The questionnaire was designed to capture data on the demographic background of herbalists, vernacular names of the plants, plant parts used, mode of preparation and administration. Face-to-face interviews with herbalists involved an interpreter, a recorder and a botanist. We also followed the face-to- face interviews with telephone conversations with the herbalists to validate information that they have previously provided. Data collection took place between September 2022–January 2023. Voucher specimens of the species of plants reported being used were collected with the herbalists from the field. The plant specimens collected were pressed and processed following standard ethnobotanical practices [43], and voucher specimens have been deposited at the Centre for Plant Medicine Research herbarium (CPMR). Plant identification was achieved via comparison of the voucher specimens collected with already identified specimens at the CPMR herbarium. Nomenclature and classification of the species of plants follow Plants of the World Online (POWO) and The Plant List databases (http://www.theplantlist.org; and https://powo. science.kew.org/accessed respectively on December 18, 2022 and July 10, 2023). Ethical statement The selection of the herbalists and the conduct of interviews were guided by the principles of the Code of Ethics of the International Society of Ethnobiology [43,44]. In this regard, the purpose of the study including methods of data collection and intention to publish data as well as an assurance of the confidentiality of the information to be provided was thoroughly explained to herbalists to enable them to make prior-informed decisions about their participation, as involvement in this study was voluntary. Only herbalists that consented to the objectives of the study were enrolled and consequently interviewed. T. Asafo-Agyei et al. http://www.theplantlist.org/ https://powo.science.kew.org/ https://powo.science.kew.org/ Heliyon 9 (2023) e22977 4 2.3. Data analysis Data were analyzed using two ethnobotanical indices, namely, Fidelity Level (FL) and Informant Consensus Factor (ICF). The Fidelity Level is a way of calculating the percentage of informants who use a particular plant for the same purpose compared to all uses of all plants, and was computed using the formula [45]: FLS = Ns/URs; where Ns is the number of informants that use a particular plant for a specific purpose, and URs is the total number of use reports for the species. Informant Consensus Factor (ICF) was employed to deduce the homogeneity of the information about plant use to treat a particular category of disease (i.e., diabetes and hypertension). The ICF was calculated using the formula [46]: ICF = (Nur − Nt)/(Nur − 1) where “Nur” refers to the total number of use reports for each disease category and “Nt” refers to the total number of species used for that category. 3. Results and discussion 3.1. Background of herbalists Information about demographic background of the 36 herbalists interviewed is summarized in Table 1. More than half (64 %) of the herbalists interviewed were males, and the majority (47 %) of the herbalists were within the age group of 41–50 years. The herbalists interviewed had attained different levels of education ranging from primary school to university level. The herbalists interviewed included Christians (92 %), traditionalists (5 %), and Muslims (3 %). About 53 % of the herbalists had practice for more than 40 years. The extensive experience (>40 years) of most of the herbalists (53 %) could indicate that the herbalists have adequate knowledge in the management of diseases [47]. The herbalists diagnosed diabetes mellitus based on symptoms such as unexplained weight loss (36 %), frequent urination (28 %), increased thirst (25 %) and extreme hunger (11 %). These symptoms are among those commonly used by traditional healers in the diagnosis of diabetes mellitus for their treatments [48,49] and used in clinical diagnosis of the disease. In Kenya, some herbalists in addition to the previously mentioned parameters relied on headache, sweating and fever in diagnosing diabetes [50]. Note that in Traditional Chinese medicine patients with chronic diseases such as diabetes are also examined using physical examination, pulse and breath odour, in addition to relying on the history of the patients [51]. Regarding the diagnosis of hypertension, herbalists mentioned irregular heartbeats (35 %), difficulty in breathing (22 %), vision problems (16 %), chest pains (14 %), fatigue (5 %), and blood in the urine (8 %). In the Maritime Region of Togo, traditional healers used a combination of symptoms including nose bleeding, headache, swarming, loss of consciousness, and shortness of breath for diagnosis of hypertension [15]. In addition, the herbalists also relied on an orthodox diagnosis of patients with diabetes and hyper- tension for their treatments. This is usually the practice if herbalists have the training and the equipment to subject patients to the clinical examination of diabetes and hypertension [50]. About 44 % of the herbalists reported that 10 patients on average per week visited their clinics for treatment of both diseases, and that they received positive feedback from the patients. This suggests that herbalists play a major role in the management of both diabetes and hypertension in Ghana, which also means that the effects of their medicines on patients must be properly investigated. 3.2. Medicinal plants A total of 39 species of plants belonging to 31 families were reported by the herbalists as being used in the management of hy- pertension and diabetes (Table 2). Most of the species of plants belong to the Apocynaceae (14 %), Fabaceae (14 %), and the others; Table 1 Background on herbalists (n = 36) interviewed. Categories Variables Number of herbalists % of herbalists Gender Male Female 23 13 64 36 Age-groups 18–30 2 6 31–40 5 14 41–50 17 47 51–60 12 33 Religion Christian 33 92 Muslim 1 3 Traditional 2 5 Educational level No formal education 2 6 Basic education 9 25 Senior High School 16 44 Tertiary 9 25 Years of practice 10–20 8 22 21–30 2 6 31–40 7 19 >41 19 53 T. Asafo-Agyei et al. Heliyon 9 (2023) e22977 5 Table 2 Medicinal plants reported used for management of diabetes and hypertension by herbalists in Ghana with information on their vernacular names, conservation status, habits, diseases treated, and how they are being used. Species (Voucher #)/Conservation Status Family (habit) Local name Disease type* Plant parts Modes of preparation Modes of administration Aframomum melegueta K. Schum. (CPMR 4945) Zingiberaceae (herb) Fam wisa (Twi) H Seeds Decoction: boil with stem bark of Khaya senegalensis and Zingiber officinale Oral: drink decoction Alchornea cordifolia (Schumach. & Thonn.) Müll.Arg (CPMR 4920) Euphorbiaceae (shrub) Ogyama (Twi) D Leaves Decoction: Boil with leaves of Psidium guajava and Citrus aurantifolia leaves Oral: drink decoction Alstonia boonei De Wild. (CPMR 4911) Apocynaceae (Tree) Nyamedua (Twi) H Stem & leaves Decoction: Boil leaves and stem together and add Zingiber officinale Oral: drink decoction Alternanthera pungens Kunth (CPMR 4906) Amaranthaceae (herb) Nkasienkasie (Asante) D Stem bark Boil with leaves of Taraxacum officinale and moringa oleifera Oral: drink decoction Anthocleista nobilis G. Don (CPMR 4930) Loganiaceae (tree) Awudifo kete (Twi) D Stem bark Boil with whole plant of Paullina pinnata, Carica papaya leaves and add lemon juice Oral: drink decoction Azadirachta indica A. Juss. (CPMR 4933) Meliaceae (tree) Nim (Fante) D Root bark Boil with leaves of Carica papaya, Gossypium arboreum leaves and seeds Xylopia aethiopica Oral: drink decoction Baphia nitida G. Lodd. (CPMR 4921) Fabaceae (tree) Odwene (Twi) H Leaves Boil leaves with Xylopia aethiopica fruits Oral: drink decoction Bryophyllum pinnatum (Lam.) Oken (CPMR 4925) Crassulaceae (herb) Egoro (Twi) H Leaves Boil with fruit Tetrapleura tetraptera Oral: drink decoction Carica papaya L. (CPMR 4917) Caricaceae (tree) Brofre (Twi) DH Leaves Boil with Khaya senegalensis stem bark, whole plant of Paullinia pinnata and Psidium guajava leaves Oral: drink decoction Cinnamomum zeylanicum Blume. (CPMR 4928) Lauraceae (tree) Anoatre dua (Twi) H Stem bark Boil with fruit Monodora myristica and dried Zingiber officinale Oral: drink decoction Cymbopogon citratus (DC.) Stapf. (CPMR 4924) Poaceae (grass) Ti-ahaban (Fante) H Whole plant Boil whole plant Oral: drink decoction Fleurya ovalifolia (Schumach. & Thonn.) Dandy (CPMR 4943) Moraceae (tree) Nsasono (Twi) DH Leaves Grind dried into granules with Carica papaya and Momordica charantia leaves Oral: drink decoction Gomphrena celosioides Mart. (CPMR 4907) Amaranthaceae (herb) Water globe (English) H Whole plant Boil whole plant Oral: drink decoction Gossypium arboreum L. (CPMR 4932) NT Malvaceae (tree) Asaawa (Twi) D Leaves Boil with root of Carica papaya, Morinda lucida and leaves of Ocimum gratissimum Oral: drink decoction Dianthera secunda (Lamb.) Griseb. (CPMR 4905) Acanthaceae (shrub) Jehovah witness tree (English) D Leaves Boil leaves with krokrodoso leaves Oral: drink decoction Khaya senegalensis (Desr.) A. Juss. (CPMR 4934) VU Meliaceae (tree) Kuntunkuri (Twi) DH Stem bark Boil with dried leaves of Carica papaya, Oral: drink decoction Kigelia africana (Lam.) Benth. (CPMR 4916) Bignoniaceae (tree) Nufuten (Asante) H Leaves, Stem bark Boil stem bark and leaves together Oral: drink decoction Lantana camara L. (CPMR 4944) Verbenaceae (shrub) Anansedokono (Akan) H Whole plant Boil with Tapinanthus banguwensis, Citrus aurantifolia leaves and Zingiber officinale Oral: drink decoction Luffa cylindrica M. Roem. (CPMR 4918) Cucurbitaceae (shrub) Sapo (Twi) H Leaves Infusion: soak fresh leaves in water. Oral: drink infusion Mangifera indica L. (CPMR 4908) Anacardiaceae (tree) Amango (Asante) DH Leaves Boil leaves and bark together with Psidium guajava leaves Oral: drink decoction Momordica charantia L.CPMR 4919 Cucurbitaceae (tree) Nyinya (Twi) D Fruit Mill fruits Oral: drink decoction Morinda citrofolia L. (CPMR 4940) Rubiaceae (tree) Noni (Hawalli) DH Fruit, Leaves Boil dried leaves and ferment the fruits. Oral: drink decoction Morinda lucida Benth. (CPMR 4939) Rubiaceae (tree) Konkroma (Asante) DH Leaves, Stem bark Mill fresh leaves and stem bark and add lemon juice Oral: drink decoction Moringa oliefera Lam. (CPMR 4935) Moringaceae (tree) Moringa (English) DH Leaves Boil freshly together with Launaea taraxacifolia or Mill dried leaves with Launaea taraxacifolia Oral: drink decoction Musa paradisiaca L. (CPMR 4936) Musaceae (tree) Brodea (Twi) H Leaves, Stem Boil with dried leaves of Mangifera indica and maize husks Oral: drink decoction Musa sapientum f. pruinosa King. (CPMR 4937) Musaceae (tree) Kwadu (Twi) D Leaves Boil together with dried leaves of carica papaya and Zingiber officinale Oral: drink decoction (continued on next page) T. Asafo-Agyei et al. Heliyon 9 (2023) e22977 6 Amaranthaceae, Cucurbitaceae, Lamiaceae, Lauraceae, Meliaceae, Musaceae, Rubiaceae and Zingiberaceae have Ten percent respectively. Trees formed the majority (55 %) of the plants being used while shrubs and herbs formed 24 % and 21 %, respectively. Of the 39 species of plants, 18 were being used for the management of only hypertension and 12 species for only diabetes. Nine species of plants, namely, Carica papaya L. Fleurya ovalifolia Schum. & Thonn., Khaya senegalensis A. Juss., Mangifera indica L., Morinda citrifolia L., Morinda lucida A. Gray., Moringa oleifera Lam., Ocimum gratissimum A Forsk. and Gymnanthemum amygdalinum (Delile) Sch.Bip was reported being used in the management of both diabetes and hypertension. The use of the same species of plants in the management of both diabetes and hypertension has been reported [52]. However, the species reported in this case is different from what has been reported elsewhere [52]. The results of literature search showed that all the species of plants reported for the management of diabetes by herbalists have been previously documented for this use [53–62]. However, major differences exist in the way the plants are being used in different areas of Ghana and elsewhere for the management of diabetes. In a recent review of the use of plants in traditional management of diabetes in Nigeria [56], only 21 of the 115 species of plants identified were reported in the present study. Moreover, plants such as Aframomum melegueta K. Schum, Cympopogon citratus (DC.) Stapf and Tapinanthus banguwensis (Engls. and K. Krause) Danscing were reported being used by the herbalists in this study but not in the management of diabetes. In a study of medicinal plants used in the management of diabetes in the Dangme West district of southern Ghana [46], only seven of the species identified were reported used in this study. Only 16 of the 76 plants reported used in the management of diabetes by [54] were reported in this study. Sometimes the plant parts used also differed in different areas. For example, the decoction of whole plant of Momordica charantia L. is used in the Dangme West district while it is the fruits that are used in the management of diabetes in this study. Understanding the use of species in different areas can assist in selecting those plants that justify further studies. Sixteen of the species of plants have been previously documented in the management of hypertension. These species were Afra- momum melegueta K. Schum. [63], Alstonia boonei De Wild [54], Kalanchoe pinnata (Lam.) Pers. [64], Cinnamomum verum J. Presl [65], Cymbopogon citiratus (DC.) Stapf. [55], Gomphrena celesioides Mart. [66], Kigelia africana (Lam.) Benth. [60], Lantana camara f. albiflora Table 2 (continued ) Species (Voucher #)/Conservation Status Family (habit) Local name Disease type* Plant parts Modes of preparation Modes of administration Ocimum gratissimum Forssk. (CPMR 4926) Lamiaceae (herb) Nunum (Twi) DH Leaves Boil dried leaves with Morinda lucida leaves Oral: drink decoction Paullinia pinnata L. (CPMR 4941) Sapindaceae (shrub) Toatin (Asante) D Whole plant Boil with Psidium guajava leaves, Carica papaya leaves Oral: drink decoction Persea americana Mill. (CPMR 4929) Lauraceae (tree) Paya (Akan) H Seed Grind dried seeds into powder. Oral: drink decoction Psidium guajava L. (CPMR 4938) Myrtaceae (tree) Oguawa (Twi) D Leaves Boil with Carica papaya and Persea americana leaves Oral: drink decoction Rauvolfia vomitoria Wennberg (CPMR 4912) Apocynaceae (tree) Kakapenpen (Twi) D Root bark Boil with Paullinia pinnata whole plant Oral: drink decoction Rosmarinus officinalis L. (CPMR 4927) Lamiaceae (herb) Rosemary (English) H Leaves Boil with leaves of Alstonia boonei, Zingiber officinale roots and stem bark of Khaya senegalensis Oral: drink decoction Senna alata (L.) Roxb. (CPMR 4922) Fabaceae(tree) Osempe (Twi) D Leaves Boil with Alchornea cordifolia leaves and whole plant of Paullinia pinnata Oral: drink decoction Strophanthus hispidus DC. (CPMR 4913) Apocynaceae (shrub) Omaatwa (Twi) H Root bark Boil roots Oral: drink decoction Tapinanthus banguwensis (Engl. & k. Krause) Danser (CPMR 4931) Loranthaceae (Climber) Nkrapan (Twi) H Whole plant Boil with Launaea taraxacifolia leaves and add Xylopia aethiopica Fruits Oral: drink decoction Launaea taraxacifolia (Willd.) Amin ex C. Jeffrey (CPMR 4915) Compositae (herb) Dandelion (English) H Leaves Boil with Moringa oleifera leaves Oral: drink decoction Tetrapleura tetraptera (Schumach. &Thonn.) Thaub. (CPMR 4923) Fabaceae (tree) Prekese (Twi) H Fruits Boil the dried fruit with leaves of Ocimum gratissimum Oral: drink decoction Trema orientalis (L.) Blume (CPMR 4942). Cannabaceae (tree) Sesea (Asante) D Leaves Decoction: boil together with roots of Morinda lucida Oral: drink decoction Gymnanthemum amygdalinum (Delile.) Sch. Bip. (CPMR 4914) Asteraceae (shrub) Anwonwene (Akan) DH Leaves Decoction: boil with leaves of Persea americana Oral: drink decoction Xylopia aethiopica (Dunal.) A. Rich (CPMR 4909) Annonaceae (tree) Hwentia (Twi) H Seed Decoction: boil with Leaves of Gossypium arboreum, roots of Morinda lucida and Carica papaya Oral: drink decoction Zanthoxylum zanthoxyloides (Lam.) Zepern.& Timler (CPMR 4910) Rutaceae (shrub) Okantor (Twi) D Stem bark Decoction: boil together with Alchornea cordifolia leaves, stem bark of Khaya senegalensis Oral: drink decoction Zingiber officinale Roscoe (CPMR 4946) Zingiberaceae (shrub) Kakaduro (Twi) H Root bark Decoction: boil with Tetrapleura tetraptera Oral: drink decoction NT= Near threatened; VU=Vulnerable; *D = Diabetes; H = hypertension. T. Asafo-Agyei et al. Heliyon 9 (2023) e22977 7 Moldenke [67] and Musa paradisiaca L. [68], Persea americana Mill. [69], Rosmarinus officinalis L. [70], Strophanthus hispidus DC. [71], Taraxacum erythrospermum Andrz. ex-Besser [72], Tetrapleura tetraptera (Schumach. & Thonn.) Taub. [73], Xylopia aethiopica (Dunal) A. Rich [74] and Zingiber officinale Roscoe [75]. However, to the best of our knowledge four species; Baphia nitida G. Lodd, Luffa aegyptiaca Mill. and Tapinanthus banguwensis (Engl. & K. Krause) Dancing are being documented for the first time in the management of hypertension (see Table 2). 3.3. Informant consensus and fidelity level A quantitative analysis of herbalist’s agreements about the use of medicinal plants for management of the diseases is presented in Table 3. The highest ICF value (0.82) was recorded for both hypertension and diabetes, followed by 0.31 for only hypertension, and 0.24 for only diabetes mellitus. These results mean that the healers agreed more on the use of plants for the management of hyper- tension compared to diabetes. A similar study by [76] reported high ICF values for hypertension (ICF = 0.90) and diabetes (0.81) among healers. ICF value may vary due to the abundance, diversity and availability of medicinal plants and their associated knowledge in a particular locality [76]. Also, constraints in the transfer of ethnobotanical knowledge from one generation or locality to another may affect ICF values [76]. Fidelity level (FL) values for the 39 medicinal plants regarding the management of the diseases are presented in Tables 4–6. The species of plants with high FL values for diabetes were Momordica charantia L. (FL = 17.3), and Psidium guajava L. (FL = 13). For hypertension, the highest FL of 15 was recorded for Tetrapleura tetraptera (Schum. ex. Thonn.) Thaub. followed by Persea americana Mill. (12.5) and Launea taraxifolia (Willd.) Amin ex C. Jeffrey (12.5). For both hypertension and diabetes, the highest FL of 23.3 % was recorded for Carica papaya L. (Table 4). These results suggest that herbalists have their preferences regarding the choice of medicinal plants for the management of diseases. It is, however, unclear what informed their choices in the selection of plants for treatments. 3.4. Formulation and application of medicinal plants The herbal medicines for the treatments of both diabetes and hypertension were commonly prepared from multiple plant pre- scriptions. The multi-component nature of herbal medicines for the treatment of hypertension is known and it is believed to improve efficacy through synergism [77]. Unlike the situation in the Endo state of Nigeria, non-plant materials like snail, potash, earthworm and native chalk were not reported added to the recipes for the management of hypertension [77] in this study. Generally, multiple plant prescriptions are very complex in terms of standardization, identification of bioactive agents, and monitoring of the uses of plants [78]. There were, however, a few instances of single plant prescriptions such as the use of Cympopogon citratus (DC.) Stapf., Gomphrena celosoides Mart., Persea americana Mill., and Strophanthus hispidus DC., for hypertension, Momordica charantia L. for diabetes, and Morinda citrofolia L. and Morinda lucida A. Gray for both diabetes and hypertension. The availability of particular plant species and knowledge of traditional healers are factors that could determine whether species of plants are used singly or in combinations [78]. Although the plant’ parts used for the management of the diseases differed, the most common parts used were leaves and stem bark (Fig. 2). Similar to the results of this study, stem bark was the most commonly used plant part in the management of diabetes in Guinea [79], and leaves formed the most frequently used plant part in the management of hypertension in nearby Togo [15] and Nigeria [77]. The plant parts used in traditional medicine could depend on the availability of the plants as well as the knowledge of local people. Scientifically, bioactive agents in plants could be related to the plant parts as secondary metabolites differ in concentration in the different plant parts. Except for the leaves of Luffa cylindrica M. Roem that were prepared in the form of an infusion for the management of hypertension, the herbal medicines were prepared by boiling the plant parts and the decoctions drunk. This observation was not surprising because most traditional medicines are prepared as decoctions for oral administration [80,81]. However, other modes of preparation and administration of herbal medicines for the management of both diabetes and hypertension have been reported elsewhere. For example, in the Dangme West District of Ghana, pulverized plant materials were added to food and eaten for the management of diabetes [48]. Also, concoctions, powders, and essence as modes of preparation of herbal medicines for hypertension have been reported [15]. 4. Review of anti-diabetic and anti-hypertensive studies on medicinal plants The results of the literature review on the bioactivity, phytochemical constituents and clinical studies about the medicinal plants identified are presented in Table 7. Out of the 39 plants reviewed, 38 have been investigated for their biological activities (14 anti- diabetic, 16 anti-hypertensive and 8 for both properties). In the last few decades, the discovery and development of phytochemi- cals intended for anti-diabetic and anti-hypertensive effects have gained some attention. Anti-diabetic and anti-hypertensive effects of medicinal plants are attributed to the group of phytochemicals or single chemical constituents of plant extracts, which work by various Table 3 Informant Consensus Factor (IFC) about medicinal plants used by herbalists in Ghana for the management of diabetes and hypertension. Disease category Number of use-reports Number of species ICF Diabetes mellitus 18 14 0.24 Hypertension 27 19 0.31 Diabetes mellitus and hypertension 45 9 0.82 T. Asafo-Agyei et al. Heliyon 9 (2023) e22977 8 mechanisms. Some phytochemicals with anti-diabetes properties for instance, work through the regulation of glucose and lipid metabolism, stimulation and regeneration of β-cells, insulin secretion, regulation of the NF-ĸB signalling pathway, inhibition of gluconeogenic enzymes and oxidative stress. Also, pharmacological effects such as regulation of potassium and calcium ion channels, adenylate cyclase, nitric oxide (NO) and adrenergic system (α and β receptors), inhibition of angiotensin-converting enzymes (ACE), serotonin (5HT), norepinephrine (NE), prostaglandins (PGs)- pathways, phosphodiesterase (PDE) and sodium ion absorption may Table 4 Fidelity level for medicinal plants reported by herbalists in Ghana as used in the management of hypertension. S/N Species Hypertension Fidelity level Urs Ns FL 1. Aframomum melegueta 40 1 2.5 2. Alstonia boonei 40 1 2.5 3. Baphia nitida 40 1 2.5 4. Bryophyllum pinnatum 40 2 5 5. Cinnamomum zeylanicum 40 1 2.5 6. Cymbopogon citiratus 40 1 2.2 7. Gomphrena celesioides 40 1 2.5 8. Kigelia africana 40 2 5 9. Lantana camara 40 1 2.5 10. Launnea officinale 40 5 12.5 11. Luffa aegyptiaca 40 1 2.5 12. Musa paradisiaca 40 2 5 13. Persea americana 40 5 12.5 14. Strophanthus hispidus 40 2 5 15. Tapinanthus banguwensis 40 2 5 16. Tetrapleura tetraptera 40 6 15 17. Xylopia aethiopica 40 3 7.5 18. Zingiber officinale 40 2 5 Table 5 Fidelity level for medicinal plants reported by herbalists in Ghana as used in the management of diabetes. S/N Species Diabetes Fidelity level Urs Ns FL 1. Alchornea cordifolia 23 1 4.3 2. Alternanthera pungens 23 1 4.3 3. Anthocleista nobilis 23 1 4.3 4. Gossypium americana 23 1 4.3 5. Momordica charantia 23 4 17.3 6. Musa sapientum 23 2 8.6 7. Paullinia pinnata 23 1 4.3 8. Psidium guajava 23 3 13 9. Rauvolfia vomitoria 23 1 4.3 10. Senna alata 23 1 4.3 11. Trema orientale 23 1 2 12. Zanthoxylum zanthoxyloides 23 1 2 Table 6 Fidelity level for medicinal plants reported by herbalists in Ghana as used in the management of hypertension. S/N Species Diabetes and Hypertension Fidelity level Urs Ns FL 1. Carica papaya 30 7 23.3 2. Fleurya ovalifolium 30 2 6.6 3. Khaya senegalensis 30 4 13.3 4. Mangifera indica 30 2 6.6 5. Morinda citrofolia 30 2 6.6 6. Morinda lucida 30 3 10 7. Moringa oliefera 30 4 13.3 8. Ocimum gratissimum 30 3 10 9. Vernonia amygdalina 30 3 10 T. Asafo-Agyei et al. Heliyon 9 (2023) e22977 9 underscore the mechanisms used by phytochemicals with anti-hypertensive properties. The groups of phytochemicals mostly investigated and reported for these activities include saponins, polyphenols, flavonoids, alkaloids, tannins, glycosides polysaccharides and stilbenes. For this review, the phytochemicals will be classified based on their comparable chemical features, without necessarily considering their common biosynthetic pathways. The classification is as follows; nitrogen-containing compounds (alkaloids), terpenes and terpenoids, polyphenolic compounds, and hydroxyl-containing compounds. 4.1. Alkaloids Alkaloids are a large family of nitrogen-containing phytochemicals with a lot of medicinal value. The antidiabetic and antihy- pertensive properties of plants such as Alstonia boonei De Wild., Alternanthera pungens Kunth, Carica papaya L., Gossypium arboreum L., Dianthera secunda (Lam.) Griseb., Kigelia africana (Lam.) Benth., Paullinia pinnata L., Strophanthus hispidus DC. and Launaea taraxacifolia (Willd.) Amin ex C. Jeffrey has been attributed to the presence of phytochemicals including, alkaloids. Some studies have related certain alkaloids with their specific molecular targets in defining their possible mode of action. In the case of antidiabetics, a special reference is made to the insulin-signaling pathway, where there is scientific data to support the activities of compounds like Nα- formylechitamidine, berberine, trigonelline, piperine, oxymatrine, vindoneline, evodiame and neferine in the regulation of insulin- signaling and other related cascades associated with β-cells, adipose tissues, myocytes and the hepatic cells [11]. Akuammicine, purified from the chloroform extract of Picralima nitida (Stapf) T. Durand & T. Durand (seeds), is known to stimulate the uptake of glucose in 3T3-L1 adipose cells [132]. This alkaloid is also detected in plants belonging to the genus Alstonia. This may partly explain why species such as Alstonia boonei De Wild. and Alstonia congensis Engl. have hypoglycemic activity. There are also reports on alkaloids which exhibit anti-hypertensive properties [54]. reported on echitamine, an alkaloid isolated from Alstonia boonei De Wild. Echitamine lowered arterial blood, relaxed the smooth muscles of the heart and induced negative chronotropic and inotropic responses [87]. Reserpine, another alkaloid isolated from Rauvolfia vomitoria Wennberg is also reported to have antihypertensive activity [88]. Reserpine decreased blood pressure by depletion of catecholamines from the peripheral sym- pathetic nerve endings thereby regulating heart rate, cardiac contractions and peripheral resistance [133]. 4.2. Terpenes and terpenoids Terpenes are a class of compounds made up of one or more isoprene units. Compounds with an exact sequence of isoprene units are strictly referred to as terpenes while those modified sequences that look like terpenes (with isoprene skeletal pattern and other functional groups) are termed terpenoids. Isoprene or isoprenoid is the simplest unit of terpenes and terpenoids and consists of 5 carbons, connected with some alkene bonds. Isoprene unit. Many terpenes and terpenoids isolated from plants have been reported to have anti-diabetic and anti-hypertensive activities. Nimbidin, lupeol, oleanolic acid, β-amyrin, glutinol, ursolic acid are a few known examples. Oleanolic acid is a pentacyclic triterpene present in the fruits, vegetables and herbs of some plants. It has been isolated from ethyl acetate fraction of Aframomum melegueta K. Schum. fruit [63], chloroform fraction of Morinda lucida Benth. ethanolic leaf extract [134] and methanolic extract of Mormodica charantia L. (gourd). The anti-diabetic activity of oleanolic acid, isolated from the fractions of various plants, has been reported [135]. Oleanolic acid, such as thymol and carvacrol extracted from Gymnanthemum amygdalinum (Delile) Sch.Bip. has been reported to show anti-diabetic activities [136,137]. Fig. 2. Plant parts used in the management of diabetes and hypertension by herbalists in Ghana. T. Asafo-Agyei et al. Heliyon9(2023)e22977 10 Table 7 Biological activity, bioactivity constituents, and clinical studies on medicinal plants reported used by herbalists in Ghana for management of diabetics and hypertension. Species Biological activity Phytochemical constituents Clinical studies Aframomum melegueta A. melegueta ethyl acetate fraction (AMEF) treatment at 300 mg/kg showed potent anti-diabetic effect in a T2D model of rats [82]. Gingeredione, oleanolic acid [63]. Lowering of cardiovascular indices such as systolic blood pressure (SBP), diastolic blood pressure (DBP). The degree of reduction was found to be within safety limits, indicating its potential usefulness in managing hypertension in young and elderly hypertensive patients [47]. Alchornea cordifolia Administration of Alchornea cordifolia leaf extract to diabetic animals significantly (p < 0.05) decreased the blood glucose level in the group treated with 200 mg/kg b w and decreased by a higher margin (p < 0.01) in animals treated with 400 and 800 mg/kg b w [83]. Anthranilic acid, protocatechuic acid, ellagic acid [84]. No previous report Alstonia boonei Aqueous extract of the stem bark caused about 44 % and 40 % reduction in the activities of hepatic glu-6-phosphatase and fru-1, 6- phosphatase, respectively. This was accompanied by about 30.5 % increase in glu-6-phosphate dehydrogenase [85]. Akuammicine, echitamidine, Nα- formylechitamidine, boonein, loganin, lupeol, ursolic acid, and β-amyrin [54]. No previous report Alternanthera pungens Treatment with 50, 200 and 300 mg kg–1 of A. pungens extract improved and restored rat serum HDL level [57]. Glycosides, alkaloids, terpenoids, flavonoids carotenoids [57]. No previous report Anthocleista nobilis The stem and root bark extracts significantly (p < 0.5) reduced fasting blood glucose concentration of diabetic animals [53]. Sweroside, secoiridoid, scopoletin [53] No previous report Azadirachta indica Aqueous extracts of neem plant showed antihyperglycemic activity in streptozotocin-induced rats and this effect was due to an increase in glucose uptake and glycogen deposition in isolated rat hemidiaphragm [86]. Nimbidin, β-sitosterol [11] No previous report Baphia nitida No previous report No previous report No previous report Bryophyllum pinnatum Both the aqueous and methanolic leaf extracts of B. pinnatum (BP, 50–800 mg/kg iv. or i.p.) produced dose related, significant (P < 0.05 - 0.001) decrease in arterial blood pressure and heart rates of anaesthetized normotensive and hypertensive rats [87]. Oleic acid, alpha-D-Glucopyranoside [64]. Using measured hypercapnic-hypoxic breathing training rehabilitation protocol in patients with mild essential hypertension leads to reduction of high blood pressure indexes [88]. Carica papaya The methanolic extract of C. papaya elicited angiotensin converting enzyme inhibitory activity. The antihypertensive effects elicited by the methanolic extract of C. papaya were similar to those of enalapril, and the baroreflex sensitivity was normalized in treated spontaneously hypertensive rats [89]. flavonoids quercetin, rutin, nicotiflorin, clitorin, and manghaslin [89]. No previous report Cinnamomum zeylanicum Acute intravenous administration of C. zeylanicum extract (5, 10 and 20 mg/kg) to L-NAME-induced hypertensive rats provoked a long- lasting decrease in blood pressure. Mean arterial blood pressure decreased by 12.5 %, 26.6 % and 30.6 % at the doses of 5, 10 and 20 mg/kg, respectively. In chronic administration, MECZ and captopril significantly prevented the increase in blood pressure and organs’ weights, as well as tissue histological damages and were able to reverse the depletion in NO tissue’s concentration [90]. Cinnamaldehyde, eugenol [65] Improves insulin potentiating activity [91]. Cymbopogon citratus A fresh leaf aqueous extract of Cymbopogon citratus administered in normal rats lowered the fasting plasma glucose and total cholesterol, triglycerides, low-density lipoproteins and very low-density lipoprotein dose dependently while raising the plasma high-density lipoprotein level in the same dose-related fashion, but with no effect on the plasma triglyceride levels [92]. Esters, aldehyde and fatty acids [55,106] No previous report Fleurya ovalifolia No previous report No previous report No previous report Gomphrena celosioides Ethanolic extract of G. celosioides (EEGC) acutely reduced Mean arterial pressure the dose of 100 mg/kg. In the 4-week assay, EEGC acted as diuretic after acute administration after 1, 2, 3 and 4 weeks of Aurantiamide, aurantiamide acetate [66] No previous report (continued on next page) T. A safo-A gyei et al. Heliyon9(2023)e22977 11 Table 7 (continued ) Species Biological activity Phytochemical constituents Clinical studies treatment. EEGC also acted as an antihypertensive and it showed significant difference already after 1 week (and after 3 and 4 weeks) compared to control, with its MAP close to pre-surgery values at the end of the experiment [93]. Gossypium arboreum Orally administered diethyl ether and ethanolic extracts of Gossypium arboreum significantly decreased blood glucose level [108. Flavonoids, phenolic compounds, tannins and alkaloids [94]. No previous report Justicia secunda Aqueous extract of J. secunda (AEJs) showed a dose dependent glucose reduction of glucose-induced hyperglycemia where a dose of 3 g/kg BW was substantially identical (P > 0.05) to that of glibenclamide at 10-2 g/kg BW. Examination of the liver-released glucose level of control normoglycemic rats and normoglycemic rats treated with AEJs and glibenclamide showed that aqueous extract of Justicia secunda and glibenclamide decreased the glucose released by the liver [58]. polyphenols, alkaloids, saponosides and sterols and polyterpenes [58]. No previous report Khaya senegalensis Treatment of diabetic groups withv organic fractions of K. senegalensis and and metformin in wistar albino rats showed significant decrease in fasting blood glucose (FBS), ameliorated hepatic and renal damages by decreasing the level of AST, ALT, ALP, Urea and creatinine compared to untreated diabetic rats and stimulated insulin secretion by β cells [95]. methyl 6-ethyl-7-hydroxy-7,8-dihydrophenan- threne-2-carboxylate [95]. No previous report Kigelia africana Significant lowering of the blood glucose levels was also expressed in mice following the administration of 50, 100, 200, and 300 mg/kg body weight of K africana [60]. phenols, flavonoids, alkaloids, tannins, terpenoids, saponins [60]. No previous report Lantana camara Ethanolic extract of Lantana camara leaves reduced workload of heart, maintained isotonic levels by negative chronotropic effect, relaxed the smooth muscles in chick and salt hypertensive rats against renal and vascular injuries [96]. Glycosides, Saponins, Tannins, Flavonoids, Terpenoids and Steroids [96]. No previous report Luffa cylindrica No previous report No previous report No previous report Mangifera indica M. indica leaf extract significantly inhibited alpha-amylase activity in a dose-dependent manner. The inhibitory effect was observed up to (51.4 ± 2.7 %) at a concentration of 200 μg/mL [97]. Mangiferin [98] No previous report Momordica charantia M. charantia improved glucose tolerance and suppressed postprandial hyperglycemia in rats [12]. Charantin, momordicin, oleanolic acid, vicine [13]. Hypoglycemic effect in only diabetic patients [99,100] Morinda citrifolia Aqueous extract of M. citrifolia significantly inhibited rat lens aldose reductase (RLAR) activities and improved free radical scavenging activities in vitro as compared to ethanolic and chloroform extracts thereby indicating a potential to inhibit cataract formation and prevent diabetic complications [101]. Lucidin, morindone [102]. No previous report Morinda lucida Administration of aqueous and methanolic extract of M. lucida significantly (p < 0.05) reduced fasting blood glucose of diabetic animals by 73.5 and 39.0 % of their initial values, respectively [103]. Steroids, anthraquinone Oleanic acid [104]. No previous report Moringa oleifera Ethanolic extract of M. oleifera leaves showed a blood pressure lowering effect in rats, mediated possibly through a calcium antagonist effect [105]. M. oleifera extract showed significant decrease in malonaldehyde and improvements in the inflammatory cytokines (TNF-α and IL-6) compared to control animals in STZ-induced diabetic rats fed with equivalent of 250 mg/kg of MO for 6 weeks [106]. Nitrile, mustard oil glycosides, thiocarbamate glycosides [105]; quercetin [107], chlorogenic Acid [108], and isothiocyanates [109]. No previous report Musa paradisiaca M. paradisiaca extracts inhibited angiotensin-I converting enzyme (ACE) activity in a dose-dependent manner (0–25 μg/ml). Unripe plantain peel (UPP) extract showed had a stronger inhibition (IC50 = 14.93 μg/ml) of ACE activity than over ripe plantain peel (OPP) and cardiac glycosides, terpenes, deoxy sugar [67]. No previous report (continued on next page) T. A safo-A gyei et al. Heliyon9(2023)e22977 12 Table 7 (continued ) Species Biological activity Phytochemical constituents Clinical studies ripe plantain peel (RPP) extracts (IC50s of 21.80 μg/ml and 21.32 μg/ ml, respectively [110]. Musa sapientum Forty-five-day treatment with M. sapientum L extract significantly reduced the fasting blood glucose and the concentration of HbA1c in diabetic rats [111]. Gallocatechin [112] No previous report Ocimum gratissimum O. gratissimum leaf extract at a dose of 200 mg/kg bw decreased the blood glucose of diabetic rats by 20.9 %, at 4 h whereas 250 mg/kg bw was able to decrease the blood glucose of diabetic rats by 29.3 % at 4 h [113]. Steroids, terpenoids, flavonoids and cardiac glycosides [114]. No previous report Paullinia pinnata P. pinnata extract (50 mg/kg) and glibenclamide (2 mg/kg) produced a significant (p < 0.05) oral glucose tolerance effect in both normoglycemic and diabetic rats. The extract produced concentration- dependent increase in antioxidant activity and had its optimum effect at 400 μ μg/mL concentration [59]. Alkaloids, flavonoids, glycosides, tannins, saponins and terpenes/sterols [59]. No previous report Persea americana The hydroalcoholic extract of the leaves of Persea americana reduced blood glucose levels and improved the metabolic state of treated animals. Additionally, PKB activation was observed in the liver and skeletal muscle of treated rats when compared with untreated rats [69]. p-coumaric acid, quercetin and epicatechin [115]. No previous report Psidium guajava Significant blood glucose lowering effects of P. guajava extract were observed after intraperitoneal injection of the extract at a dose of 10 mg/kg in both 1- and 3-month-old Lepr (db)/Lepr(db) mice [116]. Strictinin, isostrictinin, pedunculagin [117]. No previous report Rauvolfia vomitoria At 500, 700 and 1000 mg/kg ethyl acetate of R. vomitoria caused a reduction of blood glucose level of treated normoglycemic rats similar to glibenclamide at 10 mg/kg [61]. Alkaloids (eg. reserpine), flavonoids, and anthrones, anthraquinones, catechin tannins, saponins and monoterpenoids [61]. No previous report Rosmarinus officinalis Rosmarinus officinalis extract on blood glucose and serum insulin levels was studied in alloxan-induced diabetic rabbits. Of the three doses of extract, the highest dose (200 mg/kg) significantly lowered blood glucose level and increased serum insulin concentration in alloxan- diabetic rabbits [70]. Ursolic acid [118]. Both blood pressure variables of SBP and DBP reflect the clinically significant anti hypotensive effect of Rosemary essential oil that was maintained throughout the treatment period. After validation of the use of the questionnaire (Cronbach’s alpha coefficient 40.82), statistically significant differences have been found between pretreatment and post-treatment values of PSC and MSC, which indicate an improvement in these parameters that is directly related to the variation in blood pressure values [119]. Senna alata The α-glucosidase inhibitory effect of the crude extract of S. alata was far better than the standard clinically used drug, acarbose (IC (50), 107.31 ± 12.31 μg/ml) [120]. Kaempferol, kaempferol 3-O-gentiobioside [121]. No previous report Strophanthus hispidus There was a protective effect in the case of mean arterial blood pressure where, the 500 mg/Kg and 1000 mg/Kg of the plant extract did reduce the hypertension, 60.0 ± 4.80 and 50.50 ± 6.80, respectively [71]. Alkaloids, flavonoids, saponins, and cardiac and cyanogenic glycosides [122]. No previous report Tapinanthus banguwensis It is the first time it being mention for the treatment of hypertension No previous report Launaea taraxacifolia Results showed that one-off oral administration of L. taraxifolia leaf and L. taraxifolia root significantly (p < 0.05) reduced systolic, diastolic and mean arterial blood pressure. In a sub-chronic study L. taraxifolia leaves extract significantly (p < 0.05) prevented an increase in blood pressure throughout the period of treatment [72]. Saponins, flavonoids, alkaloids, phenols, triterpenoid [123] No previous report Tetrapleura tetraptera Polyphenol-rich hydroethanolic extract of Tetrapleura tetraptera (HET) reduced weight gain, fasting blood glucose and plasma insulin levels as well as homeostasis model assessment of insulin resistance (HOMA-IR) and alleviated obesity and T2DM associated oxidative stress and hypertension in rats [73]. Hytate, triterpenoid, coumarinic (scopoletin), triterpene glycoside [124]. No previous report (continued on next page) T. A safo-A gyei et al. Heliyon9(2023)e22977 13 Table 7 (continued ) Species Biological activity Phytochemical constituents Clinical studies Trema orientale Aqueous stem bark extract of T. orientalis was reported to have hypoglycemic effects in induced diabetic rats by mechanism different from that of sulfonylurea agents [125]. Flavonoids, phenolic acids [126]. No previous report Vernonia amygdalina The aqueous extract of the leaves of V. amygdalina caused a significant reduction in blood glucose levels of extract only, and allocan plus extract treated animals [127]. Flavonoids, tannins, saponins, and triterpenoids [128]. No previous report Xylopia aethiopica The anti-diabetic effect of Xylopia aethiopica has also been studied. A chloroformic extract of the dried fruits of Xylopia aethiopica administered orally at a dose of 250 mg/kg showed an 82 % reduction in the blood glucose concentration of alloxan monohydrate induced diabetic Wistar albino rats while diabetic non-treated rats and glibenclamide treated rats showed a 6.9 % and 74 % reduction respectively [74]. Methyl ester, 12-octadecanoic acid, hexadecanoic acid [129]. No previous report Zanthoxylum zanthoxyloides Z. zanthoxyloides significantly (p < 0.05) lowered blood glucose in treated animals compared to non-treated groups. Total cholesterol and LDL were significantly lower in Z. zanthoxyloides treated groups, with lowest values found in groups treated with higher concentration. It was also observed that LDH, ALP and ALT showed highest activities at 15 % of Z. zanthoxyloide feed with AST activity lowest at the highest concentration of the feed [122]. No previous report No previous report Zingiber officinale 50 mg/kg/day p.o administration of the petroleum ether and 10 mg/ kg/day p.o of toluene fraction reduced the blood pressure in unilateral nephrectomized DOCA salt and fructose-induced hypertensive rats [130]. Gingerol [131] Increase insulin receptors and enhanceβ-cell function to decrease insulin resistance of diabetic patients [75]. T. A safo-A gyei et al. Heliyon 9 (2023) e22977 14 4.3. Phenolic compounds These are secondary metabolites found in plants and consist of an aromatic ring with one or more hydroxyl groups [138]. Phenolic compounds are mostly bioactive constituents and are grouped as simple phenols, flavonoids, lignins, lignans, tannins, xanthones and coumarin [139]. Scientific evidence shows that some phenolic compounds isolated from medicinal plants such as Carica papaya L., Cinnamomum zeylanicum Blume, Gossypium arboreum, Moringa oleifera, Persea americana and Mangifera indica have cardiovascular protection making them possible anti-hypertensive agents. Phenolic compounds could also be anti-diabetic agents due to their ability to regulate glucose uptake and as well restrict the formation of islet amyloid polypeptide, amylin aggregates (IAPP) [138]. Examples of these phenolic compounds include chlorogenic acid, caffeic acid, coumaric acid, gallic acid, quercetin, isorhamnetin, kaempferol, hesperetin, naringenin, phloretin, enterolactone and enterodio [140]. Quercetin, kaempferol and their glycosides have been detected and isolated from the leaf extracts of Moringa oleifera [141]. Rutin and quercetin have been isolated from the ethanolic leaf extract of Persea americana [142]. Studies by [143] revealed some methoxy phenyl derivatives, isolated from Zingiber officinale, inhibited the enzyme aldose reductase both in vitro and in vivo, by preventing the accumulation of sorbitol and galactitol in human erythrocytes and the lenses of rats, respectively; underscoring the anti-diabetes properties of phenolic compounds. The aromatic hydroxyl group in the benzo-γ-pyran of most flavonoids has been linked to their antioxidant activity, most especially their ability to scavenge free radicals. This helps to protect against oxidative stress and enable the regeneration of vital cells. For instance, epicatechin and quercetin, two key flavonoids in green tea, protect the islet cells of the pancreas from oxidative stress and also helps regenerate β-cell [56]. Similarly [144], noted that flavonoids can promote the differentiation and mineralization of oste- oblasts at a high glucose level. 4.4. Hydroxyl containing compounds These are non-phenolic but hydroxylated compounds. A number of them have been isolated and purified from medicinal plants, and are shown to be bioactive compounds. The anti-diabetes and anti-hypertension properties of these compounds have been reported. Gingerols, isolated from Zingiber officinale, promote glucose uptake by increased expression of GLUT4 receptor [56]. Also, 6-gingerol was reported to reduce blood pressure by normalizing the expressions of hypertensive biomarkers through peroxisome proliferator-activated receptor delta (PPARδ) [145]. 5. Conclusion Ghana is bestowed with an abundance of plant biodiversity; several are used in managing diabetes and hypertension in Traditional Medicine Practice. This study has documented the current state of indigenous knowledge and medicinal plants used by herbalists for the treatment and management of diabetes and hypertension in Ghana. The results show that there is substantial preclinical evidence to support the usefulness of some of these plants as an important choice for patients with diabetes and hypertension. The reported use of medicinal plants identified in this study confirmed with previous studies could be an indication that the plants might be potent in the treatment of the diseases. Indeed, many of the plants have biological activities, and their bioactive compounds have been identified. However, clinical studies are few, and thus important that the efficacy and safety of the herbal medicines prescribed by herbalists be investigated to validate their medicinal usefulness in people with diabetes and hypertension. Similarly, Baphia nitida G. Lodd, Luffa aegyptiaca Mill. and Tapinanthus banguwensis (Engl. & k. Krause) Dancing being mentioned for the first time in the management of hypertension by the herbalists need to be investigated for their medicinal properties. By doing so, the pharmacotherapeutic potential of these plants could be harnessed towards a possible incorporation into the healthcare system. Funding statement This research did not receive any specific grant from funding agency in the public, commercial, or non-profit sectors. Data availability statement Data/supplementary material is included and referenced in the article as tables. Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. Acknowledgements The authors are grateful to members of the Ghana Federation of Traditional Medicine Practitioners who participated in this study. We are also grateful to Mrs. Susana Oteng-Mintah, Mrs. Mary-Ann Archer and Peter Atta Adjei Junior for their immense contribution to the data collection. T. Asafo-Agyei et al. Heliyon 9 (2023) e22977 15 Appendix A. Supplementary data Supplementary data to this article can be found online at https://doi.org/10.1016/j.heliyon.2023.e22977. References [1] M. Ekor, The growing use of herbal medicines: Issues relating to adverse reactions and challenges in monitoring safety, Front. Neurol. 4 (177) (2014). [2] M.A. Valdez-Solana, V.Y. Mejıa-Garcıa, A.T. Ellez-Valencia, et al., Nutritional content and elemental and phytochemical analyses of Moringa oleifera grown in Mexico, J. Chem. 2015 (2015) p9. [3] Cristian Torres-León, Ramírez Fernanda Rebolledo, A. Jorge, Aguirre-Joya, Agustina Ramírez-Moreno, L. Mónica, Chávez-González, David R. Aguillón- Gutierrez, Luis Camacho-Guerra, Nathiely Ramírez-Guzmán, Vélez Salvador Hernández, Cristóbal N. Aguilar, Saudi Pharmaceut. J. 31 (1) (2023) 21–28, https://doi.org/10.1016/j.jsps.2022.11.003. [4] A. Asase, T. Asafo-Agyei, Plants used for treatment of malaria in communities around the bobiri forest reserve in Ghana, J. Herbs, Spices, Med. Plants 17 (2) (2011) 85–106. [5] T. Asafo-Agyei, H.R. Blagogee, S.O. Mintah, M.A. Archer, F. Ayertey, A.C. Sapaty, A.A. Appiah, Ethnobotanical studies of medicinal plants used in traditional treatment of malaria by some herbalists in Ghana, J. Med. Plants Res. 13 (16) (2019) 370–383. [6] S.S. Semenya, A. Maroyi, Medicinal plants used for the treatment of tuberculosis by Bapedi traditional healers in three districts of the Limpopo Province, South Africa, Afr. J. Tradit., Complementary Altern. Med.: AJTCAM 10 (2) (2012) 316–323, https://doi.org/10.4314/ajtcam.v10i2.17.7. [7] J.M. Nguta, R. Appiah-Opong, A.K. Nyarko, D. Yeboah-Manu, P.G.A. Addo, Medicinal plants used to treat TB in Ghana, International Journal of Mycobacteriology 4 (2) (2015) 116–123, https://doi.org/10.1016/j.ijmyco.2015.02.003. [8] C.A. Philips, P. Augustine, G. Padsalgi, Herbal medicines and reactivation of chronic hepatitis B virus infection, Hepat. Mon. 18 (9) (2018), 81000, https://doi. org/10.5812/hepatmon.81000. [9] E. Bekoe, C. Agyare, J. Sarkodie, D. Dadebo, Herbal medicines used in the treatment of typhoid in the Ga east municipality of Ghana, International Journal of Tropical Disease & Health 23 (4) (2017) 1–13, https://doi.org/10.9734/IJTDH/2017/31448. [10] World Health Organization, WHO Traditional Medicine Strategy: 2014-2023, World Health Organization, 2013. https://apps.who.int/iris/handle/10665/ 92455. [11] M. Christodoulou, J. Tchoumtchoua, A. Skaltsounis, A. Scorilas, M. Halabalaki, Natural alkaloids intervening the insulin pathway: new hopes for anti-diabetic agents? Curr. Med. Chem. 26 (32) (2019) 5982–6015. [12] B. Dineshkumar, A. Mitra, M. Manjunatha, A comparative study of alpha amylase inhibitory activities of common anti-diabetic plants at Kharagpur 1 block, Int. J. Green Pharm. 4 (2) (2010), https://doi.org/10.22377/ijgp.v4i2.131. [13] M. Abdollahi, A.B.Z. Zuki, Y.M. Goh, A. Rezaeizadeh, M.M. Noordin, The effects of Momordica charantia on the liver in streptozotocin-induced diabetes in neonatal rats, Afr. J. Biotechnol. 9 (31) (2010) 5004–5012. [14] Cristian Torres-León, Ramírez Fernanda Rebolledo, A. Jorge, Aguirre-Joya, Agustina Ramírez-Moreno, L. Mónica, Chávez-González, David R. Aguillón- Gutierrez, Luis Camacho-Guerra, Nathiely Ramírez-Guzmán, Vélez Salvador Hernández, Cristóbal N. Aguilar, Saudi Pharmaceut. J. 31 (1) (2023) 21–28, https://doi.org/10.1016/j.jsps.2022.11.003. [15] H.E. Gbekley, G. Katawa, S.D. Karou, S. Anani, T. Tchadjobo, Y. Ameyapoh, K. Batawila, J. Simpore, Ethnobotanical study of plants used to treat asthma in the Maritime Region in T, Afr. J. Tradit., Complementary Altern. Med.: AJTCAM 14 (1) (2016) 196–212, https://doi.org/10.21010/ajtcam.v14i1.22. [16] World Health Organization, A global brief on hypertension; silent killer, a global public health crisis (2013) 8–34 (Accessed 3 October 2022). [17] B. Delfan, K. Saki, M. Bahmani, N. Rangsaz, M. Delfan, N. Mohseni, Z. Babaeian, A study on anti-diabetic and anti-hypertension herbs used in Lorestan province, Iran, Journal of Herb Med Pharmacology 3 (2) (2014) 71–76. [18] F. Farzaei, M.R. Morovati, F. Farjadmand, M.H. Farzaei, A mechanistic review on medicinal plants used for diabetes mellitus in traditional Persian medicine, Journal of evidence-based complementary & alternative medicine 22 (4) (2017) 944–955. [19] J.W.J. Beulens, F. Rutters, L. Rydén, et al., Risk and management of pre-diabetes, European Journal of Preventive Cardiology 26 (2_Supplement) (2019) 47–54. [20] A.J. Boulton, L. Vileikyte, l.G. Ragnarson-Tennval, J. Apelqvist, The global burden of diabetic foot disease, Lancet 366 (9498) (2005) 1719–1724. [21] C.I. Chukwuma, R. Mopuri, S. Nagiah, A.A. Chuturgoon, M.S. Islam, Erythritol reduces small intestinal glucose absorption, increases muscle glucose uptake, improves glucose metabolic enzymes activities and increases expression of Glut-4 and IRS-1 in type 2 diabetic rats, Eur. J. Nutr. (2017), https://doi.org/ 10.1007/s00394-017-1516-x. [22] Z. Hu, F. Gao, L. Qin, Y. Yang, H. Xu, A case-control study on risk factors and their Interactions with prediabetes among the elderly in rural communities of yiyang city, hunan province, 2019, J. Diabetes Res. (2019) 1–8, https://doi.org/10.1155/2019/1386048. [23] R.E. Pratley, The early treatment of type 2 diabetes, Am. J. Med. 126 (2013) S2–S9. [24] J. Bahrami, H. Gerstein, The prevalence of undiagnosed type 2 diabetes on the general medicine ward, Can. J. Diabetes 40 (5) (2016) S49–S50, https://doi. org/10.1016/j.jcjd.2016.08.139. [25] H. Jangid, S. Chaturvedi, M. Khinchi, An Overview on Diabetes Mellitus, Asian Journal of Pharmaceutical Research and Development, 2017, p. 11. [26] World Health Organisation, Obesity and Overweight, 2015. https://www.who.int/mediacentre/factsheets/fs311/en/. (Accessed 5 December 2022). [27] International Diabetes Federation Diabetes Atlas, eighth ed., 2017. Available from: https://www.idf.org/e-library/epidemiology-research/diabetes-atlas/134- idf-diabetes-atlas-8th-edition.html. (Accessed 20 July 2023). [28] D.R. Whiting, L. Guariguata, C. Weil, J. Shaw, IDF diabetes atlas: global estimates of the prevalence of diabetes for 2011 and 2030, Diabetes Res. Clin. Pract. 94 (3) (2011) 311–321, https://doi.org/10.1016/j.diabres.2011.10.029. [29] Ghana Health Service (Policy Planning Monitoring and Evaluation Division), The Health sector in Ghana facts and figures 2018, 2018. Available at: https:// ghanahealthservice.org〉Facts+Figures_2018. (Accessed 12 May 2022). [30] R.S. Vasan, A. Beiser, S. Seshadri, M.G. Larson, W.B. Kannel, The residual lifetime risk for developing hypertension in middle-aged women and men: the Framingham Heart Study, JAMA 287 (2002) 1003–1010. [31] J. Stamler, R. Stamler, J.D. Neaton, Blood pressure, systolic and diastolic, and cardiovascular risks: US population data, Arch. Intern. Med. 153 (1993) 598–615. [32] S. Douma, K. Petidis, M. Doumas, P. Papaefthimiou, A. Triantafyllou, N. Kartali, et al., Prevalence of primary hyperaldosteronism in resistant hypertension: a retrospective observational study, Lancet 371 (9628) (2008) 1921–1926. [33] B. Edvardsson, S. Persson, Reversible cerebral vasoconstriction syndrome associated with autonomic dysreflexia, J. Headache Pain 11 (3) (2010) 277–280, https://doi.org/10.1007/s10194-010-0196-1. [34] World Health Organization, Global Status Report on Non-communicable Diseases, 2011, World Health Organization, Geneva, 2010. Available at: https://apps. who.int/iris/handle/10665/44579. (Accessed 16 October 2022). [35] O.A. Carretero, S. Oparil, Essential hypertension. Part I: definition and etiology, Circulation 101 (3) (2000) 329–335, https://doi.org/10.1161/01. cir.101.3.329. [36] G. Beevers, G.Y. Lip, E. O’Brien, ABC of hypertension: the pathophysiology of hypertension, BMJ (Clinical research ed.) 322 (7291) (2001) 912–916, https:// doi.org/10.1136/bmj.322.7291.912. T. Asafo-Agyei et al. https://doi.org/10.1016/j.heliyon.2023.e22977 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref1 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref2 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref2 https://doi.org/10.1016/j.jsps.2022.11.003 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref4 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref4 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref5 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref5 https://doi.org/10.4314/ajtcam.v10i2.17.7 https://doi.org/10.1016/j.ijmyco.2015.02.003 https://doi.org/10.5812/hepatmon.81000 https://doi.org/10.5812/hepatmon.81000 https://doi.org/10.9734/IJTDH/2017/31448 https://apps.who.int/iris/handle/10665/92455 https://apps.who.int/iris/handle/10665/92455 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref11 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref11 https://doi.org/10.22377/ijgp.v4i2.131 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref13 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref13 https://doi.org/10.1016/j.jsps.2022.11.003 https://doi.org/10.21010/ajtcam.v14i1.22 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref16 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref17 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref17 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref18 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref18 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref19 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref20 https://doi.org/10.1007/s00394-017-1516-x https://doi.org/10.1007/s00394-017-1516-x https://doi.org/10.1155/2019/1386048 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref28 https://doi.org/10.1016/j.jcjd.2016.08.139 https://doi.org/10.1016/j.jcjd.2016.08.139 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref21 https://www.who.int/mediacentre/factsheets/fs311/en/ https://www.idf.org/e-library/epidemiology-research/diabetes-atlas/134-idf-diabetes-atlas-8th-edition.html https://www.idf.org/e-library/epidemiology-research/diabetes-atlas/134-idf-diabetes-atlas-8th-edition.html https://doi.org/10.1016/j.diabres.2011.10.029 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref25 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref25 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref30 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref30 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref31 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref31 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref32 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref32 https://doi.org/10.1007/s10194-010-0196-1 https://apps.who.int/iris/handle/10665/44579 https://apps.who.int/iris/handle/10665/44579 https://doi.org/10.1161/01.cir.101.3.329 https://doi.org/10.1161/01.cir.101.3.329 https://doi.org/10.1136/bmj.322.7291.912 https://doi.org/10.1136/bmj.322.7291.912 Heliyon 9 (2023) e22977 16 [37] M.J. Kim, N.K. Lim, S.J. Choi, H.Y. Park, Hypertension is an independent risk factor for type 2 diabetes: the Korean genome and epidemiology study, Hypertens. Res.: official journal of the Japanese Society of Hypertension 38 (11) (2015) 783–789, https://doi.org/10.1038/hr.2015.72. [38] W. Kooti, M. Farokhipour, Z. Asadzadeh, D. Ashtary-Larky, M. Asadi-Samani, The role of medicinal plants in the treatment of diabetes: a systematic review, Electron. Physician 8 (1) (2016) 1832–1842, https://doi.org/10.19082/1832. [39] B. Baharvand-Ahmadi, M. Asadi-Samani, A mini-review on the most important effective medicinal plants to treat hypertension in ethnobotanical evidence of Iran, Journal of nephropharmacology 6 (1) (2016) 3–8. [40] M. Karimian, Natural remedies for vascular disease, Plant Biotechnol Persa 1 (1) (2019) 1–3, https://doi.org/10.29252/pbp.1.1.1. [41] E. Karimi, S. Abbasi, N. Abbasi, Thymol polymeric nanoparticle synthesis and its effects on the toxicity of high glucose on OEC cells: involvement of growth factors and integrin-linked kinase, Drug Des. Dev. Ther. 13 (2019) 2513–2532, https://doi.org/10.2147/DDDT.S214454. [42] K.B. Barimah, O. Bonna, Traditional Medicine of Ghana, OKAD Publishing, Chalotte NC 28271, USA, 2018. [43] Recommended standards for conducting and reporting ethnopharmacological field studies, J. Ethnopharmacol., Volume 210. Pages 125-132. https://doi.org/ 10.1016/j.jep.2017.08.018. [44] The International Society of Ethnobiology (ISE), An alliance of biocultural diversity; code of ethics, Available at: https://www.ethnobiology.net/, 2016. (Accessed 16 December 2022). [45] J. Friedman, Z. Yaniv, A. Dafni, D. Palewitch, A preliminary classification of the healing potential of medicinal plants, based on a rational analysis of an ethnopharmacological field survey among Bedouins in the Negev desert, Israel, J. Ethnopharmacol. 16 (2–3) (1986) 275–287, https://doi.org/10.1016/0378- 8741(86)90094-2. [46] M. Heinrich, S. Edwards, D.E. Moerman, M. Leonti, Ethnopharmacological field studies: a critical assessment of their conceptual basis and methods, J. Ethnopharmacol. 124 (1) (2009) 1–17, https://doi.org/10.1016/j.jep.2009.03.043. [47] B. Lawal, A. Aderibigbe, G. Essiet, A. Essien, Hypotensive and antihypertensive effects of Aframomum melegueta seeds in humans, Int. J. Pharmacol. 3 (2007) 311–318, https://doi.org/10.3923/ijp.2007.311.318. [48] A. Asase, D.T. Yohonu, Ethnobotanical study of herbal medicines for management of diabetes mellitus in Dangme West District of southern Ghana, J. Herb. Med. 6 (2016) 204–209, https://doi.org/10.1016/J.HERMED.2016.07.002. [49] L.K. Keter, P.C. Mutiso, Ethnobotanical studies of medicinal plants used by traditional health practitioners in the management of diabetes in lower eastern province, Kenya, J. Ethnopharmacol. 139 (1) (2012) 74–80, https://doi.org/10.1016/j.jep.2011.10.014. [50] I.N. Chege, F.A. Okalebo, A.N. Guantai, S. Karanja, S. Derese, 2015.Management of type 2 diabetes mellitus by traditional medicine practitioners in Kenya–Key informant interviews, Pan Afr Med J 22 (2015 Oct 1) 90, https://doi.org/10.11604/pamj.2015.22.90.6485. [51] M.B. Covington, Traditional Chinese medicine in the treatment of diabetes, Diabetes Spectr. 14 (3) (2001) 154–159. [52] C.M. Arosemena, A.J. Sánchez, M.D. Tettamanti, C.D. Vasquez, A. Chang, et al., Prevalence and risk factors of poorly controlled diabetes mellitus in a clinical setting in guayaquil, Ecuador: a cross-sectional study, Int J Diabetes Clin Res 2 (2015) 34. [53] I.I. Madubunyi, K.P. Adam, H. Becker, Anthocleistol, a new secoiridoid from Anthocleista nobilis, Z. Naturforsch. C 49 (1994) 271–272. [54] J.K.P. Adotey, G.E. Adukpo, Y.O. Boahen, F.A. Armah, A review of the ethnobotany and pharmacological importance of Alstonia boonei De Wild (Apocynaceae), Pharmacol (2012), https://doi.org/10.5402/2012/587160. [55] A. Asif, E. Khodadadi, Medicinal uses and chemistry of flavonoid contents of some common edible tropical plants, JPS Summer 4 (3) (2013) 119–138, 2013. [56] U.F. Ezuruike, J.M. Prieto, The use of plants in the traditional management of diabetes in Nigeria: pharmacological and toxicological considerations, J. Ethnopharmacol. 155 (2) (2014) 857–924, https://doi.org/10.1016/j.jep.2014.05.05. [57] S.O. Owa, D.G. Oyewale, A.A. Taiwo, T.I. Edewor-Ikupoyi, J.A. Okosun, et al., Antidiabetic and antidyslipidemic effect of ethanolic extract of Alternanathera pungens on alloxan-induced diabetic rats, Asian J. Biochem. 11 (2016) 82–89, https://doi.org/10.3923/ajb.2016.82.89. [58] A. Mea, Y.H.R. Ekissi, K.J.C. Abo, G.P. Kahou Bi, Hypoglycaemiant and anti-hyperglycaemiant effect of Juscticia secunda m. vahl (acanthaceae) on glycaemia in the wistar rat, International Journal of Development Research 7 (6) (2017) 13178–13184. [59] O.S. Okwudili, N.G. Chimaobi, E.M. Ikechukwu, O.Y. Ndukaku, Antidiabetic and in vitro antioxidant effects of hydromethanol extract of Paullinia pinnata root bark in alloxan-induced diabetic rat, J. Compl. Integr. Med. 15 (2) (2017), https://doi.org/10.1515/jcim-2015-0017. [60] S.M. Njogu, W.M. Arika, A.K. Machocho, J.J.N. Ngeranwa, E.N.M. Njagi, In vivo hypoglycemic effect of Kigelia africana (Lam): studies with alloxan-induced diabetic mice, Journal of Evidence-Based Integrative Medicine 23 (2018), https://doi.org/10.1177/2515690x18768727, 2515690X1876872. [61] L.A. N’doua, K.J. Abo, S. Aoussi, L.K. Kouakou, E.E. Ehilé, Aqueous extract of rauwolfia vomitoria afzel (Apocynaceae) roots effect on blood glucose level of normoglycemic and hyperglycemic rats, American Scientific Research Journal for Engineering, Technology, and Sciences 20 (2016) 66–77. [62] M.B. Adinortey, Biochemico-physiological mechanisms underlying signs and symptoms associated with diabetes mellitus, Adv. Biol. Res. 11 (6) (2019) 382–390. [63] A. Mohammed, V.A. Gbonjubola, N.A. Koorbanally, M.S. Islam, Inhibition of key enzymes linked to type 2 diabetes by compounds isolated from Aframomum melegueta fruit, Pharmaceut. Biol. 55 (1) (2017) 1010–1016, https://doi.org/10.1080/13880209.2017.1286358. [64] R.I. Uchegbu, A.A. Ahuchaogu, O.K. Amanze, O.C. Ibe, Chemical constituents analysis of the leaves of Bryophyllum pinnatum by GC-MS, 2017, AASCIT Journal of Chemistry 3 (No. 3) (2017) 19–22. [65] A.A. Hosni, E.S. Abdel-Moneim, Abdel-Reheim, S.M. Mohamed, H. Helmy, Cinnamaldehyde potentially attenuates gestational hyperglycemia in rats through modulation of PPARγ, proinflammatory cytokines and oxidative stress, Biomed. Pharmacother. 88 (2017) 52–60. [66] D.O. Olutola, P. Onocha, O. Ekundayo, M. Ali, Isolation of aurantiamides from Gomphrena celosioides C. Mart, Iran. J. Pharm. Res. (IJPR): IJPR 13 (1) (2014) 143–147. [67] V.K. Matta, P.K. Pasala, S. Netala, S. Pandrinki, P. Konduri, Anti-Hypertensive Activity of the Ethanolic Extract of Lantana camara leaves on high salt loaded wistar albino rats, Phcog. J. 7 (5) (2015) 289–295, https://doi.org/10.5530/pj.2015.5.7. [68] U.D. Akpabio, D.S. Udiong, A.E. Akpakpan, The physicochemical characteristics of plantain (Musa paradisiaca) and banana (Musa sapientum) pseudo stem wastes, Advances in Natural and Applied Sciences 6 (2012) 167–172. [69] C.R. Lima, C.F.B. Vasconcelos, J.H. Costa-Silva, C.A. Maranhão, J. Costa, T.M. Batista, A.G. Wanderley, Anti-diabetic activity of extract from Persea americana Mill. leaf via the activation of protein kinase B (PKB/Akt) in streptozotocin-induced diabetic rats, J. Ethnopharmacol. 141 (1) (2012) 517–525, https://doi. org/10.1016/j.jep.2012.03.026. [70] T. Bakırel, U. Bakırel, O.Ü. Keleş, S.G. Ülgen, H. Yardibi, In vivo assessment of antidiabetic and antioxidant activities of rosemary (Rosmarinus officinalis) in alloxan-diabetic rabbits, J. Ethnopharmacol. 116 (1) (2008) 64–73, https://doi.org/10.1016/j.jep.2007.10.039. [71] R. Gundamaraju, R. Vemuri, R. Singla, R. Manikam, Ar Rao, S. Sekaran, Strophanthus hispidus attenuates the Ischemia-Reperfusion induced myocardial Infarction and reduces mean arterial pressure in renal artery occlusion, Phcog. Mag. 10 (39) (2014) 557, https://doi.org/10.4103/0973-1296.139782. [72] O. Aremu, C. Tata, C. Sewani-Rusike, A. Oyedeji, O. Oyedeji, E. Gwebu, B. Nkeh-Chungag, Acute and Sub-chronic Antihypertensive Properties of Taraxacum officinale Leaf (TOL) and Root (TOR), vol. 74, Transactions of the Royal Society of South Africa, 2019, pp. 132–138, https://doi.org/10.1080/ 0035919X.2019.1592031. [73] D. Kuate, A.P.N. Kengne, C.P.N. Biapa, et al., Tetrapleura tetraptera spice attenuates high-carbohydrate, high-fat diet-induced obese and type 2 diabetic rats with metabolic syndrome features, 2015, Lipids Health Dis. 14 (2015) 50, https://doi.org/10.1186/s12944-015-0051-0. [74] J.P. Fetse, W. Kofie, R. Adosraku, Ethnopharmacological importance of Xylopia aethiopica (DUNAL) A. RICH (annonaceae) - a review, Br. J. Pharmaceut. Res. 11 (2016) 1–21, https://doi.org/10.9734/BJPR/2016/24746. [75] C.W. Haas, The role of ginger in type 2 diabetes mellitus, Integrative Medicine Alert 18 (8) (2015) 85–87. [76] U. Hossain, M.O. Rahman, Ethnobotanical uses and informant consensus factor of medicinal plants in Barisal district, Bangladesh, Bangladesh J. Plant Taxon. 25 (2) (2018) 241–255, https://doi.org/10.3329/bjpt.v25i2.39530. T. Asafo-Agyei et al. https://doi.org/10.1038/hr.2015.72 https://doi.org/10.19082/1832 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref39 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref39 https://doi.org/10.29252/pbp.1.1.1 https://doi.org/10.2147/DDDT.S214454 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref42 https://doi.org/10.1016/j.jep.2017.08.018 https://doi.org/10.1016/j.jep.2017.08.018 https://www.ethnobiology.net/ https://doi.org/10.1016/0378-8741(86)90094-2 https://doi.org/10.1016/0378-8741(86)90094-2 https://doi.org/10.1016/j.jep.2009.03.043 https://doi.org/10.3923/ijp.2007.311.318 https://doi.org/10.1016/J.HERMED.2016.07.002 https://doi.org/10.1016/j.jep.2011.10.014 https://doi.org/10.11604/pamj.2015.22.90.6485 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref51 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref52 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref52 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref53 https://doi.org/10.5402/2012/587160 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref55 https://doi.org/10.1016/j.jep.2014.05.05 https://doi.org/10.3923/ajb.2016.82.89 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref58 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref58 https://doi.org/10.1515/jcim-2015-0017 https://doi.org/10.1177/2515690x18768727 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref61 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref61 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref62 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref62 https://doi.org/10.1080/13880209.2017.1286358 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref64 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref64 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref65 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref65 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref66 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref66 https://doi.org/10.5530/pj.2015.5.7 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref68 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref68 https://doi.org/10.1016/j.jep.2012.03.026 https://doi.org/10.1016/j.jep.2012.03.026 https://doi.org/10.1016/j.jep.2007.10.039 https://doi.org/10.4103/0973-1296.139782 https://doi.org/10.1080/0035919X.2019.1592031 https://doi.org/10.1080/0035919X.2019.1592031 https://doi.org/10.1186/s12944-015-0051-0 https://doi.org/10.9734/BJPR/2016/24746 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref75 https://doi.org/10.3329/bjpt.v25i2.39530 Heliyon 9 (2023) e22977 17 [77] Q. Gu, V.L. Burt, C.F. Dillon, S. Yoon, Trends in antihypertensive medication use and blood pressure control among United States adults with hypertension: the National Health and Nutrition Examination Survey, 2001 to 2010, Circulation 126 (17) (2012) 2105–2114, https://doi.org/10.1161/ CIRCULATIONAHA.112.096156. [78] A. Asase, G. Oppong-Mensah, Traditional antimalarial phytotherapy remedies in herbal markets in southern Ghana, J. Ethnopharmacol. 126 (3) (2012) 492–499. [79] A. Diallo, M.S. Traore, S.M. Keita, M.A. Balde, A. Keita, M. Camara, A.M. Balde, Management of diabetes in Guinean traditional medicine: an ethnobotanical investigation in the coastal lowlands, J. Ethnopharmacol. 144 (2) (2012) 353–361, https://doi.org/10.1016/j.jep.2012.09.020. [80] K. Busia, Fundamentals of Herbal Medicine, vols. 1 & 2, Lightning Source UK Ltd., Milton Keynes, UK, 2016. [81] A. Gurib-Fakim, Medicinal plants: traditions of yesterday and drugs of tomorrow, Mol. Aspect. Med. 27 (1) (2006) 1–93, https://doi.org/10.1016/j. mam.2005.07.008. [82] A. Mohammed, N.A. Koorbanally, M.S. Islam, Ethyl acetate fraction of Aframomum melegueta fruit ameliorates pancreatic β-cell dysfunction and major diabetes-related parameters in a type 2 diabetes model of rats, J. Ethnopharmacol. 175 (2015) 518–527, https://doi.org/10.1016/j.jep.2015.10.011. [83] R.K. Mohammed, S. Ibrahim, S.E. Atawodi, E.D. Eze, J.B. Suleiman, Anti-diabetic and Haematological Effects of N-Butanol Fraction of Alchornea cordifolia Leaf Extract in Streptozotocin-Induced Diabetic Wistar Rats, 2012, https://doi.org/10.13140/RG.2.2.35936.17921. [84] H. Mavar-Manga, J. Lejoly, Quetin-Leclercq, G.H. Schmelzer, Alchornea cordifolia (Schumach &Thonn.) Mull.Arg. Plant Resources of Tropical Africa/ Ressources vegetales de l‟Afrique tropicale, Protabase Record display, Wageningen, Netherlands, 2007. [85] Akinloye, R. Oluseyi Oshilaja, Hypoglyceamic activity of Alstonia boonei stem bark extract in mice, Agric. Biol. J. N. Am. 4 (2013) 1–5, https://doi.org/ 10.5251/abjna.2013.4.1.1.5. [86] M. Gunjan, A Comparative Study of Aloe, Kundru and Neem as an Antidiabetic Agent, Drug Invention Today, 2010. [87] J.A.O. Ojewole, Studies on the Pharmacology of Echitamine, an Alkaloid from the Stem Bark of Alstonia Boonei L. (Apocynaceae). Pharmaceutical Biology, 1984, https://doi.org/10.3109/13880208409070663. [88] C.M. Ruyter, M. Akram, I. Illahi, J. Stockigt, Investigation of the alkaloid con- tent of Rauwolfia serpentina roots from regenerated plants, Planta Med. 57 (4) (1991) 328–330. [89] G. Brasil, S. Ronchi, A. do Nascimento, E. de Lima, W. Romão, H. da Costa, T. de Andrade, Antihypertensive effect of Carica papaya via a reduction in ACE activity and improved baroreflex, Planta Med. 80 (17) (2014) 1580–1587, https://doi.org/10.1055/s-0034-1383122. [90] P. Nyadjeu, E.P. Nguelefack-Mbuyo, A.D. Atsamo, et al., Acute and chronic antihypertensive effects of Cinnamomum zeylanicum stem bark methanol extract in L-NAME-induced hypertensive rats, BMC Complement Altern Med 13 (2013) 27, https://doi.org/10.1186/1472-6882-13-27. [91] J.A. Altschuler, S.J. Casella, T.A. MacKenzie, K.M. Curtis, The effect of cinnamon on A1C among adolescents with type 1 diabetes, Diabetes Care 30 (4) (2007) 813–816, https://doi.org/10.2337/dc06-1871. [92] A.A. Adeneye, E.O. Agbaje, Hypoglycemic and hypolipidemic effects of fresh leaf aqueous extract of Cymbopogon citratus Stapf. in rats, J. Ethnopharmacol. 112 (3) (2007) 440–444, https://doi.org/10.1016/j.jep.2007.03.034. [93] S. Shah, J.M. White, S.J. Williams, Total syntheses of cis-cyclopropane fatty acids: dihydromalvalic acid, dihydrosterculic acid, lactobacillic acid, and 9,10- methylenehexadecanoic acid, Org. Biomol. Chem. 12 (46) (2014) 9427–9438, https://doi.org/10.1039/c4ob01863j. [94] P.C. de Paula Vasconcelos, C.A.S. Tirloni, R.A.C. Palozi, M.M. Leitão, M.T.S. Carneiro, M.I. Schaedler, A.O. Silva, R.I.C. Souza, M.J. Salvador, A.G. Junior, C.A. L. Kassuya, Diuretic herb Gomphrena celosioides Mart. (Amaranthaceae) promotes sustained arterial pressure reduction and protection from cardiac remodeling on rats with renovascular hypertension, J. Ethnopharmacol. 224 (2018) 126–133, https://doi.org/10.1016/j.jep.2018.05.036. [95] C. Velmurugan, A. Bhargava, Anti-diabetic activity of Gossypium herbaceum by alloxan induced model in rats, PharmaTutor 2 (4) (2014) 126–132. [96] A.J. Alhassan, Ibrahim, S. Muhammad, W. Mohammed, I. Alhassan, Idi Abdullahi, M. Aminu, S. Abubakar, A. Mohammed, I. Alexander, A. Nasir, Characterization and anti-diabetic activity of dihydrophenantherene isolated from Khaya senegalensis stem bark, Annual Research & Review in Biology 17 (2017) 1–17, https://doi.org/10.9734/ARRB/2017/35908. [97] V.K. Matta, P.K. Pasala, S. Netala, S. Pandrinki, P. Konduri, Anti-Hypertensive Activity of the Ethanolic Extract of Lantana camara leaves on high salt loaded wistar albino rats, Phcog. J. 7 (5) (2015) 289–295, https://doi.org/10.5530/pj.2015.5.7. [98] Dai-Hung Ngo, Ngo Dai-Nghiep, Nhan Vo Thi Thanh, Thanh Sang Vo, Mechanism of action of Mangifera indica leaves for anti-diabetic activity, Sci. Pharm. 87 (2) (2019) 13, https://doi.org/10.3390/scipharm87020013. [99] L. Harinantenaina, M. Tanaka, S. Takaoka, M. Oda, O. Mogami, M. Uchida, et al., Momordica charantia constituents and antidiabetic screening of the isolated major compounds, Chem. Pharm. Bull. (Tokyo) 54 (2006) 1017–1021, https://doi.org/10.1248/cpb.54.1017. [100] C.P. Ooi, Z. Yassin, T.A. Hamid, Momordica charantia for type 2 diabetes mellitus, Cochrane Database Syst. Rev. 8 (2012) CD007845, https://doi.org/ 10.1002/14651858.CD007845.pub3. (Accessed 11 January 2023). [101] V.S. Baldwa, C.M. Bhandari, A. Pangaria, R.K. Goyal, Clinical trial in patients with diabetes mellitus of an insulin-like compound obtained from plant source, Ups. J. Med. Sci. 82 (1) (1977) 39–41, https://doi.org/10.3109/03009737709179057. [102] R.N. Gacche, N.A. Dhole, Profile of aldose reductase inhibition, anti-cataract and free radical scavenging activity of selected medicinal plants: an attempt to standardize the botanicals for amelioration of diabetes complications, Food and chemical toxicology an international journal published for the British Industrial Biological Research Association 49 (8) (2011) 1806–1813, https://doi.org/10.1016/j.fct.2011.04.032. [103] K. Kamiya, W. Hamabe, S. Harada, R. Murakami, S. Tokuyama, T. Satake, Chemical constituents of Morinda citrifolia roots exhibit hypoglycemic effects in streptozotocin-induced diabetic mice, Biological & pharmaceutical bulletin 31 (5) (2008) 935–938, https://doi.org/10.1248/bpb.31.935. [104] A.A. Odutuga, J.O. Dairo, J.B.F. Minari, Anti-diabetic effect of Morinda lucida stem bark extracts on alloxan-induced diabetic rats, Res. J. Pharmacol. 4 (2010) 78–82, https://doi.org/10.3923/rjpharm.2010.78.82. [105] T.O.A. Adeyemi, O.D. Idowu, R.O. Ogboru, W.E. Iyebor, E.A. Owoeye, Phytochemical screening, nutritional and medicinal benefits of Thaumatococcus daniellii Benn (Benth.), Inter. J. Appli. Res. and Technol 3 (8) (2014) 92–97. [106] F. Anwar, S. Latif, M. Ashraf, A.H. Gilani, Moringa oleifera: a food plant with multiple medicinal uses, Phytother Res. 21 (1) (2006) 17–25, https://doi.org/ 10.1002/ptr.2023. [107] E.I. Omodanisi, Y.G. Aboua, O.O. Oguntibeju, Assessment of the anti-hyperglycaemic, anti-inflammatory and antioxidant activities of the methanol extract of Moringa oleifera in diabetes-induced nephrotoxic male wistar rats, Molecules 22 (4) (2017) 439, https://doi.org/10.3390/molecules22040439. [108] S.E. Atawodi, J.C. Atawodi, G.A. Idakwo, B. Pfundstein, R. Haubner, G. Wurtele, H. Bartsch, R.W. Owen, Evaluation of the polyphenol content and antioxidant properties of methanol extracts of the leaves, stem, and root barks of Moringa oleifera Lam, J. Med. Food 13 (3) (2010) 710–716, https://doi.org/10.1089/ jmf.2009.0057. [109] O.S. Adeyemi, T.C. Elebiyo, Moringa oleifera supplemented diets prevented nickel-induced nephrotoxicity in wistar rats, 2014, Journal of nutrition and metabolism (2014), 958621, https://doi.org/10.1155/2014/958621. [110] M.M. Almatrafi, M. Vergara-Jimenez, A.G. Murillo, G.H. Norris, C.N. Blesso, M.L. Fernandez, Moringa leaves prevent hepatic lipid accumulation and inflammation in Guinea pigs by reducing the expression of genes involved in lipid metabolism, Int. J. Mol. Sci. 18 (7) (2017) 1330. [111] S.A. Shodehinde, G. Oboh, Distribution and antioxidant activity of polyphenols in boiled unripe plantain (Musa paradisiaca) pulps, J. Food Biochem. 38 (3) (2014) 293–299. [112] S.S. Murthy, C. Felicia, Antidiabetic activity of Musa sapientum fruit peel extract on streptozotocin induced diabetic rats, Int. J. Pharma Bio Sci. 6 (2015) P537–P543. [113] J. Waghmare, A.H. Kurhade, GC-MS analysis of bioactive components from banana peel (Musa sapientum peel), Eur. J. Exp. Biol. 4 (2014) 10–15. [114] S.I.R. Okoduwa, I.A. Umar, D.B. James, H.M. Inuwa, Anti-diabetic potential of Ocimum gratissimum leaf fractions in fortified diet-fed streptozotocin treated rat model of type-2 diabetes, Medicines (Basel, Switzerland) 4 (4) (2017) 73, https://doi.org/10.3390/medicines4040073. [115] A. Akinmoladun, E. Ibukun, I. Dan-Ologe, Phytochemical constituents and antioxidant properties of extracts from the leaves of Chromolaena odorata, Scientific Research and Essay 2 (2007) 191–194. T. Asafo-Agyei et al. https://doi.org/10.1161/CIRCULATIONAHA.112.096156 https://doi.org/10.1161/CIRCULATIONAHA.112.096156 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref78 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref78 https://doi.org/10.1016/j.jep.2012.09.020 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref80 https://doi.org/10.1016/j.mam.2005.07.008 https://doi.org/10.1016/j.mam.2005.07.008 https://doi.org/10.1016/j.jep.2015.10.011 https://doi.org/10.13140/RG.2.2.35936.17921 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref101 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref101 https://doi.org/10.5251/abjna.2013.4.1.1.5 https://doi.org/10.5251/abjna.2013.4.1.1.5 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref102 https://doi.org/10.3109/13880208409070663 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref84 http://refhub.elsevier.com/S2405-8440(23)10185-X/sref84 https://doi.org/10.1055/s-0034-1383122 https://doi.org