Hindawi
Evidence-Based Complementary and Alternative Medicine
Volume 2023, Article ID 6878852, 28 pages
https://doi.org/10.1155/2023/6878852
Review Article
Medicinal Plants Used in the Management of Sexual Dysfunction,
Infertility and Improving Virility in the East African Community:
A Systematic Review
Christine Kyarimpa ,1 Christine Betty Nagawa ,2 Timothy Omara ,3 Silver Odongo ,4
Patrick Ssebugere ,4 Solomon Omwoma Lugasi ,5 and Ivan Gumula1
1
Department of Chemistry, Faculty of Science, Kyambogo University, P.O. Box 1, Kampala, Uganda
Department of Forestry, Biodiversity and Tourism, College of Agricultural and Environmental Sciences, Makerere University,
P.O. Box 7062, Kampala, Uganda
3
Chemistry Division (Food Safety aboratories), Testing Department, Standards Directorate,
Uganda National Bureau of Standards, P.O. Box 6329, Kampala, Uganda
4
Department of Chemistry, College of Natural Sciences, Makerere University, P.O. Box 7062, Kampala, Uganda
5
Department of Physical Sciences, Jaramogi Oginga Odinga University of Science and Technology, P.O. Box 210,
Bondo 40601, Kenya
2
Correspondence should be addressed to Timothy Omara; prof.timo2018@mu.ac.ke
Received 15 February 2023; Revised 13 July 2023; Accepted 27 July 2023; Published 12 August 2023
Academic Editor: Chunpeng (Craig) Wan
Copyright © 2023 Christine Kyarimpa et al. Tis is an open access article distributed under the Creative Commons Attribution
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly
cited.
Sexual disorders such as erectile dysfunction (ED), sterility, and sexual inappetence represent some of the complex reproductive
challenges that require addressing the underlying causes. Te aim of this paper was to systematically synthesize literature on the
ethnobotany, phytochemistry, bioactivities, and safety of plants used as remedies for managing sexual dysfunction and infertility,
and improving fertility and virility in the EAC. Trough an extensive review conducted in multidisciplinary electronic databases,
171 plant species were identifed to have been reported for the management of sexual inappetence (i.e., used as aphrodisiacs,
39.4%), ED (35.9%), infertility (18.7%), and increasing fertility (6.0%). Te most used plants are Mondia whitei, Acalypha
villicaulis, Combretum illairii, Erythrina abyssinica, Pappea capensis, Rhus vulgaris, and Warburgia ugandensis while roots
(44.9%), leaves (21.8%), stem and root barks (16.7%) of shrubs (35%), trees (31%), herbs (26%), and climbers (8%) are the
preferred organs for making decoctions (69%). Te research strides to date indicate that Citropsis articulata, Cola acuminata,
Ekebergia capensis, Plumbago zeylanica, Tarenna graveolens, Urtica massaica, and Zingiber ofcinale have been assessed for their
bioactivity. Te majority (71.4%) of the plants either increased testosterone levels and mounting frequency or elicited prosexual
stimulatory efects in male rats. More studies investigating the relevant pharmacological activities (aphrodisiac, fertility, and
phosphodiesterase•5 inhibitory activities), safety aspects, responsible compounds, and clinical studies are warranted to establish
the pharmacological potential of the unstudied species and elucidate the mechanism of action of the bioactive compounds.
1. Introduction
One of the universal interests enshrined in sustainable de•
velopment goal (SDG) 3 is good health and well•being. It is
linked to and afects other global goals such as SDG 1
(poverty reduction), SDG 2 (end poverty), and SDG 4
(quality and equitable education) [1]. Critical analysis of the
global disease burden shows that one•third of the total world
population has more than fve ailments [2]. Accordingly,
three in fve of the global deaths are ascribed to at least one of
the four main noncommunicable diseases (NCDs), namely,
cancer, diabetes, cardiovascular, and chronic lung diseases
[3–5]. Most global mortalities (up to 71%) are due to NCDs
[6], and 77% of these occur in low• and middle•income
2
countries due to limited access to medical services and
poverty [7]. Whereas the global focus is on the major NCDs,
conditions such as sexual dysfunction, infertility, and
anaphrodisia (sexual inappetence) represent some of the
complex health challenges.
Sexual dysfunction refers to the inability to achieve
a normal sexual intercourse. It includes orgasmic disorder,
retrograded, retarded, premature ejaculation, and erectile
dysfunction [8]. Male erectile dysfunction (ED) or impo•
tence is the inability to achieve or maintain an erection
sufcient for satisfactory sexual performance and vaginal
intercourse, typically for a period of more than six months
[9]. Tough to diferent degrees, ED afects more than 52%
of men in the age bracket of 40 and 70 years. Erectile dys•
function is linked with conditions such as diabetes, sed•
entary lifestyle, hypertension, obesity, hypercholesterolemia,
and smoking [10–12].
On the other hand, infertility is a medical condition
characterized by failure to establish a clinical pregnancy after
one year of regular and unprotected sex [13]. Infertility
afects more than 48 million couples worldwide. It can be
from either one or both partners, but 50% of all cases are due
to male infertility [14]. In women, it may be due to endo•
metriosis (premature ovarian failure) and uterine disorders
such as fbroids or thyroid diseases. In males, infertility is
associated with defective sperm function, azoospermia, low
sperm counts, varicocele, undescended testes, testicular
cancer, and low testosterone levels [13, 14]. Other risk
factors for infertility include diabetes, sexually transmitted
diseases, stress, obesity, drug abuse, age, exposure to envi•
ronmental toxins, radiotherapy, and other cancer treatments
[15, 16].
Sexual inappetence is a common reproductive challenge
that accompanies or is a direct consequence of ED and
infertility [17, 18]. Sexual inappetence (anaphrodisia or lack
of desire/libido) is one of the most common sexual dys•
functions of women. Together, ED, infertility, and sexual
inappetence are among the relatively common fecundity
challenges that afect couples medically, sexually, and psy•
chologically [17, 18]. With medical advancements in assisted
reproduction technologies, the use of synthetic agents such
as phosphodiesterase type 5 inhibitors (in intracavernosal
injection therapy for ED) and stem cell therapy (for in•
fertility) has been encouraged [13]. However, limited access
to medical services, long•term treatment tenure, and side
efects of injectable fertility drugs have limited their ac•
ceptability among the general population [19–21].
For indigenous communities in developing countries,
the use of natural products for prevention and the man•
agement of reproductive diseases and conditions are com•
mon. Te East African Community (EAC) is one of the
regions with distinguished ethnomedicinal knowledge and
use of natural products [22–25]. Te high reliance of these
communities on herbal medicine is explained by the ex•
ceptionally rich cultural heritage, acceptance, availability,
and perceived efcacy [26–28]. In this context, traditional
medicine practitioners correlate sicknesses and other
medical conditions with their possible causes [25]. For this
Evidence•Based Complementary and Alternative Medicine
reason, herbal medications and posology are prescribed
based on the supposed cause of the diseases. Critical cases, or
those due to supernatural forces, are managed through
diviners’ interventions [26, 29]. Illnesses are thought to be
induced by external polluting infuences (e.g., consumption
of tabooed foods [30], breaching of taboos, witchcraft•
related rites, fetishes or social rules, and use of objects
planted by ill people) that interfere with body physiology
[26, 31–33]. Terefore, traditional management of diseases
involves health practices, knowledge, and beliefs that utilize
plants and animal• and mineral•based remedies, dispensing
of ritually protective herbal medicines or performing rituals
for placating spirits [26, 33]. Tese perceptions are similar to
traditional medicine concepts in other parts of Africa [34].
In the EAC, chronic poverty and resource•constrained
healthcare systems are common, and the use of herbal
remedies for the treatment of sexual dysfunction (ED) and
infertility, and enhancing fertility and virility has been
sporadically mentioned in ethnobotanical studies. How•
ever, no study has systematically collated literature on
these medicinal plants with in•depth description and
analysis of their claimed efcacy, phytochemistry, and
safety. Te aim of this paper was, therefore, to system•
atically synthesize literature on ethnobotany, phyto•
chemistry, bioactivities, and the safety profle of plants
used as remedies for managing sexual dysfunction and
infertility, and improving fertility and virility in the EAC.
As part of an ongoing project, we aimed at identifying
highly cited but unstudied species that could be assessed
for their aphrodisiac, fertility and phosphodiesterase•5
inhibitory activities, bioactive phytochemicals, and tox•
icity profles. Tis could open lead to the discovery of
molecules that can be used in modern medicine.
2. Methods
2.1. Study Design, iterature Sources, and Systematic Search
Procedures. Te Preferred Reporting Items for the Sys•
tematic Reviews and Meta•Analyses (PRISMA) 2020
guidelines [35] were followed (Supplementary fle 1). Te
protocol used was registered with the International Pro•
spective Register of Systematic Reviews (PROSPERO) with
registration number CRD42022373152 (https://www.crd.
york.ac.uk/prospero/display_record.php?ID=CRD4202237
3152). Nine multidisciplinary electronic databases (Scopus,
Web of Science, PubMed, Science Direct, Google Scholar,
Wiley Online Library, Taylor and Francis Online, Springer
Link, and Scientifc Electronic Library Online) and regional
university repositories were searched to gather relevant
records on ethnobotany, phytochemistry, biological activi•
ties, and toxicity of medicinal plants exploited for the
management of sexual dysfunction and infertility, and
improving fertility and virility in the EAC. Te dates on
which we last consulted the databases were 7th January 2023,
31st December 2022, 20th November 2022, 20th January
2023, 4th January 2023, 17th January 2023, 11th November
2022, 10th January 2023, 24th November 2022, 2nd De•
cember 2022, and 2nd January 2023, respectively.
Evidence•Based Complementary and Alternative Medicine
Te EAC was considered as the region encompassing
Uganda, Kenya, Tanzania, Rwanda, Burundi, South Sudan,
and Democratic Republic of Congo (DRC) from April 2022
[36]. Te searches were performed in parallel using search
strings specifed for a comprehensive search that covered all
felds in records but broadened the scope in PubMed ad•
vanced search. Within each axis, keywords were combined
with the “OR” operator in the Boolean operator and then
linked the two axes’ search techniques to the “AND” op•
erator. Te keywords used were “plant” “erectile dysfunc•
tion” “aphrodisiac” “infertility” OR “fertility” “virility” AND
“Uganda” “Kenya” “Tanzania” “Rwanda” “Burundi” “South
Sudan” “Democratic Republic of Congo.” For example, in
Scopus, the search string used was ALL (plants, AND erectile
AND dysfunction, AND aphrodisiac, AND uganda) AND
(LIMIT•TO (AFFILCOUNTRY, “Uganda”)) OR ALL
(plants, AND erectile AND dysfunction, AND aphrodisiac,
AND Kenya) AND (LIMIT•TO (AFFILCOUNTRY,
“Kenya”)) Kenya OR ALL (plants, AND erectile AND
dysfunction, AND aphrodisiac, AND rwanda) AND
(LIMIT•TO (AFFILCOUNTRY, “Rwanda”)) OR ALL
(plants, AND erectile AND dysfunction, AND aphrodisiac,
AND burundi) AND (LIMIT•TO (AFFILCOUNTRY,
“Burundi”)) OR ALL (plants, AND erectile AND dysfunc•
tion, AND aphrodisiac, AND south Sudan) AND (LIM•
IT•TO (AFFILCOUNTRY, “South Sudan”)) OR ALL
(plants, AND erectile AND dysfunction, AND aphrodisiac,
AND Democratic Republic of Congo) AND (LIMIT•TO
(AFFILCOUNTRY, “Democratic Republic of Congo”)) OR
ALL (plants, AND erectile AND dysfunction, AND aph•
rodisiac, AND Tanzania) AND (LIMIT•TO (AFFIL•
COUNTRY,“Tanzania”)) OR ALL (plant, AND infertility
AND fertility AND uganda) AND (LIMIT•TO (AFFIL•
COUNTRY, “Uganda”)) OR ALL (plant, AND infertility
AND fertility AND Kenya) AND (LIMIT•TO (AFFIL•
COUNTRY, “Kenya”)) OR ALL (plant, AND infertility
AND fertility AND tanzania) AND (LIMIT•TO (AFFIL•
COUNTRY, “Tanzania”)) OR ALL (plant, AND infertility
AND fertility AND rwanda) AND (LIMIT•TO (AFFIL•
COUNTRY, “Rwanda”)) OR ALL (plant, AND infertility
AND fertility AND burundi) AND (LIMIT•TO (AFFIL•
COUNTRY, “Burundi”)) OR ALL (plant, AND infertility
AND fertility AND south Sudan) AND (LIMIT•TO
(AFFILCOUNTRY, “South Sudan”)) OR ALL (plant, AND
infertility AND fertility AND democratic republic of congo)
AND (LIMIT•TO (AFFILCOUNTRY, “Democratic Re•
public of Congo”)).
In addition, reference lists of the retrieved studies were
also manually searched to access additional articles which
were screened for their eligibility for inclusion in the study.
Te literature search was performed between 1st June 2022
and 20th January 2023.
2.2. Study Selection. All search results were imported into
EndNote X9 (Tomson Reuters, Philadelphia, PA, USA),
and duplicate reports were removed. Te screening was done
according to the title and abstract of the articles. Tis was
®
3
conducted independently by 4 authors (CK, CBN, TO, and
SO). Two independent reviewers (TO and SO) screened the
articles against inclusion criteria, and possible contradic•
tions during article selection and/or extraction were obvi•
ated through discussions and consensus.
2.3. Inclusion and Exclusion Criteria. To refrain the authors
from bias, (1) only full•text articles or reports published in or
translated into English and French; (2) cross•sectional
original papers or reports on the ethnobotany, phyto•
chemistry, bioactivities, and clinical trials of plants used in
the management of sexual dysfunction and infertility, and
improving fertility and virility in EAC; and (3) reports
published online until 20th January 2023 were included.
Excluded studies were those that (1) provided no data; (2)
were neither from EAC nor full•text articles; (3) reported on
the use of plants for managing conditions such as menor•
rhagia, blocked fallopian tubes, inducing twin birth or birth
to a particular sex of children; (4) narrative and systematic
reviews, or reports not based on original data (expert
opinions, editorials, and perspective papers).
2.4. Risk of Bias Assessment. Quality of the considered re•
ports (risk of bias) was established following the Joanna
Briggs Institute quality assessment tool [37]. Two authors
(TO and SO) independently assessed the quality of the
included studies. Variations in the fnal risk of bias as•
sessment among them were declared by discussing the
prespecifed criteria. Te evaluation tool consisted of seven
parameters: (1) appropriate sampling design; (2) correct
sampling technique; (3) acceptable sample size; (4) adequate
study subject and location explanation; (5) appropriate data
investigation; (6) use of valid methods for identifcation of
plants and the conditions that they treat; and (7) use of
appropriate statistical/ethnobotanical analysis indices. Be•
cause most studies met parameters 5 to 7 that were similar
across them, we relied on parameters 1 to 4 to ascertain the
risk of bias status. A study that did not meet each parameter
was scored as 1 if not 0. Te risks for biases were classifed as
either low (total score, 0•1), moderate (total score, 2), or high
(total score, 3•4) [38].
2.5. Data Extraction. Data were collated in a predesigned
Microsoft Excel 2019 standardized sheet. Information on the
reported medicinal plants, such as botanical names (and
synonyms), plant family, traditional name(s), growth habit,
part(s), and their uses (conditions treated), mode of prep•
aration and administration, isolated pure compounds, and
relevant efcacy reports were extracted. For each dataset, the
frst author’s last name, year of publication, and country
were also extracted. Missing information in some reports
such as local names, growth forms, and misspelled botanical
names was checked from Google and botanical databases
(WFO Plant List, International Plant Names Index, and
Tropicos).
4
2.6. Data Analysis. Descriptive statistical methods were used
to analyze the collected data. Results were expressed as
ranges, percentages, and frequencies and presented as tables
and charts. Tese analyses were performed in Microsoft
Excel 2019 for Windows (Microsoft Corporation, Wash•
ington, DC, USA).
3. Results and Discussion
3.1. Description of Included Studies. Our systematic search
(Figure 1) retrieved no previous review on the subject in East
Africa. From databases, registers, and other websites, the
search returned 396 unique reports published between 1962
and 2022. Te highest number of reports were from Scopus
(n � 172) and Google Scholar (n � 108), followed by Web of
Science (n � 44), Science Direct (n � 42), Wiley Online Li•
brary (n � 11), Taylor & Francis Online (n � 7), Springer Link
(n � 4), PubMed (n � 3), regional university repositories
(n � 3), and SciELO (n � 2). Of these, duplicates (n � 47) were
removed, and 349 unique articles were screened. A total of
235 articles were excluded after reading their titles and
abstracts, while 47 others were excluded because they were
not from any country within the EAC. Terefore, 67 records
were assessed for their eligibility and inclusion in the study.
Based on the inclusion and exclusion criteria, some full•text
articles were excluded with reasons, namely, (i) articles not
in English or French (n � 11), (ii) review articles (n � 9), and
(iii) those that did not provide any data (n � 8). A manual
search resulted in 7 eligible articles. Tus, data were
extracted from a total of 46 articles in this systematic review.
Regarding the assessment of the risk of bias among studies,
most reports were judged as having a low (47.8%) or
moderate risk of bias (34.8%) (Supplementary fle 2).
3.2. Inventory of Medicinal Plants Reported. Tis review
identifed 46 reports on plants used in the management and
treatment of ED and infertility, and increasing fertility and
sexual appetence (virility) in the EAC. Some of the sexual
dysfunctions captured from herbalists include erectile dis•
orders, pain during penetration, premature ejaculation, lack
of sexual arousal, and short•lasting erections (among men)
and lack of orgasm, dyspareunia, lack of sexual arousal,
atrophic vaginitis, and short orgasms among women [39].
In total, 171 plant species from 59 botanical families have
been reported for the management of sexual inappetence,
i.e., used as aphrodisiacs (39.4%), ED (35.9%), infertility
(18.7%), and increasing fertility (6.0%) (Table 1). Te highest
number of plants cited was from Kenya (96), followed by
Uganda (66), Tanzania (24), Rwanda (1), and DRC (1).
Burundi and South Sudan had no reports on plants in the
category under scrutiny. It is not surprising that Kenya
ranked the highest, as it is known to have diversifed fora
with over 7,000 plant species [23, 40]. Tis is also supported
by the fact that most of the ethnobotanical reports reviewed
(n � 25) were from Kenya as compared to Uganda (n � 18),
Tanzania (n � 7), Rwanda (n � 1), and DRC (n � 1).
Evidence•Based Complementary and Alternative Medicine
Analysis of transregional distribution of the plants
revealed that Uganda and Kenya shared 8 species and
Tanzania and Kenya shared 6 species while Kenya and
Rwanda shared one species (Tagetes minuta L.). Only one
plant (Pachycarpus robusta) was cited to be used in Uganda,
Kenya, and Tanzania [41]. Te rest of the countries did not
share any plant. Such marked divergence in the use of plants
across the region could be due to their preference which is
related to specifc cultural beliefs and traditions or centred
around human relationships [42–44].
Te majority of the plants retrieved in this study were
from families: Fabaceae (16.9%, 29 species), Euphorbiaceae
(7.0%, 12 species), Asteraceae (5.8%, 10 species), Apoc•
ynaceae, Rubiaceae (5.3%, 9 species each), and Capparaceae
(4.7%, 8 species) (Figure 2). Species from these botanical
families have been reported to have aphrodisiac and fertility
potential in ethnobotanical surveys from Ethiopia [45],
Southern Africa [46], Iran [47], and India [48]. Te dom•
inance of families, especially Fabaceae and Asteraceae, is due
to the extensive range of their distribution across global
biomes [49]. Moreover, they contain phytochemicals such as
phenolics, tannins, and alkaloids which are known to have
therapeutic efects [50, 51].
At the genus level, the most represented genera were
Acacia (6 species), Combretum (5 species), Cassia and Tragia
(3 species each), Abrus, Allium, Boscia, Cadaba, Cleome,
Croton, Impatiens, Maytenus, Sonchus, Uvaria, Vachellia,
and Vernonia (2 species each). Te commonly mentioned
plants were Mondia whitei (12 times), Warburgia ugandensis
(4 times), Acalypha villicaulis, Combretum illairii, Erythrina
abyssinica, Pappea capensis, and Rhus vulgaris (3 times
each). Some of the plants listed such as Abrus precatorius,
Allium sativum, Cola acuminata, Combretum hereroense,
Mondia whitei, Plumbago zeylanica, Ricinus communis, and
Syzygium guineense are traditionally used for treating in•
fertility and ED in South Africa [52], Ghana [53], Cameroon,
Guinea, Gabon [54], Iran [47], Benin [55], and Ethiopia [45].
It is worth mentioning that organs of some of the highly
cited species such as Abrus precatorius and Erythrina
abyssinica are used in Uganda for rituals and ceremonies of
love, weddings, and childbirth [56].
In regards to the treatment of infertility, most plan
species recorded were indicated to be used for the treatment
of female infertility (Table 2). Te most cited species were
Erythrina abyssinica and Combretum illairii (3 times each).
Interestingly, some species (Cadaba glandulosa, Cadaba
farinose, Combretum illairii, Hoslundia opposita, and Allo•
phylus pervilleria) were shown to be used for the treatment of
both female and male infertility, which could make them
good candidates for further studies of their biological
activities.
3.3. Growth Habit, Organs Used, Dosage Forms, and Posology
of the Herbal Remedies. Te plants occurred as shrubs (35%),
trees (31%), herbs (26%), and climbers (8%) (Figure 3).
Figure 4 illustrates which plant organs are widely used in
Evidence•Based Complementary and Alternative Medicine
Studies included in a previous
version of review (n = 0)
Identification of new studies from databases, registers and other websites
Records identied from;
All Databases (N = 396)
Scopus (n = 172)
Web of Science (n = 44)
PubMed (n = 3)
Science Direct (n = 42)
Wiley Online Library (n = 11)
Taylor & Francis Online (n = 7)
Springer Link (n = 4)
Google Scholar (n = 108)
SciELO (n = 2)
University repositories (n = 3)
Registers (n = 0)
Records removed before screening
Duplicate records removed (n = 47)
Eligibility
Screening
Identification
Previous studies
5
Records screened (n = 349)
Records excluded based on titles and
abstracts (n = 235)
Studies not from EAC (n = 47)
Records sought for retrieval
(n = 7)
Records not retrieved (n = 0)
Included
Records assessed for
eligibility (n = 67)
Full-text articles excluded with reasons
Articles not in English or French (n = 11)
Review articles (n = 9)
Did not provide any data (n = 8)
Total studies included in the
review (n = 46)
Figure 1: PRISMA fow diagram showing the retrieval and exclusion steps of the systematic review adapted from Page et al. [35].
preparation of the herbal remedies, that is, roots (44.9%),
leaves (21.8%), and stem and root barks (16.7%). Te fre•
quent use of roots is unsustainable but may be linked to the
fact that the conditions treated are internal to the body (are
hidden), just as root structures are hidden in the ground. On
the other hand, the relatively frequent use of leaves could be
related to their availability and the fact that they are the
photosynthetic sheet of plants that accumulate therapeutic
phytochemicals [57].
Tis review noted a tendency of including more than one
plant part and adjuvants in herbal remedies. For multiple
plant parts, a total of 13 species were encountered to be used
in combination with others. For example, in Kenya, de•
coction of Uvaria leptocladon, Boscia coriaceae, and Com•
bretum hereroense roots is used for treating ED. For
infertility in women, the roots are used with Croton
dichagamus roots [58, 59]. Similarly, the decoction of
Markhamia zanzibarica roots mixed with Uvaria acuminata
roots is administered as an aphrodisiac. For infertility in
women, it is used with Salvadora persica and Uvaria acu•
minata roots [58, 59]. A striking example of using adjuvants
is from Tanzania where roots of Polygala aphrodisiaca are
cooked with a young cock while Duosperma kilimand•
scharicum leaf and root decoction are taken with goat blood
or goat meat soup as an aphrodisiac [41]. Te use of cow and
goat milk for preparation of Morus mesozygia roots as an
aphrodisiac was also documented in Kenya [60]. In Uganda,
Acanthus pubescens leaves are taken in tonto, a traditional
beer prepared from Musa × paradisiaca L. var. sapientum
fruits [61]. Te use of more than one plant organ and ad•
juvants as witnessed in this review are tailored to various
reasons. For instance, it may be an obvious way of masking
the toxicity of herbal remedies or hiding the secrecy of the
formularies [62, 63].
Te commonest method of preparing herbal remedies is
decoctions (69%). Tis could be because decoction pro•
cedures allow for better extraction of the bioactive phyto•
chemicals in plant matrices [64]. However, the plant organs
6
Table 1: Plants used in the management of sexual disorders, infertility, and improving sexual virility and fertility in the East African Community.
Plant family
Local name
Part used
Habit
Preparation mode
Amatovu (Luganda)
Leaves
Shrub
Decoction
Duosperma
kilimandscharicum (C. B.
Clarke) Dayton
Not reported
Leaves,
roots
Alliaceae
Allium cepa L
Katunguru
(Runyankore)
Alliaceae
Allium sativum L
Tungurusumu
(Rukonjo)
Aloeaceae
Aloe volkensii Engl.
Hargeis, D’aar (Orma)
Anacardiaceae
Mangifera indica L
Anacardiaceae
Ozoroa insignis ssp.
reticulata (Baker f.) J. B.
Gillett
Acanthaceae
Acanthaceae
Annonaceae
Annonaceae
Annonaceae
Apocynaceae
Apocynaceae
Bulb, leaves,
root tuber
Stem bulb,
leaves, roots
tuber
Reference
Aphrodisiac
Uganda
[61]
Aphrodisiac
Tanzania
[41]
ED
Uganda
[39, 65]
Oral in water, and in
food
ED
Uganda
[65]
Leaves
Herb
Decoction
Used to wash genital
area thrice daily
Infertility
Kenya
[58]
Muyembe (Luganda)
Bark
Tree
Decoction
Oral
Infertility
(women)
Uganda
[22]
Not reported
Roots
Tree
Decoction
Oral
Aphrodisiac
Tanzania
[41]
Shrub
Used directly,
decoction
Oral, chewed
ED, aphrodisiac
Uganda,
Kenya
[41, 60, 65]
Oral
ED, infertility
Kenya
[61, 62]
Oral, a glass daily for
5 days
Aphrodisiac
Kenya
[59]
Oral, half a glass daily
for 5 days. For
infertility, half glass
thrice daily for 3 days
ED, infertility
(women)
Kenya
[58, 59]
Oral, taken as tea
Aphrodisiac
Tanzania,
Kenya
[64]
Oral
Aphrodisiac
Kenya
[65]
Mundagoni, murori
(Pokomo)
Sholole (Orma)
Roots
Roots
Leketetwo (Marakwet),
Carissa spinarum L.
Logetetwa (Pokot),
Roots, bark
(Synonym: Carrisa edulis
Omukuyomonza
Forssk. (Vahl))
Acokanthera schimperi
(A.D.C) Schweinf
Country
Used directly,
decoction
Mukanja (Runyankore), Bark, roots,
leaves,
Mukanza (Rukonjo),
whole plant
Musatsa (Wanga)
Ovariodendron anisatum
Ndonga (Embu)
Whole plant
Uvaria leptocladon
Herb
Decoction. Taken
with goat blood or
Oral
extract from goat
meat
Used directly,
Oral in water, and in
decoction
food or just chewed
Use
Herb
Rhus vulgaris Meikle
Uvaria acuminata Oliv
Shrub
Administration
Oral in a local brew
(tonto)
Not reported
Roots
Herb
Shrub
Shrub
Shrub
Tree
Decoction
Decoction. Used
with Markhamia
zanzibarica
Decoction. Used
with Boscia
coriaceae and
Combretum
hereroense. For
infertility, use with
Croton dichagamus
Decoction with
Elaedendron
buchanannii bark or
powder mixed with
Tragia furialis
Infusion of powder
Evidence•Based Complementary and Alternative Medicine
Anacardiaceae
Botanical name
Acanthus pubescens (T.
Toms.) Engl.
Plant family
Apocynaceae
Botanical name
Local name
andolphia swynnertonii Mokokwet (Marakwet)
Part used
Habit
Preparation mode
Administration
Roots
Shrub
Decoction
Oral
Use
Increasing
fertility
(women)
ED,
aphrodisiac,
fertility
enhancer
Country
Reference
Kenya
[66]
Uganda,
Kenya
[22, 23, 27,
39, 41, 65,
67–72]
Apocynaceae
Mondia whitei (Hook. f.)
Skeels
Omulondo (Luganda),
Omurondo
(Runyankore),
Mukombelo (Luhya)
Roots/root
bark
Vine
Used directly (chew
when raw or dry),
decoction
Oral in tea and in
food
Apocynaceae
Cryptolepis obtusa N. E.
Br
Not reported
Roots
Shrub
Decoction
(Tanzania), used
directly
Drunk, chewed
Aphrodisiac
Kenya,
Tanzania
[73]
Not reported
Roots
Climber
Used directly
Fresh root chewed
Aphrodisiac
Tanzania
[60]
Not reported
Roots
Herb
Not specifed
Not specifed
Aphrodisiac
East Africa
[41]
Not reported
Roots
Climber
Decoction
Oral, once in the
evening
Aphrodisiac
Kenya
[60]
Roots/milky Climber/
latex
liana
Decoction
Oral
Fertility
Kenya
[75]
Uganda,
Kenya
[59, 65]
Apocynaceae
Apocynaceae
Apocynaceae
Apocynaceae
Arecaceae
Asparagaceae
Asphodelaceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Dregea rubicunda K.
Schum
Pachycarpus robusta (A.
Rich.) Bullock
Parquetina nigrescens
Afzel
Periploca linearifolia Dill.
& Rich
Phoenix reclinata Jacq
Chlorophytum comosum
(Tunb.) Jacques
Aspidoglossum biforum
E. Mey
Bidens pilosa L
aunaea cornuta
(Hochst. Ex Oliv. &
Hiern) C. Jefrey
actuca inermis Forssk.
(L. Capensis Turnb.)
Microglossa pyrifolia
(Lam.) Kuntze
Sonchus asper
Psiadia punctulata (DC.)
Vatke
Sonchus schweinfurthii
Oliv. & Hiern
Sinendet (Nandi)
Akakindo, Mukindo
(Runyankore),
Mukindu (Pokomo)
Roots,
leaves
Shrub
Decoction
Nalwebe (Lusoga)
Tuber
Herb
Not specifed
Not specifed
Infertility
Uganda
[31]
Drege (Kiswahili)
Roots
Herb
Not specifed
Not specifed
Aphrodisiac
Tanzania
[41]
Mucege, Enyabarashana
(Runyankore)
Shoot,
fowers
Herb
ED, increase
fertility
Kenya,
Uganda
[27, 76]
Uthuunga (Kikamba)
Leaves,
stems
Herb
Infusion
Oral
Infertility
(women)
Kenya
[77]
Not reported
Roots
Herb
Not specifed
Not specifed
Aphrodisiac
Uganda
[56]
Omuhe/Mkuraiju
Leaves
Herb
Not specifed
Not specifed
Aphrodisiac
Tanzania
[41]
Iviuviu (Embu)
Konocho (Marakwet),
Shiro (Luhya)
Whole plant
Herb
Decoction
Oral
Kenya
[61]
Roots
Herb
Decoction
Oral
ED
Aphrodisiac,
sterility (men)
Kenya
[23]
Sungasunga
Roots
Herb
Decoction
Oral
Aphrodisiac
Tanzania
[78]
Oral, a glass daily for
ED, aphrodisiac
3 days
Decoction of young Oral, 500 ml daily for
fowers as tea
2 days for ED
Evidence•Based Complementary and Alternative Medicine
Table 1: Continued.
7
Plant family
Part used
Habit
Preparation mode
Administration
Shoot
Herb
Decoction
Oral
Kayayana (Luganda)
Leaves,
roots
Shrub
Used directly,
decoction
Shiroho
Roots
Shrub
Balanites aegyptiaca Del
Ng’oswet (Marakwet)
Roots
Balsaminaceae
Impetiens species
Entungwa baishaija
(Runyankore)
Balsaminaceae
Impatiens tinctoria A.
Rich
Chemakalbayi
Asteraceae
Asteraceae
Asteraceae
Balanitaceae
Botanical name
Tagetes minuta L
Vernonia cinerea (L.) less
(or Cyanthillium
cinereum (L.) H. Rob.)
Vernonia lasiopus O
Hofn
Local name
Nyiramunukanabi
(Kinyarwanda)
8
Table 1: Continued.
Use
Increase
fertility, ED
Country
Kenya,
Rwanda
Reference
Oral
ED
Uganda
[65]
Decoction/infusion
Oral, infusion drunk
twice a day
Aphrodisiac
Kenya
[60]
Tree
Decoction
Oral
Increasing
fertility
(women)
Kenya
[66]
Whole plant
Herb
Used directly
(chew), decoction
Oral
ED
Uganda
[39, 65]
Roots
Herb
Decoction
Oral
Fertility
Kenya
[80]
Aphrodisiac
(men),
infertility
(women)
Kenya
[58, 59]
Decoction. Used
with U. acuminata
roots. For infertility, Oral, a glass (or twice
for infertility) daily
it is used with
for 5 days
Salvadora persica
and Uvaria
acuminate
[76, 79]
Markhamia zanzibarica
Mubwoka (Pokomo)
Roots
Tree
Bignoniaceae
Spathodea campanulata
Buch. •Harm. ex DC
Kifabakazi
Bark
Tree
Decoction
Oral
Infertility (men)
Uganda
[22]
Boraginaceae
Ehretia cymosa Tonn
Roots,
leaves
Shrub
Decoction
Oral
Aphrodisiac
Kenya
[23, 75]
Boraginaceae
Kigelia africana Lam
Morori (Marakwet),
Ponponat (Pokot),
Shekhutu (Luhya)
Sausage tree (English)
Fruits, seeds
Tree
Decoction
Aphrodisiac
Tanzania
[81]
Canellaceae
Warburgia ugandensis
Sprague
Mwiha (Runyaruguru), Bark, leaves,
Mugeta (Embu)
roots
Tree
Decoction
Oral
Oral in tea, 1
spoonful thrice daily
or in porridge; 250 ml
drunk
ED
Uganda,
Kenya
[27, 61, 65,
71]
Cannabaceae
Cannabis sativa L
Njayi, olusambya
(Luganda), Njaga
(Runyankore)
Leaves,
roots
Shrub
Used directly
(chew), decoction
Oral, inhaling fumes
(smoking)
ED
Uganda
[65, 72]
Capparaceae
Boscia coriaceae Pax
Kalkacha (Orma)
Roots
Shrub
Decoction with U.
leptacladon and C.
hereroense roots
Oral, half a glass daily
for 5 days
ED
Kenya
[59]
Capparaceae
Boscia solicifolia Oliv
Chelel (Marakwet)
Roots
Tree
Decoction
Oral
Increases
fertility (male
and female)
Kenya
[66]
Evidence•Based Complementary and Alternative Medicine
Bignoniaceae
Plant family
Capparaceae
Botanical name
Cadaba glandulosa
Forssk
Capparaceae
Cadaba farinose
Capparaceae
Capparis tomentosa Lam
Capparaceae
Cleome gynandra L
Local name
Part used
Habit
Preparation mode
Alakal (Orma)
Roots
Shrub
Decoction
Kumis (Orma)
Roots
Shrub
Decoction
Roots
Climber
Decoction
Leaves,
roots,
fowers
Herb
Used directly
(chew), decoction
Oral or as food
Kumbolwop kimaget
(Marakwet)
Esobyo/Amarera
(Runkonjo), Eshogi
(Runyankore)
Administration
Use
Oral, half a glass daily Infertility (men
for 5 days
and women)
Oral, half a glass daily Infertility (men
for 3 days
and women)
Increasing
Oral
fertility
Country
Reference
Kenya
[58, 59]
Kenya
[58, 59]
Kenya
[66]
ED, aphrodisiac
Uganda
[65, 82]
Oral, one cup is taken
before food twice
daily
Aphrodisiac
Kenya
[60]
Capparaceae
Cleome usambarica Pax
Not reported
Roots
Herb
Infusion. Mixed
with roots of
Macaranga
usambarensis
Capparaceae
Maerua triphylla A. Rich
Chokotwa (Marakwet),
Chokowa (Pokot),
Olamalogi (Massai)
Stem bark,
leaves
Tree
Infusion
Oral
Aphrodisiac
Kenya
[23, 28]
Celastraceae
Catha edulis Forsk
Mairungi (Runyankore)
Leaves,
stem
Shrub
Used directly
Oral (chewed)
ED
Uganda
[39, 65]
Celastraceae
Elaeodendron buchananii
Loes
Omuharanyi
Roots
Tree
Decoction or
powder used in
porridge
Oral
Aphrodisiac
Tanzania
[64]
Maytenus putterlickioides
(Loes.) Excell &
Mendonca
Maytenus senegalensis
(Lam.) Exell
Pristimera andogensis
var. volkensii (Loes.) N.
Hallé
Muthuthi
Roots
Shrub
Decoction
Oral
Aphrodisiac
Kenya
[60]
Omuwaiswa (Lusoga)
Roots
Shrub
Not specifed
Not specifed
Infertility
Uganda
[31]
Not reported
Roots
Climber
Infusion
Oral
Aphrodisiac
Kenya
[60]
Combretaceae
Combretum constrictum
(Benth.) Laws
Not reported
Roots
Climber
Decoction with salt
or used directly
Kenya
[60]
Combretaceae
Combretum hereroense
Schinz
Konkon (Orma)
Roots
Tree
Kenya
[59, 83]
Combretaceae
Combretum illairii Engl
Mshinda alume
(Pokomo)
Root bark
Tree
Kenya
[58, 59, 83]
Combretaceae
Combretum molle R. Br.
ex G. Don
Omurama
(Runyangkore)
Leaves
Tree
Uganda
[27]
Celastraceae
Celastraceae
Celastraceae
Oral, a cup drunk
twice a day; root
Aphrodisiac
chewed
Decoction. Used
Oral, a glass daily
ED, infertility
with U. leptacladon
until efective
Oral, a glass daily for
Decoction. Used
7 days (or 2•3 times ED, infertility
with Grewia tenax
daily for 14 days for (men & women)
for men
infertility in women)
Drink 500 ml (adult)
ED
Decoction
daily
Evidence•Based Complementary and Alternative Medicine
Table 1: Continued.
9
Plant family
Botanical name
Local name
Part used
Habit
Combretaceae
Combretum pentagonum
Laws
Not reported
Roots
Climber
Cucurbitaceae
Cucurbita maxima
Ocwica (Lango)
Leaves/
seeds
Herb
Leaves
Shrub
Decoction
Roots
Shrub
Roots
Qashin a’adha,
Muuqaadhi (Orma)
Roots
Mualikaji, Muyama
(Pokomo)
Mboga (Pokot)
Roots,
leaves
Roots
Olpopongi
Ebenaceae
Euphorbiaceae
Euphorbiaceae
Flueggea virosa (Roxb. Ex
Lukandwa/mukandula
Willb.) Voigt
Acalypha villicaulis
Kaisokampanga
Hochst. ex A. Rich
(Lusoga)
Clutia abyssinica Jaub &
Kapkurelwo
Spach
(Marakwet)
Croton dichagamus
Euphorbiaceae
Croton menyharthii Pax
Euphorbiaceae
Erythrococca fscheri Pax
Euphorbia candelabrum
Kotschy
Euphorbia tirucalli L
Euphorbiaceae
Euphorbiaceae
Euphorbiaceae
Flueggea virosa (Willd.)
Voigt
Euphorbiaceae
Euphorbiaceae
Euphorbiaceae
Ricinus communis L
Tragia benthamii Baker
Tragia brevipes Pax
Not reported
Omukarara
(Runyaruguru),
Omukalali (Rukonjo)
Omukaakale (Lusoga)
Kamyu (Luganda)
Engyenyi (Runyankore)
Euphorbiaceae
Tragia furialis Boj
Mgonampili
Preparation mode
Administration
Oral, a cup drunk
Decoction with salt
twice/thrice a day or
or used directly
root is chewed
Stew eaten or raw
Decoction/used
seeds chewed twice
directly
daily
Use
Country
Reference
Aphrodisiac
Kenya
[60]
Aphrodisiac
Uganda
[82]
Oral
Infertility in
women
Uganda
[22, 65]
Infusion
Oral
ED, aphrodisiac
Uganda,
Kenya
[31, 60, 65]
Shrub
Decoction
Oral
ED
Kenya
[84]
Tree
Decoction. Used
with Uvaria
leptocladon roots
Taken, half glass 3
times daily for 6 days
Infertility in
women
Kenya
[58]
Tree
Decoction
[58]
Decoction
Infertility in
women
Infertility
Kenya
Shrub
Oral, half glass 2•3
times daily for 5 days
Oral
Kenya
[23]
Roots
Tree
Not specifed
Not specifed
Infertility
Kenya
[70]
Juice
Tree
Not specifed
Not specifed
Aphrodisiac
Tanzania
[41]
Leaves,
roots
Shrub
Decoction
Oral
ED, infertility
Uganda
[22, 65]
Leaves
Roots
Leaves
Shrub
Herb
Herb
Not specifed
Oral
Oral
ED
ED
ED
Uganda
Uganda
Uganda
[31]
[71]
[65]
Roots
Climber
Not specifed
Decoction
Decoction
Decoction. Mixed
with Elaeodendron
buchanannii or
Spathodea
campanulata and
Carisa spinarum
Oral
Aphrodisiac
Tanzania
[64]
Evidence•Based Complementary and Alternative Medicine
Euphorbiaceae
10
Table 1: Continued.
Plant family
Botanical name
Fabaceae
Abrus precatorius
Fabaceae
Abrus schimperi Hochst.
Ex Benth
Fabaceae
Acacia brevispica Harms
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Acacia abysinica Hochst
ex.Benith
Acacia drepanolobium
Harms ex Sjöstedt
Local name
Part used
Roots,
Mudanda, muturituri,
Mudwadwa (Pokomo) leaves, seeds
Not reported
Kiptare (marakwet),
Kiptara (Pokot)
Munyinya
(Runyankore)
Eluai (Massai)
Ngobgwa (Marakwet),
Kopokwo (Pokot)
Leina (Marakwet),
Acacia refciens subsp.
Panyarit (Pokot),
Misera (Vatke) Brenan
Olchurrai (Massai)
Munyinya
Acacia sieberiana Scheele
(Runyankore,
Runyaruguru)
Afzelia africana Pers
Eiya (Lugbara)
Albizia coriaria Welw ex
Omusisa (Runyankore)
Oliver
Ebinyobwa
(Runyankore),
Arachis hypogaea L
Binyebwa (Rukonjo)
Acacia nilotica (L.) Delile
Habit
Shrub
Preparation mode
Used directly. Seed
powder taken or
with seed extract or
powder of Indigofera
cordifolia or stem
powder of Tinospora
cordifolia; root also
chewed
Administration
Use
Country
Reference
Oral
Aphrodisiac
Kenya,
Tanzania
[59, 60]
Roots
Shrub
Decoction
Oral
Aphrodisiac
Tanzania
[41]
Roots
Tree
Decoction
Oral
Aphrodisiac
Kenya
[23]
Bark
Tree
Decoction
Oral
ED
Uganda
[39]
Stem bark
Shrub
Not specifed
Not specifed
For fertility
Kenya
[28]
Leaves,
bark, roots
Tree
Decoction
Oral
Aphrodisiac
Kenya
[23]
Root/stem
bark
Tree
Decoction
Oral
Aphrodisiac
Kenya
[23, 67]
Bark
Tree
Decoction
Oral
ED
Uganda
[65]
Bark
Leaves,
stem
Tree
Decoction
Oral
Aphrodisiac
Uganda
[85]
Tree
Decoction
Oral
Aphrodisiac
Uganda
[39]
Herb
Used directly (eaten
raw or roasted)
Oral
ED
Uganda
[27, 65, 72]
Oral
Aphrodisiac
Kenya
[62]
Seeds
Fabaceae
Caesalpinia volkensii
Harms
Mucuthi, Muvuthi
(Embu), Mujuthi
(Meru)
Roots
Shrub
Used directly (eaten
raw or cooked),
taken with palm
wine
Fabaceae
Cajanus cajan (L.) Millsp
Entondiirwa
(Runyankore)
Leaves
Shrub
Decoction
Oral, drink 250 ml
ED
Uganda
[27]
Fabaceae
Cassia abbreviata
Mubaraka wa guba
(Pokomo)
Roots
Tree
Decoction with
Cissampelos
mucronata roots
Oral, a glass 3 times
daily for 4 days
ED
Kenya
[59]
Evidence•Based Complementary and Alternative Medicine
Table 1: Continued.
11
Plant family
Botanical name
Fabaceae
Cassia didymobotrya
Fresen
Fabaceae
Cassia occidentalis L
Fabaceae
Desmodium salicifolium
Poir. DC
Fabaceae
Fabaceae
Fabaceae
Dolichos compressus
Wilczec
Eriosema psoraleoides
G.Don. Lam
Entada abyssinica Steud.
ex A. Rich
Local name
Mugabagaba
(Runyankore), Mukyora
(Runyaruguru), Mucora
(Rukonjo)
Mwitanzoka
(Runyankore, Rukonjo)
12
Table 1: Continued.
Habit
Preparation mode
Administration
Use
Country
Reference
Leaves,
roots
Shrub
Used directly
(chew), decoction
Oral
ED
Uganda
[65]
Leaves,
roots
Herb
Oral
ED
Uganda
[65]
Mkongorana
Leaves,
roots
Shrub
Oral, a glass taken
daily
Aphrodisiac
Tanzania
[64]
Chebugaa
Roots
Herb
Decoction
Oral
Fertility
Kenya
[80]
Orutandaigwa
Leaves,
roots
Shrub
Decoction
Oral
Aphrodisiac
Tanzania
[64]
Stem, bark
Tree
Not specifed
Not specifed
Infertility
Kenya
[60]
Bark (stem
bark), roots,
stem
Tree
Decoction
Oral, eaten
Infertility (in
women)
Kenya,
Uganda
[22, 70, 86]
Bark
Tree
Decoction
Oral
ED
Uganda
[39, 65]
Herb
Decoction
Oral
ED
Uganda
[65]
Herb
Decoction (tea)
Decoction. Used
with Zanthoxylum
usamel root bark
Oral
Aphrodisiac
Uganda
[85]
Oral, one teaspoonful
daily for 5 days
Infertility in
women
Kenya
[58]
Used directly
(chew), decoction
Decoction. Mixed
with Elaeodendron
buchananii and
Tragia furialis
Fabaceae
Dichrostachys cinereal
(L.) Wight & Arn
Macrotyloma axillare
(E.Mey.) Verdc
Mucuna pruirens (L.) DC
Jjiirikiti (Luganda),
Omutembe (Kuria),
Muhuti (Kikuyu),
Oloponi
Muremanjojo
(Runyankore)
Akaihabukuru
(Runyaruguru)
Mukuna
Fabaceae
Prosopis julifora
Mathenge
Root bark
Tree
Not reported
Roots, stem
Tree
Not specifed
Not specifed
Aphrodisiac
Kenya
[87]
Not reported
Stem bark,
roots
Tree
Decoction
Oral
Aphrodisiac
Tanzania
[41, 60]
Not reported
Roots
Tree
Decoction
Oral
Aphrodisiac
Tanzania
[41]
Bojo (Lango)
Ekalepulepu (Ateso)
Leaves
Roots
Herb
Herb
Decoction (stewed)
Decoction
Oral
Oral
Aphrodisiac
ED
Uganda
Uganda
[82]
[88]
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Flacourtiaceae
Erythrina abyssinica Lam.
Ex DC
Senegalia brevispica
(Harms) Seigler &
Ebinger
Vachellia nilotica (L.) P. J.
H. Hurter & Mabb
Vachellia sieberiana
(DC.) Kyal. & Boatwr var.
vermoesenii (De Wild.)
Keay & Brenan
Vigna unguiculata
Ocoba spinosa Forssk
Leaves,
roots
Seeds
Evidence•Based Complementary and Alternative Medicine
Part used
Plant family
Flacourtiaceae
Botanical name
Xylotheca tettensis
(Klotzsch) Gilg
Local name
Part used
Habit
Preparation mode
Decoction or used
directly
Not reported
Roots
Shrub
Not reported
Not
specifed
Herb
Decoction
Roots,
leaves
Shrub
Decoction
Leaves
Shrub
Roots
Shrub
Administration
Use
Country
Reference
Oral, taken or chewed
Aphrodisiac
Kenya
[60]
Kenya
[89]
Kenya
[23, 58, 59]
ED
Uganda
[27]
ED
Kenya
[59]
Fertility
Kenya
[80]
Genital
stimulant/
depressant
Aphrodisiac,
Oral, a glass 2•3 times
infertility (men
daily for 14 days
and women)
Lamiaceae
Becium obovatum (E.
Mey. Ex. Benth) N. E. Br
Lamiaceae
Hoslundia opposita Vahl
Lamiaceae
Ocimum suave Wild
Lamiaceae
Plectranthus barbatus
Andrews
Papaha (Pokomo),
Kan’gurwet (Markwet)
Loganiaceae
Buddleia polystachya Fres
Roots
Herb
Lythraceae
Punica granatum L
Seeds
Shrub
Decoction
Oral
ED, infertility
Kenya
[61, 62]
Malvaceae
Adansonia digitata L
Chorwet
Mukungumanga
(Embu, mbeere),
Kukumanga (Meru)
Muramba (Embu),
Mbamburi (Swahili)
Bark
Tree
Decoction
Oral
ED
Kenya
[61]
Malvaceae
Dombeya burgessiae
Gerrard ex Harv
Mukusa (Luhya)
Bark
Tree
Oral
Aphrodisiac
Kenya
[23]
Malvaceae
Hibiscus fuscus Garcke
Oral
Aphrodisiac
Kenya
[23]
Malvaceae
Sida tenuicarpa Vollesen
Ekebergia capensis
Sparrm
Oral
ED
Uganda
[65]
Oral
ED
Uganda
[69]
Kenya
[23]
Meliaceae
Simbaywa (Pokot),
Shikuma (Luhya),
Mtserere (Giriama)
Omujaaja
(Runyangkore)
Cheptelia (Marakwet),
Pkapuyan (Pokot)
Keyeyo (Rukonjo)
Roots
Herb
Leaves
Herb
Cape ash (English)
Stem bark
Tree
Decoction
Tree
Decoction (roots),
used directly (leaves,
branches and bark)
Oral
Aphrodisiac,
infertility
(women and
men)
Tree
Used directly
(exudate used)
Oral
Aphrodisiac
Tanzania
[41]
Melianthaceae
Kipset (Marakwet)
Melianthaceae
Xylocarpus benadirensis
Mattei
Not reported
Moraceae
Artocarpus integer
(Tunb.) Merr
Decoction with rock
Oral, drink 500 ml
salt
Decoction. Used
Oral, half glass daily
with C. rotundifolia
for 30 days
for frst 4 days
Decoction
Oral
Used directly
(chewed)
Used directly
(chewed)
Decoction
Bersama abyssinica
Fresen
Cissampelos micronata A.
Menispermaceae
Rich
Oral
Roots,
leaves,
branches,
bark
Unripe
fruits
Chovi, kivila kya mani
(Pokomo),
kashikiropaka
(Giriama)
Roots
Herb
Decoction. Used
with C. abbreviate
Oral, half glass daily
for 3 days
Aphrodisiac,
infertility,
azoospermia
Kenya
[59]
Fenensi (Runyangkore)
Seeds
Tree
Decoction
Oral, taken as tea
ED
Uganda
[27]
Evidence•Based Complementary and Alternative Medicine
Table 1: Continued.
13
Plant family
Botanical name
Local name
Part used
Habit
Preparation mode
Moraceae
Ficus natalensis Hochst
Ekitooma
(Runyangkore)
Roots, root
bark
Tree
Decoction
Moraceae
Morus mesozygia Stapf
Not reported
Roots
Tree
Moringaceae
Moringa oleifera Lam
Moringa (English)
Seeds,
leaves
Mujeje (Runyankore)
Roots, bark
Myricaceae
Myrtaceae
Olacaceae
Myrica salicifolia Hochst.
ex A.Rich
Syzygium guineense
(Willd.) DC
Capparis sepiaria var.
cafra
Lamaiwo (Marakwet),
Leaves, bark
Cheptimanwa (Pokot)
Hamwalika (Pokomo),
Mugwada paka
Root bark
(Giriama)
Administration
Oral, drunk 250 ml
daily or 100 ml thrice
daily (fresh root bark)
Use
Country
Reference
ED
Uganda
[27]
Decoction in cow/
goat milk
Oral
Aphrodisiac
Kenya
[60]
Tree
Decoction, teas,
food condiment
Oral; seed powder as
tea; eat leaves as
sauce; drink 100 ml
ED
Uganda
[27]
Shrub
Decoction
Oral
ED
Uganda
[65]
Oral
Aphrodisiac,
infertility
Kenya
[23, 60]
Oral, half glass daily
for 10 days
Aphrodisiac
Kenya
[59]
Tree
Shrub
Used directly (sap
used)
Decoction. used
with Grewia
plagiophylla
Mujoka (Pokomo)
Roots/stem
Climber
Decoction
Not reported
Muhoko (Runyankore),
Ruhuko (Rukonjo)
Leaves
Roots,
leaves
Herb
Not specifed
Shrub
Used directly
Piper umbellatum L
Not reported
Roots
Climber
Plumbaginaceae
Plumbago zeylanica L
Not reported
Roots
Shrub
Polygalaceae
Polygala aphrodisiaca
Gürke
Not reported
Roots
Herb
Pedaliaceae
Phytolaccaceae
Piperaceae
Polygalaceae
Polygalaceae
Polygonaceae
Polygonaceae
Polygonaceae
Polygonaceae
Polygala sphenoptera
Not reported
Roots
Fresen
Securidaca
Omukondwa (Luganda) Leaves, bark
longipedunculata Fres
Cofea species
Mwani (Runyankore)
Seeds
Hallea rubrostipulata (K.
Muziiko (Runyankore) Bark, roots
Schum.) J. F. Leroy
Mufumbagyesi
Leaves,
(Runyankore),
Rumex abyssinicus Jacq
stem
Kasekekambaju
(Luganda)
Rumex usambarensis
Kaseke kambajjo
Leaves
(Dammer) Dammer
(Luganda)
Oral, half glass daily
for 3 days
Not specifed
Smear on ripe banana
and roast
Decoction with
Oral, one cup taken
Aframomum roots
daily
and strained
Decoction
Oral
Decoction, i.e.,
cooked with a young Oral, eaten in food
cock
Infertility in
women
Aphrodisiac
Kenya
[58]
Kenya
[41]
ED
Uganda
[65]
Aphrodisiac
Kenya
[60]
ED
Uganda
[70]
Aphrodisiac
Tanzania
[41]
Herb
Infusion
Oral
Aphrodisiac
Kenya,
Tanzania
[23, 41, 60]
Tree
Decoction
Oral
ED
Uganda
[72]
Shrub
Roasted and chewed
Oral as a beverage
ED
Uganda
[65]
Tree
Decoction
Oral
ED
Uganda
[65]
Shrub
Used directly
(chewed)
Oral
ED
Uganda
[65]
Herb
Decoction
Oral
Aphrodisiac
Uganda
[61]
Evidence•Based Complementary and Alternative Medicine
Adenia gummifera
(Harv.) Harms
Sesamum indicum L
Phytolacca dodecandra
L’Her
Passiforaceae
14
Table 1: Continued.
Plant family
Polygonaceae
Pteridaceae
Ranunculaceae
Rhamnaceae
Rubiaceae
Rubiaceae
Rubiaceae
Rubiaceae
Rubiaceae
Rubiaceae
Rubiaceae
Rubiaceae
Botanical name
Tarenna graveolens (S.
Moore) Bremek
Actinopteris
semifabellata Pic. Serm
Clematis hirsuta Guill. &
Perr
Berchemia discolor
(Klotsch) Hemsl
Cofea arabica L
Cofea canephora Pierre
ex A. Froehner
(synonym: Cofea
robusta)
Craterispermum
schweinfurthii Hiern
Heinsia crinite
Molinda citrifolia Benth
Psychotria capensis subsp.
riparia (K. Schum. & K.
Krause) Verdc
Psychotria cyathicalyx
E.M. A. Petit
Psychotria lauracea (K.
Schum.) E. M. A. Petit
Local name
Munyamazi (Rukonjo,
Runyaruguru)
Part used
Leaves,
roots, bark
Mwii wa ivia (Kikamba) Whole plant
Habit
Preparation mode
Administration
Use
Country
Uganda,
Kenya
Reference
Shrub
Decoction
Oral
ED, aphrodisiac
Herb
Infusion
Oral
Infertility in
women
Kenya
[77]
[65, 92]
Omunkaamba
(Runyagkore)
Leaves
Vine
Decoction
Oral
ED
Uganda
[27]
Muchukwo (Marakwet)
Roots
Tree
Decoction
Oral
ED
Kenya
[84]
Mwani (Runyankore)
Seeds
Shrub
Oral as a beverage
ED
Uganda
[39, 65]
Oral
ED, aphrodisiac
Uganda,
Kenya
[27, 60, 72]
Oral
Aphrodisiac
Kenya
[60]
Not specifed
Oral
ED
ED
DRC
Uganda
[93]
[39]
Not reported
Roots
Shrub
Not reported
Muziiko (Runyankore)
Stem bark
Roots
Shrub
Tree
Roasted and chewed
Decoction of leaves
and fruits, used
directly (chew seeds)
or cook with food
Decoction, used
directly (chew)
Not specifed
Decoction
Not reported
Roots
Shrub
Infusion/decoction
Oral
Aphrodisiac
Kenya
[60]
Not reported
Roots
Shrub
Decoction
Oral
Aphrodisiac
Kenya
[60]
Not reported
Roots
Shrub
Decoction
Oral
Aphrodisiac
Kenya
[60]
Roots
Shrub
Decoction
Oral
ED, infertility
Kenya
[23]
Roots, bark
Tree
Uganda
[39, 61, 65]
Kenya
[58]
Leaves,
Omwaani (Runyankore) fruits, seeds,
roots
Shrub
Rubiaceae
Vangueria infausta Burch
Rutaceae
Citropsis articulata
Swingle & Kellerman
Tabirirwo (Marakwet),
Komolwo (Pokot)
Katimbolo (Luganda),
Muboro (Runyankore)
Rutaceae
Citrus sinensis (L) Osbeck
Mudimu (Giriama)
Roots/stem
bark
Tree
Rutaceae
Fagaropsis hildebrandtii
(Engl.) Milne•Redh
Muvindavindi (Kamba)
Leaves
Shrub
Decoction
Oral
Infertility
Kenya
[94]
Salicaceae
Flacourtia indica
(Burm.f.) Merr
Roots
Tree
Decoction
Oral
Infertility
Kenya
[23]
Roots
Shrub
Decoction
Kenya
[58, 59]
Sapindaceae
Allophylus pervilleria
(A.Rich) Engl
Tungururwo
(Marakwet), Tingoswa
(Pokot)
Mnyanga kitswa
(Pokomo)
Decoction, used
Oral as a beverage in
ED, aphrodisiac
directly (chew)
tea
Decoction. Mixed
Infertility in
with Acacia robusta Oral, a glass 3 times
daily for 3 days
women
and Cissus
rotundifolia roots
Oral, a glass daily for Infertility (men
7 days
and women)
Evidence•Based Complementary and Alternative Medicine
Table 1: Continued.
15
Plant family
Sapindaceae
Sapindaceae
Solanaceae
Solanaceae
Solanaceae
Sterculiaceae
Sterculiaceae
Stilbaceae
Tiliaceae
Tiliaceae
Urticaceae
Verbenaceae
Local name
Part used
Habit
Preparation mode
Administration
Use
Country
Reference
Akambula (Lusoga)
Leaves
Climber
Not specifed
Not specifed
Infertility
Uganda
[31]
Oltimigomi (Massai)
Bark
Tree
Decoction
Oral
Aphrodisiac
Kenya,
Tanzania
[28, 41, 70]
Herb
Used directly
(chew), decoction
Orally in food
ED
Uganda
[65, 72]
Herb
Used directly (chew)
Oral
ED
Kenya
[23]
Herb
Decoction
ED
Kenya
[61]
ED
Uganda
[65]
ED
Kenya
[84]
Aphrodisiac
Tanzania
[78]
Aphrodisiac
Kenya
[59]
Kamurari (Luganda),
Fruits,
Eshenda (Runyankore) leaves, bark
Labotwa (Marakwet),
Solanum incanum L
Lopotwo (Pokot),
Roots
Maduranzura (Luhya)
Solanum nigrum L
Managu (Embu)
Whole plant
Cola acuminata Schott & Engongoli (Rukonjo,
Fruits
Endl
Runyaruguru)
Sterculia africana (Lou.r)
Ililwo (Marakwet)
Seeds
Fior
Nuxia foribunda Benth
Mngogo
Roots
Grewia plagiophylla. K.
Mkoi (Pokomo)
Root bark
Schum
Mukarara
Leaves, bark
Grewia similis K. Schum
(Runyaruguru)
Deeka (Orma),
Grewia tenax (forssk.)
Mubavubavu, mukawa Root bark
Fiori
wa guba (Pokomo)
Whole
Urtica massaica Mildbr Engyenyi (Runyankore)
plant, roots
Roots, root
Clerodendrum myricoides
Munjuga iria
bark
(Hocst.) Vatke
Capsicum frutescens L
Tree
Tree
Tree
Shrub
Oral
Oral in tea, porridge,
Roasted and chewed
milk
Used directly
Oral
(chewed)
Decoction
Oral
Decoction. Used Oral, a glass daily for
with C. sepiaria
10 days
Shrub
Decoction
Oral
ED
Uganda
[65]
Shrub
Decoction. Used
with Combretum
illairii
Oral, a glass daily for
7 days
ED,
aphrodisiac,
infertility
Kenya
[58, 59]
Herb
Decoction
Oral
ED, aphrodisiac
Uganda,
Kenya
[65, 76]
Shrub
Decoction
Oral
Aphrodisiac
Kenya
[41, 76]
Kenya,
Tanzania
[59, 66]
Decoction.
Oral, a glass daily for ED, increasing
Sometimes used
7 days
female fertility
with P. barbatus for
the frst 4 days
Cissus rotundifolia
(forsk.)
Mkwembe, Maneke,
Neke (Pokomo), Arma
(Orma)
Roots
Tree
Cyphostemma adenocaule
(Steud.ex. A. Rich)
Desc.ex. Wild & R. B.
Drumm
Akabombo akatono
Bark
Herb
Decoction
Oral
ED
Uganda
[71]
Zingiberaceae
Zingiber ofcinale Roscoe
Ntangahuzi
(Runyankore)
Rhizome
Herb
Decoction
Oral in tea, milk,
porridge
ED
Uganda
[65, 72]
Zygophylaceae
Tribulus terrestris L
Kilesan (Marakwet)
Whole plant
Herb
Used directly
(chewed)
Oral
ED
Kenya
[84]
Vitaceae
Note. ED: erectile dysfunction; languages: Luganda, Lusoga, Lango, Rukonjo, and Runyankore are spoken in Uganda; Marakwet, Luhya, Nandi, Kikamba, Pokot, Orma, Wanga, Pokomo, Massai, Giriama, and
Swahili are spoken in Kenya and Kinyarwanda in Rwanda.
Evidence•Based Complementary and Alternative Medicine
Tiliaceae
Botanical name
Cardiospermum
halicacabum L
Pappea capensis Eckl. &
Zeyh. var. radlkoferi
Schinz
16
Table 1: Continued.
30
17
29
25
20
9
8
5
5
5
Polygonaceae
9
Combretaceae
10
10
Celastraceae
12
15
Capparaceae
Rubiaceae
Apocynaceae
Asteraceae
0
Euphorbiaceae
5
Fabaceae
Number of species reported
Evidence•Based Complementary and Alternative Medicine
Family
Figure 2: Major botanical families from which remedies used for treating sexual dysfunction and infertility and improving virility are
obtained in the EAC.
may also be used directly, i.e., chewed raw (16%) or prepared
as an infusion (5%) and taken (Figure 5). Te remedies are
administered orally, either by taking decoctions, infusions,
and eating or chewing. Only one study reported inhalation
of fumes from Cannabis sativa leaves for treatment of ED in
Uganda [65]. Aloe volkensii (leaf decoction) in Kenya when
utilized for treating infertility is used as a wash for genitals
[58], hinting that internally mediated fertility efects would
be unlikely when such herbal remedies are administered
orally. While most of the plants had their method of
preparation and routes of administration indicated in the
use reports, up to 8% of the species identifed did not have
specifcations of the method of preparation and adminis•
tration of the herbal remedies.
3.4. Bioactivity and Phytochemistry of the Reported Plants.
To decipher the therapeutic mechanisms and compounds
responsible for the bioactivities of the plants reported in
EAC, a holistic review of their bioactivity related to the
traditional claims and phytochemistry was undertaken.
However, only fve reports on bioactivity from EAC were
encountered for seven plants reported in this study. In this
context, the aqueous extract of Citropsis articulata root bark
was reported to increase the in vivo levels of serum tes•
tosterone and mounting frequency in male rats [66, 67].
Joseph et al. [68] found that aqueous extract of Cola acu•
minata (fruits) and Zingiber ofcinale (rhizome) had no
signifcant efect on mounting frequency and testosterone
levels in rats. Aqueous extract of Tarenna graveolens roots
increased testosterone levels but had no signifcant efect on
mounting frequency while aqueous extract of Urtica mas•
saica leaves elicited no appreciable increase in mounting
frequency and testosterone levels in male rats [68]. Other
reports were for ethanolic stem bark extract of Ekebergia
capensis which alleviated sexual dysfunction by increasing
the mounting frequency and testosterone levels of male rats
to 2.38 ± 0.02 ng/ml, 7.68 ± 0.66, and 14.5 ± 0.777 ng/mL at
doses of 300, 400, and 500 mg/kg, respectively [69]. Te latest
report is on Plumbago zeylanica, whose aqueous root extract
administered at 150, 300, and 450 mg/kg was found to elicit
prosexual stimulatory efects in male rats [70]. Tough some
of these reports supported the traditional use of the me•
dicinal plants, most studies performed preliminary phyto•
chemical screening only but not isolation and structural
elucidation of the responsible bioactive compounds. Ndukui
et al. [69], for example, found saponins and steroid glyco•
sides as the major secondary metabolites in Ekebergia
capensis stem bark. Traces of tannins, anthraquinones, al•
kaloids, carotenoids, favonoids, and anthracyanosides were
also detected. Some of these secondary metabolites (tannins,
phlobatannins, glycosides, phenols, saponins, quinones,
terpenoids, and steroids) were also detected in Plumbago
zeylanica [70]. It is worth noting that none of these studies
probed into the mechanism of action of the extracts.
We, therefore, performed further searches and retrieved
other 9 species (along with Zingiber ofcinale) cited in the
EAC that have been explored for their phytochemical
profles as well as aphrodisiac, procopulatory, and fertility
efects (Table 3). One of the most studied plants in this
context is Allium cepa (A. cepa) which is locally used in
culinary recipes. It has been reported to improve copulatory
behaviour in sexually experienced rats [71]. Malviya et al.
[72] indicated that ethyl acetate fraction of A. cepa bulb at
200 mg/kg restored the mating behaviour (ejaculatory la•
tency, postejaculatory interval, mount, intromission, and
ejaculatory frequencies and mount and intromission la•
tencies) of drug•mediated sexually dysfunctional male rats.
18
Table 2: Synopsis of the most used plant species for the treatment of infertility among men and women in the East African Community.
Medicinal plant
Parts used
Mode of
preparation
Decoction
Decoction with roots of Salvadora persica
and Uvaria acuminata
Mode of
administration
Oral, half glass thrice daily for 3 days
Group treated
(country)
Women (Kenya)
Oral
Women (Kenya)
[58, 59]
References
Roots
Markhamia zanzibarica
Roots
Spathodea campanulata Buch.•
Harm. ex DC
Mangifera indica L
Flueggea virosa (Roxb. Ex
Willb.) Voigt
Bark
Decoction
Oral
Men (Uganda)
[22]
Bark
Decoction drunk
Oral
Women (Uganda)
[22]
Leaves
Decoction drunk
Oral
Women (Uganda)
[22, 65]
Bark (stem bark),
roots, stem
Decoction, eaten directly
Cadaba glandulosa Forssk
Roots
Decoction
Cadaba farinose
Roots
Decoction
Combretum illairii Engl
Root bark
Decoction used with Grewia tenax for
men
Hoslundia opposita Vahl
Leaves
Decoction
Allophylus pervilleria (A. Rich)
Engl
Roots
Decoction
Erythrina abyssinica Lam. Ex
[58, 59]
Women (Uganda,
[22, 70, 86]
Kenya)
Women and men
[58, 59]
Oral, half a glass daily for 5 days
(Kenya)
Women and men
[58, 59]
Oral, half a glass daily for 3 days
(Kenya)
Oral, a glass daily for 7 days (or 2•3 times daily for Women and men
[58, 59, 83]
14 days for infertility in women)
(Kenya)
Women and men
[58, 59]
Oral, a glass 2•3 times daily for 14 days
(Kenya)
Women and men
[58, 59]
Oral, a glass daily for 7 days
(Kenya)
Oral
Evidence•Based Complementary and Alternative Medicine
Uvaria leptocladon
Evidence•Based Complementary and Alternative Medicine
19
Climber (vine)
8%
Herb
26%
Shrub
35%
Tree
31%
Figure 3: Life form of plants used for the preparation of remedies used in the treatment of erectile dysfunction and infertility, and increasing
fertility and virility in the EAC.
120
105
Frequency of use
100
80
60
51
39
40
20
0
11
Roots
Leaves Bark (stem
and root)
Seeds
10
Whole
plant/shoot
9
Stem
5
Fruits
2
1
Flowers Branches
Plant part
Figure 4: Plant organs used in herbal preparations for treating erectile dysfunction and infertility, and enhancing fertility and virility in the
EAC.
Quercetin (1) (Figure 6), a favonoid present in extracts of A.
cepa, enhanced sperm motility through the regulation of
protein kinase C•mediated activation of the human voltage•
gated proton channel and could explain its therapeutic efect
when used in the treatment of human infertility [14].
Similarly, S•allyl cysteine (2) isolated from Allium sativum
restored erectile function in diabetic rats through inhibiting
reactive oxygen species formation via modulation of nico•
tinamide adenine dinucleotide phosphate oxidase subunit
expression in penile tissues [73].
Te third highly investigated species is Mondia whitei. It
has been found to increase sexual arousal and copulatory
efciency and improve sexual sensation in rats [74–78]. A
follow•up study with a polyherbal formulation containing
Mondia whitei, Dracaena arborea, and Bridelia ferruginea
deduced that the administration of the formula enhanced
the sexual performances and increased the mounting and
intromission frequencies of normal rats and prediabetic
rats [79].
Zingiber ofcinale (ginger) is the most thoroughly
studied plant cited in this report. A bioactive compound
from this species (zingerone, 5) attenuated zearalenone•
induced steroidogenesis impairment in TM3 Leydig cell
lines [80] and elicited dose•dependent enhancement of
fertility in male and female rats as witnessed by increments
in gonadal weights and sperm counts [81]. A gingerol (6)•
rich fraction of ginger at 50, 100, and 200 mg/kg when
administered to male rats with carbendazim•induced tox•
icity led to increased sperm motility and count but atten•
uated sperm abnormality [82].
20
Evidence•Based Complementary and Alternative Medicine
Infusion
5%
Used directly
16%
Not specified
8%
Decoction
69%
Roasted and chewed
2%
Figure 5: Methods of preparation of herbal remedies used in the treatment of erectile dysfunction and infertility, and enhancing fertility and
virility in the EAC.
Herbal extracts from plants such as Allium cepa, Allium
sativum, Mondia whitei, and Zingiber ofcinale improve
semen quality and sperm parameters such as concentration,
viability, motility, morphology, and DNA integrity through
increment in gonadal hormone levels (testosterone and
luteinising hormone), sequestering free radicals and en•
hanced production of nitric oxide [83–85]. Such studies
substantiate that the traditional claims of using the plants in
the treatment of sexual dysfunction in EAC may be credible.
Te contraceptive efect observed in plants such as Catha
edulis (cathinone) and Cannabis sativa seed extracts is
supported by studies which instead link their use to ED [86].
Nevertheless, plant extracts from certain families have been
shown to elicit contradictory efects in fertility studies. Such
diferential bioactivities are species•specifc and may depend
on the extraction method and solvents employed [87, 88].
3.5. Clinical Studies. Clinical evaluation of herbal products is
a requirement before they are promoted and used. In this
study, we did not fnd any clinical studies in EAC that was
performed on the extracts or isolated compounds from the
cited plants. Further searches for global reports indicated
that Zingiber ofcinale is the only plant encountered in this
study that have been subjected to clinical studies in•
vestigating its efect on male ED, female sexual function, and
infertility [89]. For example, its capsules improved the sexual
function and quality of life in four weeks of a randomized,
double•blind clinical trial involving women of reproductive
age (n � 190) [90]. Another randomized double•blind
placebo•controlled trial found that 3•month oral treat•
ment using 500 mg/powder/day reduced sperm DNA
fragmentation in infertile men [91]. Such promising clinical
results demonstrate the need for more clinical trials on
species such as Mondia whitei, Acalypha villicaulis,
Combretum illairii, Erythrina abyssinica, Pappea capensis,
Rhus vulgaris, and Warburgia ugandensis that are widely
used in the region.
3.6. Adverse Side Efects and Toxicity of Medicinal Plants and
Bioactive Phytochemicals Reported. Further analysis of re•
ports considered in this systematic review showed that no
ethnobotanical survey captured the side efects of herbal
preparations used in the management of sexual dysfunction,
infertility, and improving virility in the EAC. However, some
of the plants such as Abrus precatorius (roots, leaves, and
seeds) cited in the EAC are known to contain highly poi•
sonous compounds (abrine, precatorine, and hypaphorine)
[139]. It could be positioned that the preparation of remedies
with more than one plant and plant part or with the addition
of adjuvants may be a way of masking the toxicity of the
medicinal plants [36, 93].
From available toxicological studies, extracts from six of
the investigated bioactive species have been shown to be safe
(Table 4). Four species (Abrus precatorius, Catha edulis,
Cannabis sativa, and Parquetina nigrescens) have been in•
dicated to elicit marked toxicity, indicating that their use
may lead to adverse reactions in herbal medicine practice.
For bioactive compounds identifed in the listed species
(Table 3), quercetin (1) is potentially cytotoxic and hepa•
totoxic at higher doses (100 to 2,000 mg/kg) [94, 95]. Sim•
ilarly, cathinone (3) is a psychoactive compound that is toxic
to sperm cells [96], and its abuse has been associated with
fatal renal, hepatic, and cardiac injuries [97]. On the other
hand, S•allyl cysteine (2) is considered to be safe, with very
minor acute/subacute toxicity in mice and rats
(LD50 > 54.7 mM/kg) when administered intraperitoneally
[98]. Sesamine (4) is the major lignan in sesame seeds and
has been confrmed to be safe. It attenuated reactive oxygen
Plant
Part used
Extract
Abrus precatorius
Seeds
Methanol
Allium cepa L
Bulb
Aqueous, ethyl acetate
Allium sativum L
Bulb
Aqueous, petroleum ether
Cannabis sativa
Seeds
Ethanol
Shoots, small branches
Chloroform: diethyl ether extract (1 : 3)
Kigelia africana
Fruits
Powder used directly
Mondia whitei
Root bark, roots
Aqueous, hexane
Parquetina nigrescens
Leaves
Aqueous
Sesamum indicum
Seeds
Ethanol
Zingiber ofcinale
Rhizome
Catha edulis Forsk
Bioactivity/mechanism of action
and active phytoconstituents
Antifertility efect in rats [101].
Enhanced copulatory behaviour in male rats [71, 106]. Ethyl acetate fraction of
extract at 200 mg/kg restored the mating behaviour of drug•mediated sexually
dysfunction male rats [72].
Quercetin (1) isolated from the plant•enhanced sperm motility [14].
Increased weight of seminal vesicles and epididymides in male rats [72, 106–108].
S•allyl cysteine (2) isolated from this species•promoted fertility [73].
Reduced epididymal sperm count in rats (contraceptive efect) [87, 88, 103].
Improvement of sexual behaviour and increase in plasma testosterone levels
[112–114]. Cathinone (3) is toxic to sperm cells [96].
Increase sperm count, motility, and fertilization ability in African catfsh increase in
testicular weight, body weight, testosterone levels, and follicle•stimulating hormone
[116, 117].
Increased sexual arousal, copulatory efciency, sexual sensation [74–78] through
the activation/stimulation of nitric oxide synthase activity resulting in the elevation
of levels of cyclic guanosine monophosphate [83].
Te extracts improved sexual activity, behaviour, and competence through
improving sexual hormone secretion [102, 125].
It promotes body weight gain, seminal parameters, antioxidant action, and
testosterone level [126]. Sesamin (4), a compound in this species, resisted
cyclophosphamide•induced sperm nuclear maturity and DNA damage by
increasing the expression levels of histones H2A and H2B in the testis [127].
Powder at 100 mg has been cited to elicit positive efects in folliculogenesis and
implantation [128]. Zingerone (5) isolated from the plant extract normalized
zearalenone•impaired steroidogenesis in TM3 cells [80]. Similarly, a gingerol
(6)•rich fraction of ginger enhanced sperm motility and count but attenuated sperm
abnormality in male rats with carbendazim•induced toxicity [82].
Evidence•Based Complementary and Alternative Medicine
Table 3: Bioactivity and phytochemical profle of some plants used in the treatment of ED and infertility, and enhancing virility and fertility in EAC.
21
22
Evidence•Based Complementary and Alternative Medicine
O
OH
HO
O
O
H2N
OH
S
OH
OH
OH
NH2
O
(1)
(3)
(2)
O
O
O
H
O
O
O
HO
O
H
O
(4)
(5)
O
OH
O
HO
(6)
Figure 6: Some of the bioactive molecules characterized from extracts of plants reported in EAC for treatment of ED and infertility, and
enhancing fertility and virility (based on studies outside the region). Te numbers 1 to 6 refer to the molecules mentioned in Table 3.
Table 4: Toxicity profle of plants with reports of efcacy that is used in the treatment of ED and infertility, and enhancing virility and
fertility in EAC.
Plants
Abrus precatorius
Allium cepa L
Allium sativum L
Cannabis sativa
Catha edulis Forsk
Kigelia africana
Mondia whitei
Parquetina nigrescens
Sesamum indicum
Zingiber ofcinale
Toxicity reports
Seeds contain abrin, a toxalbumin with a human lethal dose of 0.1–1 μg/kg [148].
Poisoning is characterized by severe vomiting and abdominal pain, bloody
diarrhoea, convulsions, and alteration of sensorium with depression of central
nervous system [149].
Oral administration of extracts to mice at 250 and 500 mg/kg/day for 30–90 days
had no visible toxicity symptoms. An oral dose of 30 g/kg/day for 30 days resulted
into hypothermia, tachypnea, tachycardia, piloerection, and polyuria in the treated
mice [150].
Its bulb extract induced mild alterations at 300 mg/kg in mice, indicating that it is
relatively safe [151].
Cannabidiol (a major nonpsychotropic constituent of this species) in extracts of this
species is potentially toxic through the inhibition of hepatic drug metabolism,
alterations of in vitro cell viability, reduced fertilization capacity, and decreased
activities of p•glycoprotein and other drug transporters [152].
Crude khat can damage the liver and kidneys and modulate levels of liver enzymes,
urea, creatinine, and electrolytes essential for liver and kidney functions [153].
Low to moderately toxic [154].
Low toxicity in mice exposed to the extract for 90 days [155].
Toxic to rats at 100 and 300 mg/kg of methanol leaf and aerial part extract. Renal
haemorrhage, infammation, and hepatic infammation were noted [156].
Ethanolic extract had low toxicity at 500 mg/kg body weight [157].
Extract had no toxicity at 5,000 mg/kg body weight [158].
Evidence•Based Complementary and Alternative Medicine
species and nitric oxide production in zebra fsh (LD50) [99].
Toxicity studies with zingerone (5) and gingerol (6) have
shown that they are safe [100, 104].
4. Conclusion
Te EAC has a rich ethnobotanical knowledge of herbal
remedies for the management of sexual dysfunction and
infertility, and improving fertility and virility. Tough we
retrieved 171 medicinal plants being used, most of the
species have not been subjected to phytochemical and
bioactivity studies that lend credence to traditional claims of
using them. We recommend performing toxicity studies and
clinical trials using compounds isolated from some of the
investigated species. Five highly cited unstudied species from
this review (Acalypha villicaulis, Combretum illairii,
Erythrina abyssinica, Pappea capensis, Rhus vulgaris, and
Warburgia ugandensis) have been selected for further in•
vestigation of their phytochemistry, aphrodisiac, fertility,
and phosphodiesterase•5 inhibitory activities.
Data Availability
Tis is a systematic review article, and no raw experimental
data were collected. All data generated or analyzed during
this study are included in this article.
Conflicts of Interest
Te authors declare that there are no conficts of interest.
Supplementary Materials
Supplementary fle 1: PRISMA 2020 checklist for the sys•
tematic review of medicinal plants used in the management
of sexual dysfunction and infertility, and improving virility
in the East African Community. Supplementary fle 2: Risk
of bias assessment of studies included for systematic review
on medicinal plants used in the management of sexual
dysfunction and infertility, and improving virility in the East
African Community. (Supplementary Materials)
References
[1] B. Y. F. Fong and V. T. S. Law, Sustainable Development Goal
3: Health and Well•Being of Ageing in Hong Kong, Taylor &
Francis, New York, NY, USA, 2022.
[2] T. Vos, R. M. Barber, B. Bell et al., “Global, regional, and
national incidence, prevalence, and years lived with disability
for 301 acute and chronic diseases and injuries in 188
countries, 1990–2013: a systematic analysis for the Global
Burden of Disease Study 2013,” Te ancet, vol. 386,
no. 9995, pp. 743–800, 2015.
[3] C. Hajat and E. Stein, “Te global burden of multiple chronic
conditions: a narrative review,” Preventive Medicine Reports,
vol. 12, pp. 284–293, 2018.
[4] H. Wang, M. Naghavi, C. Allen et al., “‘Global, regional, and
national life expectancy, all•cause mortality, and cause•
specifc mortality for 249 causes of death, 1980–2015:
a systematic analysis for the Global Burden of Disease Study
2015,” Te ancet, vol. 388, no. 10053, pp. 1459–1544, 2016.
23
[5] Who, “WHO reveals leading causes of death and disability
worldwide: 2000•2019,” 2020, https://www.who.int/news/
item/09•12•2020•who•reveals•leading•causes•of•death•and•
disability•worldwide•2000•2019.
[6] B. Pham, R. Jorry, N. Abori, V. D. Silas, A. D. Okely, and
W. Pomat, “Non•communicable diseases attributed mor•
tality and associated sociodemographic factors in Papua New
Guinea: evidence from the comprehensive health and epi•
demiological surveillance system,” P oS Global Public
Health, vol. 2, no. 3, 2022.
[7] Who, “Noncommunicable diseases,” 2021, https://www.who.
int/news•room/fact•sheets/detail/noncommunicable•
diseases.
[8] J. Ali, S. H. Ansari, and S. Kotta, “Exploring scientifcally
proven herbal aphrodisiacs,” Pharmacognosy Reviews, vol. 7,
no. 1, pp. 1–10, 2013.
[9] A. N. Sidawy, “Erectile dysfunction,” in Rutherford’s Vas•
cular Surgery and Endovascular Terapy, Springer, Berlin,
Germany, 2019.
[10] P. Bearelly, E. A. Phillips, S. Pan et al., “Long•term intra•
cavernosal injection therapy: treatment efcacy and patient
satisfaction,” International Journal of Impotence Research,
vol. 32, no. 3, pp. 345–351, 2020.
[11] D. Mobley, M. Khera, and N. Baum, “Recent advances in the
treatment of erectile dysfunction,” Postgraduate Medical
Journal, vol. 93, no. 1105, pp. 679–685, 2017.
[12] P. Grant, G. Jackson, I. Baig, and J. Quin, “Erectile dys•
function in general medicine,” Clinical Medicine, vol. 13,
no. 2, pp. 136–140, 2013.
[13] S. Saha, P. Roy, C. Corbitt, and S. S. Kakar, “Application of
stem cell therapy for infertility,” Cells, vol. 10, no. 7, p. 1613,
2021.
[14] M. Chae, S. J. Kang, K. P. Lee et al., “Onion (Allium cepa L.)
peel extract (OPE) regulates human sperm motility via
protein kinase C•mediated activation of the human voltage•
gated proton channel,” Andrology, vol. 5, no. 5, pp. 979–989,
2017.
[15] B. V. Rossi, M. Abusief, and S. A. Missmer, “Modifable risk
factors and infertility: what are the connections?” American
Journal of ifestyle Medicine, vol. 10, no. 4, pp. 220–231, 2016.
[16] A. Ilacqua, G. Izzo, G. P. Emerenziani, C. Baldari, and
A. Aversa, “Lifestyle and fertility: the infuence of stress and
quality of life on male fertility,” Reproductive Biology and
Endocrinology, vol. 16, no. 1, p. 115, 2018.
[17] G. Biviá•Roig, A. Boldó•Roda, R. Blasco•Sanz et al., “Impact
of the COVID•19 pandemic on the lifestyles and quality of
life of women with fertility problems: a cross•sectional
study,” Frontiers in Public Health, vol. 9, Article ID
686115, 2021.
[18] A. Starc, M. Trampuš, D. Pavan Jukić, C. Rotim, T. Jukić, and
A. Polona Mivšek, “Infertility and sexual dysfunctions:
a systematic literature review,” Acta Clinica Croatica, vol. 58,
no. 3, pp. 508–515, 2019.
[19] A. Skalkidou, T. N. Sergentanis, S. P. Gialamas et al., “Risk of
endometrial cancer in women treated with ovary•stimulating
drugs for subfertility,” Te Cochrane Database of Systematic
Reviews, vol. 3, no. 3, 2017.
[20] A. Bakhtiari, Z. Basirat, and F. Nasiri•Amiri, “Sexual dys•
function in women undergoing fertility treatment in Iran:
prevalence and associated risk factors,” Journal of Re•
production & Infertility, vol. 17, no. 1, pp. 26–33, 2016.
[21] A. Anand Ganapathy, V. M. Hari Priya, and A. Kumaran,
“Medicinal plants as a potential source of Phosphodiesterase•
24
[22]
[23]
[24]
[25]
[26]
[27]
[28]
[29]
[30]
[31]
[32]
[33]
[34]
[35]
[36]
Evidence•Based Complementary and Alternative Medicine
5 inhibitors: a review,” Journal of Ethnopharmacology,
vol. 267, Article ID 113536, 2021.
P. Tugume, E. K. Kakudidi, M. Buyinza et al., “Ethnobo•
tanical survey of medicinal plant species used by commu•
nities around Mabira central forest reserve, Uganda,” Journal
of Ethnobiology and Ethnomedicine, vol. 12, no. 1, p. 5, 2016.
Y. M. Mbuni, S. Wang, B. N. Mwangi et al., “‘Medicinal
plants and their traditional uses in local communities around
cherangani hills, western Kenya,” Plants, vol. 9, no. 3, p. 331,
2020.
T. Omara, A. K. Kiprop, R. C. Ramkat et al., “Medicinal
plants used in traditional management of cancer in Uganda:
a review of ethnobotanical surveys, phytochemistry, and
anticancer studies,” Evidence•Based Complementary and
Alternative Medicine, vol. 2020, no. 6, Article ID 3529081,
26 pages, 2020.
T. Omara, “East African quintessential plants claimed to be
used as blood purifers, cleansers, detoxifers and tonics: an
appraisal of ethnobotanical reports and correlation with
reported bioactivities,” Bulletin of the National Research
Centre, vol. 45, no. 1, p. 171, 2021.
E. Fratkin, “Traditional medicine and concepts of healing
among Samburu pastoralists of Kenya,” Journal of Ethno•
biology, vol. 16, no. 1, pp. 63–97, 1996.
H. Gumisiriza, G. Birungi, E. A. Olet, and C. D. Sesaazi,
“Medicinal plant species used by local communities around
queen elizabeth national park, maramagambo central forest
reserve and ihimbo central forest reserve, south western
Uganda,” Journal of Ethnopharmacology, vol. 239, Article ID
111926, 2019.
J. Kimondo, J. Miaron, P. Mutai, and P. Njogu, “Ethnobo•
tanical survey of food and medicinal plants of the Ilkisonko
Maasai community in Kenya,” Journal of Ethno•
pharmacology, vol. 175, pp. 463–469, 2015.
I. Sindiga, “Indigenous medical knowledge of the Maasai,”
Indigenous Knowledge and Development Monitor, vol. 2,
pp. 16–18, 1994.
H. Trant, “Food taboos in East Africa,” Te ancet, vol. 264,
no. 6840, pp. 703–705, 1954.
J. Kigenyi, “Coping with resource extinction: the case of
medicinal plants in Kawete village, Iganga district, Uganda,”
Culture and Environment in Africa Series, Vol. 9, Te Co•
logne African Studies Centre, Cologne, Germany, 2016.
S. C. Chhabra, R. L. A. Mahunnah, and E. N. Mshiu, “Plants
used in traditional medicine in eastern Tanzania. VI. An•
giosperms (sapotaceae to zingiberaceae),” Journal of Eth•
nopharmacology, vol. 39, no. 2, pp. 83–103, 1993.
S. H. Ngere, V. Akelo, K. Ondeng’e et al., “Traditional
medicine beliefs and practices among caregivers of children
under fve years•the child health and mortality prevention
surveillance (champs), western Kenya: a qualitative study,”
P oS One, vol. 17, no. 11, 2022.
S. van Vuuren and L. Frank, “Review: southern African
medicinal plants used as blood purifers,” Journal of Eth•
nopharmacology, vol. 249, Article ID 112434, 2020.
M. J. Page, J. E. McKenzie, P. M. Bossuyt et al., “Te PRISMA
2020 statement: an updated guideline for reporting sys•
tematic reviews,” International Journal of Surgery, vol. 88,
p. 105906, 2021.
T. Omara, C. K. Nakiguli, R. A. Naiyl, F. A. Opondo,
S. B. Otieno, M. L. Ndiege et al., “Medicinal plants used as
snake venom antidotes in East African Community: review
and assessment of scientifc evidences,” Journal of Medicinal
and Chemical Sciences, vol. 4, no. 2, pp. 107–144, 2021.
[37] Joanna Briggs Institute, “Checklist for prevalence studies,”
2017,
https://jbi.global/sites/default/fles/2019•05/JBI_
Critical_Appraisal•Checklist_for_Prevalence_Studies2017_
0.pdf.
[38] D. Atlaw, B. Sahiledengle, S. Degno et al., “Utilization of
provider•initiated HIV testing and counselling in Ethiopia:
a systematic review and meta•analysis,” Tropical Medicine
and Health, vol. 50, no. 1, p. 29, 2022.
[39] K. N. Kapere, M. Maud Kamatenesi, T. A. Otwine, and
N. Waisindye, “Community perceptions on the use of tra•
ditional medicine among people experiencing sexual dys•
functions in Greater Mbarara, western Uganda,” Journal of
Pharmacognosy and Phytochemistry, vol. 11, no. 2, pp. 46–59,
2022.
[40] P. Ssegawa and J. M. Kasenene, “Medicinal plant diversity
and uses in the Sango bay area, Southern Uganda,” Journal of
Ethnopharmacology, vol. 113, no. 3, pp. 521–540, 2007.
[41] J. M. Watt and M. G. Breyer•Brandwijk, “Temedicinal and
poisonous plants of Southern and Eastern Africa being an
account of theirmedicinal and other uses,” Chemical Com•
position, Pharmacological Efects and Toxicology in Man and
Animal ivingstone, Edinburgh, 1962.
[42] M. Kamatenesi•Mugisha and H. Oryem•Origa, “Traditional
herbal remedies used in the management of sexual impo•
tence and erectile dysfunction in Western Uganda,” African
Health Sciences, vol. 5, no. 1, pp. 40–49, 2005.
[43] C. K. Kaingu, J. A. Oduma, J. M. Mbaria, and S. G. Kiama,
“Medicinal plants traditionally used for the management of
female reproductive health dysfunction in Tana River
County, Kenya,” Tang Humanitarias Medicine, vol. 3, no. 2,
pp. 17.1–17.10, 2013.
[44] N. Shiracko, B. O. Owuor, M. M. Gakuubi, and W. Wanzala,
“A survey of ethnobotany of the AbaWanga people in
Kakamega County, western province of Kenya,” Indian
Journal of Traditional Knowledge, vol. 15, no. 1, pp. 93–102,
2016.
[45] P. G. Kareru, G. M. Kenji, A. N. Gachanja, J. M. Keriko,
G. Mungai, and G. Mungai, “Traditional medicines among
the Embu and Mbeere peoples of Kenya,” African Journal of
Traditional, Complementary, and Alternative Medicines:
AJTCAM, vol. 4, no. 1, pp. 75–86, 2006.
[46] J. Muriuki, “Medicinal trees in smallholder agroforestry
systems: assessing some factors infuencing cultivation by
farmers East of Mt Kenya,” Dissertation, University of
Natural Resources and Applied Life Sciences, Vienna, 2011.
[47] C. K. Kaingu, J. M. Mbaria, J. Oduma, and G. S. Kiama,
“Ethnobotanical survey of medicinal plants used for the
management of male sexual dysfunction and infertility in
tana river county, Kenya,” Te Journal of Ethnobiology and
Traditional Medicine, vol. 119, pp. 453–463, 2013.
[48] M. J. Moshi, D. F. Otieno, P. K. Mbabazi, and A. Weisheit,
“Ethnomedicine of the kagera region, north western Tan•
zania. Part 2: the medicinal plants used in katoro ward,
bukoba district,” Journal of Ethnobiology and Ethnomedicine,
vol. 6, no. 1, p. 19, 2010.
[49] G. H. Schmelzer, Medicinal Plant. Plant Resources of Tropical
Africa (PROTA), Technical Centre for Agricultural and Rural
Cooperation, Netherlands, 2008.
[50] K. J. Cheruiyot, E. Njenga, C. Mutai, C. Bii, R. Korir, and
E. Too, “Ethnobotanical survey and plant monographs of
medicinal plants used among the Elgeyo community in
Kenya,” Photon, vol. 120, pp. 633–649, 2013.
[51] J. O. Kokwaro, Medicinal Plants of East Africa, University of
Nairobi Press, Nairobi, Kenya, 3rd edition, 2009.
Evidence•Based Complementary and Alternative Medicine
[52] K. Munguti, “Indigenous knowledge in the management of
malaria and visceral leishmaniasis among the tugen of
Kenya,” Indigenous Knowledge and Development Monitoring,
vol. 5, pp. 10–12, 1997.
[53] J. G. Agea, B. Katongole, D. Waiswa, and G. N. Nabanoga,
“Market survey of Mondia whytei (mulondo) roots in
Kampala City, Uganda,” African Journal of Traditional,
Complementary, and Alternative Medicines: AJTCAM, vol. 5,
no. 4, pp. 399–408, 2008.
[54] J. K. Muthee, D. W. Gakuya, J. M. Mbaria, P. G. Kareru,
C. M. Mulei, and F. K. Njonge, “Ethnobotanical study of
anthelmintic and other medicinal plants traditionally used in
Loitoktok district of Kenya,” Journal of Ethnopharmacology,
vol. 135, no. 1, pp. 15–21, 2011.
[55] S. Asiimwe, J. Namukobe, R. Byamukama, and B. Imalingat,
“Ethnobotanical survey of medicinal plant species used by
communities around Mabira and Mpanga Central Forest
Reserves, Uganda,” Tropical Medicine and Health, vol. 49,
no. 1, p. 52, 2021.
[56] L. Ssozi, B. Kabiito, A. Byaruhanga, and W. Kanata, “Doc•
umenting baganda ethno•medicine: a step towards preser•
vation and conservation,” Journal of Applied and Advanced
Research, vol. 1, pp. 15–22, 2016.
[57] G. H. Schmelzer and A. Gurib•Fakim, “Plant resources of
tropical Africa,” Medicinal Plants 1, PROTA Foundation,
Wageningen, Netherlands, 2008.
[58] J. O. Kokwaro, Medicinal Plants of East Africa, East African
Literature Bureau, Nairobi, Kenya, 2nd edition, 1993.
[59] P. Jeruto, C. Lukhoba, G. Ouma, D. Otieno, and C. Mutai,
“An ethnobotanical study of medicinal plants used by the
Nandi people in Kenya,” Journal of Ethnopharmacology,
vol. 116, no. 2, pp. 370–376, 2008.
[60] G. N. Njoroge and R. W. Bussman, “Ethnotherapeutic
management of sexually transmitted diseases (STDs) and
reproductive health conditions in central province of
Kenya,” Indian Journal of Traditional Medicine, vol. 8, no. 2,
pp. 255–261, 2009.
[61] W. Wanzala, S. M. Syombua, and J. O. Alwala, “A survey of
the applications and use of ethnomedicinal plants and plant
products for healthcare from the Ukambani region in
Eastern
Kenya,”
Indian
Journal
of
Ethno•
phytopharmaceuticals, vol. 2, no. 2, pp. 6–58, 2016.
[62] E. K. Kakudidi, “Cultural and social uses of plants from and
around kibale national park, western Uganda,” African
Journal of Ecology, vol. 42, no. s1, pp. 114–118, 2004.
[63] R. A. Kitula, “Use of medicinal plants for human health in
udzungwa mountains forests: a case study of new dabaga
ulongambi forest reserve, Tanzania,” Journal of Ethnobiology
and Ethnomedicine, vol. 3, no. 1, p. 7, 2007.
[64] P. C. Rwangabo and P. C. Rwangabo, a médecine tradi•
tionnelle au Rwanda, vol. 258, Editions Karthala et ACCT,
Paris, 1993.
[65] S. V. Okello, R. O. Nyunja, G. W. Netondo, and
J. C. Onyango, “Ethnobotanical study of medicinal plants
used by Sabaots of Mt. Elgon Kenya,” African Journal of
Traditional, Complementary, and Alternative Medicines:
AJTCAM, vol. 7, no. 1, pp. 1–10, 2009.
[66] H. D. Neuwinger, African Ethnobotany: Poisons and Drugs:
Chemistry, Pharmacology, Toxicology, Chapman & Hall,
London, 1996.
[67] R. Nakaziba, M. K. Anyolitho, S. B. Amanya et al., “Tradi•
tional medicinal vegetables in northern Uganda: an ethno•
botanical survey,” International Journal of Food Science,
vol. 2021, Article ID 5588196, 18 pages, 2021.
25
[68] R. Korir, C. Kimani, J. Gathirwa, M. Wambura, and C. Bii,
“In vitro antimicrobial properties of methanol extracts of
three medicinal plants from Kilif district, Kenya,” African
Journal of Health Sciences, vol. 20, pp. 4–10, 2012.
[69] W. Kipkore, B. Wanjohi, H. Rono, and G. Kigen, “A study of
the medicinal plants used by the Marakwet community in
Kenya,” Journal of Ethnobiology and Ethnomedicine, vol. 10,
no. 1, p. 24, 2014.
[70] G. Anywar, E. Kakudidi, R. Byamukama, J. Mukonzo,
A. Schubert, and H. Oryem•Origa, “Indigenous traditional
knowledge of medicinal plants used by herbalists in treating
opportunistic infections among people living with HIV/
AIDS in Uganda,” Journal of Ethnopharmacology, vol. 246,
Article ID 112205, 2020.
[71] J. Nankaya, J. Nampushi, S. Petenya, and H. Balslev, “Eth•
nomedicinal plants of the loita Maasai of Kenya,” Envi•
ronment, Development and Sustainability, vol. 22, no. 3,
pp. 2569–2589, 2019.
[72] A. S. Delbanco, N. D. Burgess, and A. Cuni•Sanchez,
“Medicinal plant trade in Northern Kenya: economic im•
portance, uses, and origin,” Economic Botany, vol. 71, no. 1,
pp. 13–31, 2017.
[73] K. Philip, M. Elizabeth, P. Cheplogoi, and K. Samuel,
“Ethnobotanical survey of antimalarial medicinal plants used
in Butebo county, Eastern Uganda,” European Journal of
Medicinal Plants, vol. 21, no. 4, pp. 1–22, 2017.
[74] D. O. Okach, A. R. O. Nyunja, and G. Opande, “Phyto•
chemical screening of some wild plants from Lamiaceae and
their role in traditional medicine in Uriri district–Kenya,”
International Journal of Herbal Medicine, vol. 1, no. 5,
pp. 135–143, 2013.
[75] J. G. Ndukui, H. Muwonge, and L. F. Sembajwe, “Aphro•
disiac potential and phytochemical profle of <i&gt;
Ekebergia capensis&lt;/i&gt; (Cape ash) in male
albino rats,” Spatula DD, vol. 2, no. 4, pp. 237–243, 2012.
[76] P. Onen, D. Ocira, T. Omara, J. Nyeko, and A. Okwir,
“Preliminary phytochemical screening of plumbagozeylanica
L. Roots and its aphrodisiac efect in male rats,” Asian
Journal of Applied Chemistry Research, vol. 8, no. 3,
pp. 24–31, 2021.
[77] E. Odongo, N. Mungai, P. Mutai, E. Karumi, J. Mwangi, and
J. Omale, “Ethnobotanical survey of medicinal plants used in
Kakamega County, western Kenya,” Applied Medical Re•
search, vol. 4, no. 1, pp. 22–40, 2018.
[78] P. Tshisekedi Tshibangu, P. Mutwale Kapepula, M. Kabongo
Kapinga et al., “Antiplasmodial activity of Heinsia crinita
(Rubiaceae) and identifcation of new iridoids,” Journal of
Ethnopharmacology, vol. 196, pp. 261–266, 2017.
[79] W. Musila, D. Kisangau, and J. Muema, “Conservation status
and use of medicinal plants by traditional medical practi•
tioners in machakos district, Kenya,” in Indigenous
Knowledge Conference Proceedings, p. 22, Pennsylvania State
University. Traditional Aspects of Health and Wellness,
Pennsylvania, PA, USA, 2004.
[80] MEWNR, “Kenya biodiversity atlas. Ministry of envi•
ronment natural resources and regional developement
authorities,” 2015, https://webfles.york.ac.uk/KITE/
Kenya%20Atlas/Kenyas%20Natural%20Atlas%20•%20A
%20Biodiversity%20Atlas.pdf.
[81] T. Omara, S. Kagoya, A. Openy et al., “Antivenin plants used
for treatment of snakebites in Uganda: ethnobotanical re•
ports and pharmacological evidences,” Tropical Medicine
and Health, vol. 48, no. 1, pp. 6–16, 2020.
26
[82] K. Medius, K. Esther, B. C. Anthony, and H. Robert,
“Medicinal plants and herbalist preferences around bwindi
impenetrable national park,” Journal of Medicinal Plants
Research, vol. 11, no. 8, pp. 161–170, 2017.
[83] T. Omara, “Plants used in antivenom therapy in rural Kenya:
ethnobotany and future perspectives,” Journal of Toxicology,
vol. 2020, Article ID 1828521, 9 pages, 2020.
[84] D. Asmerom, T. H. Kalay, T. Y. Araya, D. M. Desta,
D. Z. Wondafrash, and G. G. Tafere, “Medicinal plants used
for the treatment of erectile dysfunction in Ethiopia: a sys•
tematic review,” BioMed Research International, vol. 2021,
Article ID 6656406, 12 pages, 2021.
[85] S. S. Semenya and M. J. Potgieter, “Ethnobotanical survey of
medicinal plants used by Bapedi traditional healers to treat
erectile dysfunction in the Limpopo Province, South Africa,”
Journal of Medicinal Plants Research, vol. 7, pp. 349–357,
2013.
[86] M. Nimrouzi, A. M. Jaladat, and M. M. Zarshenas, “A
panoramic view of medicinal plants traditionally applied for
impotence and erectile dysfunction in Persian medicine,”
Journal of Traditional and Complementary Medicine, vol. 10,
no. 1, pp. 7–12, 2020.
[87] N. S. Chauhan, V. Sharma, V. K. Dixit, and M. Takur, “A
review on plants used for improvement of sexual perfor•
mance and virility,” BioMed Research International,
vol. 2014, pp. 1–19, 2014.
[88] A. A. Ajao, N. P. Sibiya, and A. N. Moteetee, “Sexual prowess
from nature: a systematic review of medicinal plants used as
aphrodisiacs and sexual dysfunction in sub•Saharan Africa,”
South African Journal of Botany, vol. 122, pp. 342–359, 2019.
[89] D. Tungmunnithum, A. Tongboonyou, A. Pholboon, and
A. Yangsabai, “Flavonoids and other phenolic compounds
from medicinal plants for pharmaceutical and medical as•
pects: an overview,” Medicines, vol. 5, no. 3, p. 93, 2018.
[90] C. Tanase, S. Coşarcă, and D. L. Muntean, “A critical review
of phenolic compounds extracted from the bark of woody
vascular plants and their potential biological activity,”
Molecules, vol. 24, no. 6, p. 1182, 2019.
[91] B. Van Wyk and P. Van Wyk, Field Guide to Trees of
Southern Africa, Struik publishers Ltd, Pretoria, South
Africa, 1997.
[92] M. Ofosuhene, “Assessment of the efects of Mondia whitei
extracts on some biochemical processes associated with
penile erection,” MPhil. Tesis, Department of Biochemistry,
University of Ghana, Ghana, 2005.
[93] J. Adjanohoum, N. Aboubaka, K. Dramane, N. E. Ebot,
J. A. Ekpere, and E. G. Enow•Orock, Traditional Medicine
and Pharmacopoeia. Contribution to Ethnobotanical and
Floristic Studies in Cameroon OUA/STRC, Lagos, Nigeria,
1996.
[94] E. Agbodjento, J. R. Klotoé, T. I. Sacramento et al., “Eth•
nobotanical knowledge of medicinal plants used in the
treatment of male infertility in southern Benin,” Advances in
Traditional Medicine, vol. 21, no. 4, pp. 655–673, 2020.
[95] R. Machado, I. Alves•Pereira, and R. Ferreira, “Plant growth,
phytochemical accumulation and antioxidant activity of
substrate•grown spinach,” Heliyon, vol. 4, no. 8, 2018.
[96] K. A. M. Kuria, S. De Coster, G. Muriuki et al., “Antimalarial
activity of Ajuga remota Benth (Labiatae) and Caesalpinia
volkensii Harms (Caesalpiniaceae): in vitro confrmation of
ethnopharmacological use,” Journal of Ethnopharmacology,
vol. 74, no. 2, pp. 141–148, 2001.
Evidence•Based Complementary and Alternative Medicine
[97] T. Omara, “Antimalarial plants used across Kenyan com•
munities,” Evidence•Based Complementary and Alternative
Medicine, vol. 2020, Article ID 4538602, 31 pages, 2020.
[98] Q. W. Zhang, L. G. Lin, and W. C. Ye, “Techniques for
extraction and isolation of natural products: a comprehen•
sive review,” Chinese Medicine, vol. 13, no. 1, p. 20, 2018.
[99] O. Joseph, E. A. Paul, A. Martin, K. T. Julius, O. C. E. Joseph,
and G. A. Amon, “Efects of aqueous root bark extract of
Citropsis articulata (Swingle Kellerman) on sexual function
in male rats,” African Journal of Pharmacy and Pharma•
cology, vol. 9, no. 29, pp. 723–729, 2015.
[100] P. Vudriko, M. K. Baru, J. Kateregga, and J. G. Ndukui,
“Crude ethanolic leaf extracts of Citropsis articulata: a po•
tential phytomedicine for treatment of male erectile dys•
function associated with testosterone defciency,”
International Journal of Basic & Clinical Pharmacology,
vol. 3, no. 1, pp. 120–123, 2014.
[101] O. Joseph, J. K. Tanayen, K. Barbra et al., “Phytochemical and
efcacy study on four herbs used in erectile dysfunction:
mondia whiteii, Cola acuminata, Urtica massaica, and
Tarenna graveolens,” African Journal of Pharmacy and
Pharmacology, vol. 10, no. 37, pp. 785–790, 2016.
[102] Y. Gigani, A. Vekaria, and S. A. Amir, “Efect of Abrus
precatorius and Amaranthus spinosus combination treat•
ment on fertility in male rats,” Journal of Pharmacology and
Pharmacotherapeutics, vol. 3, no. 3, pp. 272•273, 2012.
[103] M. Z. Allouh, H. M. Daradka, M. M. A. Barbarawi, and
A. G. Mustafa, “Fresh onion juice enhanced copulatory
behavior in male rats with and without paroxetine•induced
sexual dysfunction,” Experimental Biology and Medicine,
vol. 239, no. 2, pp. 177–182, 2014.
[104] O. I. Adeyemi, O. O. Ige, E. Agbede, and C. A. Adebajo, “Te
efect of tardalafl on the aphrodisiac properties of Allium
sativum and Allium cepa using behavioural models in rats,”
Nigerian Journal of Natural Products and Medicine, vol. 21,
pp. 14–20, 2017.
[105] N. Malviya, S. Jain, V. B. Gupta, and S. Vyas, “Management
of drug induced sexual dysfunction in male rats by ethyl
acetate fraction of onion,” Acta Poloniae Pharmaceutica,
vol. 70, no. 2, pp. 317–322, 2013.
[106] A. M. Al•Bekairi, A. H. Shah, and S. Qureshi, “Efect of
Allium sativum on epididymal spermatozoa, estradiol•
treated mice and general toxicity,” Journal of Ethno•
pharmacology, vol. 29, no. 2, pp. 117–125, 1990.
[107] V. W. Pooja, J. Saravanan, T. K. Praveen, R. Emdormi, and
S. Deepa, “Evaluation of aphrodisiac activity of Allium
sativum in male rats,” International Journal Of Scientifc &
Technology Research, vol. 8, no. 10, pp. 1683–1686, 2019.
[108] J. Yang, T. Wang, J. Yang et al., “S•allyl cysteine restores
erectile function through inhibition of reactive oxygen
species generation in diabetic rats,” Andrology, vol. 1, no. 3,
pp. 487–494, 2013.
[109] M. R. Sailani and H. Moeini, “Efect of Ruta graveolens and
Cannabis sativa alcoholic extract on spermatogenesis in the
adult wistar male rats,” Indian Journal of Urology, vol. 23,
no. 3, pp. 257–260, 2007.
[110] N. Lotf, M. Khazaei, S. M. A. Shariatzadeh, M. Soleimani
Mehranjani, and A. Ghanbari, “Te efect of Cannabis sativa
hydroalcoholic extract on sperm parameters and testis his•
tology in rats,” International Journal of Morphology, vol. 31,
no. 1, pp. 82–86, 2013.
[111] A. O. Ige, D. T. Oluwole, M. O. Olaoye, and E. O. Adewoye,
“Testicular function following oral exposure to Tramadol and
Cannabis sativa ethanol extracts in male Wistar rats,”
Evidence•Based Complementary and Alternative Medicine
[112]
[113]
[114]
[115]
[116]
[117]
[118]
[119]
[120]
[121]
[122]
[123]
[124]
[125]
Research Journal of Health Sciences, vol. 8, no. 2, pp. 63–72,
2020.
M. Abdulwaheb, E. Makonnen, A. Debella, and D. Abebe,
“Efect of Catha edulis foresk (khat) extracts on male rat
sexual behavior,” Journal of Ethnopharmacology, vol. 110,
no. 2, pp. 250–256, 2007.
S. A. Taha, A. M. Ageel, M. W. Islam, and O. T. Ginawi,
“Efect of (•)•cathinone, a psychoactive alkaloid from khat
(Catha edulis forsk.) and cafeine on sexual behaviour in
rats,” Pharmacological Research, vol. 31, no. 5, pp. 299–303,
1995.
A. Mohammed and E. Engidawork, “Reproductive param•
eters are diferentially altered following subchronic admin•
istration of Catha edulis F. (Khat) extract and cathinone in
male rats,” Journal of Ethnopharmacology, vol. 134, no. 3,
pp. 977–983, 2011.
M. W. Islam, M. Tariq, A. M. Ageel, F. El•Feraly, I. Al•
Meshal, and I. Ashraf, “An evaluation of the male re•
productive toxicity of cathinone,” Toxicology, vol. 60, no. 3,
pp. 223–234, 1990.
O. O. Azu, F. I. O. Duru, A. A. Osinubi et al., “Histo•
morphometric efects of Kigelia africana (Bignoniaceae) fruit
extract on the testis following short•term treatment with
cisplatin in male Sprague–Dawley rats,” Middle East Fertility
Society Journal, vol. 15, no. 3, pp. 200–208, 2010.
E. O. Adeparusi, A. A. Dada, and O. V. Alale, “Efects of
medicinal plant (kigelia africana) on sperm quality of african
catfsh Clarias gariepinus (burchel, 1822) broodstock,”
Journal of Agricultural Science, vol. 2, no. 1, pp. 193–199,
2010.
P. Watcho, P. Kamtchouing, S. D. Sokeng et al., “Androgenic
efect of Mondia whitei roots in male rats,” Asian Journal of
Andrology, vol. 6, no. 3, pp. 269–272, 2004.
P. Watcho, F. Zelefack, T. B. Nguelefack et al., “Efects of the
aqueous and hexane extracts of mondia whitei on the sexual
behaviour and some fertility parameters of sexually in•
experienced male rats,” African Journal of Traditional,
Complementary, and Alternative Medicines: AJTCAM, vol. 4,
no. 1, pp. 37–46, 2006.
P. Watcho, D. Fotsing, F. Zelefack et al., “Efects of Mondia
whitei extracts on the contractile responses of isolated rat vas
deferens to potassium chloride and adrenaline,” Indian
Journal of Pharmacology, vol. 38, no. 1, pp. 33–37, 2006.
P. Watcho, F. Zelefack, and T. B. Nguelefack, “Efects of the
hexane extract of mondia whitei on the reproductive organs
of male rat,” African Journal of Traditional, Complementary
and Alternative Medicines, vol. 2, pp. 302–311, 2005.
G. M. Gundidza, V. M. Mmbengwa, M. L. Magwa et al.,
“Aphrodisiac properties of some Zimbabwean medicinal
plants formulations,” African Journal of Biotechnology, vol. 8,
no. 22, pp. 6402–6407, 2009.
O. Quasie, O. N. Martey, A. K. Nyarko, W. S. Gbewonyo, and
L. K. Okine, “Modulation of penile erection in rabbits by
Mondia whitei: possible mechanism of action,” African
Journal of Traditional, Complementary, and Alternative
Medicines: AJTCAM, vol. 7, no. 3, pp. 241–252, 2010.
O. T. Oyelowo, O. V. Fabiyi, O. M. Jimoh, and B. V. Owoyele,
“Aphrodisiac and male sexual characteristics in albino rats
treatedwith the aqueous extract of Parquetina nigrescens
root,” Nigerian Journal of Natural Products and Medicine,
vol. 16, pp. 18–25, 2012.
O. T. Kayode and M. T. Yakubu, “Parquetina nigrescens
leaves: chemical profle and infuence on the physical and
biochemical indices of sexual activity of male Wistar rats,”
27
[126]
[127]
[128]
[129]
[130]
[131]
[132]
[133]
[134]
[135]
[136]
[137]
[138]
[139]
[140]
Journal of Integrative Medicine, vol. 15, no. 1, pp. 64–76,
2017.
E. Ashamu, E. Salawu, O. Oyewo, A. Alhassan, O. Alamu,
and A. Adegoke, “Efcacy of vitamin C and ethanolic extract
of Sesamum indicum in promoting fertility in male Wistar
rats,” Journal of Human Reproductive Sciences, vol. 3, no. 1,
pp. 11–14, 2010.
D. M. Hai, J. W. Ren, Y. N. Chi et al., “Protective efects of
sesamin on cytoxan•induced spermatogenesis dysfunction
by regulating RNF8•ubH2A/ubH2B pathways in male mice,”
Frontiers in Pharmacology, vol. 12, Article ID 708467, 2021.
B. Seven, H. Timur, M. N. Kalem, Z. Kalem, O. Han, and
B. Bilezikci, “Ginger (zingiber ofcinale) might improve
female fertility: a rat model,” Journal of the Chinese Medical
Association, vol. 81, no. 10, pp. 905–911, 2018.
M. Shahidi, A. Moradi, and P. Dayati, “Zingerone attenuates
zearalenone•induced steroidogenesis impairment and apo•
ptosis in TM3 Leydig cell line,” Toxicon, vol. 211, pp. 50–60,
2022.
M. Salihu, B. O. Ajayi, I. A. Adedara, D. de Souza,
J. B. T. Rocha, and E. O. Farombi, “6•Gingerol•rich fraction
from Zingiber ofcinale ameliorates carbendazim•induced
endocrine disruption and toxicity in testes and epididymis of
rats,” Andrologia, vol. 49, no. 5, 2017.
P. Watcho, G. M. A. Tchuenchie, and D. P. B. Defo, “Sexual
stimulant efects of the mixture of Mondia whitei, Dracaena
arborea, and Bridelia ferruginea in normal and prediabetic
male Wistar rats,” Journal of Basic and Clinical Physiology
and Pharmacology, vol. 30, no. 4, 2019.
B. Ghazi Eid, A. Hanafy, A. Hasan, and T. Neamatalla,
“Zingerone enhances fertility markers in both male and
female rats and increases aryl hydrocarbon receptor ex•
pression,” International Journal of Pharmacology, vol. 16,
no. 3, pp. 267–275, 2020.
S. A. Banihani, “Efect of ginger (Zingiber ofcinale) on
semen quality,” Andrologia, vol. 51, no. 6, 2019.
S. A. Banihani, “Testosterone in males as enhanced by onion
(Allium cepa L.),” Biomolecules, vol. 9, no. 2, p. 75, 2019.
D. Pizzol, J. Demurtas, B. Stubbs et al., “Relationship between
Cannabis use and erectile dysfunction: a systematic review
and meta•analysis,” American Journal of Men’s Health,
vol. 13, no. 6, Article ID 155798831989246, 2019.
M. Gholami•Ahangaran, M. Karimi•Dehkordi, A. Akbari
Javar, M. Haj Salehi, and M. Ostadpoor, “A systematic review
on the efect of Ginger (Zingiber ofcinale) on improvement
of biological and fertility indices of sperm in laboratory
animals, poultry and humans,” Veterinary Medicine and
Science, vol. 7, no. 5, pp. 1959–1969, 2021.
Z. Afshar, S. Shahali, and H. Rastad, “Efects of oral ginger
capsule on sexual function and sexual quality of life in
women: a double•blinded, randomized, placebo•controlled
trial,” Sexologies, vol. 31, no. 4, pp. 387–393, 2022.
J. Hosseini, A. Mardi Mamaghani, H. Hosseinifar,
M. A. Sadighi Gilani, F. Dadkhah, and M. Sepidarkish, “Te
infuence of ginger (Zingiber ofcinale) on human sperm
quality and DNA fragmentation: a double•blind randomized
clinical trial,” International Journal of Reproductive Bio•
medicine, vol. 14, no. 8, pp. 533–540, 2016.
V. Kuete, Physical, Hematological, and Histopathological
Signs of Toxicity Induced by African Medicinal Plants, Tox•
icological Survey of African Medicinal Plants, Africa, 2014.
L. L. Chen, R. Verpoorte, H. R. Yen et al., “Efects of pro•
cessing adjuvants on traditional Chinese herbs,” Journal of
Food and Drug Analysis, vol. 26, no. 2, pp. S96–S114, 2018.
28
[141] A. Karthikeyan and S. D. Amalnath, “Abrus precatorius
poisoning: a retrospective study of 112 patients,” Indian
Journal of Critical Care Medicine, vol. 21, no. 4, pp. 224•225,
2017.
[142] L. Reedman, R. D. Shih, and O. Hung, “Survival after an
intentional ingestion of crushed abrus seeds,” Te Western
Journal of Emergency Medicine, vol. 9, no. 3, pp. 157–159,
2008.
[143] S. Alqasoumi, T. H. Khan, M. Al•Yahya, I. Al•Mofeh, and
S. Rafatullah, “Efect of acute and chronic treatment of
common spices in Swiss albino mice: a safety assessment
study,” International Journal of Pharmacology, vol. 8, no. 2,
pp. 80–90, 2012.
[144] B. Lawal, O. K. Shittu, F. I. Oibiokpa et al., “Antimicrobial
evaluation, acute and sub•acute toxicity studies of Allium
sativum,” Journal of Acute Disease, vol. 5, no. 4, pp. 296–301,
2016.
[145] M. Machado Bergamaschi, R. Helena Costa Queiroz,
A. Waldo Zuardi, and J. Alexandre S Crippa, “Safety and side
efects of cannabidiol, a Cannabis sativa constituent,” Cur•
rent Drug Safety, vol. 6, no. 4, pp. 237–249, 2011.
[146] E. Muema, J. Mbaria, J. Nguta et al., “Toxicity and safety of
khat (Catha edulis) consumption during pregnancy using
olive baboons (Papio anubis) as experimental models:
a prospective randomised study,” Greener Journal of Epi•
demiology and Public Health, vol. 4, no. 3, pp. 061–070, 2016.
[147] S. Atawodi and O. Olowoniyi, “Pharmacological and ther•
apeutic activities of kigelia africana (lam.) benth,” Annual
Research & Review in Biology, vol. 5, pp. 1–17, 2015.
[148] J. Oloro, J. K. Tanayen, K. Barbra et al., “Toxicity of four
herbs used in erectile dysfunction;Mondia whiteii,Cola
acuminata,Urtica massaica, and Tarenna graveolensin male
rats,” African Journal of Pharmacy and Pharmacology, vol. 9,
no. 30, pp. 756–763, 2015.
[149] L. Adu•Amoah, C. Agyare, E. Kisseih, P. G. Ayande, and
K. B. Mensah, “Toxicity assessment of Erythrophleum
ivorense and Parquetina nigrescens,” Toxicology Reports,
vol. 1, pp. 411–420, 2014.
[150] K. C. Uruakpa, K. E. Obeten, M. Eru, and A. O. Igiri, “Te
toxicity study of ethanolic leaf extract of Sesamum indicum
on the histomorphology of the liver of adult Wistar rats,”
Global Journal of Biology, Agriculture and Health Sciences,
vol. 23, pp. 42–46, 2013.
[151] T. Plengsuriyakarn, V. Viyanant, V. Eursitthichai et al.,
“Cytotoxicity, toxicity, and anticancer activity of Zingiber
ofcinale Roscoe against cholangiocarcinoma,” Asian Pacifc
Journal of Cancer Prevention, vol. 13, no. 9, pp. 4597–4606,
2012.
[152] R. Chen, J. Lin, J. Hong et al., “Potential toxicity of quercetin:
the repression of mitochondrial copy number via decreased
POLG expression and excessive TFAM expression in irra•
diated murine bone marrow,” Toxicology Reports, vol. 1,
pp. 450–458, 2014.
[153] P. Singh, S. Sharma, and S. K. Rath, “A versatile favonoid
Quercetin: study of its toxicity and diferential gene ex•
pression in the liver of mice,” Phytomedicine Plus, vol. 2,
no. 1, Article ID 100148, 2022.
[154] A. L. Riley, K. H. Nelson, P. To et al., “Abuse potential and
toxicity of the synthetic cathinones (i.e., “Bath salts”),”
Neuroscience & Biobehavioral Reviews, vol. 110, pp. 150–173,
2020.
[155] Y. Kodera, A. Suzuki, O. Imada et al., “Physical, chemical,
and biological properties of s•allylcysteine, an amino acid
Evidence•Based Complementary and Alternative Medicine
derived from garlic,” Journal of Agricultural and Food
Chemistry, vol. 50, no. 3, pp. 622–632, 2002.
[156] W. Kitipaspallop, P. Phuwapraisirisan, W. K. Kim,
C. Chanchao, and W. Pimtong, “Sesamin lacks zebrafsh
embryotoxicity but exhibits evidence of anti•angiogenesis,
anti•oxidant and anti•infammatory activities,” Comparative
Biochemistry and Physiology Part C: Toxicology & Pharma•
cology, vol. 269, Article ID 109637, 2023.
[157] V. A. S. Jesudoss, S. V. A. Santiago, K. Venkatachalam, and
P. Subramanian, “Zingerone (ginger extract): antioxidant
potential for efcacy in gastrointestinal and liver disease,” in
Gastrointestinal Tissue. Oxidative Stress and Dietary Anti•
oxidants, pp. 289–297, 2017.
[158] N. Promdam and P. Panichayupakaranant, “[6]•Gingerol:
a narrative review of its benefcial efect on human health,”
Food Chemistry Advances, vol. 1, Article ID 100043, 2022.