Fadogia agrestis herb tested in animal studies for libido enhancement
Fadogia agrestis has been found to have aphrodisiac benefits in rodent studies.
As of October 2009, we have not seen human studies with Fadogia agrestis herb.
Fadogia agrestis herb sexual benefits
Aphrodisiac potentials of the aqueous extract of Fadogia agrestis (Schweinf.
Ex Hiern) stem in male albino rats.
Asian J Androl. 2005 Dec;7(4):399-404. Yakubu MT, Akanji MA, Oladiji AT.
Medicinal Plants Research Laboratory, Department of Biochemistry, University of
Ilorin, PMB 1515, Ilorin, Nigeria.
To evaluate the phytochemical constituents and the aphrodisiac potential of the
aqueous extract of Fadogia agrestis (Rubiaceae) stem in male albino rats. The
aqueous stem extract of the plant was screened for phytochemical constituents.
Male rats were orally dosed with 18 mg/kg, 50 mg/kg and 100 mg/kg body weight,
respectively, of the extract at 24 h intervals and their sexual behavior
parameters and serum testosterone concentration were evaluated at days 1, 3 and
5. Phytochemical screening revealed the presence of alkaloids and saponins while
anthraquinones and flavonoids are weakly present. All the doses resulted in
significant increase in mount frequency, intromission frequency and
significantly prolonged the ejaculatory latency (P 0.05) and reduced mount and
intromission latency. There was also a significant increase in serum
testosterone concentrations in all the groups in a manner suggestive of
dose-dependence. The aqueous extract of Fadogia agrestis stem increased the
blood testosterone concentrations and this may be the mechanism responsible for
its aphrodisiac effects and various masculine behaviors. It may be used to
modify impaired sexual functions in animals, especially those arising from
hypotestosteronemia.
Fadogia agrestis
caution and safety concerns
Effects of oral administration of aqueous extract of Fadogia agrestis (Schweinf.
Ex Hiern) stem on some testicular function indices of male rats.
J Ethnopharmacol. 2008 Jan 17; Yakubu MT, Akanji MA, Oladiji AT.Medicinal
Plants Research Laboratory, Department of Biochemistry, University of Ilorin,
P.M.B. 1515 Ilorin, Nigeria.
The effects of administration of aqueous extract of Fadogia agrestis (Schweinf.
Ex Hiern) stem on some testicular function indices of male rats (Rattus
norvegicus) and their recovery potentials for 10 days were investigated.
Compared with the control, extract administration for 28 days at all the doses
resulted in significant increase in percentage testes-body weight ratio,
testicular cholesterol, sialic acid, glycogen, acid phosphatase and gamma-glutamyl
transferase activities while there was significant decrease in the activities of
testicular alkaline phosphatase, acid phosphatase, glutamate dehydrogenase and
concentrations of protein. Recoveries were made by the animals on some of the
testicular function indices mainly at 18 mg/kg body weight. The alterations
brought about by the aqueous extract of Fadogia agrestis stem are indications of
adverse effects on the male rat testicular function and this may adversely
affect the functional capacities of the testes. The recovery made at the dose of
18 mg/kg body weight as used in folklore medicine suggests that it does not
exhibit permanent toxicity at this dose.
Aphrodisiac herbs available over
the counter
These include maca, tongkat ali, butea superba, cnidium monnieri, tribulus terrestris extract,
mucuna pruriens, horny goat weed, avena sativa, LJ100, muira puama, catuaba,
ginger, cistanches, and yohimbe bark extract.
Mode of cellular toxicity of aqueous extract of Fadogia
agrestis (Schweinf. Ex Hiern) stem in male rat liver and kidney.
Hum Exp Toxicol. 2009 Aug; Yakubu MT, Oladiji AT, Akanji MA. Phytomedicine
and Toxicology Research Laboratory, Department of Biochemistry, University of
Ilorin, Ilorin, Nigeria.
The mode of cellular toxicity of aqueous extract of Fadogia agrestis stem in
male rats was investigated. Rats were grouped into four: A, B, C and D where A
(the control) received orally 1 mL of distilled water; B, C and D (test groups)
received orally 18, 50 and 100 mg/kg body weight of the extract, respectively,
for 28 days. Infrared spectroscopy indicated the presence of hydroxyl (OH) and
primary amine (CONH). Clinical toxicity symptoms such as respiratory distress,
epistasis, salivation, hypo- and hyperactivity were not observed at any period
of the experiment. No mortality was also recorded. Extract administration
significantly reduced (p < .05) the activities of alkaline phosphatase, lactate
dehydrogenase and gamma glutamyl transferase in the liver and kidney with
corresponding increases in the serum. Serum malondialdehyde also increased
significantly in all the extract-treated groups. The liver and kidney body
weight ratios of the extract-treated animals compared well with their controls
throughout the experimental period. The extract did not cause any swelling,
atrophy or hypertrophy of the organs. The other evidence in this study suggests
disruption of the ordered lipid bilayer of the plasma membranes of the
hepatocytes and nephrons. This might have resulted from peroxidation of the
polyunsaturated fatty acids on the membranes of the hepatocytes and nephrons
made possible by the functional groups or the product of metabolism of the
extract. This may be responsible for the compromise of the integrity of the
plasma membranes of the hepatocytes and nephrons.