Arch Pharm Res 1998
Dec;21(6):779-81
Eurycoma longifolia
increases sexual motivation in sexually naive male
rats.
Ang HH, Sim
MK.
School of
Pharmaceutical Sciences, University of Science, Malaysia,
Minden, Singapore.
The aim of this study
is to provide evidence on the aphrodisiac property of Eurycoma
longifolia Jack. An electric grid was used as an obstruction
in the electrical copulation cage in order to determine how
much an aversive stimulus the sexually naive male rat for both
the treated with E. longifolia Jack and control groups were
willing to overcome to reach the estrous receptive female in
the goal cage. The intensity of the grid current was
maintained at 0.12 mA and this was the intensity in which the
male rats in the control group failed to crossover to reach
the goal cage. Results showed that E. longifolia Jack
continued to enhance and also maintain a high level of both
the total number of successful crossovers, mountings,
intromissions and ejaculations during the 9-12th week
observation period. In conclusion, these results further
enhanced and strengthened the aphrodisiac property of E.
longifolia Jack.
PMID: 9868556 [PubMed
- indexed for MEDLINE]
Arch Pharm Res 2001
Oct;24(5):437-40
Effects of Eurycoma
longifolia jack on laevator ani muscle in both uncastrated and
testosterone-stimulated castrated intact male rats.
Ang HH, Cheang HS.
School of
Pharmaceutical Sciences, University Science Malaysia, Minden,
11800, Penang, Malaysia. hhang@usm.my
It has been reported
that Eurycoma longifolia Jack commonly known as Tongkat Ali
has gained notoreity as a symbol of man's ego and strength by
the Malaysian men because it increases male virility and
sexual prowess during sexual activities. As such, the effects
of 200, 400 and 800 mg/kg of butanol, methanol, water and
chloroform fractions of E. longifolia Jack were studied on the
laevator ani muscle in both uncastrated and
testosterone-stimulated castrated intact male rats after
dosing them for 12 consecutive weeks. Results showed that 800
mg/kg of butanol, methanol, water and chloroform fractions of
E. longifolia Jack significantly increased (p<0.05) the
leavator ani muscle to 58.56+/-1.22, 58.23+/-0.31, 60.21
+/-0.86 and 62.35 +/-0.98 mg/100 g body weight, respectively,
when compared with the control (untreated) in the uncastrated
intact male rats and 49.23+/-0.82, 52.23+/-0.36, 50.21+/-0.66
and 52.35+/-0.58 mg/100 g body weight, respectively, when
compared to control (untreated) in the testosterone-stimulated
castrated intact male rats. Hence, the pro-androgenic effect
as shown by this study further supported the traditional use
of this plant as an aphrodisiac.
PMID: 11693547 [PubMed
- indexed for MEDLINE]
Biol Pharm Bull 1998
Feb;21(2):153-5
Eurycoma longifolia
JACK and orientation activities in sexually experienced male
rats.
Ang HH, Sim MK.
School of
Pharmaceutical Sciences, University of Science Malaysia,
Penang.
The effects of
Eurycoma longifolia JACK were studied on the orientation
activities of sexually experienced male rats towards receptive
females (mounting, licking, anogenital sniffing), environment
(exploration, raring, climbing), themselves (genital grooming,
non-genital grooming) and mobility (unrestricted, restricted)
after dosing them with 200, 400 and 800 mg/kg body weight
twice daily for 10 d prior to the test. The results showed
that E. longifolia JACK modified the orientation activities of
the treated male rats in that they significantly displayed
more frequent and vigorous mounting, licking and anogenital
sniffing towards the receptive females, and it further
intensified self orientation as indicated by the increased
grooming of the genitals compared to the controls (p<0.05).
In addition, rats treated with 800 mg/kg of methanol, water
and butanol extracts of E. longifolia JACK continued to show
confinement to a particular area of the cage (around the
female), thus showing restriction in movement as compared to
the controls (p<0.05). However, the treated males possessed
a lack of interest in the external environment as indicated by
a reduction in exploration, raring and climbing on the cage
wall. Hence, the present study further supports the folk use
of E. longifolia JACK as an aphrodisiac.
PMID: 9514610 [PubMed
- indexed for MEDLINE]
Exp Anim 1997
Oct;46(4):287-90
Eurycoma longifolia
Jack enhances libido in sexually experienced male rats.
Ang HH, Sim MK.
School of
Pharmaceutical Sciences, University of Science Malaysia,
Penang, Malaysia.
The effects of
Eurycoma longifolia Jack were studied on the libido of
sexually experienced male rats after dosing them with 200, 400
and 800 mg/kg body weight twice daily of different fractions
of E. longifolia Jack for 10 days. Results showed that E.
longifolia Jack produced a dose-dependent increase in mounting
frequency of the treated animals with 400 mg/kg of chloroform,
methanol, water and butanol fractions resulting in mounting
frequencies of 5.3 +/- 1.2, 4.9 +/- 0.7, 4.8 +/- 0.7 and 5.2
+/- 0.1, and 800 mg/kg further increased them to 5.4 +/- 0.8,
5.4 +/- 0.8, 5.2 +/- 0.6 and 5.3 +/- 0.2 respectively but
there were no erections, intromissions, ejaculations or
seminal emissions during the 20-min observation period which
allowed for the measurement of sexual arousal reflected by
mounting frequency uninfluenced by other behavioural
components. This study provides evidence that E.
longifolia Jack is a potent stimulator of sexual arousal
in sexually vigorous male rats in the absence of feedback from
genital sensation.
PMID: 9353636 [PubMed
- indexed for MEDLINE]
Exp Anim 2000
Jan;49(1):35-8
Effects of Eurycoma
longifolia Jack (Tongkat Ali) on the initiation of sexual
performance of inexperienced castrated male rats.
Ang HH, Cheang HS,
Yusof AP.
School of
Pharmaceutical Sciences, University Science Malaysia, Penang,
Malaysia.
We studied the effects
of Eurycoma longifolia Jack, commonly known as Tongkat Ali in
Malaysia, on the initiation of sexual performance and the
weights of sexual accessories in inexperienced castrated male
rats. The doses of 200, 400 and 800 mg/kg body weight, which
were extracted from E. longifolia Jack, were orally
administered to the rats twice daily for 10 days prior to the
tests and continued throughout the test period. Testosterone
was used as a positive control after injecting 15 mg/kg daily
subcutaneously for 32 days. Results showed that E. longifolia
Jack produced a dose-dependent increase in sexual performance
of the treated animals, but the E. longifolia Jack groups
showed lower sexual performance in mounting, intromission and
ejaculation than the testosterone group. Further results also
showed that E. longifolia Jack promoted the growth of both
ventral prostate and seminal vesicles as compared with the
control, but the growth of sexual accessories at 800 mg/kg of
butanol, methanol, water and chloroform fractions of E.
longifolia Jack was less than that of testosterone treated
group. The present study therefore gives further evidence of
the folkuse of E. longifolia as an aphrodisiac.
PMID: 10803359 [PubMed
- indexed for MEDLINE]
Fundam Clin Pharmacol
2001 Aug;15(4):265-8
Aphrodisiac
evaluation in non-copulator male rats after chronic
administration of Eurycoma longifolia Jack.
Ang HH, Ngai TH.
School of
Pharmaceutical Sciences, University of Science Malaysia,
Minden, 11800, Penang, Malaysia.
The aphrodisiac effect
of Eurycoma longifolia Jack (0.5 g/kg) was evaluated in
noncopulator male rats using an electrical cage. Fractions of
E. longifolia Jack decreased the hesitation time of
noncopulator male rats, throughout the investigation period.
Furthermore, it possessed a transient increase in the
percentage of the male rats responding to the right choice,
more than 50% of the male rats scored "right choice" after 3
weeks post-treatment and the effect became more prominent
after 8 weeks post-treatment (only 40-50% of the control male
rats responded to the right choice) using the electrical
copulation cage. Hence, this study lends further support to
the use of the plant by indigenous populations as a
traditional medicine for its aphrodisiac property.
PMID: 11564133 [PubMed
- indexed for MEDLINE]
Int J Androl 2000;23 Suppl 2:82-4 Related Articles,
Books, LinkOut
Phytochemicals and
the breakthrough of traditional herbs in the management of
sexual dysfunctions.
Adimoelja A.
School of medicine
'Hang Tuah' University, Teaching and Naval Hospital,Surabaya,
Indonesia.
Traditional herbs have
been a revolutionary breakthrough in the management of
erectile dysfunction and have become known world-wide as an
'instant' treatment. The modern view of the management of
erectile dysfunction subscribes to a single etiology, i.e. the
mechanism of erection. A large number of pharmacological
agents are orally consumed and vasoactive agents inserted
intraurethrally or injected intrapenially to regain good
erection. Modern phytochemicals have developed from
traditional herbs.
Phytochemicals focus their mechanism
of healing action to the root cause, i.e. the inability to
control the proper function of the whole body system. Hence
phytochemicals manage erectile dysfunction in the frame of
sexual dysfunction as a whole entity.
Protodioscin is a
phytochemical agent derived from Tribulus terrestris L plant,
which has been clinically proven to improve sexual desire and
enhance erection via the conversion of protodioscine to DHEA
(De-Hydro-Epi-Androsterone). Preliminary observations suggest
that Tribulus terrestris L grown on different soils does not
consistently produce the active component Protodioscin.
Further photochemical studies of many other
herbal plants are needed to explain the inconsistent results
found with other herbal plants, such as in diversities of
Ginseng, Eurycoma longifolia, Pimpinella pruacen, Muara puama,
Ginkgo biloba, Yohimbe etc.
PMID: 10849504 [PubMed
- indexed for MEDLINE]
J Ethnopharmacol 2002
Sep 1;82(1):55 Related Articles, Books, LinkOut
In vitro anti-tumor
promoting and anti-parasitic activities of the quassinoids
from Eurycoma longifolia, a medicinal plant in Southeast Asia.
Jiwajinda S,
Santisopasri V, Murakami A, Kawanaka M, Kawanaka H, Gasquet M,
Eilas R, Balansard G, Ohigashi H.
Central Laboratory and
Greenhouse Complex, Kasetsart University, Kamphaeng Saen
Campus, 73140, Nakhon Pathom, Thailand
Some
quassinoids (1-6) isolated previously as plant growth
inhibitors from the leaves of Eurycoma longifolia Jack.
(Simaroubaceae) were subjected to in vitro tests on anti-tumor
promoting, antischistosomal and plasmodicidal activities. The
most active compound for inhibition of tumor promoter-induced
Epstein-Barr virus activation (anti-tumor promotion) was
14,15beta-dihydroxyklaineanone (5, IC(50)=5 &mgr;M).
Longilactone (1) gave significant antischistosomal effect at a
concentration of 200 &mgr;g/ml. 11-Dehydroklaineanone (3)
and 15beta-O-acetyl-14-hydroxyklaineanone (6) showed potent
plasmodicidal activity (IC(50)=2 &mgr;g/ml).
Thus it was suggested that E. longifolia possesses high
medicinal values due to the occurrence of a variety of
quassinoids.
PMID: 12169407 [PubMed
- as supplied by publisher]
J Nat Prod 1991
Sep-Oct;54(5):1360-7Related Articles, Books,
LinkOut
Cytotoxic and antimalarial constituents of the roots of
Eurycoma longifolia.
Kardono LB,
Angerhofer CK, Tsauri S, Padmawinata K, Pezzuto JM, Kinghorn
AD.
Department of
Medicinal Chemistry and Pharmacognosy, College of Pharmacy,
University of Illinois, Chicago 60612.
By
bioactivity-directed fractionation, five cytotoxic
constituents have been characterized from the roots of
Eurycoma longifolia collected in Kalimantan, Indonesia. Four
canthin-6-one alkaloids, namely, 9-methoxycanthin-6-one,
9-methoxycanthin-6-one-N-oxide, 9-hydroxycanthin-6-one, and
9-hydroxycanthin-6-one-N-oxide, and one quassinoid,
eurycomanone, were found to be cytotoxic principles. Each of
these compounds was evaluated against a panel of cell lines
comprising a number of human cancer cell types [breast, colon,
fibrosarcoma, lung, melanoma, KB, and KB-V1 (a multi-drug
resistant cell line derived from KB)] and murine lymphocytic
leukemia (P-388). The canthin-6-ones 1-4 were found to be
active with all cell lines tested except for the KB-V1 cell
line. Eurycomanone was inactive against murine lymphocytic
leukemia (P-388) but was significantly active against the
human cell lines tested. Two additional isolates, the
beta-carboline alkaloids beta-carboline-1-propionic acid and
7-methoxy-beta-carboline-1-propionic acid, were not
significantly active with these cultured cells. However,
compounds 5 and 7 were found to demonstrate significant
antimalarial activity as judged by studies conducted with
cultured Plasmodium falciparum strains. The structures of the
novel compounds 2-4 and 7 were established by spectral and
chemical methods.
PMID:
1800638 [PubMed - indexed for MEDLINE]