E. longifolia prefers acid and sandy soils at low altitude up to 700 m above sea level. Plants usually grow in beach forests, primary and secondary forests, mixed dipterocarp forests and also in heath forests. In Riau Province, Sumatra, 1991, the author found that plants were growing in areas with an average temperature of 25C and 86% humidity. The soils in this area were found to be poor in nutrients, but mycorrhizal fungi were found growing near the plants and may indicate an association. Seedlings require shade, during which time they develop an extensive root system. Following juvenile stages, plants need stronger light to develop vegetative and reproductive parts. E. longifolia flowers and fruits throughout the year, with peak flowering from June-July and peak fruiting in September.
E. longifolia originates from South East Asia, including Indonesia, Malay Peninsula, Thailand, Laos, Cambodia and Vietnam. In Indonesia, this species only occurs naturally in Sumatra and Kalimantan.
Though E. longifolia is currently mostly known as an aphrodisiac, in South East Asia, all parts of E. longifolia plants have long been used medicinally. The plant is commonly used throughout the region as a tonic after childbirth. The bark of the roots is used in the Malay Peninsula to cure fever, ulcers in the mouth, and intestinal worms. The Malays also use the paste of the plant to relieve headache, stomachache, pain caused by syphilis, and many other general pains.
One of the most unique uses for E. longifolia is that of the Sakai ethnic group in Sumatra who use the plant as an amulet to protect people from the smallpox virus.
The active constituents in E. longifolia, and many other species in the Family Simaroubaceae, include quassin, neo-quassin, glaukarubin, sedrin, eurycomanol that are mostly derivatives from compounds with 20 carbon atoms.
Clinical Studies - References
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]