TONGKAT ALI AND APHRODISIAC PROPERTY: FACT OR FOLKLORE?
VI. TONGKAT ALI AND APHRODISIAC PROPERTY: FACT OR FOLKLORE?
The possibility of bioactive aphrodisiacs, substances that stimulate sexual desire and that may be derived from animals, minerals, and plants (55), has been attractive throughout recorded history and the passion of man since time immemorial.
Most of these ideas originated from the ancient belief in the therapeutic efficacy of ‘‘signature’’—the notion that plants or animal organs resembling
the genitalia would impart sexual powers. As such, among them are rhinoc-
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eros horn and reindeer antler, which have been extensively used by men to enhance sexual drive, based on the association between their shapes and the erect penis.
Reindeer shed their antlers annually; collected shedded antlers are im- ported from Canada, Finland, Norway, and Sweden into Japan for aphro- disiac purpose. Although the fresh antlers are supposed to be more powerful, removal of live antlers from the animals is forbidden in Scandinavia. There- fore, live reindeers have been imported to provide the best possible aphrodis- iac quality (56).
Rhinoceros horn is considered a panacea in East Asia and the horns are widely used to increase male sexual capacity including the capacity for erection. Chemical analysis of powdered horn extracts reveals only polypep- tides, sugars, phosphorus, ethanolamine, and free amino acids such as aspartic acid, threonine, ornithine, lysine, histidine, and arginine (which has been suggested to increase the intensity of sensation during sex) (57). Rhinoc- eros horn is, after all, only a modified epidermis.
Mylabris, an alcoholic extract from the dried bodies of China blister beetles (Pan mao), or Spanish fly (the generic name for a variety of species of beetles including Cantharis vesicatoria, Lytta vesicatoria, Epicauta funebris, and Mylabris phalerata), is used in China today as an aphrodisiac and to in- duce abortions. The active principle, called cantharidin, is a potent vesicant with an estimated fatal dose in humans of 32 mg. It causes irritation of the urethra, resulting in priapism (58).
Other popular aphrodisiacs include lion-tailed macaque (59), tiger penis, bear paws, and snake bile (60). The study of plants exhibiting aphrodisiac property is becoming more important because of international pressure against the slaughter of animals since this eventually will cause many animals to become endangered or extinct.
Punica granatum has been a symbol of love, fertility, and immorality in Oriental regions (61). The yohimbine-rich bark of Corynanthe yohimbe, indigenous to West Africa, has been employed for centuries as an aphrodisiac (62). It contains the indole alkaloid, which has been used as a sexual stimulant for domestic animals and, more recently, to treat impotence in men (63–66).
Chelidonium majus , Heracleum sphondylium, and Satureja montana have been formulated into topical preparations by the European community for vaginal douches to increase sexual desire in women (67). Similarly, Hindu medicine still claims that Aristolochia indica, Crocus sativus, Alpinia galanga, and Allium cepa are potent aphrodisiacs (68).
In Malaysia, tongkat Ali has also gained notoriety as a male aphrodisiac and this has caused rampant, excessive, and uncontrolled encroachments into forest reserves. The raids have become so frequent and massive that the
Eurycoma Iongifolia Jack (Tongkat Ali) 649
Forestry Department in Malaysia is worried that the plant species may become extinct if immediate steps are not taken to stop the wanton uprooting (69).
Numerous scientific investigations pertaining to the aphrodisiac prop- erty of this plant have been exhaustively carried out using both the in vivo and in vitro animal models. However, the definitive criteria used to establish the aphrodisiac value of a compound still remain elusive. Nevertheless, it was found that higher erectile function observed in a treated animal provides evidence for responses and an increase in sexual pleasure (70).
Male sexual activity evaluation of the effect of this plant showed that in the absence of receptive females, sexually normal male rodents treated with various extracts of this plant did not exhibit any homosexuality during the observation period (71), unlike PCPA ( p-chlorophenylalanine ester), which did lead to homosexuality (72). In addition, the treated male rodents exhibited increase in the penile erection index (71), using the methods previously described (73,74), in an observation cage (75).
In addition, the effects of this plant on the pendiculation activities (act of yawning and stretching) in the male rodents were studied following the method previously described (74), since it is pertinent that yawning, alone or associated with stretching, is considered to be an ancestral vestige surviving throughout evolution, which subserves the purpose of sexual arousal (76). Results showed that the extracts enhanced pendiculation activities in sexually normal male rodents (77) as well as in middle-aged, 9-month-old, retired breeder male rodents, but to a smaller degree (78). Thus, these results provided further evidence of erectile responses and increase in sexual pleasure (70).
The above interesting results led to further investigations on the masculine copulatory behavior of treated sexually normal (79) and middle- aged (80) male rodents in the presence of receptive females (81,82). Results showed that treated sexually normal male rodents exhibited increase in ejaculation latencies-1, -2, and -3 (79), thus suggesting that these extracts increased the sexual performance of the male rodents by extending the duration of coitus (83,84). In addition, the increase in the above three parameters and also decrease in both postejaculatory intervals -1 and -2 (79) led to the conclusion that these extracts intensified the sexual activity of the male rodents in a sustained manner by decreasing the refractory period between the different series of copulation. This was also observed in middle- aged rodents but to a smaller degree (80).
Further investigations were also carried out pertaining to the effect of this plant on the libido of sexually experienced male rodents. Sexual arousal or motivation with mount tests following penile anesthetization is a reliable index of pure libido unaffected by the reinforcing effect of genital sensation (85,86). Results showed that these extracts enhanced the libido of sexually
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experienced male rodents, providing evidence that this plant is a potent stimulator of sexual arousal in intact, sexually vigorous male rodents in the absence of feedback from genital sensation (87).
Further studies were also carried out pertaining to the orientation activities of the treated sexually experienced male rodents using the methods previously described (88,89) because modification of orientation activities is one of the criteria in determining male sexual behavior (88,90). Results showed that this plant enhanced the orientation activities of treated males toward receptive females by causing them to display vigorous anogenital investigatory behavior, and further intensified self-orientation as evidenced by increased grooming of their own genitalia (91). These improved the sexual performance of treated sexually experienced male rodents (84,92).
In addition, there was an enhancement of the sexual motivation in the treated sexually naı¨ve male mice (93), middle-aged male rats (94), and noncopulator male rats (95).
Similarly, there was also a slow and transient reduction in the hesitation time before the treated sexually naı¨ve male mice crossed the electrical grid (maintained at 0.12 mA) in the copulation cage to reach the goal cage, besides an increase in the percentage of sexually naı¨ve male mice scoring ‘‘right choice’’ (goal cage with an estrous female mouse) throughout the investiga- tion period (96). An electrical grid was used as an obstruction in the copu- lation cage to determine how much a negative stimulus (crossing an electrical grid) a male mouse was willing to overcome to reach the sexual contact. Sim- ilar results were obtained in sexually naı¨ve male rats (97) and noncopulator male rats (98). Longitudinal study showed that these extracts were able to maintain sexual activity in aging rats (99).
Further results also indicated that these extracts promoted the growth of accessory sexual organs , viz. ventral prostate and seminal vesicles in the inexperienced castrated male rats (100), penis in the sexually experienced castrated male rats (101), levator ani muscle in both the uncastrated and testosterone-stimulated castrated intact male rats (102).
Potency activity of the aphrodisiac property was also evaluated in male rats treated with these extracts. Results showed that these extracts produced a dose-dependent, recurrent, and significant increase in the episodes of penile reflexes as evidenced by increase in quick flips, long flips, and erections during the observation period (103).
Other scientific investigators pursued the study of the aphrodisiac effects of aqueous extract of the roots in male rodents and found that they showed intense copulatory behavior and a 480% increase in the serum testosterone (104,105).
In addition, the sperm quality and parameters were also investigated after the rodents were dosed with extracts from this plant (106,107). Results
Eurycoma Iongifolia Jack (Tongkat Ali) 651
showed that there was a significant increase in the total sperm count, motility, forward velocity, and fructose concentration in the cauda epididymal semen, which were probably due to an increase of androgen, caused by the proan- drogenic effect of these extracts, which enhanced the physiological matura- tion of sperms (107).
The total sperm count and motility were calculated using the method previously described (108) and the forward velocity was calculated using the method previously described (109). Fructose concentration in the cauda epi- didymal semen was analyzed according to the method previously described (110).
In conclusion, the above studies clearly showed that various extracts from E. longifolia Jack had aphrodisiac property and this may be attributed to the presence of the active compounds in more than one fraction.
Although these studies lend further support for the use of this plant by the indigenous population as a traditional aphrodisiac, it is suggested that a detailed toxicological study should also be carried.
REFERENCES 1. Traditional medicines now a global worry. The Sun, Friday, May 17, 2002, 5.
2. Herbal products enjoying growing demand: Dr. Lim. The New Straits Times, Wednesday, August 21, 2002, B6. 3. Melchior H. Engler’s Syllabus der Pflauzenfamilien. Vol. 2. Berlin: Gebruder Borntrager, 1964. 4. Nooteboom HP. Flora Malesiana 1962; 6(ser. 1):193. 5. Cronquist A. An Integrated System of Classification of Flowering Plants. New York: Columbia University Press, 1981. 6. Corner EJH. Wayside Trees of Malaya. Kuala Lumpur: Government Printing Office, 1952. 7. Jack W. Description of Malayan Plants III. Leiden: Boerhaave Press, 1977. 8. Steenis V. Flora Malesiana 1972; 6:203. 9. Malaysian Herbal Monograph. Vol 1. Kuala Lumpur: Malaysian Monograph Committee, 1999. 10. http://www.bogor.indo.net.id/kri/eurycoma.htm (verified on November 1, 2002). 11. Goh SH, Chuah CH, Mok JSL, Soepadmo E. Malaysian Medicinal Plants for the Treatment of Cardiovascular Diseases. Selangor: Pelanduk Publication Sdn Bhd, 1995. 12. Nooteboom L. Simaroubaceae. In: Steenis JV ed. Flora Malesiana. 6th ed. Groningen: Wolters-Woordhoff Publishing, 1972:205. 13. Gimlette JD, Thomson HW, eds. A Dictionary of Malayan Medicine. Kuala Lumpur: Oxford University Press, 1977:183. 14. Standard of ASEAN Herbal Medicine. Vol. 1. Jakarta: ASEAN Countries, 1993.
652 Ang 15. Perry LM, ed. Medicinal Plants of East and Southeast Asia. Attributed
Properties and Uses. Boston: MIT Press, 1980:389. 16. Thoi LV, Suong NN. Constituents of Eurycoma longifolia Jack. J Org Chem 1970; 35:1104–1109. 17. Burkill IH, Haniff M. Gard Bull Straits Settl, 1930; 182. 18. Gimlette JD, Burkill IH. Gard Bull Straits Settl, 1930; 6:329. 19. Marziah M. Tanaman Perubatan Tradisional. Serdang: Universiti Pertanian Malaysia, 1987. 20. Burkill IH. A Dictionary of the Economic Products of the Malay Peninsula. Vol. 1 and 2. Malaysia: Ministry of Agriculture, 1966. 21. Jagananth JB, Ng LT. Herbs The Green Pharmacy of Malaysia. Kuala Lumpur: Vinpress Sdn. Bhd. and Malaysian Research And Development Insti- tute, 2000. 22. Research: Tongkat Ali may be effective against cancer and HIV. The New Sunday Times, Sunday, July 21, 2002; 1–2. 23. Ensuring steady supply. The STAR, Thursday, July 4, 2002; 13. 24. Darise M, Kohda H, Mitzutani K, Tanaka O. Eurycomanone and eurycoma- nol, quassinoids from the roots of Eurycoma longifolia. Jack. Phytochemistry 1982; 21:2091–2093. 25. Suong NN, Bhatnagar S, Polonsky J, Vuilhorgne M, Prange T, Pascard C.
Structure of laurycolactone A and B, new C 18 -quassinoids from Eurycoma longifolia and revised structure of eurycomalactone (X-ray analysis). Tetrahe- dron Lett 1982; 23:5159–5162. 26. Darise M, Kodha H, Mitzutani K, Tanaka O. Revision of configuration of the 12-hydroxyl group of eurycomanone and eurycomanol, quassinoids from Eurycoma longifolia . Phytochemistry 1983; 22:1514. 27. Bates RB, Linz GS, Tempesta MS. Structures of eurycomalactone and related terpenoids. J Org Chem 1984; 49:2820–2821. 28. Chan KL, O’Neill MJ, Phillipson JD, Warhurst DC. Plants as sources of antimalarial drugs. Part 3. Eurycoma longifolia Jack. Planta Med 1986; 52:105– 107. 29. Chan KL, Lee SP, Sam TW, Han BH, Isolation and structural elucidation of
eurycomanol-2-O-h- D -glucopyranoside from Eurycoma longifolia Jack. UNESCO subregional seminar/workshop on the systematic identification of natural products, Bangi, Malaysia, June 13–17, 1988. 30. Chan KL, Lee SP, Sam TW, Han BH. A quassinoid glycoside from the roots of Eurycoma longifolia . Phytochemistry 1989; 28:2857–2859. 31. Morita H, Kishi E, Takeya K, Itokawa H, Tanaka O. New quassinoids from the roots of Eurycoma longifolia. Chem Lett 1990; 749–752. 32. Chan KL, Lee SP, Sam TW, Tan SC, Noguchi H, Sankawa U. 13h, 18- Dihydroeurycomanol, a quassinoid from Eurycoma longifolia. Phytochemistry 1991; 30:3138–3141. 33. Kardono LBS, Angerhofer CK, Tsauri S, Padmawinata K, Pezzuto JM, Kinghorn AD. Cytotoxic and antimalarial constituents of the roots of Eurycoma longifolia . J Nat Prod 1991; 54:1360–1367.
Eurycoma Iongifolia Jack (Tongkat Ali) 653 34. Tada H, Yasuda F, Otani K, Doteuchi M, Ishihara Y, Shiro M. New antiulcer
quassinoids from Eurycoma longifolia. Eur J Med Chem 1991; 26:345–349. 35. Chan KL, Iitaka Y, Noguchi H, Sugiyama H, Saito I, Sankawa U. 6a- Hydroxyeurycomalactone, a quassinoid from Eurycoma longifolia. Phytochem- istry 1992; 31:4295–4298. 36. Itokawa H, Kishi E, Morita H, Takeya K. Cytotoxic quassinoids and tirucallane-type triterpenes from the woods of Eurycoma longifolia. Chem Pharm Bull 1992; 40:1053–1055. 37. Morita H, Kishi E, Takeya K, Itokawa H, Iitaka Y. Highly oxygenated quassinoids from Eurycoma longifolia. Phytochemistry 1993; 33:691–696. 38. Itokawa H, Qin XR, Morita H, Takeya K, Iitaka Y. Novel quassinoids from Eurycoma longifolia . Chem Pharm Bull 1993; 41:403–405.
39. Itokawa H, Qin XR, Morita H, Takeya K. C 18 and C 19 quassinoids from Eurycoma longifolia . J Nat Prod 1993; 56:1766–1771. 40. Chan KL, Lee,SP, Yuen KH, Antipyretic Activity of Quassinoids from Eury- coma longifolia Jack. 11th Chemical Seminar on Natural Products, UNIMAS, Sarawak, Malaysia, June 25–28, 1995. 41. Ang HH, Chan KL, Mak JW. In vitro antimalarial activity of quassinoids from Eurycoma longifolia against Malaysian chloroquine-resistant Plasmodium falciparum Isolates. Planta Med 1995; 61:177–178. 42. Ang HH, Hitotsuyanagi Y, Takeya K. Eurycolactones A–C, novel quassinoids from Eurycoma longifolia. Tetrahedron Lett 2000; 41:6849–6853. 43. Jiwajinda S, Santisopasri V, Murakami A, Hirai N, Ohigashi H. Quassinoids from Eurycoma longifolia Jack as plant growth inhibitors. Phytochemistry 2001; 58:959–962. 44. Ang HH, Hitotsuyanagi Y, Fukaya H, Takeya K. Quassinoids from Eurycoma longifolia . Phytochemistry 2002; 59:833–837. 45. Jiwajinda S, Santisopasri V, Murakami A, Kawanaka M, Kawanaka H, Gasquet M, Eilas R, Balansard G, Ohigashi H. In vitro anti-tumor promoting and anti-parasitic activities of the quassinoids from Eurycoma longifolia, a medicinal plant in Southeast Asia. J Ethnopharmacol 2002; 82:55–58. 46. Itokawa H, Kishi E, Morita H, Takeya K, Iitaka Y. Eurylene, a new squalene- type triterpene from Eurycoma longifolia. Tetrahedron Lett 1991; 32:1803–1804. 47. Itokawa H, Kishi E, Morita H, Takeya K, Iitaka Y. A new squalene-type triterpene from the woods of Eurycoma longifolia. Chem Lett 1991; 2221–2222. 48. Morita H, Kishi E, Takeya K, Itokawa H, Iitaka Y. Squalene derivatives from Eurycoma longifolia . Phytochemistry 1993; 34:765–771. 49. Morita H, Kishi E, Takeya K, Itokawa H. Biphenylneolignans from wood of Eurycoma longifolia . Phytochemistry 1992; 31:3993–3995. 50. Mitsunaga K, Koike K, Tanaka T, Ohkawa Y, Kobayashi Y, Sawaguchi T, Ohmoto T. Canthin-6-one alkaloids from Eurycoma longifolia. Phytochemistry 1994; 35:799–802. 51. Ang HH, Characterisation of local Plasmodium falciparum isolates by cloning and susceptibility studies against antimalarial drugs. Ph.D dissertation, Uni- versity Science Malaysia, Penang, Malaysia, 1992.
654 Ang 52. Okano M, Fukamiya N, Lee KH. Biologically active compounds from sima-
roubaceous plants. In: Rahman Atta-ur-, ed. Studies in Natural Products Chemistry. Vol. 7. Amsterdam: Elsevier Science Publishers, 1990:369–404. 53. Trager W, Jensen JB. Human malaria parasites in continuous culture. Science 1976; 193:673–675. 54. Trager W, Jensen JB. Cultivation of erythrocyte stage. Bull WHO 1997; 5:363– 365. 55. Taberner PV. Aphrodisiacs: The Science and the Myth. London: Croom Helm, 1985.
56. http://www.santesson.com/aphrodis/animal.htm (verified on November 1, 2002).
57. Inagaki I, Oida N, Nagoya Shiritsu Daigaku, Yakugakuba Kenkyu Nempo, 1970; 57. 58. Taberner PV. Sex and drugs–Aphrodite’s legacy. Trends Pharmacol Sci 1985; 6:49–54. 59. Ramachandran KK, Easa PS, Vijayakumaran P. Nair, Management of Periya Tiger Reserve—problems and perspective. Tigerpaper 1987; 14:25–33. 60. Animal rights? Wrong. Asia Mag April 4–6, 1997; 30. 61. Farnsworth NR, Bingel AS, Cordell GA, Crane FA, Fong HHS. Potential value of plants as sources of new antifertility agents II. J Pharm Sci 1975; 64:717–753. 62. Johanson DN, Diamond M. Yohimbine and sexual stimulation in the male rats. Physiol Behav 1968; 4:411–413. 63. Reid K, Surridge DH, Morales A. Double-blind trial of yohimbine in treatment of psychogenic impotence. Lancet 1987; 2:241–243. 64. Morales A, Condra M, Owen JA, Surridge DH, Fenemore J, Harris C. Is yohimbine effective in the treatment of organic impotence? J Urol 1987; 137:1168–1172. 65. Susset JG, Tessier CD, Wineze J. Effect of yohimbine in the treatment of erectile impotence: a double-blind study. J Urol 1989; 141:1360–1363. 66. Sonda LP, Mazo R, Chancellor MB. The role of yohimbine in the treatment of erectile dysfunction. J Sex Marital Ther 1990; 16:15–21. 67. Messegne M. Man and Plants. New York: Macmillan, 1973. 68. Puri HS. Vegetable aphrodisiacs of India. Q J Crude Drug Res 1971; 11:1742– 1748. 69. Dept to root out problem of ‘‘tongkat Ali’’ pilferage. The STAR, Tuesday January 30, 2001; 6. 70. Argiolas AM, Melis MR, Gessa GL. Yawning and penile erection: central dopamine-oxytocin-adrenocorticotropin connection. Ann NY Acad Sci 1988; 525:330–337. 71. Ang HH, Sim MK. Effects of Eurycoma longifolia Jack on penile erection index and homosexual mountings in rats. Pharm Sci 1997; 3:117–119. 72. Whalen RE, Luttge WG. p-Chlorophenylalanine methyl ester: an aphrodisiac? Science 1970; 169:1000–1001. 73. Benassi Benelli A, Ferrari F, Pellegrini Quarantotti B. Penile erection induced
Eurycoma Iongifolia Jack (Tongkat Ali) 655 by apomorphine and N-n-propylnorapomorphine in rats. Arch Int Pharmaco-
dyn 1979; 242:241–247. 74. Baggio G, Ferrari F. The role of dopaminergic receptors in the behavioral effects induced by lisuride in male rats. Psychopharmacology 1983; 80:38–42. 75. Mendelson SD, Gorzalka BB. An improved chamber for the observation and analysis of the sexual behavior of the female rat. Physiol Behav 1987; 39:67–71. 76. Ferrari W, Gessa GL, Vargiu L. Behavioural effects induced by intracisternally injected ACTH and MSH. Ann NY Acad Sci 1963; 104:330–345. 77. Ang HH, Sim MK. Evaluation of pendiculation activities in male rats after oral administration of Eurycoma longifolia Jack. Pharm Biol 1998; 36:144–146. 78. Ang HH, Lee KL. Eurycoma longifolia intensifies sexual arousal in middle aged male rats. The Science Conference, Yemeni Scientific Research Foundation, Sana’a, Republic of Yemen, Oct 11–13, 2001. 79. Ang HH, Sim MK. Effects of Eurycoma longifolia Jack on sexual behaviour of male rats. Arch Pharm Res 1997; 20:656–658. 80. Ang HH, Lee KL. Effects of Eurycoma longifolia Jack on masculine copulatory behaviour in middle aged male rats—a comparison study. Nat Prod Sci 2002; 8:44–47. 81. Meyerson BJ, Lindstrom L, In: James VHT, Martini L, eds. Hormonal Ste- roids. Excerpta Medical International Congress, 1971; serial no. 219. 82. Meyerson BJ, Lindstrom L. Sexual motivation in the female rat. Acta Physiol Scand 1973; 389(suppl):1–80. 83. Beach EA, Whalen RE. Effect of ejaculation on sexual behaviour in the male rat. J Comp Physiol Psychol 1959; 52:249–252. 84. Ferrari F, Baggio G, Mangiafico V. The dopamine autoreceptor agonist B-HT 920 markedly stimulates sexual behaviour in male rats. Experientia 1985; 41:636–638. 85. Alder N, Bermant G. Sexual behaviour of male rats: effects of reduced sensory feedback. J Comp Physiol Psychol 1966; 61:240–243. 86. Davidson JM, Gray GD, Smith ER. Animal models in the endocrinology of reproductive behaviour. In: Alexander NJ, ed. Animal Models for Research on Contraception and Fertility. New York: Harper & Row, 1978:61–62. 87. Ang HH, Sim MK. Eurycoma longifolia Jack enhances libido in sexually experienced male rats. Exp Anim 1997; 46:287–290. 88. Malminas CO. Monoaminergic influence on testosterone activated copulatory behaviour in the male rats. Acta Physiol Scand 1973; 89:1–128. 89. Hull EM, Nishita JK, Bitran D. Perinatal dopamine-related drugs demasculin- ized rats. Science 1984; 9:1011–1013. 90. Morales A, Surridge DHC, Marshall PG, Fenemote J. Non-hormonal pharmacological treatment of organic impotence. J Urol 1982; 128:45–47. 91. Ang HH, Sim MK. Eurycoma longifolia Jack and orientation activities in sexually experienced male rats. Biol Pharm Bull 1998; 21:153–155. 92. Doherty PC, Baum MJ, Todd RB. Effects of chronic hypoprolactinemia on sexual arousal and erectile function in male rats. Neuroendocrinology 1986; 42:368–375.
656 Ang 93. Ang HH, Chan KL, Gan EK, Yuen KH. Enhancement of sexual motivation in
sexually naı¨ve male mice by Eurycoma longifolia Jack. Int J Pharmacog 1997; 35:144–146. 94. Ang HH, Cheang HS. Effects of chronic administration of Eurycoma longifolia Jack on the copulatory behavior in middle aged male rats. J Herbs Species Med Plants 2002; 9:109–114. 95. Ang HH, Sim MK. Aphrodisiac effect of Eurycoma longifolia Jack in non- copulator male rats. Fitoter 1998; 69:445–447. 96. Ang HH, Sim MK. Aphrodisiac evaluation in sexually naı¨ve male mice after chronic administration of Eurycoma longifolia Jack (tongkat Ali). Nat Prod Sci 1998; 4:58–61. 97. Ang HH, Sim MK. Eurycoma longifolia Jack increases sexual motivation in sexually naı¨ve male rats. Arch Pharm Res 1998; 21:779–781. 98. Ang HH, Ngai TH. Aphrodisiac evaluation in non-copulator male rats after chronic administration of Eurycoma longifolia Jack. Fund Clin Pharmacol 2001; 15:265–268. 99. Ang HH, Cheang HS. Promotion of sexual activity in rats with Eurycoma longifolia Jack. J Herbs Spices Med Plants 1999; 6:23–28.
100. Ang HH, Cheang HS, Yusof APM. Effects of Eurycoma longifolia Jack (tongkat Ali) on the initiation of sexual performance of inexperienced castrated male rats. Exp Anim 2000; 49:35–38.
101. Ang HH, Cheang HS. Effects of Eurycoma longifolia Jack in maintaining mating behavior of sexually experienced castrated male rats. Nat Prod Sci 1999; 5:138–141.
102. Ang HH, Cheang HS. Effects of Eurycoma longifolia Jack on laevator ani muscle in both uncastrated and testosterone-stimulated castrated intact male rats. Arch Pharm Res 2001; 24:437–440.
103. Ang HH, Ikeda S, Gan EK. Evaluation of the potency activity of Eurycoma longifolia Jack. Phytother Res 2001; 15:435–436. 104. Kwan TK, Saad JM, Farizaturradiah O, Koh BH, The effect of Eurycoma longifolia on rat and human testicular steroidogenesis. National Medicinal Plants Convention, Kuala Lumpur, Malaysia, Oct 13–15, 1995.
105. Thambi MIM, Update on current tongkat Ali research. 11th Malaysian Uro- logical Conference, Kuantan, Pahang, Malaysia, Nov 7–11, 2001. 106. Mahanem MN, Lukman CH, The effects of Eurycoma longifolia Jack (tongkat Ali) on sexual behaviour of male rats and its sperm quality. MPS Pharmacy Scientific Conference, Penang, Malaysia, Oct 31–Nov 2, 2002.
107. Ang HH, Lee KL, Matsumoto K, Sperm parameters changes induced by Eury- coma longifolia Jack. 19th Congress of FAPA, Seoul, Korea, Oct 5–8, 2002. 108. Besley MA, Eliarson R, Gallegos AJ, Moghissi KS, Paulsen CA, Prasad MRN. Laboratory Manual for the Examination of Human Semen and Semen Cervical Mucus Interaction. Singapore: WHO Press, 1980.
109. Ratnasoorya WD. Effect of atropine on fertility of female rat and sperm motility. Indian J Exp Biol 1984; 22:463–466. 110. Bauer JD, Ackerman PG, Toro G. Clinical Laboratory Methods. St. Louis: Mosby Co., 1974.