effects of short term administration of tulsi leaves on sexual
Transcription
effects of short term administration of tulsi leaves on sexual
Indian J Physiol LETTER Pharmacol 1999; 43 (3) : 398-400 TO THE EDITOR EFFECTS OF SHORT TERM ADMINISTRATION SEXUAL BEHAVIOUR IN FEMALE RATS OF TULSI LEAVES ON Sir, ( Received on October 10, 1996) estrous cycle. Every day during fixed period each of these female rats were presented with healthy male rats of proven reproductive activity. The female rat was kept with male rats for a total time of 10 minutes. During this time L.Q. was measured (5). The leaves of ocimum sanctum (Tulsi) have antifertility and abortifacient effect in female rats (1-3). These also decrease the sexual behavioural score in male rats (4). However, in none of these studies (1-3) the reproductory behaviour was measured in terms of Lordosis quotient (L.Q) in female rats. The present study was therefore undertaken to study the alterations in reproductory behaviour in terms of LQ after administration of Tulsi extract in adult female albino rats. After control study of 8 days these rats were given fresh Tulsi leaves extract (ocimum sanctum Linn). Each rat was given orally 80 mgs of fresh Tulsi leaves extract prepared in 15 ml of 5% glucose per day for two weeks (4). After 2 weeks Tulsi leaves were discontinued and they were given only water for a period of another 2 weeks. During this entire period of study their estrous cycle was studied and reproductive behaviour in terms of LQ was quantitatively measured. The Estrous cycle was disrupted 15 adult female albino rats weighing between 180 and 220 grams were taken. These rarts were separated in individual plastic cages and were given food and water ad libitum. Their Estrous cycle was studied everyday by taking vaginal smears. All of them were found to be having normal TABLE Group Number L.Q. *P<0.05; Control I: Effect of Tulsi leaves on Lordosis Quotient (x-SEM) (LQ). Tusli administration stopped but water adminiatered Tulsi administration 1st week 2nd week 1st week 2nd week 15 15 15 15 15 38 ± 5.2 24 ± 3.8 **P<O.OOI 20.0 ± 4* 6 ± 1.2** 6±1.1** Indian J Physiol Pharmacol Letter to the Editor 1999; 43(3) after the administration of Tulsi and finally the rats showed only the diestrus phase. In control rats, LQ was maxium during proesturs followed by estrus and metestrus, the least-being in diestrus phase. After administration of Tulsi, LQ decreased (P<O.05) and this decrease continued further even the stoppage of Tulsi (P<O.OOl) (Table I). In the present study the estrous cycle of rats was disrupted from second week of tulsi administration finally showing a continuous diestrous phase. This is probably due to tulsi leaves extract inhibiting ovarian hormones. Smith et al reported that the hormonal conditions during estrous as well as estrogen-progresterone treatment in ovariectomized female rats significantly potentiated the three immobility responses viz. Lordosis, tonic immobility and dorsal immobility response, and suggested that the ovarian hormones act through a common mechanism shared by all three responses (6). This explains why LQ is maximum during proestrous followed by estrous, metestrous and least diestrous 399 phase. The LQ decreased markedly after administration of Tulsi leaves. This is probably due to inhibition of ovarian hormones by Tulsi leaves. Lordosis behaviour is a sequense of sensorimotor reflexes. Dopamine system in striatum and forebrain is believed to inhibit the lordosis response (7). It was seen that selective destruction of dopamine system with 60HDA (8) or blockadge with dopamine antagonist (haloperiool) (9) facilitates Lordosis behaviour; while dopamine receptor agonist (d-amploetamine) blocked Lordosis (10). It is also documented that acute exposure to estrogen suppressed behaviours mediated by dopamine systems (11, 12). Thus in our study administration of tulsi leaves probably inhibited affects of ovarian hormones on dopamine system. Therefore, Lordosis quotient decreased after .administration of tulsi leaves. This effect of Tulsi leaves is probably long lasting and so after discontinuing tulsi leaves Lordosis quotient remained suppressed for two weeks. SANDIP R. SARDESSAI*, ABHAYA S. BaRKER AND MARJORIE E. ABRAHAM Department of Physiology, Goa Medical College, Bambolim, Goa - 403 202 REFERENCES 1. Chopra RN, Nayar SL, Chora IC. Glossary oflndian Medicinal Plants, CSIR 1956. 2. Nadkarni AK. Nadharnis Indian Material Medica in: Nadk arni AK. Bombay Popoular Book Depot 1954; 868. 3. Vora SB, Garg SK, Chaudhary RR. Indian Journol of Medical Research 57; 1969. *Corresponding Author 4. Kantak NM, Gogate MG. Effect of sho rt term administration of' Tul si (ocimum sanctum Linn) on rep roduct ive behaviour of adult male rats. Indian J Physiol Phurmacol 1992; 36 109-111. 5. Kuchn RE, Beach FA. Quantitative measurement of sexual receptivity in female rats. Behaviour 1963; 21: 282-299. 400 Letter to the Editor 6. Smith RL, Webster DG, Van Eartesveldt C, Majer ME. Effects of estrous, estrogen; progesterone priming and viginal stimulation on tonic immobility, dorsal immobility and Lordosis in female rat. Physial Behav 1985; 35: 570-581. 7. Pednekar JR, Mascarenhas JF. Role of striatal Dopamine in the Lordosis behaviour. Indian J Pliysiol Pharmacal 1993; 333-336. 8. Caggiula AR, Herndon JG, Scanlon R, Greenstone D, Bradshaw W, Sharp D. Dissociation of active from immobility components of sexual behaviour in female rats by central 6-hydroxdopamine implications Io r CA involvement in sexual behaviour and sensorimotor responsiveness. Brain Res 1979: 172. 9. Aolenius S, Engal J, Eriksson H, Medigh K, Sodarstem P. Importance of central catecholamines Indian J Physiol Pharmacol 1999; 43(3) in the mediation of Lordosis behaviour in ovariectomized rats treated with estrogen and inhibitors of monoamine synthesis. J Neural Tranum. 1972; 33: 247-255. 10. Everitt BJ, Fuxe K. Dopamine and sexual behaviour in Female rats. Effects of dopamine receptor agonists and solpiride. Neurosol lett 1977; 4: 209-213. 11. Joyee IN, Van Hartesveldt G. Behaviors induced by intrastriatal dopamine vary independently across estrous cycle. Pharmacal Biocheni Behav 1984; 20: 551-557. 12. Smith RL, Van Hartesveldt C. Effets of ovariectomy and estrogen replacement an intrastriatal dopamine elicited postural deviation. Pharmacal Biochem Behao 1985; 22: 689-694.