Tamura K, Abe Y, Kogo H
Department of Pharmacology, Tokyo University of Pharmacy and Life Science 1432-1, Horinouchi, Hachioji-shi, 192-0392, Tokyo, Japan.
Eur J Pharmacol. 2000 Jun 16;398(2):317-22. doi: 10.1016/s0014-2999(00)00312-5.
This study was planned to determine the effects and possible mechanism of action of phenytoin on development of the reproductive tract and first ovulation in immature rats. Rats were injected s.c. with 5 IU of equine chorionic gonadotrophin (equine CG) on day 26 to induce ovarian and uterine development. Treatment with phenytoin (140 mg/kg) at 1200 h on day 28, which induces serum levels approximately twice those reached with the clinical dose as anticorvulsant drug for humans, was effective for inhibiting the first ovulation and normal secretion of serum follicle - stimulating hormone and luteinizing hormone (LH) on day 29 as well as the preovulatory gonadotrophin surge on day 28. The block of ovulation was overcome by administration of human chorionic gonadotrophin or LH-releasing hormone on day 28. Simultaneous treatment with equine CG and phenytoin at 0800 h on day 26 did not affect either ovarian weight or ovarian hormones secretion, whereas phenytoin clearly inhibited the normal increase in uterine weight on day 27. Furthermore, phenytoin suppressed uterine growth after 17beta-oestradiol injection. These results indicate that phenytoin inhibits the first ovulation by inhibiting the gonadotrophin surge and further, that the drug impairs the stimulatory effects of oestrogen on uterine proliferation in the gonadotropin-induced ovulation model.
本研究旨在确定苯妥英钠对未成熟大鼠生殖道发育和首次排卵的影响及其可能的作用机制。在第26天给大鼠皮下注射5国际单位的马绒毛膜促性腺激素(马CG)以诱导卵巢和子宫发育。在第28天1200时用苯妥英钠(140mg/kg)进行治疗,该剂量诱导的血清水平约为作为人类抗惊厥药物临床剂量时所达到水平的两倍,其有效地抑制了第29天的首次排卵以及血清促卵泡激素和黄体生成素(LH)的正常分泌,以及第28天排卵前促性腺激素激增。在第28天给予人绒毛膜促性腺激素或促黄体激素释放激素可克服排卵阻滞。在第26天0800时同时用马CG和苯妥英钠治疗,既不影响卵巢重量也不影响卵巢激素分泌,而苯妥英钠明显抑制了第27天子宫重量的正常增加。此外,苯妥英钠抑制了注射17β-雌二醇后的子宫生长。这些结果表明,苯妥英钠通过抑制促性腺激素激增来抑制首次排卵,并且进一步表明,在促性腺激素诱导的排卵模型中,该药物损害了雌激素对子宫增殖的刺激作用。