Naess O, Cusan L, Brekke I, Purvis K, Torjesen P, Hansson V
Int J Androl. 1981 Dec;4(6):685-90. doi: 10.1111/j.1365-2605.1981.tb00752.x.
In the present study we have examined the effects of gonadotrophin releasing hormone (LHRH), sex steroids and glucocorticoids on the binding of LHRH to receptors in the pituitary of male intact and castrated rats. In intact rats, LHRH (10 microgram/day) treatment for 11 days caused a significant increase in LHRH binding, whereas testosterone (500 microgram/day) or oestradiol (50 microgram/day) were inhibitory. 17-hydroxyprogesterone and dexamethasone were without effects. In castrated rats, LHRH caused a marginal decrease in LHRH binding. Much greater inhibition was observed with testosterone and oestradiol. 17-hydroxyprogesterone reduced binding to that of intact controls, whereas dexamethasone was ineffective. When different doses of sex steroids were tested, both oestradiol, testosterone and 5 alpha-dihydrotestosterone inhibited LHRH in a dose-dependent manner. The lowest doses of steroids causing significant inhibition of LHRH binding in castrated animals were 0.5, 50 and 500 microgram/day for oestradiol, 5 alpha-dihydrotestosterone and testosterone, respectively. The present study shows that pituitary receptors for LHRH are regulated both by sex steroids and LHRH itself.
在本研究中,我们检测了促性腺激素释放激素(LHRH)、性类固醇和糖皮质激素对雄性未阉割及阉割大鼠垂体中LHRH与受体结合的影响。在未阉割大鼠中,连续11天每天注射10微克LHRH可使LHRH结合显著增加,而睾酮(每天500微克)或雌二醇(每天50微克)则具有抑制作用。17-羟孕酮和地塞米松无作用。在阉割大鼠中,LHRH使LHRH结合略有下降。观察到睾酮和雌二醇的抑制作用更强。17-羟孕酮使结合降至未阉割对照水平,而地塞米松无作用。当测试不同剂量的性类固醇时,雌二醇、睾酮和5α-二氢睾酮均以剂量依赖方式抑制LHRH。在阉割动物中导致LHRH结合显著抑制的最低类固醇剂量分别为:雌二醇每天0.5微克、5α-二氢睾酮每天50微克和睾酮每天500微克。本研究表明,垂体中的LHRH受体受性类固醇和LHRH自身的调节。