Hall R W, Steinberger E
Neuroendocrinology. 1977;24(5-6):325-32. doi: 10.1159/000122719.
Normal, castrate and estradiol benzoate (EB; 1 microgram/100 g b.w. x 6d, s.c.)-treated castrate male rats were utilized to study the short term effects of these treatments upon the incorporation of 3H-glycine into LH-RH in vitro. The rise in serum LH and FSH observed in the untreated castrates was prevented by EB therapy. The treatment had no significant effect upon serum LH-RH levels or the incorporation of 3H-gly into LH-RH. EB treatment markedly (p less than 0.01) increased the hypothalamic LH-RH concentration and significantly lowered the specific activity (nCi/ng) of the 3H-gly-LH-RH (p less than 0.05). These results suggest that EB acts both on the pituitary and hypothalamus to suppress gonadotropin (Gn) release, but that, at the time period studied, neither castration or EB-treatment had any apparent effect upon hypothalamic LH-RH synthesis.
正常雄性大鼠、去势雄性大鼠以及接受苯甲酸雌二醇(EB;1微克/100克体重×6天,皮下注射)处理的去势雄性大鼠被用于研究这些处理对体外3H-甘氨酸掺入促性腺激素释放激素(LH-RH)的短期影响。未处理的去势大鼠血清促黄体生成素(LH)和促卵泡生成素(FSH)升高的情况可被EB治疗所阻止。该处理对血清LH-RH水平或3H-甘氨酸掺入LH-RH没有显著影响。EB处理显著(p<0.01)提高了下丘脑LH-RH浓度,并显著降低了3H-甘氨酸-LH-RH的比活性(nCi/ng)(p<0.05)。这些结果表明,EB作用于垂体和下丘脑以抑制促性腺激素(Gn)释放,但在所研究的时间段内,去势或EB处理对下丘脑LH-RH合成均无明显影响。