Spona J
Endocrinol Exp. 1975 Sep;9(3):167-76.
Intact male rats (I) and rats 30 days after orchidectomy (OR) were treated in vivo with a single dose of 1.5 or 0.5 mg testosterone propionate (TP), 22.5 or 7.5 mug estradiol benzoate (EB) and a mixture of TP plus EB, respectively. The release of LH and FSH from anterior pituitaries of steroid hormone pretreated animals induced by the administration of LH-RH was studied in vitro. LH-RH stimulated FSH release from pituitaries of I and OR was inhibited by higher doses of EB or a mixture of EB plus TP. On the other hand, EB and combination of EB plus TP stimulated LH release in I, whereas EB and TP inhibited LH-RH induced release of LH in OR. At the lower dose levels no inhibition of LH-RH stimulated FSH release from pituitaries of steroid pretreated I or OR animals occured. LH-RH induced LH release was only observed at thise dose level in I pretreated with TP and OR pretreated with EB. On the other hand, pretreatment of ovariectomized rats (OV) with sex steroids (5 mug 17 beta-estradiol, 3 mg progesterone, and mixture of 5 mug 17 beta-estradiol and 3 mg progesterone, resp., each injected through 6 days) resulted in restoration of LH-RH induced FSH release lost 30 days after ovariectomy. Furthermore, LH-RH induced release of LH and FSH from male rat pituitaries at different times after orc dectomy exhibited a pattern from that recorded for ovariectomized animals. [125I] LH-RH binding assays with anterior pituitary plasma membrane fractions isolated from I revealed two binding sites with apparent affinity constants of 4.3 x 10(-9) M and 2.2 x 10(-8) M, respectively. The low affinity binding site is lost upon orchidectomy. Scatchard plot analyses of binding data obtained for LH-RH reaction with plasma membrane fractions isolated from anterior pituitaries of OR pretreated with sex steroids showed that the second binding site could be regenerated by treatment with the low dose of TP. From the present experiments it is concluded that: 1. LH-RH induced gonadotropin release is affected by sex steroids at the pituitary plasma membrane level. 2. One hypothalamic hormone may well specifically control LH and FSH release. 3. Mechanisms controlling LH-RH induced gonadotropin release are different in the male and female.
完整雄性大鼠(I组)和去势30天后的大鼠(OR组)分别接受单剂量1.5或0.5毫克丙酸睾酮(TP)、22.5或7.5微克苯甲酸雌二醇(EB)以及TP加EB的混合物的体内处理。研究了给予促黄体生成素释放激素(LH - RH)后,经类固醇激素预处理动物的垂体前叶中LH和FSH的释放情况。LH - RH刺激I组和OR组垂体释放FSH,但高剂量的EB或EB加TP的混合物会抑制这种释放。另一方面,EB以及EB加TP的组合刺激I组中的LH释放,而EB和TP抑制OR组中LH - RH诱导的LH释放。在较低剂量水平时,未观察到对LH - RH刺激的、经类固醇预处理的I组或OR组动物垂体释放FSH的抑制作用。仅在经TP预处理的I组和经EB预处理的OR组中,在此剂量水平观察到LH - RH诱导的LH释放。另一方面,用性类固醇(分别为5微克17β - 雌二醇、3毫克孕酮以及5微克17β - 雌二醇和3毫克孕酮的混合物,每种均连续注射6天)对去卵巢大鼠(OV组)进行预处理,可使去卵巢30天后丧失的LH - RH诱导的FSH释放得以恢复。此外,去势后不同时间点雄性大鼠垂体中LH - RH诱导的LH和FSH释放呈现出与去卵巢动物记录的模式不同的模式。用从I组分离的垂体前叶质膜部分进行的[125I]LH - RH结合试验显示有两个结合位点,其表观亲和常数分别为4.3×10⁻⁹ M和2.2×10⁻⁸ M。去势后低亲和力结合位点消失。对用性类固醇预处理的OR组垂体前叶质膜部分与LH - RH反应获得的结合数据进行Scatchard图分析表明,低剂量的TP处理可使第二个结合位点再生。从目前的实验得出以下结论:1. LH - RH诱导的促性腺激素释放受垂体质膜水平的性类固醇影响。2. 一种下丘脑激素很可能特异性地控制LH和FSH的释放。3. 控制LH - RH诱导的促性腺激素释放的机制在雄性和雌性中有所不同。