Knecht M, Katz M S, Catt K J
J Biol Chem. 1981 Jan 10;256(1):34-6.
Ovarian granulosa cells obtained from hypophysectomized, diethylstilbestrol-treated rats were cultured in the presence of ovine follicle-stimulating hormone (FSH) and gonadotropin-releasing hormone (GnRH). FSH stimulated the production and accumulation of both cAMP and cGMP, as well as progesterone, during a 48-h incubation period. Addition of GnRH or an agonist analog, [D-Ala6]des-Gly10-GnRH N-ethylamide (GnRHa), did not influence the cyclic nucleotide response to FSH in the first 6 h of incubation, but caused dose-dependent inhibition of the FSH-induced rise in cyclic nucleotide production from 24 to 48 h of incubation. Cellular production of both cyclic nucleotides and progesterone was decreased by GnRHa concentrations as low as 10(-12) M, with maximum inhibition at 10(-9) M GnRHa. These results suggest that the in vitro antigonadal actions of GnRH and related peptides are expressed through inhibition of cyclic nucleotide production.
从经垂体切除、己烯雌酚处理的大鼠获取的卵巢颗粒细胞,在羊促卵泡激素(FSH)和促性腺激素释放激素(GnRH)存在的情况下进行培养。在48小时的孵育期内,FSH刺激了环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)以及孕酮的产生和积累。添加GnRH或激动剂类似物[D - Ala6]去甘氨酸10 - GnRH N - 乙基酰胺(GnRHa),在孵育的最初6小时内不影响对FSH的环核苷酸反应,但在孵育24至48小时期间导致FSH诱导的环核苷酸产生增加呈剂量依赖性抑制。GnRHa浓度低至10^(-12) M时,环核苷酸和孕酮的细胞产生均减少,在10^(-9) M GnRHa时抑制作用最大。这些结果表明,GnRH和相关肽的体外抗性腺作用是通过抑制环核苷酸产生来表达的。