Conti M, Harwood J P, Hsueh A J, Dufau M L, Catt K J
J Biol Chem. 1976 Dec 10;251(23):7729-31.
Gonadotropin receptor sites and adenylate cyclase activity were analyzed in luteinized rat ovaries following injection of human chorionic gonadotropin (hCG). Gonadotropin binding capacity and hormonal stimulation of adenylate cyclase declined rapidly to a minimum at 6 to 12 h, remained depressed for 4 days, and returned to the control level between 5 and 7 days. Total adenylate cyclase activity measured in the presence of fluoride fell by 50% within a few hours but returned to normal by 24 h. A close correlation was observed between the number of gonadotropin receptors and the ability of adenylate cyclase to be stimulated by hormone. Assay of tissue-bound hormone showed that the initial loss of hormone sensitivity and binding capacity was associated with occupancy of luteinizing hormone receptor sites, but that the prolonged changes in these activities were not attributable to receptor occupancy. These studies have demonstrated that induction of a refractory or desensitized state in ovarian adenylate cyclase by gonadotropin results from the loss of specific hormone receptor sites.
在注射人绒毛膜促性腺激素(hCG)后,对黄体化大鼠卵巢中的促性腺激素受体位点和腺苷酸环化酶活性进行了分析。促性腺激素结合能力和腺苷酸环化酶的激素刺激在6至12小时迅速下降至最低水平,在4天内持续降低,并在5至7天恢复到对照水平。在氟化物存在下测得的总腺苷酸环化酶活性在数小时内下降了50%,但在24小时恢复正常。观察到促性腺激素受体数量与腺苷酸环化酶受激素刺激的能力之间存在密切相关性。组织结合激素的测定表明,激素敏感性和结合能力的最初丧失与促黄体生成素受体位点的占据有关,但这些活性的长期变化并非归因于受体占据。这些研究表明,促性腺激素诱导卵巢腺苷酸环化酶产生不应期或脱敏状态是由于特异性激素受体位点的丧失。