Luttge W G, Sheets C S
Pharmacol Biochem Behav. 1977 Dec;7(6):563-6. doi: 10.1016/0091-3057(77)90255-6.
Sexual receptivity in ovariectomized CD-1 mice induced by chronic daily injections of estradiol benzoate (E2B) was inhibited in a dose related fashion by daily injections of dihydrotestosterone (DHT) given concurrently with the E2B. Administration of the progestins, progesterone and dihydroprogesterone (DHP), and of the hypothalamic decapeptide, LH-RH, 6 hr prior to testing restored receptivity to varying degrees in these E2B + DHT treated mice. Of these treatments progesterone was clearly the most effective, followed by LH-RH and finally DHP in restoring estrogen-induced receptivity. Results were discussed in terms of a proposed essential role for LH-RH in the induction of sexual receptivity in mice.
通过每日慢性注射苯甲酸雌二醇(E2B)诱导去卵巢的CD-1小鼠出现性接受能力,若在注射E2B的同时每日注射二氢睾酮(DHT),则其性接受能力会受到剂量相关方式的抑制。在测试前6小时给予孕激素(孕酮和二氢孕酮(DHP))以及下丘脑十肽促黄体生成素释放激素(LH-RH),可使这些经E2B + DHT处理的小鼠的性接受能力不同程度地恢复。在恢复雌激素诱导的性接受能力方面,这些处理中孕酮显然最有效,其次是LH-RH,最后是DHP。根据所提出的LH-RH在诱导小鼠性接受能力中的重要作用对结果进行了讨论。