Cusan L, Auclair C, Belanger A, Ferland L, Kelly P A, Seguin C, Labrie F
Endocrinology. 1979 May;104(5):1369-76. doi: 10.1210/endo-104-5-1369.
Following previous observations of the potent antifertility effects of acute treatment with LHRH or its agonistic analogs in male and female rats, this study describes the effect of long term (up to 12 weeks) treatment with an LHRH agonist, [D-Ala6, des-Gly-NH210]LHRH ethylamide (LHRH-A), on testicular and ovarian gonadotropin receptor levels and function in the rat. Treatment of adult male rats with 100 ng LHRH-A every third day led to a progressive decrease of testis, seminal vesicle, and prostate weight up to 12 weeks of treatment, while the inhibitory effect (70%) on LH receptor levels was already maximal at 1 week. When adult female rats were injected daily with 5 microgram LHRH-A for 12 weeks, ovarian LH, FSH, and PRL receptor levels were reduced 50--90%, while plasma estradiol and progesterone levels were inhibited 60% (compared with diestrus day 1). The effect of chronic administration of a low dose (5 IU) of hCG in the male rat was transient. By contrast, no sign of resistance developed up to 12 weeks of treatment with the LHRH agonist in either male or female animals.
继先前观察到促性腺激素释放激素(LHRH)或其激动剂类似物对雄性和雌性大鼠进行急性处理具有强大的抗生育作用之后,本研究描述了用LHRH激动剂[D - Ala6,des - Gly - NH210]LHRH乙酰胺(LHRH - A)进行长期(长达12周)处理对大鼠睾丸和卵巢促性腺激素受体水平及功能的影响。每隔一天用100 ng LHRH - A处理成年雄性大鼠,直至处理12周,睾丸、精囊和前列腺重量逐渐下降,而对促黄体生成素(LH)受体水平的抑制作用(70%)在1周时已达到最大。当成年雌性大鼠每天注射5微克LHRH - A,持续12周时,卵巢LH、促卵泡生成素(FSH)和催乳素(PRL)受体水平降低50% - 90%,而血浆雌二醇和孕酮水平受到60%的抑制(与动情间期第1天相比)。在雄性大鼠中,慢性给予低剂量(5国际单位)人绒毛膜促性腺激素(hCG)的作用是短暂的。相比之下,在雄性或雌性动物中,用LHRH激动剂处理长达12周均未出现耐药迹象。