Ekholm C, Hillensjö T, Isaksson O
Endocrinology. 1981 May;108(5):2022-4. doi: 10.1210/endo-108-5-2022.
The acute effects in vivo of gonadotropin releasing hormone (GnRH) and a potent agonistic analogue (GnRHa) were tested in PMSG-treated immature female rats, hypophysectomized on the morning of proestrus. The rats were injected once with either LH, GnRH, or GnRHa 3-4 h after surgery, and the effects on oocyte meiosis, ovulation, and plasma progesterone were investigated. LH (25 microgram) and GnRHa (12.0 and 1.2 microgram) caused a high rate of meiosis, while GnRH (100 microgram) or GnRHa (0.12 microgram) caused a partial response. LH and GnRHa produced ovulation in all of the treated rats and caused a prolonged increase in plasma progesterone levels. It is concluded that GnRH agonists exert acute stimulatory effects in the ovarian follicle, independent of pituitary factors.
在动情前期上午进行垂体切除的孕马血清促性腺激素(PMSG)处理的未成熟雌性大鼠中,测试了促性腺激素释放激素(GnRH)和一种强效激动剂类似物(GnRHa)的体内急性效应。术后3 - 4小时,给大鼠单次注射促黄体生成素(LH)、GnRH或GnRHa,研究其对卵母细胞减数分裂、排卵和血浆孕酮的影响。LH(25微克)和GnRHa(12.0微克和1.2微克)引起高减数分裂率,而GnRH(100微克)或GnRHa(0.12微克)引起部分反应。LH和GnRHa使所有处理大鼠排卵,并导致血浆孕酮水平持续升高。结论是,GnRH激动剂在卵巢卵泡中发挥急性刺激作用,独立于垂体因素。