Stewart S F, Tornaben J A, Kopia S, Edgren R A
Prostaglandins. 1976 Sep;12(3):427-41. doi: 10.1016/0090-6980(76)90023-x.
Pseudopregnancy was induced in 26 day old female rats by giving 30 IU of PMS followed 56 hours later with 5 IU of hCG. Day 1 of pseudopregnancy was considered established 72 hours after PMS administration. Pseudopregnancy lasted 14 to 15 days. Ovarian weights increased for 4 to 8 times due to treatment. Histological examiniation of the corpora lutea (CL) of pseudopregnancy suggested luteolysis began on day 6 and extended to day 8. A "new" crop of CL appeared on day 9 suggesting the duration of pseudopregnancy was supported by more than one generation of CL or by CL maturing at different rates. Twice daily administration of 1 mg PGF2alpha on days 5 to 8 prevented the appearance of the "new" CL on day 9, and increased signs of luteolysis in the initially formed CL. Lower doses (0.01 and 0.1 mg, b.i.d., X 4 days) delayed the appearance of "new" CL until day 10. Blood samples withdrawn between 0930 and 1100 hours were analysed for FSH, LH and prolactin. Animals treated with 0.01 and 0.1 mg of PGF2alpha, b.i.d., X 4 days had increased LH values on day 8, thus the PG appeared luteotrophic. Rats treated with 1 mg of PGF2alpha, b.i.d., X 4 days had decreased LH values on day 7 and the CL showed subsequent luteolysis. FSH levels were relatively constant during pseudopregnancy. However, all doses of PGF2alpha reduced FSH levels on day 7. An associated decrease in uterine weight occurred, possibly due to reduced follicular development. Prolactin levels fell in response to PGF2alpha treatment which undoubtedly contributed to the observed luteolysis. The signs of early cessation of pseudopregnancy were: increased serum FSH on days 9 and 10; increasing uterine weight; and the reappearance of follicular growth. These data suggest that PGF2alpha reduced the duration of pseudopregnancy primarily by inhibiting the secretion of FSH, LH and prolactin.
通过给26日龄雌性大鼠注射30国际单位孕马血清促性腺激素(PMS),并在56小时后注射5国际单位人绒毛膜促性腺激素(hCG)来诱导假孕。假孕第1天被认为是在注射PMS 72小时后确立。假孕持续14至15天。由于治疗,卵巢重量增加了4至8倍。对假孕黄体(CL)的组织学检查表明,黄体溶解于第6天开始并持续到第8天。第9天出现“新的”一批黄体,这表明假孕的持续时间由不止一代黄体或不同速率成熟的黄体所维持。在第5至8天每天两次给予1毫克前列腺素F2α(PGF2α)可防止第9天出现“新的”黄体,并增加最初形成的黄体中的黄体溶解迹象。较低剂量(0.01和0.1毫克,每日两次,共4天)将“新的”黄体出现推迟到第10天。在0930至1100小时之间采集血样分析促卵泡激素(FSH)、促黄体生成素(LH)和催乳素。每日两次给予0.01和0.1毫克PGF2α,共4天的动物在第8天LH值升高,因此PG表现出促黄体作用。每日两次给予1毫克PGF2α,共4天的大鼠在第7天LH值降低,且黄体随后出现黄体溶解。在假孕期间FSH水平相对恒定。然而,所有剂量的PGF2α在第7天均降低了FSH水平。子宫重量随之下降,可能是由于卵泡发育减少。催乳素水平因PGF2α治疗而下降,这无疑促成了观察到的黄体溶解。假孕早期终止的迹象为:第9天和第10天血清FSH升高;子宫重量增加;以及卵泡生长重新出现。这些数据表明,PGFα主要通过抑制FSH、LH和催乳素的分泌来缩短假孕的持续时间。