首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Differential depletion of cytoplasmic high affinity oestrogen receptors after the in vivo administration of the antioestrogens clomiphene MER-25 and tamoxifen.
【2h】

Differential depletion of cytoplasmic high affinity oestrogen receptors after the in vivo administration of the antioestrogens clomiphene MER-25 and tamoxifen.

机译:在体内施用抗雌激素克罗米芬MER-25和他莫昔芬后细胞质高亲和力雌激素受体的差异耗竭。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

1 The in vivo actions of the oestrogen antagonists, MER-25 and tamoxifen upon the cytosol oestrogen receptors prepared from amygdala, hypothalamus, pituitary and uterus of rats were studied 24 h after drug administration. 2 There was a dose-related depletion of cytosol oestrogen receptors. However, the uterine and pituitary receptors were consistently affected at a lower dose than were those from the brain. 3 The ratios of the combined central ED50 to the combined peripheral ED50 were clomiphene 169 greater than MER-25 19.2 greater than tamoxifen 2.13. 4 The receptor changes were not related to biological activity monitored by serum luteinizing hormone levels and uterotrophic response. 5 The possible role of these drug effects in the induction of ovulation and future developments are discussed.
机译:1在给药后24小时,研究了雌激素拮抗剂MER-25和他莫昔芬对从大鼠杏仁体,下丘脑,垂体和子宫制备的胞浆雌激素受体的体内作用。 2剂量相关的细胞溶质雌激素受体耗竭。但是,子宫和垂体受体的剂量始终低于大脑的剂量。 3组合的中心ED50与组合的外围ED50之比是克罗米芬169大于MER-25 19.2大于他莫昔芬2.13。 4受体变化与血清黄体生成激素水平和子宫营养反应所监测的生物学活性无关。 5讨论了这些药物作用在诱导排卵和未来发展中的可能作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号