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ICI 182,780:一种纯粹的抗雌激素,它能影响大鼠的行为和能量平衡,且不作用于大脑。

ICI 182,780: a pure antiestrogen that affects behaviors and energy balance in rats without acting in the brain.

作者信息

Wade G N, Blaustein J D, Gray J M, Meredith J M

机构信息

Department of Psychology, University of Massachusetts, Amherst 01003.

出版信息

Am J Physiol. 1993 Dec;265(6 Pt 2):R1392-8. doi: 10.1152/ajpregu.1993.265.6.R1392.

Abstract

ICI 182,780 is one of a new class of steroidal antiestrogens that differs from nonsteroidal antiestrogens, such as tamoxifen, in a number of respects. 1) It is bound by estrogen receptors with a high affinity, similar to that for estradiol. 2) It is a "pure" antiestrogen in that it does not mimic any of the effects of estradiol. 3) This class of antiestrogens does not seem to be bound by antiestrogen binding sites. 4) ICI 182,780 may not be active in the brain after peripheral administration. Indeed, ICI 182,780 blocked in vivo cell nuclear binding of [3H]estradiol in uterus, pituitary, and adipose tissue but not in hypothalamus-preoptic area. In vitro, ICI 182,780 competed for binding by neural estrogen receptors with an affinity comparable with that for estradiol. When given to ovariectomized rats, ICI 182,780 did not mimic any of the actions of estradiol. Instead, ICI 182,780 treatment completely blocked the uterotrophic effects of estradiol and attenuated the actions of estradiol on linear growth, carcass fat content, fat pad weight, and sexual receptivity. Treatment with ICI 182,780 also attenuated the estrogenic effects of tamoxifen on food intake, body weight and composition, linear growth, and uterine weight. These findings support the concept that, in addition to its actions in the brain, estradiol can act peripherally to modulate regulatory behaviors, energy balance, and estrous behavior. They are also consistent with the hypothesis that nonsteroidal antiestrogens, such as tamoxifen, affect energy balance via estrogen receptors, rather than antiestrogen binding sites.

摘要

ICI 182,780是一类新型甾体抗雌激素药物之一,它在许多方面与非甾体抗雌激素药物(如他莫昔芬)不同。1)它与雌激素受体具有高亲和力结合,类似于与雌二醇的结合。2)它是一种“纯粹”的抗雌激素,因为它不会模拟雌二醇的任何作用。3)这类抗雌激素似乎不会与抗雌激素结合位点结合。4)外周给药后,ICI 182,780在大脑中可能没有活性。实际上,ICI 182,780在体内阻断了子宫、垂体和脂肪组织中[3H]雌二醇的细胞核结合,但在下丘脑-视前区没有阻断。在体外,ICI 182,780与神经雌激素受体竞争结合,其亲和力与雌二醇相当。给去卵巢大鼠注射ICI 182,780后,它不会模拟雌二醇的任何作用。相反,ICI 182,780治疗完全阻断了雌二醇的子宫营养作用,并减弱了雌二醇对线性生长、胴体脂肪含量、脂肪垫重量和性接受能力的作用。ICI 182,780治疗还减弱了他莫昔芬对食物摄入、体重和组成、线性生长以及子宫重量的雌激素作用。这些发现支持了这样一种观点,即除了在大脑中的作用外,雌二醇还可以在周围发挥作用来调节调节行为、能量平衡和发情行为。它们也与非甾体抗雌激素药物(如他莫昔芬)通过雌激素受体而非抗雌激素结合位点影响能量平衡的假设一致。

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