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2-羟基雌二醇-17β、2-羟基雌二醇-17α和4-羟基雌酮对大鼠排卵前促黄体生成素激增的影响:激动剂和拮抗剂作用。

Effects of 2-hydroxyestradiol-17 beta, 2-hydroxyestradiol-17 alpha, and 4-hydroxyestrone on the preovulatory luteinizing hormone surge in the rat: agonist and antagonist actions.

作者信息

Okatani Y, Fishman J

出版信息

Endocrinology. 1984 Sep;115(3):1090-4. doi: 10.1210/endo-115-3-1090.

Abstract

Four-day cycling rats equipped with intracardiac catheters were injected with 2-hydroxyestradiol-17 beta (2OHE2-17 beta) at 0800, 0900, 1000, and 1200 h on the morning of proestrus. The administration at 0800 and 0900 h resulted in abolition of the afternoon preovulatory LH surge in virtually all animals. Injections given at 1000 and 1200 h were ineffective in this respect. The isomeric catechol estrogen 4-hydroxyestrone effectively inhibited the LH surge when given at 0900 h, but not if injected at 1000 or 1200 h. In contrast, the nonestrogenic 2-hydroxyestradiol-17 alpha was effective in blocking the LH surge when given at 0900 or 1000 h. Rats treated with 2OHE2-17 beta at 1000 h responded normally to exogenous LHRH administration in the afternoon, indicating that the action of 2OHE2-17 beta is at the hypothalamic level. 2OHE2-17 beta and 4-hydroxyestrone, which are potent estrogens, may act in this instance first as estrogen agonists, advancing the "time window" when their catechol antagonist properties in blocking the LH surge can be functional. The nonuterotropic 2-hydroxyestradiol-17 alpha and 2-hydroxyestrone act solely as catechol estrogens and inhibit the preovulatory LH surge if administered at a time when they be present during this physiological window, which is thought to involve events at the estrogen-catecholaminergic interphase.

摘要

给配备心内导管的4日龄周期性发情大鼠在发情前期上午8点、9点、10点和12点注射17β - 2 - 羟基雌二醇(2OHE2 - 17β)。上午8点和9点给药几乎使所有动物下午的排卵前促黄体生成素(LH)峰消失。在这方面,10点和12点注射无效。同分异构儿茶酚雌激素4 - 羟基雌酮在上午9点给药时能有效抑制LH峰,但在10点或12点注射则无效。相比之下,非雌激素性的17α - 2 - 羟基雌二醇在上午9点或10点给药时能有效阻断LH峰。在10点用2OHE2 - 17β处理的大鼠下午对外源性促性腺激素释放激素(LHRH)给药反应正常,这表明2OHE2 - 17β的作用在下丘脑水平。2OHE2 - 17β和4 - 羟基雌酮是强效雌激素,在这种情况下可能首先作为雌激素激动剂起作用,提前“时间窗”,在此期间它们阻断LH峰的儿茶酚拮抗剂特性才能发挥作用。非促子宫生长的17α - 2 - 羟基雌二醇和2 - 羟基雌酮仅作为儿茶酚雌激素起作用,如果在它们存在于这个生理窗口的时间给药,就能抑制排卵前LH峰,这个生理窗口被认为涉及雌激素 - 儿茶酚胺能界面的事件。

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