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雌二醇增强记忆作用的分子机制。

Molecular mechanisms underlying the memory-enhancing effects of estradiol.

作者信息

Frick Karyn M

机构信息

Department of Psychology, University of Wisconsin-Milwaukee, 2441 E. Hartford Ave., Milwaukee, WI 53211, USA.

出版信息

Horm Behav. 2015 Aug;74:4-18. doi: 10.1016/j.yhbeh.2015.05.001. Epub 2015 May 8.

Abstract

This article is part of a Special Issue "Estradiol and cognition". Since the publication of the 1998 special issue of Hormones and Behavior on estrogens and cognition, substantial progress has been made towards understanding the molecular mechanisms through which 17β-estradiol (E2) regulates hippocampal plasticity and memory. Recent research has demonstrated that rapid effects of E2 on hippocampal cell signaling, epigenetic processes, and local protein synthesis are necessary for E2 to facilitate the consolidation of object recognition and spatial memories in ovariectomized female rodents. These effects appear to be mediated by non-classical actions of the intracellular estrogen receptors ERα and ERβ, and possibly by membrane-bound ERs such as the G-protein-coupled estrogen receptor (GPER). New findings also suggest a key role of hippocampally-synthesized E2 in regulating hippocampal memory formation. The present review discusses these findings in detail and suggests avenues for future study.

摘要

本文是《雌二醇与认知》特刊的一部分。自1998年《激素与行为》关于雌激素与认知的特刊发表以来,在理解17β - 雌二醇(E2)调节海马可塑性和记忆的分子机制方面已取得了重大进展。最近的研究表明,E2对海马细胞信号传导、表观遗传过程和局部蛋白质合成的快速作用,对于E2促进去卵巢雌性啮齿动物的物体识别和空间记忆巩固是必要的。这些作用似乎是由细胞内雌激素受体ERα和ERβ的非经典作用介导的,也可能是由膜结合雌激素受体如G蛋白偶联雌激素受体(GPER)介导的。新发现还表明海马合成的E2在调节海马记忆形成中起关键作用。本综述详细讨论了这些发现,并提出了未来研究的方向。

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