Molecular signature of rapid estrogen regulation of synaptic connectivity and cognition

被引:60
作者
Sellers, Katherine [1 ]
Raval, Pooja [1 ]
Srivastava, Deepak P. [1 ]
机构
[1] Kings Coll London, Dept Basic & Clin Neurosci, James Black Ctr, Inst Psychiat Psychol & Neurosci, London SE5 9NU, England
基金
英国医学研究理事会;
关键词
17; beta-Estradiol; Estrogen receptor alpha; Estrogen receptor beta; GPER1 (G-protein estrogen receptor); GPR30; Dendritic spine; Cortex; Hippocampus; AMPA receptor; NMDA receptor; HIPPOCAMPAL DENDRITIC SPINES; HEALTH INITIATIVE MEMORY; ELEMENT-BINDING PROTEIN; CENTRAL-NERVOUS-SYSTEM; ESTRADIOL-INDUCED ENHANCEMENT; CONJUGATED EQUINE ESTROGENS; RANDOMIZED-CONTROLLED TRIAL; 2-STEP WIRING PLASTICITY; LONG-TERM POTENTIATION; COUPLED RECEPTOR 30;
D O I
10.1016/j.yfrne.2014.08.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
There is now a growing appreciation that estrogens are capable of rapidly activating a number of signaling cascades within the central nervous system. In addition, there are an increasing number of studies reporting that 17 beta-estradiol, the major biologically active estrogen, can modulate cognition within a rapid time frame. Here we review recent studies that have begun to uncover the molecular and cellular framework which contributes to estrogens ability to rapidly modulate cognition. We first describe the mechanisms by which estrogen receptors (ERs) can couple to intracellular signaling cascades, either directly, or via the transactivation of other receptors. Subsequently, we review the evidence that estrogen can rapidly modulate both neuronal function and structure in the hippocampus and the cortex. Finally, we will discuss how estrogens may influence cognitive function through the modulation of neuronal structure, and the implications this may have on the treatment of a range of brain disorders. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:72 / 89
页数:18
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