Molecular mechanisms underlying the memory-enhancing effects of estradiol

被引:136
作者
Frick, Karyn M. [1 ]
机构
[1] Univ Wisconsin, Dept Psychol, Milwaukee, WI 53211 USA
关键词
Estrogen; Hippocampus; Estrogen receptor; Cell signaling; Epigenetic; ERK; mTOR; Histone acetylation; DNA methylation; GPER; ESTROGEN-RECEPTOR-BETA; ACTIVATED PROTEIN-KINASE; DENDRITIC SPINE DENSITY; SIGNAL-REGULATED KINASE; HIPPOCAMPAL SYNAPTIC PLASTICITY; OBJECT RECOGNITION MEMORY; IMPAIRS FEAR EXTINCTION; LONG-TERM POTENTIATION; SPATIAL-LEARNING TASK; HISTONE ACETYLATION;
D O I
10.1016/j.yhbeh.2015.05.001
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
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 17 beta-estradiol (E-2) regulates hippocampal plasticity and memory. Recent research has demonstrated that rapid effects of E-2 on hippocampal cell signaling, epigenetic processes, and local protein synthesis are necessary for E-2 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 ER alpha and ER beta, 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 E-2 in regulating hippocampal memory formation. The present review discusses these findings in detail and suggests avenues for future study. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:4 / 18
页数:15
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