The impact of ERα action on muscle metabolism and insulin sensitivity - Strong enough for a man, made for a woman

被引:45
|
作者
Hevener, Andrea L. [1 ]
Zhou, Zhenqi [1 ]
Moore, Timothy M. [1 ]
Drew, Brian G. [1 ]
Ribas, Vicent [1 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Div Endocrinol Diabet & Hypertens, Los Angeles, CA 90095 USA
来源
MOLECULAR METABOLISM | 2018年 / 15卷
基金
美国国家卫生研究院;
关键词
Estrogen action; Estrogen receptors; Insulin sensitivity; Metabolic homeostasis; ESTROGEN-RECEPTOR-ALPHA; ACTIVATED PROTEIN-KINASE; EXTRANUCLEAR STEROID-RECEPTORS; POSTMENOPAUSAL HORMONE-THERAPY; GENOME-WIDE IDENTIFICATION; GLUCOSE-TRANSPORTER GLUT4; SKELETAL-MUSCLE; AROMATASE DEFICIENCY; REPLACEMENT THERAPY; REGULATED KINASE;
D O I
10.1016/j.molmet.2018.06.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The incidence of chronic disease is elevated in women after menopause. Natural variation in muscle expression of the estrogen receptor (ER)alpha is inversely associated with plasma insulin and adiposity. Moreover, reduced muscle ER alpha expression levels are observed in women and animals presenting clinical features of the metabolic syndrome (MetSyn). Considering that metabolic dysfunction impacts nearly a quarter of the U.S. adult population and elevates chronic disease risk including type 2 diabetes, heart disease, and certain cancers, treatment strategies to combat metabolic dysfunction and associated pathologies are desperately needed. Scope of the review: This review will provide evidence supporting a critical and protective role for skeletal muscle ER alpha in the regulation of metabolic homeostasis and insulin sensitivity, and propose novel ER alpha targets involved in the maintenance of metabolic health. Major conclusions: Studies identifying ER alpha-regulated pathways essential for disease prevention will lay the important foundation for the rational design of novel therapeutics to improve the metabolic health of women while limiting secondary complications that have plagued traditional hormone replacement interventions. (C) 2018 Published by Elsevier GmbH.
引用
收藏
页码:20 / 34
页数:15
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