Impact of Estrogens on the Regulation of White, Beige, and Brown Adipose Tissue Depots

被引:29
作者
Bernasochi, Gabriel B. [1 ]
Bell, James R. [1 ]
Simpson, Evan R. [3 ]
Delbridge, Lea M. D. [1 ]
Boon, Wah Chin [2 ]
机构
[1] Univ Melbourne, Sch Biomed Sci, Cardiac Phen Lab, Melbourne, Vic, Australia
[2] Florey Inst Neurosci & Mental Hlth, Parkville, Vic, Australia
[3] Hudson Inst Med Res, Clayton, Vic, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
BODY-FAT DISTRIBUTION; MESSENGER-RIBONUCLEIC-ACID; GROWTH-FACTOR RECEPTOR; DEFICIENT ARKO MICE; ALPHA ER-ALPHA; BREAST-CANCER; AROMATASE EXPRESSION; VISCERAL FAT; G-PROTEIN; GENE-EXPRESSION;
D O I
10.1002/cphy.c180009
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
As adipose tissue depots are active endocrine organs, they secrete a variety of hormones (including estrogens from white adipose) and inflammatory mediators, which have important implications in numerous obesity-associated diseases. Adipose tissues are broadly characterized as consisting of white, beige, and brown depot types. The endocrine, metabolic, and inflammatory profiles of adipose are depot dependent and influenced by the estrogenic and androgenic status of the adipose tissue. Estrogen receptors mediate both the genomic and nongenomic actions of estrogens and are expressed in the brain, heart, and other peripheral tissues. All three known estrogen receptor alpha (ER alpha) and estrogen receptor beta (ER beta), and the G-protein coupled estrogen receptor (GPER/GPR30) are expressed in white adipose and can modulate adipose mass. Expression of each receptor is dependent on depot location, adipose cell type, and estrogen levels. Estrogen receptor expression profiles in beige and brown adipocytes are less well established. This review will discuss the effects of estrogens on the differential deposition of the major adipose tissues and the impact of estrogens within white adipose depots. (C) 2019 American Physiological Society.
引用
收藏
页码:457 / 475
页数:19
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