Estrogen and mitochondria function in cardiorenal metabolic syndrome.

Abstract:

:The cardiorenal metabolic syndrome (CRS) consists of a constellation of cardiac, renal, and metabolic disorders including insulin resistance (IR), obesity, metabolic dyslipidemia, high-blood pressure, and evidence of early cardiac and renal disease. Mitochondria dysfunction often occurs in the CRS, and this dysfunction is promoted by excess reactive oxygen species, genetic factors, IR, aging, and altered mitochondrial biogenesis. Recently, it has been shown that there are important sex-related differences in mitochondria function and metabolic, cardiovascular, and renal components. Sex differences in the CRS have mainly been attributed to the estrogen's effects that are mainly mediated by estrogen receptor (ER) α, ERβ, and G-protein coupled receptor 30. In this review, we discuss the effects of estrogen on the mitochondrial function, insulin metabolic signaling, glucose transport, lipid metabolism, and inflammatory responses from liver, pancreatic β cells, adipocytes, skeletal muscle, and cardiovascular tissue.

authors

Jia G,Aroor AR,Sowers JR

doi

10.1016/B978-0-12-394625-6.00009-X

subject

Has Abstract

pub_date

2014-01-01 00:00:00

pages

229-49

eissn

1877-1173

issn

1878-0814

pii

B978-0-12-394625-6.00009-X

journal_volume

127

pub_type

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