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ERα in the Control of Mitochondrial Function and Metabolic Health.
Hevener, Andrea L; Ribas, Vicent; Moore, Timothy M; Zhou, Zhenqi.
Afiliação
  • Hevener AL; David Geffen School of Medicine, Department of Medicine, Division of Endocrinology, Diabetes, and Hypertension, University of California, Los Angeles, CA 90095, USA; Iris Cantor-UCLA Women's Health Research Center, University of California, Los Angeles, CA 90095, USA. Electronic address: ahevener@me
  • Ribas V; David Geffen School of Medicine, Department of Medicine, Division of Endocrinology, Diabetes, and Hypertension, University of California, Los Angeles, CA 90095, USA.
  • Moore TM; David Geffen School of Medicine, Department of Medicine, Division of Endocrinology, Diabetes, and Hypertension, University of California, Los Angeles, CA 90095, USA.
  • Zhou Z; David Geffen School of Medicine, Department of Medicine, Division of Endocrinology, Diabetes, and Hypertension, University of California, Los Angeles, CA 90095, USA.
Trends Mol Med ; 27(1): 31-46, 2021 01.
Article em En | MEDLINE | ID: mdl-33020031
ABSTRACT
Decrements in metabolic health elevate disease risk, including type 2 diabetes, heart disease, and certain cancers. Thus, treatment strategies to combat metabolic dysfunction are needed. Reduced ESR1 (estrogen receptor, ERα) expression is observed in muscle from women, men, and animals presenting clinical features of the metabolic syndrome. Human studies of natural expression of ESR1 in metabolic tissues show that muscle expression of ESR1 is positively correlated with markers of metabolic health, including insulin sensitivity. Herein, we highlight the important impact of ERα on mitochondrial form and function and present how these actions of the receptor govern metabolic homeostasis. Studies identifying ERα-regulated pathways for disease prevention will lay the foundation for the design of novel therapeutics to improve the health of women while limiting secondary complications that have plagued traditional hormone replacement interventions.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptor alfa de Estrogênio / Metabolismo Energético / Homeostase / Doenças Metabólicas / Mitocôndrias Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptor alfa de Estrogênio / Metabolismo Energético / Homeostase / Doenças Metabólicas / Mitocôndrias Idioma: En Ano de publicação: 2021 Tipo de documento: Article