Antioxidants and Redox Signaling · 2021 · 54 citations · 136 references
MedicineBiochemistryEndocrinologyMetabolic RegulationReproductive EndocrinologyReproductive PhysiologyAdipose TissueHepatic PathophysiologyInsulin ResistanceLipid MetabolismLiver DiseaseLiver PhysiologyEstrogen ExposureEstrogen MetabolismEstrogen ReceptorsHepatic Insulin ResistanceHepatic Metabolic RegulationLipid Metabolism PathwaysLiver Metabolism RegulationSex Steroid Physiology
Significance: Nonalcoholic fatty liver disease (NAFLD) is a hepatic and systemic disorder with a complex multifactorial pathogenesis. Owing to the rising incidence of obesity and diabetes mellitus, the prevalence of NAFLD and its impact on global health care are expected to increase in the future. Differences in NAFLD exist between males and females, and among females depending on their reproductive status. Clinical and preclinical data show that females in the fertile age are more protected against NAFLD, and studies in postmenopausal women and ovariectomized animal models support a protective role for estrogens. Recent Advances: An efficient crosstalk between the liver and adipose tissue is necessary to regulate lipid and glucose metabolism, protecting the liver from steatosis and insulin resistance contributing to NALFD. New advances in the knowledge of sexual dimorphism in liver and adipose tissue are providing interesting clues about the sex differences in NAFLD pathogenesis that could inspire new therapeutic strategies. Critical Issues: Sex hormones influence key master regulators of lipid metabolism and oxidative stress in liver and adipose tissue. All these sex-biased metabolic adjustments shape the crosstalk between liver and adipose tissue, contributing to the higher protection of females to NAFLD. Future Directions: The development of novel drugs based on the protective action of estrogens, but without its feminizing or undesired side effects, might provide new therapeutic strategies for the management of NAFLD. Antioxid. Redox Signal. 35, 753–774.
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