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Irisin, a Link among Fatty Liver Disease, Physical Inactivity and Insulin Resistance

期刊

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
卷 15, 期 12, 页码 23163-23178

出版社

MDPI
DOI: 10.3390/ijms151223163

关键词

non-alcoholic fatty liver disease; insulin resistance; aerobic exercise; irisin; brown-fat-like development; muscle; FNDC5 (fibronectin type III domain-containing 5 transmembrane receptor); PPAR gamma (peroxisome proliferator-activated receptor gamma); PGC-1 alpha (peroxisome proliferator-activated receptor gamma coactivator-1 alpha)

资金

  1. Instituto de Salud Carlos III [PI12/02026]

向作者/读者索取更多资源

Nonalcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease in industrialized countries. The increasing prevalence of NAFLD mirrors the outbreak of obesity in western countries, highlighting the connection between these two conditions. Nevertheless, there is currently no specific pharmacotherapy for its treatment. Accepted management begins with weight loss and exercise. Moreover, exercise can provide metabolic benefits independently of weight loss. It is known how long-term aerobic training produces improvements in hepatic triglycerides, visceral adipose tissue and free fatty acids, even if there is no weight reduction. A recent study from Bostrom et al. unravels a potential molecular mechanism that may explain how exercise, independently of weight loss, can potentially improve metabolic parameters through a new messenger system (irisin) linking muscle and fat tissue. Irisin has been proposed to act as a hormone on subcutaneous white fat cells increasing energy expenditure by means of a program of brown-fat-like development. Moreover, it was also shown that irisin plasma concentration was higher in people who exercise, suggesting a molecular mechanism by which exercise may improve metabolism. The present systematic review is based on the possibility that irisin might represent a hypothetical connection between NAFLD pathogenesis and disease progression.

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