Swimming training induces liver adaptations to oxidative stress and insulin sensitivity in rats submitted to high-fat diet

Redox Rep. 2017 Nov;22(6):515-523. doi: 10.1080/13510002.2017.1315513. Epub 2017 Apr 13.

Abstract

Oxidative stress, physical inactivity and high-fat (FAT) diets are associated with hepatic disorders such as metabolic syndrome (MS). The therapeutic effects of physical training (PT) were evaluated in rats with MS induced by FAT diet for 13 weeks, on oxidative stress and insulin signaling in the liver, during the last 6 weeks. FAT-sedentary (SED) rats increased body mass, retroperitoneal fat, mean arterial pressure (MAP) and heart rate (HR), and total cholesterol, serum alanine aminotransferase, glucose and insulin. Livers of FAT-SED rats increased superoxide dismutase activity, thiobarbituric acid-reactive substances, protein carbonyl and oxidized glutathione (GSSG); and decreased catalase activity, reduced glutathione/GSSG ratio, and the mRNA expression of insulin receptor substrate 1 (IRS-1) and serine/threonine kinase 2. FAT-PT rats improved in fitness and reduced their body mass, retroperitoneal fat, and glucose, insulin, total cholesterol, MAP and HR; and their livers increased superoxide dismutase and catalase activities, the reduced glutathione/GSSG ratio and the expression of peroxisome proliferator-activated receptor gamma and insulin receptor compared to FAT-SED rats. These findings indicated adaptive responses to PT by restoring the oxidative balance and insulin signaling in the liver and certain biometric and biochemical parameters as well as MAP in MS rats.

Keywords: Physical training; high-fat diet; insulin signaling pathway; liver; oxidative stress.

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Catalase / metabolism
  • Diet, High-Fat
  • Glutathione / metabolism
  • Glutathione Disulfide / metabolism
  • Insulin / metabolism*
  • Liver / metabolism*
  • Male
  • Oxidative Stress / physiology
  • Rats
  • Superoxide Dismutase / metabolism
  • Swimming / physiology*

Substances

  • Antioxidants
  • Insulin
  • Catalase
  • Superoxide Dismutase
  • Glutathione
  • Glutathione Disulfide

Grants and funding

This study was supported by the Universidade Federal de Ouro Preto (UFOP), Pró-Reitoria de Pós-Graduação (PROPP-UFOP), FAPEMIG (Fundação de Amparo à Pesquisa do Estado de Minas Gerais)-Rede Toxifar, CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico), FAPEMIG-Universal and Pronex Project Grant (FAPEMIG/ CNPq). Aline Cruz Zacarias is a Master’s Degree student in the Programa de Pós-graduação – Ciências Biológicas, NUPEB, UFOP; CNPq: [Grant Number Universal472497/2013-8]; FAPEMIG: [Grant Number APQ-3384-3.13/07].