Central and peripheral effects of physical exercise without weight reduction in obese and lean mice

Biosci Rep. 2018 Mar 5;38(2):BSR20171033. doi: 10.1042/BSR20171033. Print 2018 Apr 27.

Abstract

To investigate the central (hypothalamic) and peripheral effects of exercise without body weight change in diet-induced obesity (DIO). Twelve-week-old male C57Bl/6 mice received a control (C) or a high-fat diet (H). Half of them had free access to running wheels for 5 days/week for 10 weeks (CE) and HE, respectively). Hypothalamic expression of genes related to energy homeostasis, and leptin (Stat3 and p-Stat3) and insulin (Akt and p-Akt) signaling were evaluated. Glucose and leptin tolerance, peripheral insulin sensitivity, and plasma insulin, leptin and adiponectin were determined. Perigonadal and retroperitoneal fat depots were increased by diet but reduced by exercise despite lack of effect of exercise on body weight. Blood glucose during intraperitoneal glucose tolerance test (ipGTT) was higher and glucose decay during intraperitoneal insulin tolerance test (ipITT) was lower in H and HE compared with C and CE. Exercise increased liver p-Akt expression and reduced fast glycemia. High-fat diet increased plasma insulin and leptin. Exercise had no effect on insulin but decreased leptin and increased adiponectin. Leptin inhibited food intake in all groups. Hypothalamic total and p-Stat3 and Akt were similar amongst the groups despite higher plasma levels of leptin and insulin in H and HE mice. High-fat diet modulated gene expression favoring a positive energy balance. Exercise only marginally changed the gene expression. Exercise induced positive changes (decreased fast glycemia and fat depots; increased liver insulin signaling and adiponectin concentration) without weight loss. Thus, despite reducing body weight could bring additional benefits, the effects of exercise must not be overlooked when weight reduction is not achieved.

Keywords: energy balance; hypothalamus; insulin; leptin; obesity; physical exercise.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Weight*
  • Dietary Fats / adverse effects*
  • Dietary Fats / pharmacology
  • Gene Expression Regulation*
  • Hypothalamus / metabolism*
  • Insulin / metabolism
  • Leptin / metabolism
  • Male
  • Mice
  • Obesity / chemically induced
  • Obesity / metabolism*
  • Physical Conditioning, Animal*
  • Proto-Oncogene Proteins c-akt / metabolism
  • STAT3 Transcription Factor / metabolism

Substances

  • Dietary Fats
  • Insulin
  • Leptin
  • STAT3 Transcription Factor
  • Stat3 protein, mouse
  • Proto-Oncogene Proteins c-akt