Diet-induced obesity causes hypothalamic neurochemistry alterations in Swiss mice

Metab Brain Dis. 2019 Apr;34(2):565-573. doi: 10.1007/s11011-018-0337-9. Epub 2019 Jan 11.

Abstract

The aim of this study was to assess inflammatory parameters, oxidative stress and energy metabolism in the hypothalamus of diet-induced obese mice. Male Swiss mice were divided into two study groups: control group and obese group. The animals in the control group were fed a diet with adequate amounts of macronutrients (normal-lipid diet), whereas the animals in the obese group were fed a high-fat diet to induce obesity. Obesity induction lasted 10 weeks, at the end of this period the disease model was validated in animals. The animals in the obese group had higher calorie consumption, higher body weight and higher weight of mesenteric fat compared to control group. Obesity showed an increase in levels of interleukin 1β and decreased levels of interleukin 10 in the hypothalamus. Furthermore, increased lipid peroxidation and protein carbonylation, and decreased level of glutathione in the hypothalamus of obese animals. However, there was no statistically significant difference in the activity of antioxidant enzymes, superoxide dismutase and catalase. The obese group had lower activity of complex I, II and IV of the mitochondrial respiratory chain, as well as lower activity of creatine kinase in the hypothalamus as compared to the control group. Thus, the results from this study showed changes in inflammatory markers, and dysregulation of metabolic enzymes in the pathophysiology of obesity.

Keywords: Energy metabolism; Hypothalamus; Inflammation; Obesity; Oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / pharmacology
  • Biomarkers / metabolism
  • Diet, High-Fat / adverse effects*
  • Energy Intake / drug effects
  • Energy Metabolism / physiology*
  • Hypothalamus / metabolism*
  • Inflammation / metabolism
  • Male
  • Mice
  • Neurochemistry / methods
  • Obesity / metabolism*
  • Oxidative Stress / drug effects

Substances

  • Antioxidants
  • Biomarkers