Switching from high-fat feeding (HFD) to regular diet improves metabolic and behavioral impairments in middle-aged female mice

Behav Brain Res. 2021 Feb 1:398:112969. doi: 10.1016/j.bbr.2020.112969. Epub 2020 Oct 16.

Abstract

Obesity represents a risk factor for metabolic syndrome and cardiovascular and psychiatric disorders. Excessive caloric intake, particularly in dietary fats, is an environmental factor that contributes to obesity development. Thus, the observation that switching from long-standing dietary obesity to standard diet (SD) can ameliorate the high-fat diet-induced metabolic, memory, and emotionality-related impairments are particularly important. Herein we investigated whether switching from the high-fat diet (HFD) to SD could improve the metabolic and behavioral impairments observed in middle-aged females C57Bl/6 mice. During twelve weeks, the animals received a high-fat diet (61 % fat) or SD diet. After 12-weeks, the HFD group's diet was switched to SD for an additional four weeks. It was observed a progressive deleterious effect of HFD in metabolic and behavioral parameters in mice. After four weeks of HFD-feeding, the animals showed glucose intolerance and increased locomotor activity. A subsequent increase in the body mass gain, hyperglycemia, and depressive-like behavior was observed after eight weeks, and memory impairments after twelve weeks. After replacing the HFD to SD, it was observed an improvement of metabolic (loss of body mass, normal plasma glucose levels, and glucose tolerance) and behavioral (absence of memory and emotional alterations) parameters. These results demonstrate the temporal development of metabolic and behavioral impairments following HFD in middle-age female mice and provide new evidence that these alterations can be improved by switching back the diet to SD.

Keywords: Behavioral; Depression; Glucose; High-fat diet (HFD); Memory; Obesity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Animals
  • Behavior, Animal / physiology
  • Cognitive Dysfunction / diet therapy
  • Cognitive Dysfunction / etiology*
  • Depression / diet therapy
  • Depression / etiology*
  • Diet, High-Fat / adverse effects*
  • Disease Models, Animal
  • Female
  • Glucose Intolerance / blood
  • Glucose Intolerance / diet therapy
  • Glucose Intolerance / etiology
  • Hyperglycemia / blood
  • Hyperglycemia / diet therapy
  • Hyperglycemia / etiology*
  • Locomotion / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Motivation / physiology*
  • Obesity / etiology*
  • Spatial Memory / physiology*