Chronic Variable Stress and Cafeteria Diet Combination Exacerbate Microglia and c-fos Activation but Not Experimental Anxiety or Depression in a Menopause Model

Int J Mol Sci. 2024 Jan 25;25(3):1455. doi: 10.3390/ijms25031455.

Abstract

The menopause transition is a vulnerable period for developing both psychiatric and metabolic disorders, and both can be enhanced by stressful events worsening their effects. The present study aimed to evaluate whether a cafeteria diet (CAF) combined with chronic variable stress (CVS) exacerbates anxious- or depressive-like behavior and neuronal activation, cell proliferation and survival, and microglia activation in middle-aged ovariectomized (OVX) rats. In addition, body weight, lipid profile, insulin resistance, and corticosterone as an index of metabolic changes or hypothalamus-pituitary-adrenal (HPA) axis activation, and the serum pro-inflammatory cytokines IL-6, IL-β, and TNFα were measured. A CAF diet increased body weight, lipid profile, and insulin resistance. CVS increased corticosterone and reduced HDL. A CAF produced anxiety-like behaviors, whereas CVS induced depressive-like behaviors. CVS increased serum TNFα independently of diet. A CAF and CVS separately enhanced the percentage of Iba-positive cells in the hippocampus; the combination of factors further increased Iba-positive cells in the ventral hippocampus. A CAF and CVS increased the c-fos-positive cells in the hippocampus; the combination of factors increased the number of positive cells expressing c-fos in the ventral hippocampus even more. The combination of a CAF and CVS generates a slight neuroinflammation process and neuronal activation in a hippocampal region-specific manner and differentially affects the behavior.

Keywords: Iba-positive cells; anxiety; c-fos; chronic variable stress; menopause model; obesity.

MeSH terms

  • Animals
  • Anxiety / etiology
  • Anxiety / psychology
  • Body Weight
  • Corticosterone*
  • Depression / etiology
  • Diet / adverse effects
  • Female
  • Insulin Resistance*
  • Lipids
  • Menopause* / metabolism
  • Microglia* / metabolism
  • Proto-Oncogene Proteins c-fos* / metabolism
  • Rats
  • Stress, Psychological / metabolism
  • Tumor Necrosis Factor-alpha

Substances

  • Corticosterone
  • Lipids
  • Tumor Necrosis Factor-alpha
  • Proto-Oncogene Proteins c-fos