Sleep restriction promotes brain oxidative stress and inflammation, and aggravates cognitive impairment in insulin-resistant mice

Psychoneuroendocrinology. 2024 Aug:166:107065. doi: 10.1016/j.psyneuen.2024.107065. Epub 2024 Apr 29.

Abstract

Sleep deprivation and insulin resistance (IR) are two risk factors for Alzheimer's disease. As the population of people with IR increases and sleep restriction (SR) due to staying up late becomes the "new normal", it is necessary to investigate the effects and molecular pathogenesis of chronic SR on cognitive function in insulin resistance. In this study, 4-week-old mice were fed a high-fat diet (HFD) for 8 weeks to establish IR model, and then the mice were subjected to SR for 21 days, and related indicators were assessed, including cognitive capacity, apoptosis, oxidative stress, glial cell activation, inflammation, blood-brain barrier (BBB) permeability and adiponectin levels, for exploring the potential regulatory mechanisms. Compared with control group, IR mice showed impaired cognitive capacity, meanwhile, SR not only promoted Bax/Bcl2-induced hippocampal neuronal cell apoptosis and Nrf2/HO1- induced oxidative stress, but also increased microglia activation and inflammatory factor levels and BBB permeability, thus aggravating the cognitive impairment in IR mice. Consequently, changing bad living habits and ensuring sufficient sleep are important intervention strategies to moderate the aggravation of IR-induced cognitive impairment.

Keywords: Sleep restriction (SR); cognitive impairment; inflammation; insulin resistant (IR); oxidative stress.

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Blood-Brain Barrier* / metabolism
  • Brain* / metabolism
  • Cognitive Dysfunction* / etiology
  • Cognitive Dysfunction* / metabolism
  • Cognitive Dysfunction* / physiopathology
  • Diet, High-Fat* / adverse effects
  • Disease Models, Animal
  • Hippocampus / metabolism
  • Inflammation* / metabolism
  • Insulin Resistance* / physiology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Microglia / metabolism
  • Oxidative Stress* / physiology
  • Sleep Deprivation* / complications
  • Sleep Deprivation* / metabolism
  • Sleep Deprivation* / physiopathology