Sleep fragmentation promotes NADPH oxidase 2-mediated adipose tissue inflammation leading to insulin resistance in mice

Abstract

BackgroundShort sleep has been implicated in higher risk of obesity in humans, and is associated with insulin resistance. However, the effects of fragmented sleep (SF) rather than curtailed sleep on glucose homeostasis are unknown.MethodsWild type and NADPH oxidase 2 (Nox2) null male mice were subjected to SF or sleep control (SC) conditions for 3 days-3 weeks. Systemic and visceral adipose tissue (VAT) insulin sensitivity tests, glucose tolerance test, FACS and immunohistochemistry for macrophages and sub-types (M1 and M2) and Nox expression and activity were examined.ResultsHere show that SF in the absence of sleep curtailment induces time-dependent insulin resistance, in vivo and also in vitro in VAT. Oxidative stress pathways were up-regulated by SF in VAT, and were accompanied by M1 macrophage polarization. SF-induced oxidative stress, inflammation, and insulin resistance in VAT were completely abrogated in genetically altered mice lacking Nox2 activity.ConclusionsThese studies imply that SF, a frequent occurrence in many disorders and more specifically in sleep apnea, is a potent inducer of insulin resistance via activation of oxidative stress and inflammatory pathways, thereby opening the way for therapeutic strategies.