Microglia are the resident immune cells in the brain where they play essential roles in the development and maintenance of physiological functions of this organ. Aberrant activation of microglia is speculated to be involved in the pathogenesis of a variety of neurological disorders, including alcohol use disorders. Repeated binge ethanol consumption can have a profound impact on the function and integrity of the brain resulting in changes in behaviors such as withdrawal and reward. However, the microglial molecular and cellular pathways associated with ethanol binge consumption remain poorly understood.
In this study, adult C57BL/6J male and female mice were subjected daily to a gelatin-based drinking-in-the-dark voluntary ethanol consumption paradigm (3-hours/day for 4 months) to characterize ethanol consumption and withdrawal-associated and anxiety-like behaviors. Brain microglia were isolated at the end and analyzed for protein expression profile changes using unbiased mass spectrometry-based proteomic analysis.
Both male and female mice consistently consumed binge quantities of ethanol daily, resulting in blood ethanol levels >80 mg/dl measured at the end of the 3-hour daily consumption period. Although female mice consumed a significantly greater amount of ethanol than male mice, ethanol withdrawal-associated anxiety-like behaviors measured by marble burying, light-dark box, and elevated plus maze tests were predominantly observed in male mice. Proteomic analysis of microglia isolated from the brains of animals at the end of the 4-month binge ethanol consumption identified 117 and 37 proteins that were significantly up or down-regulated in ethanol-exposed male and female mice, respectively, compared to their pair-fed controls. Protein expression profile-based pathway analysis identified several cellular pathways that may underlie the sex-specific and ethanol withdrawal-associated behavioral abnormalities.
Taken together, our findings revealed sex-specific changes in ethanol withdrawal-associated behaviors and signaling pathways in the mouse brain microglia and may help advance our understanding of the molecular, cellular, and behavioral changes related to human binge ethanol consumption.
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