Melatonin prevents neuroinflammation and relieves depression by attenuating autophagy impairment through FOXO3a regulation

Abstract

Major depressive disorder (MDD) is a life‐threatening illness characterized by mood changes and high rates of suicide. Although the role of neuroinflammation in MMD has been studied, the mechanistic interplay between antidepressants, neuroinflammation, and autophagy is yet to be investigated. The present study investigated the effect of melatonin on LPS‐induced neuroinflammation, depression, and autophagy impairment. Our results showed that in mice, lipopolysaccharide (LPS) treatment induced depressive‐like behaviors and caused autophagy impairment by dysregulating ATG genes. Moreover, LPS treatment significantly increased the levels of cytokines (TNFα, IL‐1β, IL‐6), enhanced NF‐ᴋB phosphorylation, caused glial (astrocytes and microglia) cell activation, dysregulated FOXO3a expression, increased the levels of redox signaling molecules such as ROS/TBARs, and altered expression of Nrf2, SOD2, and HO‐1. Melatonin treatment significantly abolished the effects of LPS, as demonstrated by improved depressive‐like behaviors, normalized autophagy‐related gene expression, and reduced levels of cytokines. Further, we investigated the role of autophagy in LPS‐induced depressive‐like behavior and neuroinflammation using autophagy inhibitors 3‐MA and Ly294002. Interestingly, inhibitor treatment significantly abolished and reversed the anti‐depressive, pro‐autophagy, and anti‐inflammatory effects of melatonin. The present study concludes that the anti‐depressive effects of melatonin in LPS‐induced depression might be mediated via autophagy modulation through FOXO3a signaling.