Inhibition of Connexin 36 attenuates HMGB1‐mediated depressive‐like behaviors induced by chronic unpredictable mild stress

Abstract

Abstract Background High mobility group box 1 (HMGB1) released by neurons and microglia was demonstrated to be an important mediator in depressive‐like behaviors induced by chronic unpredictable mild stress (CUMS), which could lead to the imbalance of two different metabolic approaches in kynurenine pathway (KP), thus enhancing glutamate transmission and exacerbating depressive‐like behaviors. Evidence showed that HMGB1 signaling might be regulated by Connexin (Cx) 36 in inflammatory diseases of central nervous system (CNS). Our study aimed to further explore the role of Cx36 in depressive‐like behaviors and its relationship with HMGB1. Methods After 4‐week chronic stress, behavioral tests were conducted to evaluate depressive‐like behaviors, including sucrose preference test (SPT), tail suspension test (TST), forced swimming test (FST), and open field test (OFT). Western blot analysis and immunofluorescence staining were used to observe the expression and location of Cx36. Enzyme‐linked immunosorbent assay (ELISA) was adopted to detect the concentrations of inflammatory cytokines. And the excitability and inward currents of hippocampal neurons were recorded by whole‐cell patch clamping. Results The expression of Cx36 was significantly increased in hippocampal neurons of mice exposed to CUMS, while treatment with glycyrrhizinic acid (GZA) or quinine could both down‐regulate Cx36 and alleviate depressive‐like behaviors. The proinflammatory cytokines like HMGB1, tumor necrosis factor alpha (TNF‐α), and interleukin‐1β (IL‐1β) were all elevated by CUMS, and application of GZA and quinine could decrease them. In addition, the enhanced excitability and inward currents of hippocampal neurons induced by lipopolysaccharide (LPS) could be reduced by either GZA or quinine. Conclusions Inhibition of Cx36 in hippocampal neurons might attenuates HMGB1‐mediated depressive‐like behaviors induced by CUMS through down‐regulation of the proinflammatory cytokines and reduction of the excitability and intracellular ion overload.

Keywords

• chronic unpredictable mild stress
• Connexin 36
• depressive disorder
• hippocampal neurons
• HMGB1