4.7 Article

The connexin hemichannel inhibitor D4 produces rapid antidepressant-like effects in mice

期刊

JOURNAL OF NEUROINFLAMMATION
卷 20, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12974-023-02873-z

关键词

Depression; Connexin hemichannels; Glia; Stress; Antidepressant

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In this study, the researchers found that using a selective Cx hemichannel inhibitor called D4 can reduce neuroinflammation and alleviate depressive-like behaviors by normalizing neuronal activity. The results suggest that glial Cx hemichannels may be potential therapeutic targets for depression.
Depression is a common mood disorder characterized by a range of clinical symptoms, including prolonged low mood and diminished interest. Although many clinical and animal studies have provided significant insights into the pathophysiology of depression, current treatment strategies are not sufficient to manage this disorder. It has been suggested that connexin (Cx)-based hemichannels are candidates for depression intervention by modifying the state of neuroinflammation. In this study, we investigated the antidepressant-like effect of a recently discovered selective Cx hemichannel inhibitor, a small organic molecule called D4. We first showed that D4 reduced hemichannel activity following systemic inflammation after LPS injections. Next, we found that D4 treatment prevented LPS-induced inflammatory response and depressive-like behaviors. These behavioral effects were accompanied by reduced astrocytic activation and hemichannel activity in depressive-like mice induced by repeated low-dose LPS challenges. D4 treatment also reverses depressive-like symptoms in mice subjected to chronic restraint stress (CRS). To test whether D4 broadly affected neural activity, we measured c-Fos expression in depression-related brain regions and found a reduction in c-Fos(+) cells in different brain regions. D4 significantly normalized CRS-induced hypoactivation in several brain regions, including the hippocampus, entorhinal cortex, and lateral septum. Together, these results indicate that blocking Cx hemichannels using D4 can normalize neuronal activity and reduce depressive-like symptoms in mice by reducing neuroinflammation. Our work provides evidence of the antidepressant-like effect of D4 and supports glial Cx hemichannels as potential therapeutic targets for depression.

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