Depression-like phenotypes in mice following common bile duct ligation: Insights into the gut-liver-brain axis via the vagus nerve.
Yong Yang, Akifumi Eguchi, Chisato Mori, Kenji Hashimoto
Neurobiology of disease March 1, 2024 DOI: 10.1016/j.nbd.2024.106433 via PubMed
Summary
AI-generated from the abstractDepression often accompanies liver cirrhosis, but the underlying reasons are unclear. In mice with cirrhosis induced by common bile duct ligation (CBDL), depression-like behaviors, inflammation, reduced synaptic proteins in the prefrontal cortex, gut microbiota imbalance, and altered blood metabolites were observed. These changes were reversed by severing the subdiaphragmatic vagus nerve, and a single injection of arketamine improved the depression-like behaviors. The findings suggest that the gut-liver-brain axis, via the vagus nerve, mediates depression in cirrhosis, and arketamine may offer a new treatment.
Study at a glance
| Characteristics | Animal study Peer reviewed |
|---|---|
| Population | Mice with liver cirrhosis induced by common bile duct ligation |
| Interventions | subdiaphragmatic vagotomy arketamine |
| Dose | single injection |
| Duration | Behavioral tests conducted 10 days after surgery |
| Topics | Depression Ketamine |
| Keywords | Gut microbiota Liver cirrhosis Metabolites |
| Key finding | CBDL-induced depression-like phenotypes in mice are mediated through the gut-liver-brain axis via the subdiaphragmatic vagus nerve, and arketamine improved these behaviors. |
Abstract
Depression frequently occurs in patients with liver cirrhosis, yet the reasons for this correlation are not fully understood. Dysbiosis of gut microbiota has been implicated in depression through the gut-brain axis via the vagus nerve. This study explored the potential role of the gut-liver-brain axis via the vagus nerve in depression-like phenotypes in mice with liver cirrhosis. These mice underwent common bile duct ligation (CBDL), a method used to stimulate liver cirrhosis. To assess depression-like behaviors, behavioral tests were conducted 10 days following either sham or CBDL surgeries. The mice with CBDL displayed symptoms such as splenomegaly, elevated plasma levels of interleukin-6 and tumor necrosis factor-α, depression-like behaviors, decreased levels of synaptic proteins in the prefrontal cortex (PFC), disrupted gut microbiota balance, and changes in blood metabolites (or lipids). Additionally, there were positive or negative correlations between the relative abundance of microbiome and behavioral data or blood metabolites (or lipids). Significantly, these changes were reversed in CBDL mice by performing a subdiaphragmatic vagotomy. Intriguingly, depression-like phenotypes in mice with CBDL were improved after a single injection of arketamine, a new antidepressant. These results suggest that CBDL-induced depression-like phenotypes in mice are mediated through the gut-liver-brain axis via the subdiaphragmatic vagus nerve, and that arketamine might offer a new treatment approach for depression in liver cirrhosis patients.