AI Article Synopsis

  • The gut microbiota influences depression by affecting the brain-gut axis, with specific changes observed in a mouse model of depression known as the subchronic and mild social defeat stress (sCSDS) model.
  • In this study, researchers used liquid chromatography/mass spectrometry (LC/MS) to analyze fecal bile acid profiles in sCSDS mice, finding increased levels of deoxycholic acid (DCA) and lithocholic acid (LCA), linked to altered gut microbiota.
  • The results demonstrated that higher levels of certain bile acids correlated negatively with social interaction scores, indicating that gut changes due to sCSDS affect behavior associated with stress vulnerability.

Article Abstract

The gut microbiota plays a crucial role in both the pathogenesis and alleviation of host depression by modulating the brain-gut axis. We have developed a murine model of human depression called the subchronic and mild social defeat stress (sCSDS) model, which impacts not only behavior but also the host gut microbiota and gut metabolites, including bile acids. In this study, we utilized liquid chromatography/mass spectrometry (LC/MS) to explore the effects of sCSDS on the mouse fecal bile acid profile. sCSDS mice exhibited significantly elevated levels of deoxycholic acid (DCA) and lithocholic acid (LCA) in fecal extracts, leading to a notable increase in total bile acids and 7α-dehydroxylated secondary bile acids. Consequently, a noteworthy negative correlation was identified between the abundances of DCA and LCA and the social interaction score, an indicator of susceptibility in stressed mice. Furthermore, analysis of the colonic microbiome unveiled a negative correlation between the abundance of CDCA and . Additionally, DCA and LCA exhibited positive correlations with and but negative correlations with the group. These findings suggest that sCSDS impacts the bidirectional interaction between the gut microbiota and bile acids and is associated with reduced social interaction, a behavioral indicator of susceptibility in stressed mice.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11220325PMC
http://dx.doi.org/10.12938/bmfh.2023-095DOI Listing

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