4.7 Article

Gut Microbiota-Mediated Elevated Production of Secondary Bile Acids in Chronic Unpredictable Mild Stress

Journal

FRONTIERS IN PHARMACOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2022.837543

Keywords

CUMS; bile acid; gut microbiota; depression; Ruminococcaceae

Funding

  1. Natural Science Foundation of China [82173879]
  2. Jiangsu Pharmaceutical Association [Q202019, H202122]
  3. Lift Project for Discipline Construction of The Second Affiliated Hospital of Soochow University [XKTJ-XK202010]
  4. Second Affiliate Hospital of Soochow University Talent Promotion Project [XKTJ-RC202013, XKTJ-RC202014]
  5. Suzhou Science Foundation [SYS2019058]
  6. Suzhou Health Talent Project [GSW2020025]
  7. Suzhou Science and Technology Development Plan [SS2019042]

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A study using a mouse model of depression induced by chronic stress found that the bile acid and energy metabolism pathways were significantly affected. The study also revealed that chronic stress promoted the deconjugation of conjugated bile acid and increased the levels of secondary bile acid. Furthermore, the increased secondary bile acid levels were found to be positively correlated with specific bacterial abundance. These findings suggest that changes in bile acid metabolism may play a role in the progression of depression.
A growing body of evidence suggests that gut microbiota could participate in the progression of depression via the microbiota-gut-brain axis. However, the detailed microbial metabolic profile changes in the progression of depression is still not fully elucidated. In this study, a liquid chromatography coupled to mass spectrometry-based untargeted serum high-throughput metabolomics method was first performed to screen for potential biomarkers in a depressive-like state in a chronic unpredictable mild stress (CUMS)-induced mouse model. Our results identified that the bile acid and energy metabolism pathways were significantly affected in CUMS progression. The detailed bile acid profiles were subsequently quantified in the serum, liver, and feces. The results showed that CUMS significantly promoted the deconjugation of conjugated bile acid and secondary bile acid biosynthesis. Furthermore, 16S rRNA gene sequencing revealed that the increased secondary bile acid levels in the feces positively correlated with Ruminococcaceae_UCG-010, Ruminococcus, and Clostridia_UCG-014 abundance. Taken together, our study suggested that changes in family Ruminococcaceae abundance following chronic stress increased biosynthesis of deoxycholic acid (DCA), a unconjugated secondary bile acid in the intestine. Aberrant activation of secondary bile acid biosynthesis pathway thereby increased the hydrophobicity of the bile acid pool, which might, in turn, promoted metabolic disturbances and disease progression in CUMS mice.

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