4.7 Article

Association of Short-Chain Fatty Acids with Gut Microbiota and Lipid Metabolism in Mice with Diarrhea Induced by High-Fat Diet in a Fatigued State

Journal

MOLECULAR NUTRITION & FOOD RESEARCH
Volume -, Issue -, Pages -

Publisher

WILEY
DOI: 10.1002/mnfr.202300452

Keywords

diarrhea; gut microbiota; high-fat diet; lipid metabolic; SCFAs

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Preliminary research suggests that a high-fat diet in a fatigued state can trigger diarrhea, but the exact mechanism is unclear. This study investigates the composition and metabolomics of the gut microbiota to understand the pathogenesis of diarrhea. The results show that an HFD in a fatigued state causes changes in gut microbiota, deprivation of short-chain fatty acids, increased inflammation, and dysregulated lipid metabolism, all of which may contribute to the development of diarrhea.
ScopePreliminary research finds that a high-fat diet (HFD) in a fatigued state triggers diarrhea, but the exact mechanism has not been clarified. To address concerns about the pathogenesis of diarrhea, the study evaluates the composition and metabolomics of the gut microbiota.Methods and resultsThe study uses the multiple platform apparatus device to induce fatigue in mice, combined with intragastric administration of lard-caused diarrhea. Subsequently, the characteristics and interaction relationship of gut microbiota, short-chain fatty acids (SCFAs), inflammatory biomarkers, brain-gut peptides, and lipid metabolism are analyzed at the end of the experiment. HFD in a fatigued state results in a significant increase in interleukin-17, interleukin-6, cholecystokinin, somatostatin, and malondialdehyde content in mice (p < 0.05), along with a substantial decrease in high-density lipoprotein (p < 0.05). Additionally, an HFD in a fatigued state causes changes in the structure and composition of the gut microbiota, with Lactobacillus murinus as its characteristic bacteria, and reduces the production of SCFAs.ConclusionsAn HFD in a fatigued state triggers diarrhea, possibly associated with gut content microbiota dysbiosis, SCFAs deprivation, increased inflammation, and dysregulated lipid metabolism.

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