4.7 Article

Erchen Decoction alleviates obesity-related hepatic steatosis via modulating gut microbiota-drived butyric acid contents and promoting fatty acid beta-oxidation

Journal

JOURNAL OF ETHNOPHARMACOLOGY
Volume 317, Issue -, Pages -

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2023.116811

Keywords

Obesity; Hepatic steatosis; Erchen Decoction; Gut microbiota; Butyric acid; Fatty acid beta-oxidation

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This study investigates the therapeutic effect and molecular mechanism of Erchen decoction (ECD) in a rat model of high-fat diet-induced obesity. The results demonstrate that ECD treatment improves lipid metabolic disorders and hepatic steatosis. Furthermore, ECD promotes the abundance of beneficial bacteria that produce short-chain fatty acids and reduces the abundance of disease-related bacteria. ECD also increases total short-chain fatty acids levels, particularly butyric acid. The mechanism may involve an increase in acetyl-histone 3-lysine 9 levels, promoting fatty acid beta-oxidation in the liver.
Ethnopharmacological relevance: Erchen decoction (ECD) is a traditional Chinese medicine formula comprising six distinct herbs and has been documented to possess a protective effect against obesity. The study conducted previously demonstrated that ECD has the potential to effectively modulate the composition of gut microbiota and levels of short-chain fatty acids (SCFAs) in obese rat. However, the regulatory mechanism of ECD on gut microbiota and SCFAs and further improvement of obesity have not been thoroughly explained. Aim of the study: The objective of this study was to examine the therapeutic effect and molecular mechanism of ECD in a rat model of high-fat diet (HFD) feeding. Materials and methods: Rats with HFD-induced obesity were treated with ECD. Upon completion of the study, serum and liver samples were procured to conduct biochemical, pathological, and Western blotting analyses. The investigation of alterations in the gut microbiota subsequent to ECD treatment was conducted through the utilization of 16S rRNA sequencing. The metabolic alterations in the cecal contents were examined through the utilization of mass spectrometry-ultraperformance liquid chromatography. Results: ECD treatment improved lipid metabolic disorders and reduced hepatic steatosis in HFD-induced obese rats. Obese rat treated with ECD showed a higher abundance of SCFA-producing bacteria, including Lactobacillus, Bifidobacterium, and Butyricicoccus, and lower abundance of disease-related bacteria, such as Bacteroides, Parabacteroides, and Sediminibacterium. Additionally, ECD caused an increase in total SCFAs levels; in particular, butyric acid was dramatically increased in the HFD group. Rats treated with ECD also exhibited significantly increased butyric acid concentrations in the serum and liver. The subsequent reduction in histone deacetylase 1 expression and increase in acetyl-histone 3-lysine 9 (H3K9ac) levels contributed to the promotion of fatty acid beta-oxidation (FAO) in liver by ECD. Conclusion: This study demonstrates that ECD regulates the gut microbiota and promotes butyric acid production to ameliorate obesity-related hepatic steatosis. The mechanism might be related to the promotion of FAO via a butyric acid-mediated increase in H3K9ac levels in the liver.

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