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昼夜节律紊乱影响肝脂代谢、肠道微生物群,并促进小鼠胆固醇结石形成。

Circadian Rhythm Disruption Influenced Hepatic Lipid Metabolism, Gut Microbiota and Promoted Cholesterol Gallstone Formation in Mice.

机构信息

Center of Gallstone Disease, Shanghai East Hospital, Institution of Gallstone Disease, School of Medicine, Tongji University, Shanghai, China.

出版信息

Front Endocrinol (Lausanne). 2021 Oct 21;12:723918. doi: 10.3389/fendo.2021.723918. eCollection 2021.

Abstract

BACKGROUND

Hepatic lipid metabolism regulates biliary composition and influences the formation of cholesterol gallstones. The genes and , which encode key liver enzymes, are regulated by circadian rhythm-related transcription factors. We aimed to investigate the effect of circadian rhythm disruption on hepatic cholesterol and bile acid metabolism and the incidence of cholesterol stone formation.

METHODS

Adult male C57BL/6J mice were fed either a lithogenic diet (LD) only during the sleep phase (time-restricted lithogenic diet feeding, TRF) or an LD (non-time-restricted lithogenic diet feeding, nTRF) for 4 weeks. Food consumption, body mass gain, and the incidence of gallstones were assessed. Circulating metabolic parameters, lipid accumulation in the liver, the circadian expression of hepatic clock and metabolic genes, and the gut microbiota were analyzed.

RESULTS

TRF caused a dysregulation of the circadian rhythm in the mice, characterized by significant differences in the circadian expression patterns of clock-related genes. In TRF mice, the circadian rhythms in the expression of genes involved in bile acid and cholesterol metabolism were disrupted, as was the circadian rhythm of the gut microbiota. These changes were associated with high biliary cholesterol content, which promoted gallstone formation in the TRF mice.

CONCLUSION

Disordered circadian rhythm is associated with abnormal hepatic bile acid and cholesterol metabolism in mice, which promotes gallstone formation.

摘要

背景

肝脏脂质代谢调节胆汁成分,并影响胆固醇胆结石的形成。编码关键肝脏酶的基因和受昼夜节律相关转录因子调控。我们旨在研究昼夜节律紊乱对肝脏胆固醇和胆汁酸代谢以及胆固醇结石形成的影响。

方法

成年雄性 C57BL/6J 小鼠仅在睡眠阶段(时间限制致石饮食喂养,TRF)或非时间限制致石饮食(非时间限制致石饮食喂养,nTRF)下接受致石饮食喂养 4 周。评估食物消耗、体重增加和胆结石的发生率。分析循环代谢参数、肝脏脂质积累、肝脏时钟和代谢基因的昼夜表达以及肠道微生物群。

结果

TRF 导致小鼠昼夜节律失调,表现为时钟相关基因的昼夜表达模式存在显著差异。在 TRF 小鼠中,胆汁酸和胆固醇代谢相关基因的表达昼夜节律被打乱,肠道微生物群的昼夜节律也被打乱。这些变化与高胆汁胆固醇含量有关,促进了 TRF 小鼠的胆结石形成。

结论

紊乱的昼夜节律与小鼠异常的肝胆汁酸和胆固醇代谢有关,从而促进胆结石形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee0e/8567099/e1b7cf0809bd/fendo-12-723918-g001.jpg

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