Obesity induced disruption on diurnal rhythm of insulin sensitivity via gut microbiome-bile acid metabolism

IF 3.9 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochimica et biophysica acta. Molecular and cell biology of lipids Pub Date : 2023-11-10 DOI:10.1016/j.bbalip.2023.159419
Xiaozhen Guo , Jiawen Wang , Hualing Xu , Yangyang Wang , Yutang Cao , Yingquan Wen , Jiaqi Li , Yameng Liu , Kanglong Wang , Jue Wang , Xianchun Zhong , Chuying Sun , Yongxin Zhang , Jingyi Xu , Cuina Li , Pengxiang Mu , Lingyan Xu , Cen Xie
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Abstract

The disruption of the diurnal rhythm has been recognized as a significant contributing factor to metabolic dysregulation. The important role of gut microbiota and bile acid metabolism has attracted extensive attention. However, the function of the gut microbiota-bile acid axis in regulating the diurnal rhythms of metabolic homeostasis remains largely unknown. Herein, we aimed to investigate the interplay between rhythmicity of host metabolism and gut microbiota-bile acid axis, as well as to assess the impact of obesity on them. We found that high fat diet feeding and Leptin gene deficiency (ob/ob) significantly disturbed the rhythmic patterns of insulin sensitivity and serum total cholesterol levels. The bile acid profiling unveiled a conspicuous diurnal rhythm oscillation of ursodeoxycholic acid (UDCA) in lean mice, concomitant with fluctuations in insulin sensitivity, whereas it was absent in obese mice. The aforementioned diurnal rhythm oscillations were largely desynchronized by gut microbiota depletion, suggesting the indispensable role of gut microbiota in diurnal regulation of insulin sensitivity and bile acid metabolism. Consistently, 16S rRNA sequencing revealed that UDCA-associated bacteria exhibited diurnal rhythm oscillations that paralleled the fluctuation in insulin sensitivity. Collectively, the current study provides compelling evidence regarding the association between diurnal rhythm of insulin sensitivity and gut microbiota-bile acid axis. Moreover, we have elucidated the deleterious effects of obesity on gut microbiome-bile acid metabolism in both the genetic obesity model and the diet-induced obesity model.

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肥胖通过肠道微生物群-胆汁酸代谢导致胰岛素敏感性的昼夜节律紊乱。
昼夜节律的中断已被认为是代谢失调的一个重要因素。肠道菌群在胆汁酸代谢中的重要作用已引起广泛关注。然而,肠道微生物-胆汁酸轴在调节代谢稳态的昼夜节律中的功能仍然很大程度上未知。本研究旨在探讨宿主代谢节律性与肠道微生物-胆汁酸轴之间的相互作用,并评估肥胖对它们的影响。我们发现高脂饮食喂养和瘦素基因缺乏(ob/ob)显著扰乱胰岛素敏感性和血清总胆固醇水平的节律模式。胆红酸谱揭示了瘦小鼠熊去氧胆酸(UDCA)的昼夜节律振荡,同时伴有胰岛素敏感性波动,而肥胖小鼠则没有。上述昼夜节律振荡在很大程度上被肠道菌群消耗所破坏,这表明肠道菌群在胰岛素敏感性和胆酸代谢的昼夜调节中起着不可或缺的作用。一致地,16S rRNA测序显示,udca相关细菌表现出与胰岛素敏感性波动平行的昼夜节律振荡。总的来说,目前的研究为胰岛素敏感性的昼夜节律与肠道微生物-胆汁酸轴之间的关系提供了令人信服的证据。此外,我们还在遗传肥胖模型和饮食诱导肥胖模型中阐明了肥胖对肠道微生物群-胆汁酸代谢的有害影响。
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来源期刊
CiteScore
11.00
自引率
2.10%
发文量
109
审稿时长
53 days
期刊介绍: BBA Molecular and Cell Biology of Lipids publishes papers on original research dealing with novel aspects of molecular genetics related to the lipidome, the biosynthesis of lipids, the role of lipids in cells and whole organisms, the regulation of lipid metabolism and function, and lipidomics in all organisms. Manuscripts should significantly advance the understanding of the molecular mechanisms underlying biological processes in which lipids are involved. Papers detailing novel methodology must report significant biochemical, molecular, or functional insight in the area of lipids.
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