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高脂肪饮食诱导的结肠细胞功能障碍会加剧微生物群衍生的三甲胺氧化物。

High-fat diet-induced colonocyte dysfunction escalates microbiota-derived trimethylamine -oxide.

机构信息

Vanderbilt Institute for Infection, Immunology, and Inflammation, Vanderbilt University Medical Center, Nashville, TN 37232, USA.

Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.

出版信息

Science. 2021 Aug 13;373(6556):813-818. doi: 10.1126/science.aba3683.


DOI:10.1126/science.aba3683
PMID:34385401
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8506909/
Abstract

A Western-style, high-fat diet promotes cardiovascular disease, in part because it is rich in choline, which is converted to trimethylamine (TMA) by the gut microbiota. However, whether diet-induced changes in intestinal physiology can alter the metabolic capacity of the microbiota remains unknown. Using a mouse model of diet-induced obesity, we show that chronic exposure to a high-fat diet escalates choline catabolism by altering intestinal epithelial physiology. A high-fat diet impaired the bioenergetics of mitochondria in the colonic epithelium to increase the luminal bioavailability of oxygen and nitrate, thereby intensifying respiration-dependent choline catabolism of In turn, choline catabolism increased levels of circulating trimethlamine -oxide, which is a potentially harmful metabolite generated by gut microbiota.

摘要

西式高脂肪饮食会促进心血管疾病,部分原因是它富含胆碱,胆碱可被肠道微生物群转化为三甲胺(TMA)。然而,饮食引起的肠道生理变化是否会改变微生物群的代谢能力尚不清楚。本研究使用饮食诱导肥胖的小鼠模型,结果表明,慢性高脂肪饮食通过改变肠道上皮生理来加速胆碱代谢。高脂肪饮食损害了结肠上皮细胞中线粒体的生物能量学,增加了腔内氧气和硝酸盐的生物利用度,从而加剧了依赖呼吸的胆碱代谢。反过来,胆碱代谢增加了循环三甲胺氧化物的水平,三甲胺氧化物是肠道微生物群产生的一种潜在有害代谢物。

相似文献

[1]
High-fat diet-induced colonocyte dysfunction escalates microbiota-derived trimethylamine -oxide.

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[2]
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[3]
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[6]
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[7]
Intestinal microbiota composition modulates choline bioavailability from diet and accumulation of the proatherogenic metabolite trimethylamine-N-oxide.

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[8]
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[9]
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[1]
Gut Microbiota-Associated Metabolites Affected the Susceptibility to Heart Health Abnormality in Young Migrants at High-Altitude: Gut Microbiota and Associated Metabolites Impart Heart Health in Plateau.

Exploration (Beijing). 2025-6-12

[2]
Impact of Obesity on Immunity to the Influenza Virus: Gut Microbiota, Mechanisms, and Novel Therapeutic Strategies.

Diseases. 2025-8-19

[3]
HIF-1 attenuates high-fiber diet-mediated proliferation and stemness of colonic epithelium.

Gut Microbes. 2025-12

[4]
Mechanisms conferring multi-layered protection against intestinal Salmonella Typhimurium infection.

FEMS Microbiol Rev. 2025-1-14

[5]
The role of trimethylamine N-oxide in disease pathogenesis and the therapeutic potential of traditional Chinese medicine.

Front Pharmacol. 2025-7-24

[6]
Linking Short-Chain Fatty Acids to Systemic Homeostasis: Mechanisms, Therapeutic Potential, and Future Directions.

J Nutr Metab. 2025-7-28

[7]
Assessing Choline, Carnitine, and Betaine Intake and Their Effects on Trimethylamine N-Oxide Levels: Validation of a Dietary Questionnaire in a Central European Population.

Nutrients. 2025-7-9

[8]
Unraveling the complexities of diet induced obesity and glucolipid dysfunction in metabolic syndrome.

Diabetol Metab Syndr. 2025-7-22

[9]
Role of oral and gut microbiomes in enterosalivary nitrate metabolism and their effects on systemic disease.

Front Cell Infect Microbiol. 2025-7-3

[10]
High-Fat Diet with Normal Caloric Intake Elevates TMA and TMAO Production and Reduces Microbial Diversity in Rats.

Nutrients. 2025-7-5

本文引用的文献

[1]
Dysbiosis: from fiction to function.

Am J Physiol Gastrointest Liver Physiol. 2019-9-11

[2]
Microbiota-Nourishing Immunity: A Guide to Understanding Our Microbial Self.

Immunity. 2019-8-20

[3]
Endogenous Enterobacteriaceae underlie variation in susceptibility to Salmonella infection.

Nat Microbiol. 2019-3-25

[4]
Colonocyte metabolism shapes the gut microbiota.

Science. 2018-11-30

[5]
Gut microbe-generated metabolite trimethylamine-N-oxide as cardiovascular risk biomarker: a systematic review and dose-response meta-analysis.

Eur Heart J. 2017-10-14

[6]
Microbiota-activated PPAR-γ signaling inhibits dysbiotic Enterobacteriaceae expansion.

Science. 2017-8-11

[7]
Respiration of Microbiota-Derived 1,2-propanediol Drives Salmonella Expansion during Colitis.

PLoS Pathog. 2017-1-5

[8]
Virulence factors enhance Citrobacter rodentium expansion through aerobic respiration.

Science. 2016-9-16

[9]
Intestinal dysbiosis contributes to the delayed gastrointestinal transit in high-fat diet fed mice.

Cell Mol Gastroenterol Hepatol. 2016-5

[10]
High Fat Diets Induce Colonic Epithelial Cell Stress and Inflammation that is Reversed by IL-22.

Sci Rep. 2016-6-28

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