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胆碱代谢产物——氧化三甲胺对炎症性肠病免疫代谢的影响。

Effects of choline metabolite-trimethylamine N-oxide on immunometabolism in inflammatory bowel disease.

作者信息

Wang Siyu, Ni Yifan, Zhou Shuwei, Peng Huiping, Cao Ying, Zhu Yue, Gong Jing, Lu Qiulu, Han Zhongyu, Lin Yumeng, Wang Yaodong

机构信息

Department of Preventive Medicine, Kunshan Hospital of Chinese Medicine, Kunshan, China.

Suzhou Key Laboratory of Integrated Traditional Chinese and Western Medicine for Digestive Diseases, Kunshan, China.

出版信息

Front Immunol. 2025 Jul 17;16:1591151. doi: 10.3389/fimmu.2025.1591151. eCollection 2025.


DOI:10.3389/fimmu.2025.1591151
PMID:40746564
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12310921/
Abstract

Trimethylamine N-oxide (TMAO), a key metabolite derived from the gut microbial metabolism of choline, has recently been implicated as a significant contributor to the development of several chronic diseases, including diabetes, cardiovascular disease, and chronic kidney disease. Its detrimental effects have garnered widespread attention in the scientific community. Inflammatory bowel disease (IBD), marked by persistent and recurring gastrointestinal inflammation, is a significant global health issue. Emerging evidence highlights a critical role for TMAO in the pathogenesis of IBD. This review comprehensively summarizes current research on the association between TMAO and IBD, with a particular focus on the mechanisms by which TMAO regulates immunometabolism in diseases.

摘要

氧化三甲胺(TMAO)是胆碱经肠道微生物代谢产生的一种关键代谢产物,最近被认为是包括糖尿病、心血管疾病和慢性肾脏病在内的几种慢性疾病发展的重要促成因素。其有害影响已在科学界引起广泛关注。炎症性肠病(IBD)以持续反复的胃肠道炎症为特征,是一个重大的全球健康问题。新出现的证据凸显了TMAO在IBD发病机制中的关键作用。本综述全面总结了目前关于TMAO与IBD关联的研究,特别关注TMAO在疾病中调节免疫代谢的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ed/12310921/a533ff602094/fimmu-16-1591151-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ed/12310921/414e8fa6120e/fimmu-16-1591151-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ed/12310921/b8d16eaf66ef/fimmu-16-1591151-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ed/12310921/a533ff602094/fimmu-16-1591151-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ed/12310921/414e8fa6120e/fimmu-16-1591151-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ed/12310921/b8d16eaf66ef/fimmu-16-1591151-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ed/12310921/a533ff602094/fimmu-16-1591151-g003.jpg

相似文献

[1]
Effects of choline metabolite-trimethylamine N-oxide on immunometabolism in inflammatory bowel disease.

Front Immunol. 2025-7-17

[2]
TMAO and the gut microbiome: implications for the CVD-CKD-IBD axis.

Ann Med. 2025-12

[3]
Gut microbiota-dependent metabolite trimethylamine N-oxide (TMAO) and cardiovascular risk in patients with suspected functionally relevant coronary artery disease (fCAD).

Clin Res Cardiol. 2022-6

[4]
Gut microbial metabolite trimethylamine N-oxide induces aortic dissection.

J Mol Cell Cardiol. 2024-4

[5]
The gut microbe-derived metabolite trimethylamine-N-oxide induces aortic valve fibrosis via PERK/ATF-4 and IRE-1α/XBP-1s signaling in vitro and in vivo.

Atherosclerosis. 2024-4

[6]
Gut microbial metabolite trimethylamine N-oxide as a novel predictor for adverse cardiovascular events after PCI: a systematic review and dose-response meta-analysis.

Nutr J. 2025-6-16

[7]
Dietary Nitrogen and Its Role in the Gut Microbiome and Inflammatory Bowel Disease: A Narrative Review.

Nutrients. 2025-7-20

[8]
Microbiota-derived metabolites in inflammatory bowel disease.

Semin Immunopathol. 2025-3-4

[9]
Gut Microbiota Metabolites and Risk of Major Adverse Cardiovascular Disease Events and Death: A Systematic Review and Meta-Analysis of Prospective Studies.

J Am Heart Assoc. 2017-6-29

[10]
Trimethylamine N-oxide reduction is related to probiotic strain specificity: A systematic review.

Nutr Res. 2022-8

本文引用的文献

[1]
Effect of acarbose and vildagliptin on plasma trimethylamine N-oxide levels in patients with type 2 diabetes mellitus: a 6-month, two-arm randomized controlled trial.

Front Endocrinol (Lausanne). 2025-5-6

[2]
Association of TMAO levels with indicators of ulcerative colitis activity.

Caspian J Intern Med. 2024-10-19

[3]
The Effects of Interventions with Glucosinolates and Their Metabolites in Cruciferous Vegetables on Inflammatory Bowel Disease: A Review.

Foods. 2024-11-1

[4]
Alterations of the Gut Microbiome and TMAO Levels in Patients with Ulcerative Colitis.

J Clin Med. 2024-9-28

[5]
Ulcerative colitis: molecular insights and intervention therapy.

Mol Biomed. 2024-10-10

[6]
Microbiome- and Host Inflammasome-Targeting Inhibitor Nanoligomers Are Therapeutic in the Murine Colitis Model.

ACS Pharmacol Transl Sci. 2024-8-30

[7]
Trimethylamine N-oxide induces non-alcoholic fatty liver disease by activating the PERK.

Toxicol Lett. 2024-10

[8]
Obesity-associated inflammation countered by a Mediterranean diet: the role of gut-derived metabolites.

Front Nutr. 2024-6-24

[9]
Trimethylamine N-Oxide in Aquatic Foods.

J Agric Food Chem. 2024-7-3

[10]
Ultra-processed foods: increasing the risk of inflammation and immune dysregulation?

Nat Rev Immunol. 2024-7

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