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三甲胺/氧化三甲胺:饮食与心血管疾病之间的关键因素

Trimethylamine/Trimethylamine-N-Oxide as a Key Between Diet and Cardiovascular Diseases.

作者信息

He Siyu, Jiang Hong, Zhuo Caili, Jiang Wei

机构信息

West China School of Medicine, West China Hospital, Sichuan University, Chengdu, 610041, People's Republic of China.

The Laboratory of Cardiovascular Diseases, Molecular Medicine Research Center, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, People's Republic of China.

出版信息

Cardiovasc Toxicol. 2021 Aug;21(8):593-604. doi: 10.1007/s12012-021-09656-z. Epub 2021 May 18.


DOI:10.1007/s12012-021-09656-z
PMID:34003426
Abstract

Trimethylamine (TMA) is a gut microbiota-derived metabolite which comes from diets rich of choline, betaine or L-carnitine and could be further converted to Trimethylamine-N-oxide (TMAO) in the liver. As the function of gut microbiota and its metabolites being explored so far, studies suggest that TMAO may be a potential risk factor of cardiovascular diseases independent of other traditional risk factors. However, the precise role of TMAO is controversial as some converse results were discovered. In recent studies, it is hypothesized that TMA may also participate in the progression of cardiovascular diseases and some cytotoxic effect of TMA has been discovered. Thus, exploring the relationship between TMA, TMAO and CVD may bring a novel insight into the diagnosis and therapy of cardiovascular diseases. In this review, we discussed the factors which influence the TMA/TMAO's process of metabolism in the human body. We have also summarized the pathogenic effect of TMA/TMAO in cardiovascular diseases, as well as the limitation of some controversial discoveries.

摘要

三甲胺(TMA)是一种由肠道微生物群产生的代谢产物,它来自富含胆碱、甜菜碱或左旋肉碱的饮食,并可在肝脏中进一步转化为氧化三甲胺(TMAO)。随着目前对肠道微生物群及其代谢产物功能的探索,研究表明,TMAO可能是心血管疾病的一个潜在风险因素,独立于其他传统风险因素。然而,由于发现了一些相反的结果,TMAO的确切作用存在争议。在最近的研究中,有人假设TMA也可能参与心血管疾病的进展,并且已经发现了TMA的一些细胞毒性作用。因此,探索TMA、TMAO与心血管疾病之间的关系可能会为心血管疾病的诊断和治疗带来新的见解。在这篇综述中,我们讨论了影响人体中TMA/TMAO代谢过程的因素。我们还总结了TMA/TMAO在心血管疾病中的致病作用,以及一些有争议发现的局限性。

相似文献

[1]
Trimethylamine/Trimethylamine-N-Oxide as a Key Between Diet and Cardiovascular Diseases.

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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[10]
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本文引用的文献

[1]
Sacubitril/Valsartan Decreases Atrial Fibrillation Susceptibility by Inhibiting Angiotensin II-Induced Atrial Fibrosis Through p-Smad2/3, p-JNK, and p-p38 Signaling Pathways.

J Cardiovasc Transl Res. 2022-2

[2]
The Health Effects of Vitamin D and Probiotic Co-Supplementation: A Systematic Review of Randomized Controlled Trials.

Nutrients. 2020-12-30

[3]
Vascular reactivity stimulated by TMA and TMAO: Are perivascular adipose tissue and endothelium involved?

Pharmacol Res. 2021-1

[4]
Gut microbiota-associated metabolite trimethylamine N-Oxide and the risk of stroke: a systematic review and dose-response meta-analysis.

Nutr J. 2020-7-30

[5]
TMAO, a seafood-derived molecule, produces diuresis and reduces mortality in heart failure rats.

Elife. 2020-6-8

[6]
Metabolic endotoxemia and cardiovascular disease: A systematic review about potential roles of prebiotics and probiotics.

Clin Exp Pharmacol Physiol. 2020-6

[7]
Role of Claudin Proteins in Regulating Cancer Stem Cells and Chemoresistance-Potential Implication in Disease Prognosis and Therapy.

Int J Mol Sci. 2019-12-20

[8]
Gut Microbiota-Dependent Marker TMAO in Promoting Cardiovascular Disease: Inflammation Mechanism, Clinical Prognostic, and Potential as a Therapeutic Target.

Front Pharmacol. 2019-11-19

[9]
Trimethylamine N-Oxide Binds and Activates PERK to Promote Metabolic Dysfunction.

Cell Metab. 2019-9-19

[10]
TMA (trimethylamine), but not its oxide TMAO (trimethylamine-oxide), exerts haemodynamic effects: implications for interpretation of cardiovascular actions of gut microbiome.

Cardiovasc Res. 2019-12-1

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