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三甲基胺 N-氧化物——动脉粥样硬化性血管疾病的标志物。

Trimethylamine N-oxide-a marker for atherosclerotic vascular disease.

机构信息

Institute of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine, 301617 Tianjin, China.

Graduate School, Tianjin University of Traditional Chinese Medicine, 301617 Tianjin, China.

出版信息

Rev Cardiovasc Med. 2021 Sep 24;22(3):787-797. doi: 10.31083/j.rcm2203085.

Abstract

As a potential causative factor in various cardiovascular diseases, the gut microbe-generated metabolite trimethylamine N-oxide (TMAO) has courted considerable research interest as a potential biomarker. TMAO is a small molecule considered to be beneficial for the health of deep-water animals due to its ability to protect proteins against hydrostatic pressure stress. However, it may cause deleterious effects in humans as mounting evidence suggests that TMAO may enhance atherosclerosis, independent of traditional risk factors. This may be mediated by its capacity to enhance inflammation, platelet activation and thrombosis, and inhibit reverse cholesterol transport. In humans, circulating levels of TMAO have been found to be associated with increased risk of developing atherosclerotic diseases such as carotid atherosclerosis, coronary atherosclerotic heart disease, stroke, and peripheral arteriosclerosis. This review aims to discuss the current role of TMAO in the atherosclerosis process, using animal models and clinical studies, with special attention to determining whether TMAO could be used as a marker for monitoring severity and prognosis in atherosclerosis and to evaluate evidence for its role as a mediator in the pathogenesis of atherosclerotic vascular disease.

摘要

作为各种心血管疾病的潜在致病因素,肠道微生物产生的代谢物三甲胺 N-氧化物(TMAO)作为一种潜在的生物标志物引起了相当大的研究兴趣。TMAO 是一种小分子,由于其能够保护蛋白质免受静压应激的影响,被认为对深海动物的健康有益。然而,越来越多的证据表明,TMAO 可能会增强动脉粥样硬化,而与传统的危险因素无关,因此它可能会对人体造成有害影响。这可能是由于它能够增强炎症、血小板激活和血栓形成,并抑制胆固醇逆转运。在人类中,循环 TMAO 水平与发展为动脉粥样硬化疾病的风险增加有关,如颈动脉粥样硬化、冠状动脉粥样硬化性心脏病、中风和外周动脉硬化。本综述旨在讨论 TMAO 在动脉粥样硬化过程中的作用,使用动物模型和临床研究,并特别关注确定 TMAO 是否可用于作为监测动脉粥样硬化严重程度和预后的标志物,并评估其作为动脉粥样硬化性血管疾病发病机制中介物的证据。

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