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血浆 TMAO 水平升高是否是心血管疾病中静水压力和渗透压力应激的代偿反应?

Is increased plasma TMAO a compensatory response to hydrostatic and osmotic stress in cardiovascular diseases?

机构信息

Department of Experimental Physiology and Pathophysiology, Laboratory of Centre for Preclinical Research, Medical University of Warsaw, Warsaw, Poland.

Department of Experimental Physiology and Pathophysiology, Laboratory of Centre for Preclinical Research, Medical University of Warsaw, Warsaw, Poland.

出版信息

Med Hypotheses. 2019 Sep;130:109271. doi: 10.1016/j.mehy.2019.109271. Epub 2019 Jun 11.

Abstract

Recent clinical studies show a positive correlation between elevated plasma TMAO and increased cardiovascular risk. However, the mechanism of the increase and biological effects of TMAO in the circulatory system are obscure. Plasma TMAO level depends mostly on the following three factors. First, the liver produces TMAO from TMA, a gut bacteria metabolite of dietary choline and carnitine. Second, plasma TMAO increases after ingestion of dietary TMAO from fish and seafood. Finally, plasma TMAO depends on TMAO and TMA excretion by the kidneys. Ample evidence highlights protective functions of TMAO, including the stabilization of proteins and cells exposed to hydrostatic and osmotic stresses, for example in fish exposed to hydrostatic stress (deep water) and osmotic stress (salty water). Osmotic stress and hydrostatic stresses are augmented in cardiovascular diseases such as hypertension. In hypertensive subjects a diastole-systole change in hydrostatic pressure in the heart may exceed 220 mmHg with a frequency of 60-220/min. This produces environment in which hydrostatic pressure changes over 100,000 times per 24 h. Furthermore, cardiovascular diseases are associated with disturbances in water-electrolyte balance which produce changes in plasma osmolarity. Perhaps, the increase in plasma TMAO in cardiovascular diseases is analogous to increased level of plasma natriuretic peptide B, which is both a cardiovascular risk marker and a compensatory response producing beneficial effects for pressure/volume overloaded heart. In this regard, there is some evidence that a moderate increase in plasma TMAO due to TMAO supplementation may be beneficial in animal model of hypertension-related heart failure. Finally, increased plasma TMAO is present in humans consuming seafood-rich diet which is thought to be health-beneficial. We hypothesize that increased plasma TMAO serves as a compensatory response mechanism which protects cells from hydrostatic and osmotic stresses.

摘要

最近的临床研究表明,血浆 TMAO 水平升高与心血管风险增加呈正相关。然而,TMAO 在循环系统中增加的机制和生物学效应尚不清楚。血浆 TMAO 水平主要取决于以下三个因素。首先,肝脏将 TMA 转化为 TMAO,TMA 是肠道细菌代谢膳食胆碱和肉碱的产物。其次,摄入富含鱼和海鲜的膳食 TMAO 后,血浆 TMAO 增加。最后,血浆 TMAO 取决于肾脏排泄的 TMAO 和 TMA。大量证据强调了 TMAO 的保护功能,包括暴露于静水和渗透压应激下的蛋白质和细胞的稳定,例如在暴露于静水(深水)和渗透压(咸水)应激下的鱼类中。静水和渗透压应激在高血压等心血管疾病中增加。在高血压患者中,心脏的静水压在舒张期-收缩期的变化可能超过 220mmHg,频率为 60-220/min。这会产生静水压力变化超过 100000 次/24 小时的环境。此外,心血管疾病与水-电解质平衡紊乱有关,这些紊乱会导致血浆渗透压变化。也许,心血管疾病中血浆 TMAO 的增加类似于血浆利钠肽 B 水平的升高,后者既是心血管风险标志物,也是产生对压力/容量超负荷心脏有益影响的代偿反应。在这方面,有一些证据表明,由于 TMAO 补充而导致的血浆 TMAO 适度增加可能对高血压相关心力衰竭的动物模型有益。最后,摄入富含海鲜的饮食会导致人类血浆 TMAO 增加,而这种饮食被认为是有益健康的。我们假设增加的血浆 TMAO 作为一种代偿反应机制,保护细胞免受静水和渗透压应激。

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