镁与心血管生物学:心血管危险因素和动脉粥样硬化之间的重要联系。

B M Altura, B T Altura
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引用次数: 0

摘要

在这篇综述中,提出了高胆固醇血症、高血压、糖尿病、终末期肾病、肾透析和长期应激如何导致动脉粥样硬化、缺血性心脏病和中风的基本原理。这些数据表明,由不良饮食和/或镁代谢错误引起的镁缺乏可能是多种心血管危险因素与动脉粥样硬化之间缺失的一环。来自我们实验室和其他实验室的数据表明,细胞外和细胞内游离Mg离子(Mg2+)的减少可以诱导一系列已知在动脉粥样硬化中重要的病理生理现象,即血管痉挛,血管反应性增加,[Ca2+]i升高,促炎剂的形成,氧自由基,血小板聚集,心脏生物能量的减少,心力衰竭,脂蛋白氧化,与性别相关的内皮源性放松因子/NO的调节,膜脂肪酸饱和度的变化,膜磷脂原和n -磷脂的变化(提示细胞内磷脂信号的变化),以及可能的转录因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Magnesium and cardiovascular biology: an important link between cardiovascular risk factors and atherogenesis.

In this review, a rationale is presented for how hypercholesterolemia, hypertension, diabetes mellitus, end-stage renal disease, renal dialysis, and prolonged stress can all lead to atherosclerosis, ischemic heart disease, and stroke. The data indicate that Mg deficiency caused either by poor diet and/or errors in Mg metabolism may be a missing link between diverse cardiovascular risk factors and atherosclerosis. Data from our laboratories and others indicate that reduction in extracellular and intracellular free Mg ions (Mg2+) can induce an entire array of pathophysiological phenomena known to be important in atherogenesis, that is, vasospasm, increased vascular reactivity, elevation in [Ca2+]i, formation of proinflammatory agents, oxygen radicals, platelet aggegation, reduction in cardiac bioenergetics, cardiac failure, oxidation of lipoproteins, gender-related modulation of endothelial-derived relaxing factor/NO, changes in membrane fatty acid saturation, changes in membrane plasmalogens and N-phospholipids (suggesting changes in intracellular phospholipid signals), and probably transcription factors.

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