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首页> 外文期刊>Danish Medical Bulletin. Bibliographical Supplement >Magnesium in arterial thrombosis, ischaemia-reperfusion injury, and atherosclerosis - evidence from experimental studies
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Magnesium in arterial thrombosis, ischaemia-reperfusion injury, and atherosclerosis - evidence from experimental studies

机译:镁在动脉血栓形成,缺血再灌注损伤和动脉粥样硬化中的作用-实验研究的证据

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Magnesium is a trace mineral with an atomic number of 12 and a mass of 24.32 Dalton. It is the fourth most abundant cation in the body and the second most abundant cation in intracellular fluid. Magnesium is an important cofactor for more than 300 enzymatic reactions involving energy metabolism and protein synthesis (Elin, 1994). It is also involved in several processes including: gating of calcium channels, transmembrane ion flux and regulation of adeny-late cyclase, muscle contraction, control of vasomotor tone, and cardiac excitability (Fawcett et al, 1999). In many of the cardiovascular effects magnesium reflect an antagonism of calcium-initiated processes, which has led to the characterisation of magnesium as "nature's physiological calcium blocker" (Iseri and French, 1984). In humans magnesium is distributed principally between bone (53%) and intracellular compartments of muscle (27%) and soft tissues (19%); and less than 1% is found in serum and red blood cells (Elin, 1994). Only approximately 0.3% of total body magnesium is found in serum, where it is present in three states: 1) free ionised magnesium (62%; the physiologically active form), 2) protein bound (33%; mainly albumin), and 3) complexed to anions (5%; such as citrate and phosphate). Sources rich in magnesium include, grain, cereals, and vegetables and the absorption occurs principally in the ileum and colon. The amount absorbed is inversely correlated to the intake. Excretion and serum magnesium control occur via the kidney (Fawcett et al, 1999). Assessment of magnesium status is a complex area as the ion is predominantly located intracellularly. Description of the laboratory tests available for total body magnesium measurement is beyond the scope of this review (see ref. Elin, 1994). The intention of the present work is to summarise the pharmacological effects of magnesium on the cardiovascular system, particularly the potential antithrom-botic and the myocardial protective effect. In this respect magnesium should be seen as a therapeutic substance, where treatment is given irrespective of the actual magnesium status in the individual.
机译:镁是微量元素,原子序数为12,质量为24.32道尔顿。它是人体内第四大最丰富的阳离子,也是细胞内液中第二大最丰富的阳离子。镁是涉及能量代谢和蛋白质合成的300多种酶促反应的重要辅助因子(Elin,1994)。它也参与几个过程,包括:钙通道的门控,跨膜离子通量和腺苷酸环化酶的调节,肌肉收缩,血管舒张压的控制和心脏兴奋性(Fawcett等,1999)。在许多心血管疾病中,镁反映了钙引发过程的拮抗作用,这已导致镁表征为“自然的生理钙阻滞剂”(Iseri和French,1984)。在人体中,镁主要分布在骨骼(53%)与肌肉的细胞内区室(27%)和软组织(19%)之间;在血清和红细胞中发现的比例不到1%(Elin,1994)。在血清中仅发现约0.3%的体内镁,并以三种状态存在:1)游离离子化的镁(62%;生理活性形式),2)结合蛋白(33%;主要是白蛋白)和3 )与阴离子(5%;例如柠檬酸根和磷酸根)络合。富含镁的来源包括谷物,谷类和蔬菜,吸收主要发生在回肠和结肠。吸收的量与摄入量成反比。排泄和血清镁的控制通过肾脏发生(Fawcett等,1999)。镁状态的评估是一个复杂的领域,因为离子主要位于细胞内。可用于全身镁测量的实验室测试的描述超出了本文的范围(参见参考文献Elin,1994)。本工作的目的是总结镁对心血管系统的药理作用,特别是潜在的抗血栓形成和心肌保护作用。在这方面,应将镁视为治疗性物质,无论个人的实际镁状况如何,都应给予治疗。

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