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在胱氨酸和半胱氨酸存在的情况下,同型半胱氨酸会强烈增强金属催化的低密度脂蛋白氧化。

Homocysteine strongly enhances metal-catalyzed LDL oxidation in the presence of cystine and cysteine.

作者信息

Pfanzagl Beatrix, Tribl Florian, Koller Elisabeth, Möslinger Thomas

机构信息

Institute of Physiology, University of Wien, Schwarzspanierstrasse 17, Austria.

出版信息

Atherosclerosis. 2003 May;168(1):39-48. doi: 10.1016/s0021-9150(03)00057-1.

Abstract

Here we show that homocysteine stimulates low density lipoprotein (LDL) oxidation at copper(II) concentrations causing only a slight oxidation of LDL lipids. LDL oxidation by homocysteine and copper(II) is further enhanced in the presence of cystine, although cystine alone does not stimulate LDL oxidation with copper(II). Similarly, a combination of cysteine with homocysteine provoked a more than additive increase of oxidation. Simultaneous presence of cysteine and homocystine also resulted in a more than additive oxidative effect which was not statistically significant, however. Stimulation of LDL oxidation in the presence of homocysteine by cystine was also observed with iron(III) at acidic pH and when LDL oxidation was initiated by azo-compound generated peroxyl radicals. At pH 7.4 histidine is able to prevent LDL oxidation by copper(II) in a thiol mixture similar to the one found in human plasma if present in tenfold excess over homocysteine, but loses its inhibitory effect at higher homocysteine concentrations. The synergistic effect on metal-catalyzed LDL oxidation observed with mixtures of homocysteine and cystine or cysteine sustains the hypothesis that the epidemiological association between raised homocysteine levels and risk of cardiovascular disease is caused by an increase in oxidative stress.

摘要

在此我们表明,同型半胱氨酸在仅引起低密度脂蛋白(LDL)脂质轻微氧化的铜(II)浓度下刺激LDL氧化。在胱氨酸存在的情况下,同型半胱氨酸和铜(II)对LDL的氧化作用进一步增强,尽管单独的胱氨酸不会刺激LDL与铜(II)发生氧化反应。同样,半胱氨酸与同型半胱氨酸的组合引发了超过相加效应的氧化增加。半胱氨酸和同型胱氨酸同时存在也导致了超过相加的氧化作用,不过在统计学上并不显著。在酸性pH条件下,当LDL氧化由偶氮化合物产生的过氧自由基引发时,用铁(III)也观察到胱氨酸在同型半胱氨酸存在的情况下对LDL氧化的刺激作用。在pH 7.4时,如果组氨酸的存在量比同型半胱氨酸过量十倍,它能够在类似于人血浆中发现的硫醇混合物中防止铜(II)介导的LDL氧化,但在同型半胱氨酸浓度较高时会失去其抑制作用。同型半胱氨酸与胱氨酸或半胱氨酸混合物对金属催化的LDL氧化的协同作用支持了这样一种假说,即同型半胱氨酸水平升高与心血管疾病风险之间的流行病学关联是由氧化应激增加引起的。

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