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对氧磷酶1(PON1)基因多态性对高密度脂蛋白(HDL)抗氧化能力的影响会随着年龄增长而减弱。

Effect of PON1 polymorphism on HDL antioxidant potential is blunted with aging.

作者信息

Cherki Mounia, Berrougui Hicham, Isabelle Maxim, Cloutier Martin, Koumbadinga Gérémy Abdull, Khalil Abdelouahed

机构信息

Research Centre on Aging, Sherbrooke Geriatric University Institute, 1036 Belvedere South, Sherbrooke, Quebec, Canada.

出版信息

Exp Gerontol. 2007 Aug;42(8):815-24. doi: 10.1016/j.exger.2007.04.006. Epub 2007 Apr 24.

Abstract

Paraoxonase1 is a HDL-associated enzyme, which is responsible for their antioxidant property. This study was aimed to investigate the effect of PON1 [Q192R] and [L55M] genotypes on susceptibility of LDL and HDL to lipid peroxidation and on antioxidant activity of HDL as a function of aging. Seventy-eight healthy subjects distributed in two age groups, young (20-30 years) and elderly (60-89 years) were recruited. PON1 activities and genotype polymorphisms were determined for each subject. LDL and HDL susceptibility to lipid peroxidation was evaluated by the measure of lag-phase (LP) for conjugated diene formation. HDL antioxidant property was evaluated by the measure of their capacity to protect LDL against lipid peroxidation. Our results show that LP for LDL and HDL peroxidation decreased with age of donors. Moreover, PON1 genotypes affect significantly the susceptibility of LDL and HDL to lipid peroxidation. Furthermore, basal- and salt-stimulated paraoxonase as well arylesterase activities were significantly reduced in elderly compared to young subjects. These results show a beneficial effect of PON1 towards susceptibility of HDL to oxidation as well to their antioxidant effect. However, this PON1 protective effect seems to be blunted with advancing age. Altogether our results suggest that the decrease in the PON1 protective effect with aging may contribute to the acceleration of the atherosclerosis process in elderly.

摘要

对氧磷酶1是一种与高密度脂蛋白(HDL)相关的酶,负责HDL的抗氧化特性。本研究旨在探讨对氧磷酶1 [Q192R]和[L55M]基因型对低密度脂蛋白(LDL)和HDL脂质过氧化易感性以及HDL抗氧化活性随年龄变化的影响。招募了78名健康受试者,分为两个年龄组,即年轻组(20 - 30岁)和老年组(60 - 89岁)。测定了每位受试者的对氧磷酶1活性和基因型多态性。通过测量共轭二烯形成的滞后期(LP)来评估LDL和HDL对脂质过氧化的易感性。通过测量HDL保护LDL免受脂质过氧化的能力来评估HDL的抗氧化特性。我们的结果表明,LDL和HDL过氧化的LP随供体年龄的增加而降低。此外,对氧磷酶1基因型显著影响LDL和HDL对脂质过氧化的易感性。此外,与年轻受试者相比,老年受试者的基础对氧磷酶和盐刺激的对氧磷酶以及芳基酯酶活性显著降低。这些结果表明对氧磷酶1对HDL氧化易感性及其抗氧化作用具有有益影响。然而,随着年龄的增长,这种对氧磷酶1的保护作用似乎减弱。总之,我们的结果表明,随着年龄增长对氧磷酶1保护作用的降低可能有助于加速老年人动脉粥样硬化进程。

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