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自由基的体外电子顺磁共振表征:与运动诱导的脂质过氧化的相关性及抗坏血酸预防的意义

In vitro electron paramagnetic resonance characterization of free radicals: relevance to exercise-induced lipid peroxidation and implications of ascorbate prophylaxis.

作者信息

Davison Gareth W, Ashton Tony, Davies Bruce, Bailey Damian M

机构信息

Sport and Exercise Sciences Research Institute, University of Ulster Jordanstown, Newtownabbey, UK.

出版信息

Free Radic Res. 2008 Apr;42(4):379-86. doi: 10.1080/10715760801976618.

DOI:10.1080/10715760801976618
PMID:18404537
Abstract

This study tested the hypothesis that exercise-induced oxidative stress is caused by free radical-mediated damage to polyunsaturated fatty acids (PUFA) which can be prevented following ascorbate prophylaxis. Hyperfine coupling constants (HCC) of alpha-phenyl-tert-butylnitrone (PBN)-adducts were measured via room temperature electron paramagnetic resonance (EPR) spectroscopy in the venous blood of 12 subjects at rest and following maximal exercise during a randomized double-blind placebo-controlled trial and compared to those observed following room-air incubation (2 h at 37 degrees C) of L-alpha-phosphatidycholine, linoleic acid, alpha-linolenic acid and arachidonic acid. All adducts exhibited similar HCC [a(N) 13.6 Gauss (G) and a beta(H) 1.8 G] with the exception of L-alpha-phosphatidycholine [a(N1)=13.4 G, a beta(H1)=1.6 G (37%) and a(N2)=14.9 G, a beta(H2)=0.3 G (63%)] consistent with the trapping of lipid-derived alkoxyl and oleate radicals, respectively. Ascorbate pre-treatment ablated radical formation in both systems. These findings identify circulating PUFA as a potential source of secondary radicals that are capable of initiating oxidative stress in the exercising human.

摘要

本研究检验了以下假设

运动诱导的氧化应激是由自由基介导的对多不饱和脂肪酸(PUFA)的损伤所致,而抗坏血酸预防可防止这种损伤。在一项随机双盲安慰剂对照试验中,通过室温电子顺磁共振(EPR)光谱法测量了12名受试者在静息状态下以及最大运动后的静脉血中α-苯基叔丁基硝酮(PBN)加合物的超精细偶合常数(HCC),并与在37℃下空气中孵育2小时后的L-α-磷脂酰胆碱、亚油酸、α-亚麻酸和花生四烯酸所观察到的HCC进行比较。除L-α-磷脂酰胆碱外,所有加合物均表现出相似的HCC [a(N) 13.6高斯(G)和aβ(H) 1.8 G] [L-α-磷脂酰胆碱:a(N1)=13.4 G,aβ(H1)=1.6 G(37%)和a(N2)=14.9 G,aβ(H2)=0.3 G(63%)],分别与脂质衍生的烷氧基和油酸自由基的捕获一致。抗坏血酸预处理消除了两个系统中的自由基形成。这些发现确定循环中的PUFA是继发性自由基的潜在来源,这些自由基能够在运动的人体中引发氧化应激。

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