Keaney J F, Xu A, Cunningham D, Jackson T, Frei B, Vita J A
Evans Memorial Department of Medicine, Boston University Medical Center, Massachusetts 02118, USA.
J Clin Invest. 1995 Jun;95(6):2520-9. doi: 10.1172/JCI117953.
Excess vascular oxidative stress and the local formation of oxidized LDL (ox-LDL) have been implicated in the development of impaired endothelium-dependent arterial relaxation in hypercholesterolemia and atherosclerosis. Dietary antioxidants limit LDL oxidation in vitro and treatment of cholesterol-fed rabbits with dietary antioxidants preserves endothelium-derived relaxing factor (EDRF) action. To investigate the mechanism(s) responsible for these observations, we examined EDRF action, vascular oxidative stress, and antioxidant protection in male New Zealand White rabbits using four dietary treatments. Animals consumed standard chow (chow group) or chow supplemented with: (a) 0.5% cholesterol (0.5% cholesterol group); (b) 1% cholesterol (1% cholesterol group); or (c) 1% cholesterol and 1% probucol (probucol group). After 28 d of dietary treatment, segments of thoracic aorta from the 0.5 and 1% cholesterol groups demonstrated impairment of acetylcholine-mediated endothelium-dependent arterial relaxation compared to chow-fed animals (57 +/- 11% and 45 +/- 9% vs 78 +/- 3%, respectively; P < 0.05). In contrast, vessels from the probucol group demonstrated normal relaxation to acetylcholine (83 +/- 5%). Plasma cholesterol levels and the extent of atherosclerosis were similar among all cholesterol-fed groups. Probucol treatment was associated a threefold increase in LDL resistance to copper-induced oxidative modification (P < 0.05) and a reduction in tissue lipid peroxidation (as assessed by thiobarbituric acid-reactive substances; P < 0.05) compared to animals fed cholesterol alone. Most importantly, both of these changes were strongly correlated with preserved EDRF action. Moreover, cholesterol feeding was associated with a dose-dependent increase in vascular superoxide generation and lysophosphatidylcholine content, both of which were prevented by probucol treatment. From these findings, we conclude that probucol, a lipid-soluble antioxidant, preserves EDRF action in cholesterol-fed rabbits in association with limiting vascular oxidative stress and superoxide generation.
血管氧化应激过度以及氧化型低密度脂蛋白(ox-LDL)的局部形成与高胆固醇血症和动脉粥样硬化中内皮依赖性动脉舒张功能受损的发展有关。膳食抗氧化剂在体外可限制低密度脂蛋白氧化,用膳食抗氧化剂治疗喂食胆固醇的兔子可保留内皮衍生舒张因子(EDRF)的作用。为了研究导致这些观察结果的机制,我们使用四种饮食处理方法,对雄性新西兰白兔的EDRF作用、血管氧化应激和抗氧化保护进行了研究。动物食用标准饲料(饲料组)或添加了以下成分的饲料:(a)0.5%胆固醇(0.5%胆固醇组);(b)1%胆固醇(1%胆固醇组);或(c)1%胆固醇和1%普罗布考(普罗布考组)。经过28天的饮食处理后,与喂食标准饲料的动物相比,0.5%和1%胆固醇组的胸主动脉段显示乙酰胆碱介导的内皮依赖性动脉舒张功能受损(分别为57±11%和45±9%,而喂食标准饲料的动物为78±3%;P<0.05)。相比之下,普罗布考组的血管对乙酰胆碱表现出正常的舒张反应(83±5%)。所有喂食胆固醇的组中血浆胆固醇水平和动脉粥样硬化程度相似。与单独喂食胆固醇的动物相比,普罗布考处理使低密度脂蛋白对铜诱导的氧化修饰的抵抗力增加了三倍(P<0.05),并降低了组织脂质过氧化(通过硫代巴比妥酸反应性物质评估;P<0.05)。最重要的是,这两种变化都与EDRF作用的保留密切相关。此外,喂食胆固醇与血管超氧化物生成和溶血磷脂酰胆碱含量的剂量依赖性增加有关,而普罗布考处理可预防这两种情况。从这些发现中,我们得出结论,脂溶性抗氧化剂普罗布考通过限制血管氧化应激和超氧化物生成,在喂食胆固醇的兔子中保留了EDRF的作用。