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慢性补充线粒体抗氧化剂(MitoQ)可改善健康老年人的血管功能。

Chronic Supplementation With a Mitochondrial Antioxidant (MitoQ) Improves Vascular Function in Healthy Older Adults.

机构信息

From the Department of Integrative Physiology, University of Colorado Boulder (M.J.R., J.R.S.-P., C.A.C.S., N.Z.B., L.M.C., H.L.R., K.A.W., R.A.G.-R., D.R.S.)

From the Department of Integrative Physiology, University of Colorado Boulder (M.J.R., J.R.S.-P., C.A.C.S., N.Z.B., L.M.C., H.L.R., K.A.W., R.A.G.-R., D.R.S.).

出版信息

Hypertension. 2018 Jun;71(6):1056-1063. doi: 10.1161/HYPERTENSIONAHA.117.10787. Epub 2018 Apr 16.

Abstract

UNLABELLED

Excess reactive oxygen species production by mitochondria is a key mechanism of age-related vascular dysfunction. Our laboratory has shown that supplementation with the mitochondrial-targeted antioxidant MitoQ improves vascular endothelial function by reducing mitochondrial reactive oxygen species and ameliorates arterial stiffening in old mice, but the effects in humans are unknown. Here, we sought to translate our preclinical findings to humans and determine the safety and efficacy of MitoQ. Twenty healthy older adults (60-79 years) with impaired endothelial function (brachial artery flow-mediated dilation <6%) underwent 6 weeks of oral supplementation with MitoQ (20 mg/d) or placebo in a randomized, placebo-controlled, double-blind, crossover design study. MitoQ was well tolerated, and plasma MitoQ was higher after the treatment versus placebo period (<0.05). Brachial artery flow-mediated dilation was 42% higher after MitoQ versus placebo (<0.05); the improvement was associated with amelioration of mitochondrial reactive oxygen species-related suppression of endothelial function (assessed as the increase in flow-mediated dilation with acute, supratherapeutic MitoQ [160 mg] administration; n=9; <0.05). Aortic stiffness (carotid-femoral pulse wave velocity) was lower after MitoQ versus placebo (<0.05) in participants with elevated baseline levels (carotid-femoral pulse wave velocity >7.60 m/s; n=11). Plasma oxidized LDL (low-density lipoprotein), a marker of oxidative stress, also was lower after MitoQ versus placebo (<0.05). Participant characteristics, endothelium-independent dilation (sublingual nitroglycerin), and circulating markers of inflammation were not different (all >0.1). These findings in humans extend earlier preclinical observations and suggest that MitoQ and other therapeutic strategies targeting mitochondrial reactive oxygen species may hold promise for treating age-related vascular dysfunction.

CLINICAL TRIAL REGISTRATION

URL: http://www.clinicaltrials.gov. Unique identifier: NCT02597023.

摘要

目的

线粒体产生的过量活性氧是与年龄相关的血管功能障碍的关键机制。我们的实验室已经表明,补充线粒体靶向抗氧化剂 MitoQ 通过减少线粒体活性氧来改善血管内皮功能,并改善老年小鼠的动脉僵硬,但在人类中的效果尚不清楚。在这里,我们试图将我们的临床前发现转化为人类,并确定 MitoQ 的安全性和有效性。

方法

20 名内皮功能受损(肱动脉血流介导的扩张 <6%)的健康老年人(60-79 岁)接受了为期 6 周的口服 MitoQ(20mg/d)或安慰剂治疗,采用随机、安慰剂对照、双盲、交叉设计研究。

结果

MitoQ 耐受性良好,治疗后血浆 MitoQ 高于安慰剂期(<0.05)。与安慰剂相比,MitoQ 后肱动脉血流介导的扩张增加了 42%(<0.05);这种改善与改善与线粒体活性氧相关的内皮功能抑制有关(评估为急性、超治疗剂量 MitoQ [160mg]给药时血流介导的扩张增加;n=9;<0.05)。与基线水平较高(颈动脉-股动脉脉搏波速度>7.60m/s;n=11)的参与者相比,MitoQ 后主动脉僵硬(颈动脉-股动脉脉搏波速度)较低。与安慰剂相比,MitoQ 后血浆氧化型 LDL(低密度脂蛋白),一种氧化应激标志物,也较低(<0.05)。参与者特征、内皮非依赖性扩张(舌下硝酸甘油)和循环炎症标志物无差异(均>0.1)。这些在人类中的发现扩展了早期的临床前观察结果,并表明 MitoQ 和其他靶向线粒体活性氧的治疗策略可能有希望治疗与年龄相关的血管功能障碍。

临床试验注册

网址:http://www.clinicaltrials.gov。唯一标识符:NCT02597023。

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