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慢性α-硫辛酸治疗可改善高脂饮食喂养小鼠主动脉内皮依赖性血管舒张功能。

Chronic Treatment with α-Lipoic Acid Improves Endothelium-Dependent Vasorelaxation of Aortas in High-Fat Diet-Fed Mice.

机构信息

Department of Pharmacology, Kawasaki Medical School.

Laboratory of Physiology, Faculty of Pharmaceutical Sciences, Josai University.

出版信息

Biol Pharm Bull. 2019;42(9):1456-1463. doi: 10.1248/bpb.b18-00800.

DOI:10.1248/bpb.b18-00800
PMID:31474707
Abstract

α-Lipoic acid (ALA) is used as a dietary supplement and known as an anti-oxidant. The present study aimed to examine whether ALA improves endothelial dysfunction in high-fat diet-fed obese mice. After feeding a high-fat diet to Institute of Cancer Research (ICR) mice for 4 weeks, the mice were maintained with a high-fat diet (group HF) or a high-fat diet containing ALA (25 mg/d, group HF + ALA) for an additional 20 weeks. Age-matched normal diet-fed mice were also used (group Normal). Chronic oral treatment with ALA did not affect various plasma parameters or body weights. As compared with the aortas of Normal mice, those from HF mice showed impaired endothelium-dependent relaxation in response to clonidine. However, such an impairment was not observed in the aortas from HF + ALA mice. The plasma levels of thiobarbituric acid reactive substances, an indicator of oxidative stress, were significantly decreased in HF + ALA mice compared with HF mice, confirming the anti-oxidative effects of ALA. In addition, when the impaired clonidine-induced vasorelaxation of aortas from normal mice under high glucose conditions was used as a model of acute oxidative stress, the vasorelaxation responses were improved in the presence of ALA at 100 µM. Our results suggested that the chronic oral administration of ALA improves endothelial dysfunction in high-fat diet-fed obese mice possibly through the reduction in oxidative stress in vivo.

摘要

α-硫辛酸(ALA)被用作膳食补充剂,是一种抗氧化剂。本研究旨在探讨 ALA 是否能改善高脂肪饮食喂养肥胖小鼠的内皮功能障碍。将 ICR 小鼠用高脂肪饮食喂养 4 周后,将其继续用高脂肪饮食(HF 组)或含 ALA(25mg/d)的高脂肪饮食喂养 20 周(HF+ALA 组)。同时还使用了年龄匹配的正常饮食喂养的小鼠(正常组)。慢性口服 ALA 治疗不影响各种血浆参数或体重。与正常组小鼠的主动脉相比,HF 组小鼠对可乐定的内皮依赖性松弛反应受损。然而,HF+ALA 组小鼠的主动脉中并未观察到这种损伤。与 HF 组相比,HF+ALA 组小鼠的血浆硫代巴比妥酸反应物质(氧化应激的一个指标)水平显著降低,证实了 ALA 的抗氧化作用。此外,当正常小鼠在高葡萄糖条件下的受损可乐定诱导血管松弛反应被用作急性氧化应激模型时,在 100µM 的 ALA 存在下,血管松弛反应得到改善。我们的结果表明,慢性口服 ALA 可改善高脂肪饮食喂养肥胖小鼠的内皮功能障碍,可能是通过减少体内氧化应激。

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