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硫辛酸可改善慢性间歇性低氧暴露小鼠的内皮功能和氧化应激。

Alpha Lipoic Acid Improves Endothelial Function and Oxidative Stress in Mice Exposed to Chronic Intermittent Hypoxia.

机构信息

Department of Anesthesiology, Pharmacology and Therapeutics, The University of British Columbia, Vancouver, Canada.

Divisions of Critical Care and Respiratory Medicine, Department of Medicine, The University of British Columbia, Vancouver, BC, Canada.

出版信息

Oxid Med Cell Longev. 2019 Apr 9;2019:4093018. doi: 10.1155/2019/4093018. eCollection 2019.


DOI:10.1155/2019/4093018
PMID:31093313
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6481039/
Abstract

OBJECTIVE: Obstructive sleep apnea (OSA) is characterized by recurrent airway collapse that causes chronic intermittent hypoxia (CIH). OSA is associated with systemic inflammation and oxidative stress resulting in endothelial dysfunction and cardiovascular disease (CVD). Alpha lipoic acid (ALA) is a potent antioxidant with anti-inflammatory properties. We hypothesized that dietary ALA can improve endothelial function of mice exposed to CIH. METHODS: Mice were exposed to either CIH or intermittent air (IA) and treated with dietary ALA (0.2% /) or a regular chow diet for 8 weeks. Endothelial function, endothelial nitric oxide (eNOS) uncoupling, systemic oxidative stress, systemic inflammation, aortic expression of inflammatory cytokines, and antioxidant enzymes were measured after 8 weeks. RESULTS: Mice exposed to CIH exhibited endothelial dysfunction accompanied by systemic oxidative stress and inflammation as well as increased aortic expression of inflammatory cytokines. Furthermore, CIH led to eNOS uncoupling. Treatment with dietary ALA reversed endothelial dysfunction in mice exposed to CIH, lowered systemic oxidative stress and inflammation, prevented the increases of inflammatory cytokine gene expression, increased the expression of antioxidant enzymes, and preserved eNOS in a coupled state. CONCLUSION: ALA attenuates endothelial dysfunction by preventing oxidative stress and inflammation and restoring nitric oxide bioavailability in mice exposed to CIH. Our data suggests the potential beneficial use of ALA as adjunctive therapy in OSA.

摘要

目的:阻塞性睡眠呼吸暂停(OSA)的特征是反复发生气道塌陷,导致慢性间歇性低氧(CIH)。OSA 与全身炎症和氧化应激有关,导致内皮功能障碍和心血管疾病(CVD)。α-硫辛酸(ALA)是一种具有抗炎特性的强效抗氧化剂。我们假设饮食中的 ALA 可以改善暴露于 CIH 的小鼠的内皮功能。

方法:将小鼠暴露于 CIH 或间歇性空气(IA)中,并接受饮食 ALA(0.2% /)或常规饮食治疗 8 周。8 周后测量内皮功能、内皮型一氧化氮合酶(eNOS)解偶联、全身氧化应激、全身炎症、主动脉炎症细胞因子表达和抗氧化酶。

结果:暴露于 CIH 的小鼠表现出内皮功能障碍,伴有全身氧化应激和炎症,以及主动脉炎症细胞因子表达增加。此外,CIH 导致 eNOS 解偶联。饮食中添加 ALA 可逆转暴露于 CIH 的小鼠的内皮功能障碍,降低全身氧化应激和炎症,防止炎症细胞因子基因表达增加,增加抗氧化酶的表达,并使 eNOS 保持偶联状态。

结论:ALA 通过预防氧化应激和炎症,恢复 CIH 暴露小鼠中一氧化氮的生物利用度,减轻内皮功能障碍。我们的数据表明,ALA 作为 OSA 的辅助治疗具有潜在的有益作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0356/6481039/6a8e0a2b89bd/OMCL2019-4093018.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0356/6481039/0b378a32c4c6/OMCL2019-4093018.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0356/6481039/004fad91ebb9/OMCL2019-4093018.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0356/6481039/edf297aad0da/OMCL2019-4093018.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0356/6481039/39b7086ea06c/OMCL2019-4093018.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0356/6481039/59ae3b4caeac/OMCL2019-4093018.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0356/6481039/922581e094d0/OMCL2019-4093018.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0356/6481039/6a8e0a2b89bd/OMCL2019-4093018.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0356/6481039/0b378a32c4c6/OMCL2019-4093018.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0356/6481039/004fad91ebb9/OMCL2019-4093018.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0356/6481039/edf297aad0da/OMCL2019-4093018.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0356/6481039/39b7086ea06c/OMCL2019-4093018.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0356/6481039/59ae3b4caeac/OMCL2019-4093018.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0356/6481039/922581e094d0/OMCL2019-4093018.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0356/6481039/6a8e0a2b89bd/OMCL2019-4093018.007.jpg

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[1]
Uncoupling of Vascular Nitric Oxide Synthase Caused by Intermittent Hypoxia.

Oxid Med Cell Longev. 2016

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Sleep Med Rev. 2014-7-24

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Diabetol Metab Syndr. 2014-7-28

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