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氧化应激在糖尿病性血管内皮功能障碍中的作用。

The role of oxidative stress in diabetes mellitus-induced vascular endothelial dysfunction.

机构信息

Department of Endocrinology and Metabolism, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, 646000, China.

Metabolic Vascular Disease Key Laboratory of Sichuan Province, Luzhou, Sichuan, 646000, China.

出版信息

Cardiovasc Diabetol. 2023 Sep 2;22(1):237. doi: 10.1186/s12933-023-01965-7.


DOI:10.1186/s12933-023-01965-7
PMID:37660030
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10475205/
Abstract

Diabetes mellitus is a metabolic disease characterized by long-term hyperglycaemia, which leads to microangiopathy and macroangiopathy and ultimately increases the mortality of diabetic patients. Endothelial dysfunction, which has been recognized as a key factor in the pathogenesis of diabetic microangiopathy and macroangiopathy, is characterized by a reduction in NO bioavailability. Oxidative stress, which is the main pathogenic factor in diabetes, is one of the major triggers of endothelial dysfunction through the reduction in NO. In this review, we summarize the four sources of ROS in the diabetic vasculature and the underlying molecular mechanisms by which the pathogenic factors hyperglycaemia, hyperlipidaemia, adipokines and insulin resistance induce oxidative stress in endothelial cells in the context of diabetes. In addition, we discuss oxidative stress-targeted interventions, including hypoglycaemic drugs, antioxidants and lifestyle interventions, and their effects on diabetes-induced endothelial dysfunction. In summary, our review provides comprehensive insight into the roles of oxidative stress in diabetes-induced endothelial dysfunction.

摘要

糖尿病是一种代谢性疾病,其特征是长期高血糖,导致微血管和大血管病变,并最终增加糖尿病患者的死亡率。内皮功能障碍已被认为是糖尿病微血管和大血管病变发病机制中的关键因素,其特征是一氧化氮生物利用度降低。氧化应激是糖尿病的主要致病因素之一,通过减少一氧化氮,它是内皮功能障碍的主要触发因素之一。在这篇综述中,我们总结了糖尿病血管中四种来源的活性氧簇和潜在的分子机制,高血糖、高脂血症、脂肪因子和胰岛素抵抗等致病因素如何在糖尿病环境下诱导内皮细胞发生氧化应激。此外,我们还讨论了针对氧化应激的干预措施,包括降糖药物、抗氧化剂和生活方式干预,以及它们对糖尿病引起的内皮功能障碍的影响。总之,我们的综述提供了对氧化应激在糖尿病引起的内皮功能障碍中的作用的全面了解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2322/10475205/939235534955/12933_2023_1965_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2322/10475205/e1033b2210ff/12933_2023_1965_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2322/10475205/0811a7a66ed8/12933_2023_1965_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2322/10475205/7610af3980ce/12933_2023_1965_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2322/10475205/939235534955/12933_2023_1965_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2322/10475205/e1033b2210ff/12933_2023_1965_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2322/10475205/0811a7a66ed8/12933_2023_1965_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2322/10475205/7610af3980ce/12933_2023_1965_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2322/10475205/939235534955/12933_2023_1965_Fig4_HTML.jpg

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本文引用的文献

[1]
Dapagliflozin prevents oxidative stress-induced endothelial dysfunction via sirtuin 1 activation.

Biomed Pharmacother. 2023-9

[2]
Synergistic effect of elevated glucose levels with SARS-CoV-2 spike protein induced NOX-dependent ROS production in endothelial cells.

Mol Biol Rep. 2023-7

[3]
Rosiglitazone reduces diabetes angiopathy by inhibiting mitochondrial dysfunction dependent on regulating HSP22 expression.

iScience. 2023-2-13

[4]
Molecular Mechanism of Fucoidan Nanoparticles as Protector on Endothelial Cell Dysfunction in Diabetic Rats' Aortas.

Nutrients. 2023-1-21

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25-hydroxyvitamin D3 inhibits oxidative stress and ferroptosis in retinal microvascular endothelial cells induced by high glucose through down-regulation of miR-93.

BMC Ophthalmol. 2023-1-13

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The vicious circle of UHRF1 down-regulation and KEAP1/NRF2/HO-1 pathway impairment promotes oxidative stress-induced endothelial cell apoptosis in diabetes.

Diabet Med. 2023-4

[7]
The Effect of Allograft Inflammatory Factor-1 on Inflammation, Oxidative Stress, and Autophagy via miR-34a/ATG4B Pathway in Diabetic Kidney Disease.

Oxid Med Cell Longev. 2022

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miR-351 promotes atherosclerosis in diabetes by inhibiting the ITGB3/PIK3R1/Akt pathway and induces endothelial cell injury and lipid accumulation.

Mol Med. 2022-9-30

[9]
Endothelial reactive oxygen-forming NADPH oxidase 5 is a possible player in diabetic aortic aneurysm but not atherosclerosis.

Sci Rep. 2022-7-7

[10]
Positive regulation of endothelial Tom70 by metformin as a new mechanism against cardiac microvascular injury in diabetes.

Mitochondrion. 2022-7

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