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晚期氧化蛋白产物在动脉粥样硬化中的特征与作用

The Characteristics and Roles of Advanced Oxidation Protein Products in Atherosclerosis.

作者信息

Ou Hanxiao, Huang Zhuping, Mo Zhongcheng, Xiao Ji

机构信息

Department of Histology and Embryology, Laboratory of Reproductive Medicine, University of South China, Hengyang, 421001, China.

Department of Anesthesiology, Loudi Central Hospital, Loudi, 417000, China.

出版信息

Cardiovasc Toxicol. 2017 Jan;17(1):1-12. doi: 10.1007/s12012-016-9377-8.

Abstract

Advanced oxidation protein products (AOPPs) are novel biomarkers of oxidative damage to proteins and a novel class of inflammatory mediators. AOPPs can promote oxidative stress (OS) and inflammation and thus participate in many pathophysiological disease processes. Atherosclerosis is a chronic inflammatory disease of blood vessels that is characterized by low-density lipoprotein infiltration into the endothelial intima and the formation of atherosclerotic plaques. Inflammation and OS are established risk factors for the formation of atherosclerosis. Accumulated studies show that AOPPs can accelerate the progression of atherosclerosis through OS and inflammation. Additionally, AOPPs can accelerate the formation of atherosclerotic plaques by inhibiting high-density lipoprotein receptor scavenger receptor class B type I-mediated high-density lipoprotein cholesterol reverse transport, leading to metabolic disturbances. Some studies have suggested that plasma AOPPs levels are independently positively correlated with blood pressure and are also independent risk factors for cardiovascular disease. AOPPs can trigger oxidative bursts of neutrophils, monocytes and phagocytic cells, increase the generation of reactive oxygen species and promote the secretion of cytokines to accelerate endothelial cell injury. Detecting the levels and inhibiting the formation of AOPPs may provide a novel approach to monitor the progress and improve the prognosis of atherosclerosis.

摘要

晚期氧化蛋白产物(AOPPs)是蛋白质氧化损伤的新型生物标志物,也是一类新型炎症介质。AOPPs可促进氧化应激(OS)和炎症反应,从而参与多种病理生理疾病过程。动脉粥样硬化是一种血管慢性炎症性疾病,其特征是低密度脂蛋白浸润到内皮内膜并形成动脉粥样硬化斑块。炎症和OS是动脉粥样硬化形成的既定危险因素。累积研究表明,AOPPs可通过OS和炎症加速动脉粥样硬化的进展。此外,AOPPs可通过抑制高密度脂蛋白受体B族I型清道夫受体介导的高密度脂蛋白胆固醇逆向转运,加速动脉粥样硬化斑块的形成,导致代谢紊乱。一些研究表明,血浆AOPPs水平与血压独立正相关,也是心血管疾病的独立危险因素。AOPPs可触发中性粒细胞、单核细胞和吞噬细胞的氧化爆发,增加活性氧的生成,并促进细胞因子的分泌,从而加速内皮细胞损伤。检测AOPPs水平并抑制其形成可能为监测动脉粥样硬化的进展和改善预后提供一种新方法。

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