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首页> 外文期刊>Cardiovascular Drugs and Therapy >LOX-1: A Critical Player in the Genesis and Progression of Myocardial Ischemia
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LOX-1: A Critical Player in the Genesis and Progression of Myocardial Ischemia

机译:LOX-1:心肌缺血的发生和发展中的关键角色。

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摘要

Myocardial ischemia is the most common cause of mortality and morbidity in the developed countries and rapidly becoming a common malady in the developing countries. Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1), encoded by the OLR1 gene, is a scavenger receptor that plays a fundamental role in the genesis and progression of atherosclerosis and its complications. LOX-1 has been identified as a major receptor for oxidized low-density lipoprotein (ox-LDL) in endothelial cells, cardiomyocytes and fibroblast. In vitro and in vivo studies show that LOX-1 is upregulated during acute myocardial ischemia, and continues to be upregulated during chronic ischemia. Further, LOX-1 inhibition reduces ischemic myocardial injury and limits cardiac remodeling. LOX-1 inhibition decreases oxidative stress and inflammatory response to injury resulting in limitation of ischemic injury. Molecular studies show that LOX-1 inhibition reduces release of pro-inflammatory cytokines and expression of angiotensin II type 1 receptor via inhibition of redox-sensitive pathways. These alterations limit cardiomyocyte hypertrophy and collagen accumulation in the ischemic regions. These alterations in molecular signaling and physical alterations can result in improved cardiac function and better survival after ischemic myocardial injury.
机译:心肌缺血是发达国家死亡和发病的最常见原因,并迅速成为发展中国家的常见疾病。由OLR1基因编码的类凝集素样氧化型低密度脂蛋白受体1(LOX-1)是一种清除剂受体,在动脉粥样硬化的发生,发展及其并发症中起着基本作用。 LOX-1已被确定为内皮细胞,心肌细胞和成纤维细胞中氧化型低密度脂蛋白(ox-LDL)的主要受体。体外和体内研究表明,LOX-1在急性心肌缺血期间被上调,并且在慢性缺血期间继续被上调。此外,LOX-1抑制作用可减少缺血性心肌损伤并限制心脏重塑。 LOX-1抑制作用降低了氧化应激和对损伤的炎症反应,从而限制了缺血性损伤。分子研究表明,LOX-1抑制通过抑制氧化还原敏感途径而减少促炎性细胞因子的释放和1型血管紧张素II受体的表达。这些改变限制了缺血区域中心肌细胞的肥大和胶原蛋白的积累。分子信号传导和物理改变的这些改变可导致心脏功能改善和缺血性心肌损伤后更好的生存。

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