Madahian Sepideh, Navab Kaveh Daniel, Pourtabatabaei Nasim, Seyedali Seyedehsara, Safar Sheila, Vazirian Samra, Hough Greg
David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA.
Curr Med Chem. 2014;21(25):2902-9. doi: 10.2174/0929867321666140414105530.
High density lipoprotein (HDL) has two important roles: a) it modulates inflammation, and, b) it promotes reverse cholesterol transport. HDL-cholesterol levels are inversely correlated with the risk of cardiovascular events. The main component of HDL, apolipoprotein A-I (apo A-I), is largely responsible for reverse cholesterol transport through the macrophage ATP-binding cassette transporter ABCA1. Apo A-I can be damaged by oxidative mechanisms, which render the protein less able to promote cholesterol efflux. HDL also contains a number of other proteins that are affected by the oxidative environment of the acute-phase response. Modification of the protein components of HDL can convert it from an anti-inflammatory to a pro inflammatory and dysfunctional particle. Small peptides that mimic some of the properties of apo A-I have been shown in preclinical models to improve HDL function and reduce atherosclerosis without altering HDL-cholesterol levels. Endothelium is the interface between the blood and the extra vascular environment regulating the traffic of vital molecules between the blood and tissues. Oxidative stress and excess levels of reactive oxygen species disrupt the normal function of endothelium. HDL and other antioxidant/anti-inflammatory systems prevent endothelial dysfunction and maintain the critical balance needed for normal vascular function.
高密度脂蛋白(HDL)具有两个重要作用:a)调节炎症,以及b)促进胆固醇逆向转运。HDL胆固醇水平与心血管事件风险呈负相关。HDL的主要成分载脂蛋白A-I(apo A-I)在很大程度上负责通过巨噬细胞ATP结合盒转运体ABCA1进行胆固醇逆向转运。Apo A-I可被氧化机制破坏,从而使该蛋白促进胆固醇流出的能力降低。HDL还包含许多其他受急性期反应氧化环境影响的蛋白质。HDL蛋白质成分的修饰可使其从抗炎性颗粒转变为促炎性和功能失调性颗粒。在临床前模型中已表明,模拟apo A-I某些特性的小肽可改善HDL功能并减少动脉粥样硬化,而不会改变HDL胆固醇水平。内皮是血液与血管外环境之间的界面,调节着血液与组织之间重要分子的运输。氧化应激和活性氧的过量水平会破坏内皮的正常功能。HDL和其他抗氧化/抗炎系统可预防内皮功能障碍,并维持正常血管功能所需的关键平衡。