University of Cincinnati Metabolic Diseases Institute, Cincinnati, Ohio 45237, USA.
Curr Opin Endocrinol Diabetes Obes. 2012 Apr;19(2):109-14. doi: 10.1097/MED.0b013e32835056d4.
To review recently published advances in the development of apolipoprotein A-I (apoA-I) mimetic peptides as a potential treatment for cardiovascular diseases.
Various apoA-I mimetic peptides are currently in development and these display potent cardioprotective features that can rival or even surpass those of full length apoA-I and high-density lipoproteins (HDLs). These features include the ability to efflux cholesterol from various cell types as well as anti-inflammatory and antioxidative properties. Recent work has been aimed at identifying the structural features of these peptides that are responsible for these various functions and also for determining the operational mechanisms. There is also interesting new data suggesting that the intestine may be playing an important role in the action of these peptides.
In the last year, there have been many important advances in the relatively new field of apoA-I mimetic therapy. These findings support a strong potential for their development as treatment for not only cardiovascular disease but other disease states involving chronic inflammation and oxidation as well.
综述最近发表的载脂蛋白 A-I(apoA-I)模拟肽在心血管疾病治疗中的研究进展。
目前正在开发各种 apoA-I 模拟肽,这些肽具有很强的心脏保护作用,可以与全长 apoA-I 和高密度脂蛋白(HDL)相媲美,甚至超过它们。这些特性包括从各种细胞类型中流出胆固醇的能力以及抗炎和抗氧化特性。最近的工作旨在确定这些肽的结构特征,这些结构特征决定了它们的各种功能,也确定了它们的作用机制。还有一些有趣的新数据表明,肠道可能在这些肽的作用中发挥重要作用。
在过去的一年中,apoA-I 模拟治疗这一相对较新的领域取得了许多重要进展。这些发现为它们的开发提供了强有力的潜力,不仅可用于治疗心血管疾病,还可用于治疗涉及慢性炎症和氧化的其他疾病状态。