Yamagishi Sho-ichi
Department of Pathophysiology and Therapeutics of Diabetic Vascular Complications, Kurume University School of Medicine, Kurume, Japan.
Ther Apher Dial. 2009 Dec;13(6):534-9. doi: 10.1111/j.1744-9987.2009.00775.x.
Reducing sugars can react non-enzymatically with amino groups of protein to form Amadori products. These early glycation products undergo further complex reactions, such as rearrangement, dehydration, and condensation, to become irreversibly cross-linked, heterogeneous fluorescent derivatives, termed advanced glycation end products (AGEs). The formation and accumulation of AGEs have been known to progress at an accelerated rate in patients with diabetes mellitus, thus being involved in the development and progression of diabetic micro- and macroangiopathy. Indeed, there is accumulating evidence that an interaction between an AGE and its receptor (RAGE) generates oxidative stress and subsequently evokes vascular inflammation and thrombosis, thereby playing a central role in diabetic vascular complications. In this paper, we review the pathophysiological role of AGE-RAGE-oxidative stress system and its therapeutic interventions in diabetic micro- and macroangiopathy.
还原糖可与蛋白质的氨基发生非酶反应,形成阿马多里产物。这些早期糖基化产物会经历进一步的复杂反应,如重排、脱水和缩合,从而变成不可逆交联的、异质性的荧光衍生物,即晚期糖基化终末产物(AGEs)。已知糖尿病患者体内AGEs的形成和积累会加速进行,进而参与糖尿病微血管和大血管病变的发生和发展。事实上,越来越多的证据表明,AGE与其受体(RAGE)之间的相互作用会产生氧化应激,随后引发血管炎症和血栓形成,从而在糖尿病血管并发症中起核心作用。在本文中,我们综述了AGE-RAGE-氧化应激系统在糖尿病微血管和大血管病变中的病理生理作用及其治疗干预措施。