Li Jian-Mei, Shah Ajay M
Department of Cardiology, Guy's King's & St Thomas's School of Medicine, King's College London, London, United Kingdom.
J Am Soc Nephrol. 2003 Aug;14(8 Suppl 3):S221-6. doi: 10.1097/01.asn.0000077406.67663.e7.
Oxidative stress has emerged as an important pathogenic factor in the development of long-term complications, such as atherosclerosis and nephropathy, in patients with diabetes. Whereas multiple enzymes and processes can contribute to oxidative stress, recent studies indicate that a multicomponent phagocyte-type NADPH oxidase is a major source of reactive oxygen species (ROS) production in many nonphagocytic cells, including fibroblasts, vascular smooth muscle cells, endothelial cells, renal mesangial cells, and tubular cells. Under physiologic conditions, nonphagocytic NADPH oxidases have very low-level constitutive activity. However, enzyme activity can be upregulated both acutely and chronically in response to stimuli such as growth factors, cytokines, high glucose, and hyperlipidemia. ROS production by the oxidase may serve a signaling role or may lead to oxidative damage. This article reviews current knowledge of the nonphagocyte-NADPH oxidases at both structural and biochemical levels and discusses the possible role of these enzymes in the pathophysiology of diabetic nephropathy.
氧化应激已成为糖尿病患者长期并发症(如动脉粥样硬化和肾病)发展过程中的一个重要致病因素。虽然多种酶和过程都可能导致氧化应激,但最近的研究表明,一种多组分吞噬细胞型NADPH氧化酶是许多非吞噬细胞(包括成纤维细胞、血管平滑肌细胞、内皮细胞、肾系膜细胞和肾小管细胞)中活性氧(ROS)产生的主要来源。在生理条件下,非吞噬性NADPH氧化酶具有非常低水平的组成性活性。然而,酶活性可因生长因子、细胞因子、高血糖和高脂血症等刺激而急性和慢性上调。氧化酶产生的ROS可能起到信号传导作用,也可能导致氧化损伤。本文综述了目前关于非吞噬细胞NADPH氧化酶在结构和生化水平方面的知识,并讨论了这些酶在糖尿病肾病病理生理学中的可能作用。