Deshane Jessy, Wright Marcienne, Agarwal Anupam
Department of Medicine, Nephrology Research and Training Center, Division of Nephrology, University of Alabama at Birmingham, Birmingham, AL, USA.
Acta Biochim Pol. 2005;52(2):273-84. Epub 2005 May 31.
Heme oxygenase-1 (HO-1) is an enzyme which catalyzes the rate-limiting step in heme degradation resulting in the formation of iron, carbon monoxide and biliverdin, which is subsequently converted to bilirubin by biliverdin reductase. The biological effects exerted by the products of this enzymatic reaction have gained much attention. The anti-oxidant, anti-inflammatory and cytoprotective functions associated with HO-1 are attributable to one or more of its degradation products. Induction of HO-1 occurs as an adaptive and beneficial response to several injurious stimuli including heme and this inducible nature of HO-1 signifies its importance in several pathophysiological disease states. The beneficial role of HO-1 has been implicated in several clinically relevant disease states involving multiple organ systems as well as significant biological processes such as ischemia-reperfusion injury, inflammation/immune dysfunction and transplantation. HO-1 has thus emerged as a key target molecule with therapeutic implications.
血红素加氧酶-1(HO-1)是一种催化血红素降解限速步骤的酶,该步骤会生成铁、一氧化碳和胆绿素,随后胆绿素由胆绿素还原酶转化为胆红素。这种酶促反应产物所发挥的生物学效应备受关注。与HO-1相关的抗氧化、抗炎和细胞保护功能归因于其一种或多种降解产物。HO-1的诱导是对包括血红素在内的多种损伤性刺激的适应性有益反应,HO-1的这种可诱导特性表明其在多种病理生理疾病状态中具有重要意义。HO-1的有益作用已涉及多种临床相关疾病状态,包括多个器官系统以及诸如缺血再灌注损伤、炎症/免疫功能障碍和移植等重要生物学过程。因此,HO-1已成为具有治疗意义的关键靶分子。