Regulation and role of heme oxygenase in oxidative injury.

P A Dennery
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引用次数: 148

Abstract

The HO-1 isoenzyme is an early stress response gene regulated by many forms of oxidative stress. The HO-2 isoenzyme is predominantly a constitutive enzyme, which may serve to sequester heme as well as degrade it. All HO enzyme activity results in the degradation of heme and the production of antioxidant bile pigments, which would favor an antioxidant role for the enzyme. In fact, in oxidative stress in vitro, HO-1 is protective (91-94) but within a narrow threshold of overexpression (93,94) in some models, since iron released in the HO reaction may obviate any cytoprotective effect (Fig. 3). So far, HO-2 appears to be beneficial in oxygen toxicity in vivo, but the consequences of HO-2 overexpression have not yet been tested. It will be important to better define the role of each HO isoenzyme in oxidative stress so as to determine whether enhancing these complex systems could alleviate some of the cellular changes seen as a result of oxidative injury. Furthermore, prior to considering therapeutic maneuvers to enhance HO, a complete understanding of the physiologic consequences of HO-1 induction and associated reactions, in each particular setting, will be crucial.

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血红素加氧酶在氧化损伤中的调控作用。
HO-1同工酶是由多种形式的氧化应激调节的早期应激反应基因。HO-2同工酶主要是一种组成酶,它可以隔离血红素,也可以降解血红素。所有HO酶的活性都导致血红素的降解和抗氧化胆汁色素的产生,这有利于酶的抗氧化作用。事实上,在体外氧化应激中,HO-1具有保护作用(91-94),但在一些模型中,HO-1的过表达阈值很窄(93,94),因为HO反应中释放的铁可能会消除任何细胞保护作用(图3)。到目前为止,HO-2似乎对体内氧毒性有益,但HO-2过表达的后果尚未得到测试。更好地定义每个HO同工酶在氧化应激中的作用,以确定增强这些复杂系统是否可以减轻氧化损伤引起的一些细胞变化,这将是很重要的。此外,在考虑提高HO的治疗策略之前,对每种特定情况下HO-1诱导和相关反应的生理后果的全面了解将是至关重要的。
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