首页> 美国卫生研究院文献>Frontiers in Pharmacology >The Role of Human Aldo-Keto Reductases in the Metabolic Activation and Detoxication of Polycyclic Aromatic Hydrocarbons: Interconversion of PAH Catechols and PAH o-Quinones
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The Role of Human Aldo-Keto Reductases in the Metabolic Activation and Detoxication of Polycyclic Aromatic Hydrocarbons: Interconversion of PAH Catechols and PAH o-Quinones

机译:人醛基酮还原酶在多环芳烃代谢活化和脱毒中的作用:多环芳烃邻苯二酚和多环芳烃邻喹啉的相互转化

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摘要

Polycyclic aromatic hydrocarbons (PAH) are ubiquitous environmental pollutants. They are procarcinogens requiring metabolic activation to elicit their deleterious effects. Aldo-keto reductases (AKR) catalyze the oxidation of proximate carcinogenic PAH trans-dihydrodiols to yield electrophilic and redox-active PAH o-quinones. AKRs are also found to be capable of reducing PAH o-quinones to form PAH catechols. The interconversion of o-quinones and catechols results in the redox-cycling of PAH o-quinones to give rise to the generation of reactive oxygen species and subsequent oxidative DNA damage. On the other hand, PAH catechols can be intercepted through phase II metabolism by which PAH o-quinones could be detoxified and eliminated. The aim of the present review is to summarize the role of human AKRs in the metabolic activation/detoxication of PAH and the relevance of phase II conjugation reactions to human lung carcinogenesis.
机译:多环芳烃(PAH)是普遍存在的环境污染物。它们是致癌物,需要代谢活化才能引起其有害作用。醛基酮还原酶(AKR)催化最接近致癌的PAH反式二氢二醇的氧化,从而产生亲电和具有氧化还原活性的PAH邻醌。还发现AKR能够还原PAH邻醌以形成PAH邻苯二酚。邻苯二酚和邻苯二酚的相互转化导致PAH邻苯二酚的氧化还原循环,从而引起活性氧的产生和随后的氧化DNA损伤。另一方面,PAH儿茶酚可以通过II期代谢被拦截,PAH邻醌可以被解毒并消除。本综述的目的是总结人类AKR在PAH的代谢活化/解毒中的作用以及II期缀合反应与人类肺癌发生的相关性。

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