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肝脏中的解毒途径。

Detoxification pathways in the liver.

作者信息

Grant D M

机构信息

Division of Clinical Pharmacology and Toxicology, Hospital for Sick Children, Toronto, Ontario, Canada.

出版信息

J Inherit Metab Dis. 1991;14(4):421-30. doi: 10.1007/BF01797915.

Abstract

The liver plays an important rôle in protecting the organism from potentially toxic chemical insults through its capacity to convert lipophiles into more water-soluble metabolites which can be efficiently eliminated from the body via the urine. This protective ability of the liver stems from the expression of a wide variety of xenobiotic biotransforming enzymes whose common underlying feature is their ability to catalyse the oxidation, reduction and hydrolysis (Phase I) and/or conjugation (Phase II) of functional groups on drug and chemical molecules. The broad substrate specificity, isoenzyme multiplicity and inducibility of many of these enzyme systems make them particularly well adapted to handling the vast array of different chemical structures in the environment to which we are exposed daily. However, some chemicals may also be converted to more toxic metabolites by certain of these enzymes, implying that variations in the latter may be important predisposing factors for toxicity. Pharmacogenetic defects of xenobiotic biotransformation enzymes, a subclass of inborn errors of metabolism which are manifested only upon drug challenge, introduce marked variation into human populations for the pharmacokinetics and pharmacodynamics of therapeutic and toxic agents, and thus may have important clinical consequences for drug efficacy and toxicity.

摘要

肝脏在保护机体免受潜在有毒化学物质侵害方面发挥着重要作用,它能够将亲脂性物质转化为水溶性更高的代谢产物,这些代谢产物可通过尿液有效地从体内排出。肝脏的这种保护能力源于多种外源性生物转化酶的表达,这些酶的共同基本特征是能够催化药物和化学分子上功能基团的氧化、还原和水解(I相)以及/或结合反应(II相)。许多这些酶系统具有广泛的底物特异性、同工酶多样性和可诱导性,这使得它们特别适合处理我们每天接触到的环境中大量不同的化学结构。然而,某些化学物质也可能被其中某些酶转化为毒性更强的代谢产物,这意味着这些酶的变异可能是毒性的重要易感因素。外源性生物转化酶的药物遗传学缺陷是代谢先天性疾病的一个亚类,仅在药物激发时才会表现出来,它会给人群中治疗药物和毒性药物的药代动力学和药效学带来显著差异,因此可能对药物疗效和毒性产生重要的临床影响。

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