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药物在人药物代谢酶催化反应中形成潜在毒性代谢物。

Formation of potentially toxic metabolites of drugs in reactions catalyzed by human drug-metabolizing enzymes.

机构信息

, Haulikova 6, HR 10 000, Zagreb, Croatia.

Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, 37232-0146, USA.

出版信息

Arch Toxicol. 2024 Jun;98(6):1581-1628. doi: 10.1007/s00204-024-03710-9. Epub 2024 Mar 23.

Abstract

Data are presented on the formation of potentially toxic metabolites of drugs that are substrates of human drug metabolizing enzymes. The tabular data lists the formation of potentially toxic/reactive products. The data were obtained from in vitro experiments and showed that the oxidative reactions predominate (with 96% of the total potential toxication reactions). Reductive reactions (e.g., reduction of nitro to amino group and reductive dehalogenation) participate to the extent of 4%. Of the enzymes, cytochrome P450 (P450, CYP) enzymes catalyzed 72% of the reactions, myeloperoxidase (MPO) 7%, flavin-containing monooxygenase (FMO) 3%, aldehyde oxidase (AOX) 4%, sulfotransferase (SULT) 5%, and a group of minor participating enzymes to the extent of 9%. Within the P450 Superfamily, P450 Subfamily 3A (P450 3A4 and 3A5) participates to the extent of 27% and the Subfamily 2C (P450 2C9 and P450 2C19) to the extent of 16%, together catalyzing 43% of the reactions, followed by P450 Subfamily 1A (P450 1A1 and P450 1A2) with 15%. The P450 2D6 enzyme participated in an extent of 8%, P450 2E1 in 10%, and P450 2B6 in 6% of the reactions. All other enzymes participate to the extent of 14%. The data show that, of the human enzymes analyzed, P450 enzymes were dominant in catalyzing potential toxication reactions of drugs and their metabolites, with the major role assigned to the P450 Subfamily 3A and significant participation of the P450 Subfamilies 2C and 1A, plus the 2D6, 2E1 and 2B6 enzymes contributing. Selected examples of drugs that are activated or proposed to form toxic species are discussed.

摘要

本文介绍了作为人体药物代谢酶底物的药物潜在毒性代谢物的形成。表格数据列出了潜在毒性/反应性产物的形成。这些数据来自于体外实验,结果表明氧化反应占主导地位(占潜在毒化反应的 96%)。还原反应(例如,将硝基还原为氨基和还原脱卤)的参与度为 4%。在酶中,细胞色素 P450(P450,CYP)酶催化了 72%的反应,髓过氧化物酶(MPO)占 7%,黄素单加氧酶(FMO)占 3%,醛氧化酶(AOX)占 4%,磺基转移酶(SULT)占 5%,还有一组次要参与酶占 9%。在 P450 超家族中,P450 亚家族 3A(P450 3A4 和 3A5)的参与度为 27%,亚家族 2C(P450 2C9 和 P450 2C19)的参与度为 16%,共同催化了 43%的反应,其次是 P450 亚家族 1A(P450 1A1 和 P450 1A2)占 15%。P450 2D6 酶参与的程度为 8%,P450 2E1 为 10%,P450 2B6 为 6%。其他所有酶的参与度均为 14%。数据表明,在所分析的人体酶中,P450 酶在催化药物及其代谢物的潜在毒性反应中占主导地位,其中 P450 亚家族 3A 起主要作用,P450 亚家族 2C 和 1A 也有显著参与,加上 2D6、2E1 和 2B6 酶的贡献。本文还讨论了一些被激活或被提议形成毒性物质的药物的实例。

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