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致癌物与双香豆素:对大鼠肝脏NAD(P)H脱氢作用的相反影响。

Carcinogens and dicumarol: opposite effects on rat liver NAD(P)H dehydrogenation.

作者信息

Schor N A, Boh E, Burke V T

出版信息

Enzyme. 1978;23(4):217-24. doi: 10.1159/000458583.

Abstract

The carcinogens, N-acetyl-aminofluorene, 7,12-dimethylbenzanthracene, 3,4-benzpyrene and 3-methylcholanthrene, increase the activity of the soluble enzyme D-T-diaphorase. This action is observed 24 h after the administration of these chemicals to rats. Dicumarol blocks this effect. Dicumarol does not inhibit the increase in activity of the microsomal aryl hydrocarbon hydroxylase system as elicited by 3,4-benz(a)pyrene and 3-methylcholanthrene. The functional significance of these findings and the possible role of cytosolic enzymic changes in chemical toxicity are discussed.

摘要

致癌物N-乙酰氨基芴、7,12-二甲基苯并蒽、3,4-苯并芘和3-甲基胆蒽可增加可溶性酶D-T-黄递酶的活性。在给大鼠施用这些化学物质24小时后可观察到这种作用。双香豆素可阻断这种效应。双香豆素并不抑制由3,4-苯并(a)芘和3-甲基胆蒽引起的微粒体芳烃羟化酶系统活性的增加。本文讨论了这些发现的功能意义以及胞质酶变化在化学毒性中可能发挥的作用。

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