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给大鼠施用烟酰胺对肝脏微粒体药物代谢酶的影响。

Effect of nicotinamide administration to rats on the liver microsomal drug metabolizing enzymes.

作者信息

Nomura K, Shin M, Sano K, Umezawa C, Shimada T

出版信息

Int J Vitam Nutr Res. 1983;53(1):36-43.

PMID:6222007
Abstract

A single injection or 3 successive injections of nicotinamide (500 mg/kg body wt) increased NADPH-cytochrome c reductase and aniline hydroxylase activities of rat liver microsomes without changing cytochrome P-450 content. Oral administration of nicotinamide for 2 weeks resulted in significant increase in cytochrome P-450, indicating that nicotinamide was an inducer of cytochrome P-450 though its potency was weak. A kinetic study indicated that microsomes isolated from control rats contained only high affinity (low Km) form of aniline hydroxylase while microsomes isolated from nicotinamide-treated rats contained more high affinity form and a newly appeared-low affinity (high Km) form. These results suggest that there exist at least 2 different cytochrome P-450s participating in aniline hydroxylation in rat liver microsomes and nicotinamide induces the high Km form. Ethanol or nicotinamide consumption for 2 weeks resulted in enhancement of high affinity form and appearance of low affinity form but with slightly different Km values.

摘要

单次注射或连续3次注射烟酰胺(500毫克/千克体重)可增加大鼠肝脏微粒体的NADPH - 细胞色素c还原酶和苯胺羟化酶活性,而细胞色素P - 450含量不变。口服烟酰胺2周导致细胞色素P - 450显著增加,表明烟酰胺是细胞色素P - 450的诱导剂,尽管其效力较弱。动力学研究表明,从对照大鼠分离的微粒体仅含有高亲和力(低Km)形式的苯胺羟化酶,而从烟酰胺处理的大鼠分离的微粒体含有更多的高亲和力形式和新出现的低亲和力(高Km)形式。这些结果表明,大鼠肝脏微粒体中至少存在2种不同的细胞色素P - 450参与苯胺羟化,且烟酰胺诱导高Km形式。连续2周摄入乙醇或烟酰胺会导致高亲和力形式增强和低亲和力形式出现,但Km值略有不同。

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