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Heterogeneity of hepatic nicotine oxidase.

作者信息

Nakayama H, Nakashima T, Kurogochi Y

出版信息

Biochim Biophys Acta. 1982 Apr 13;715(2):254-7. doi: 10.1016/0304-4165(82)90367-1.

DOI:10.1016/0304-4165(82)90367-1
PMID:7074142
Abstract

When rats were pretreated with 3-methylcholanthrene of beta-naphthoflavone, hepatic nicotine oxidase activity per cytochrome P-448 molecule decreased, but the specific activity of the enzyme remained unchanged. After phenobarbital pretreatment, the specific activity of nicotine oxidase increased while the activity of the enzyme per cytochrome P-450 molecule decreased. alpha-Naphthoflavone selectively inhibited the activities of phenobarbital-induced nicotine oxidase and constitutive form(s) of the enzyme. These results show that phenobarbital-induced cytochrome P-450 and constitutive form(s) of the enzyme may be active in hepatic nicotine oxidation.

摘要

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引用本文的文献

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Arch Toxicol. 1991;65(1):68-72. doi: 10.1007/BF01973505.
2
Increased cotinine elimination and cotinine-N-oxide formation by phenobarbital induction in rat and mouse.苯巴比妥诱导大鼠和小鼠增加可替宁的消除及可替宁-N-氧化物的形成。
Clin Investig. 1992 Mar-Apr;70(3-4):175-81. doi: 10.1007/BF00184648.