Cytochrome P450 2E1/2A6-Selective Inhibition by Halogenated Anilines on Metabolic Activation of Dimethylnitrosamine in Human Liver Microsomes
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- Ohashi Yohei
- Graduate School of Pharmaceutical Sciences, Nagoya City University
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- Kato Taka-aki
- Graduate School of Pharmaceutical Sciences, Nagoya City University
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- Yamada Katsuya
- Graduate School of Pharmaceutical Sciences, Nagoya City University
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- Mizutani Takaharu
- Graduate School of Pharmaceutical Sciences, Nagoya City University
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- Saeki Ken-ichi
- Graduate School of Pharmaceutical Sciences, Nagoya City University
書誌事項
- 公開日
- 2006
- DOI
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- 10.1248/jhs.52.623
- 公開者
- 公益社団法人 日本薬学会
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説明
Nine halogenated anilines, consisting of di- and tri-substituted fluoro-, chloro-, and bromoanilines, were subjected to analysis of their cytochrome P450 (CYP) 2E1/2A6-selective inhibitory effects on metabolic activation of dimetylnitrosamine (DMN) in human liver microsomes. Inhibitory activities (IC50) of these anilines on human recombinant CYP2E1 ranged from 8.0 to 549 μM. However, most of these anilines showed no remarkable inhibition of CYP1A2, while their IC50 values on CYP2A6 ranged from 2.9 to 232 μM. The CYP2E1 selectivity of these anilines in terms of the ratio of the IC50 values of these anilines on CYP2A6 to those on CYP2E1, ranged from 0.1- to 5.2-fold. Their CYP2E1 selectivity decreased in the following order: 3,4,5-trifluoroaniline (3,4,5-triF-A) > 3,5-diF-A >> 3,5-dichloroaniline (3,5-diCl-A) > 3,4-diCl-A > 2,6-diCl-A > 2,3,4-trichloroaniline (2,3,4-triCl-A) > 2,4,6-triCl-A > 2,6-dibromoaniline (2,6-diBr-A) > 3,4,5-triCl-A. The inhibitory effects of these anilines on metabolic activation of DMN were analyzed using human liver microsomes. The IC50 values of these anilines on demethylation metabolism of DMN correlated with those of these anilines on CYP2E1. These results suggest that these halogenated anilines may be useful as indicators of CYP-selectivity involved in metabolic activation of nitrosamines. <br>
収録刊行物
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- JOURNAL OF HEALTH SCIENCE
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JOURNAL OF HEALTH SCIENCE 52 (5), 623-627, 2006
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390282679474380672
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- NII論文ID
- 110004809618
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- NII書誌ID
- AA11316464
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- ISSN
- 13475207
- 13449702
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- NDL書誌ID
- 8073902
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDLサーチ
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- 使用不可

