CYP3A4参与溴哌啶醇体外代谢。

S Sato, T Someya, O Shioiri, T Koitabashi, Y Inoue
{"title":"CYP3A4参与溴哌啶醇体外代谢。","authors":"S Sato,&nbsp;T Someya,&nbsp;O Shioiri,&nbsp;T Koitabashi,&nbsp;Y Inoue","doi":"10.1034/j.1600-0773.2000.d01-27.x","DOIUrl":null,"url":null,"abstract":"<p><p>In this study, human cytochrome P450 isoenzymes (CYP1A2, CYP2C19, CYP2D6, and CYP3A4) expressed in a cell line were used to elucidate their roles in the metabolism of bromperidol. We found that CYP3A4 catalyzes the N-dealkylation of bromperidol and its metabolite, reduced bromperidol. CYP3A4 also catalyzes the dehydration of bromperidol to bromperidol 1,2,3,6-tetrahydropyridine, metabolizes bromperidol to bromperidol pyridinium, and catalyzes the oxidation of reduced bromperidol back to bromperidol. CYP1A2, CYP2C19, and CYP2D6 do not catalyze these reactions.</p>","PeriodicalId":19876,"journal":{"name":"Pharmacology & toxicology","volume":"86 3","pages":"145-8"},"PeriodicalIF":0.0000,"publicationDate":"2000-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Involvement of CYP3A4 in the metabolism of bromperidol in vitro.\",\"authors\":\"S Sato,&nbsp;T Someya,&nbsp;O Shioiri,&nbsp;T Koitabashi,&nbsp;Y Inoue\",\"doi\":\"10.1034/j.1600-0773.2000.d01-27.x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In this study, human cytochrome P450 isoenzymes (CYP1A2, CYP2C19, CYP2D6, and CYP3A4) expressed in a cell line were used to elucidate their roles in the metabolism of bromperidol. We found that CYP3A4 catalyzes the N-dealkylation of bromperidol and its metabolite, reduced bromperidol. CYP3A4 also catalyzes the dehydration of bromperidol to bromperidol 1,2,3,6-tetrahydropyridine, metabolizes bromperidol to bromperidol pyridinium, and catalyzes the oxidation of reduced bromperidol back to bromperidol. CYP1A2, CYP2C19, and CYP2D6 do not catalyze these reactions.</p>\",\"PeriodicalId\":19876,\"journal\":{\"name\":\"Pharmacology & toxicology\",\"volume\":\"86 3\",\"pages\":\"145-8\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2000-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pharmacology & toxicology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1034/j.1600-0773.2000.d01-27.x\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmacology & toxicology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1034/j.1600-0773.2000.d01-27.x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

摘要

本研究利用细胞系中表达的人细胞色素P450同工酶(CYP1A2、CYP2C19、CYP2D6和CYP3A4)来阐明它们在溴哌啶醇代谢中的作用。我们发现CYP3A4可以催化溴哌啶醇的n -脱烷基反应及其代谢产物,还原溴哌啶醇。CYP3A4还催化溴peridol脱水生成溴peridol 1,2,3,6-四氢吡啶,将溴peridol代谢为溴peridol吡啶,并催化还原溴peridol氧化回溴peridol。CYP1A2、CYP2C19和CYP2D6不催化这些反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Involvement of CYP3A4 in the metabolism of bromperidol in vitro.

In this study, human cytochrome P450 isoenzymes (CYP1A2, CYP2C19, CYP2D6, and CYP3A4) expressed in a cell line were used to elucidate their roles in the metabolism of bromperidol. We found that CYP3A4 catalyzes the N-dealkylation of bromperidol and its metabolite, reduced bromperidol. CYP3A4 also catalyzes the dehydration of bromperidol to bromperidol 1,2,3,6-tetrahydropyridine, metabolizes bromperidol to bromperidol pyridinium, and catalyzes the oxidation of reduced bromperidol back to bromperidol. CYP1A2, CYP2C19, and CYP2D6 do not catalyze these reactions.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
A screening study on the liability of eight different female sex steroids to inhibit CYP2C9, 2C19 and 3A4 activities in human liver microsomes. Gastrointestinal and systemic uptake of bismuth in mice after oral exposure. NordTox 2003. Abstracts of the 7th Nordic Conference of the Nordic Societies of Toxicology and Environmental Mutagenesis. Bornholm, Denmark, June 15-18, 2003. Distribution of zinc-binding metallothionein in cirrhotic liver of rats administered zinc. Ethanol in blood after ingestion of light alcoholic beverages (maximal 2.25 % v/v).
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1