• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[人类细胞色素P450。在药理学中的应用]

[Human cytochromes P450. Applications in pharmacology].

作者信息

Beaune P

机构信息

INSERM U 75, CHU, Necker-Enfants-Malades, Université René Descartes, Paris.

出版信息

Therapie. 1993 Nov-Dec;48(6):521-6.

PMID:8091338
Abstract

Cytochromes P450 (P450) are hemoproteins which catalyze essentially monooxygenation reactions. These enzymes may metabolize either endogenous compounds such as steroids, or exogenous compounds. This review will concentrate on P450 metabolizing xenobiotics. They are found mainly in endoplasmic reticulum of hepatocytes. Purification and cloning of the different isoforms allowed to set up an international nomenclature based on sequences similarities between these P450. Ten families are known in mammals and 4 (CYP 1 to 4) metabolize xenobiotics. Each family may include several subfamilies (A, B, ...). Numerous factors cause variations in the expression of these P450: genetic, environmental, physiopathologic. Several genetic polymorphism have been described, P450, 2D6, 2C and may be 1A2 and 2E1. Some P450 (3A, 1A, 2E, ...) are inducible by compounds such as phenobarbital, rifampicin, aromatic hydrocarbon, ethanol, or omeprazole. Finally, P450 expression and inducibility vary depending on tissues. It is now possible to determine which isoform(s) is (are) responsible of the production of a metabolite. Specific tests are now available to evaluate the level of P450 in vivo in man (1A, 3A, 2D6, 2C).

摘要

细胞色素P450(P450)是一类血红素蛋白,主要催化单加氧反应。这些酶可代谢内源性化合物,如类固醇,也可代谢外源性化合物。本综述将聚焦于代谢外源性物质的P450。它们主要存在于肝细胞的内质网中。不同同工型的纯化和克隆使得基于这些P450之间的序列相似性建立了国际命名法。哺乳动物中已知有十个家族,其中4个家族(CYP 1至4)代谢外源性物质。每个家族可能包括几个亚家族(A、B等)。许多因素会导致这些P450表达的变化:遗传、环境、生理病理因素。已经描述了几种基因多态性,如P450、2D6、2C,可能还有1A2和2E1。一些P450(3A、1A、2E等)可被苯巴比妥、利福平、芳香烃、乙醇或奥美拉唑等化合物诱导。最后,P450的表达和诱导性因组织而异。现在有可能确定是哪种同工型负责代谢物的产生。现在有特定的检测方法可用于评估人体体内P450的水平(1A、3A、2D6、2C)。

相似文献

1
[Human cytochromes P450. Applications in pharmacology].[人类细胞色素P450。在药理学中的应用]
Therapie. 1993 Nov-Dec;48(6):521-6.
2
[Role of human cytochrome P-450 enzymes in the metabolism of xenobiotics].[人类细胞色素P-450酶在外源化学物代谢中的作用]
Acta Pharm Hung. 1995 Sep;65(5):147-56.
3
Identification of multiple constitutive and inducible hepatic cytochrome P450 enzymes in market weight swine.市售体重猪中多种组成型和诱导型肝细胞色素P450酶的鉴定
Drug Metab Dispos. 2001 Jun;29(6):908-15.
4
[Cytochromes P450: xenobiotic metabolism, regulation and clinical importance].[细胞色素P450:外源性物质代谢、调节及临床意义]
Ann Biol Clin (Paris). 2006 Nov-Dec;64(6):535-48.
5
Cytochrome P450 enzyme levels in HepG2 cells and cryopreserved primary human hepatocytes and their induction in HepG2 cells.HepG2细胞和冷冻保存的原代人肝细胞中的细胞色素P450酶水平及其在HepG2细胞中的诱导作用。
Toxicol In Vitro. 2007 Dec;21(8):1581-91. doi: 10.1016/j.tiv.2007.05.014. Epub 2007 Jun 8.
6
Redox cycling in the metabolism of the environmental pollutant and suspected human carcinogen o-anisidine by rat and rabbit hepatic microsomes.大鼠和兔肝微粒体对环境污染物及疑似人类致癌物邻甲氧基苯胺代谢中的氧化还原循环。
Chem Res Toxicol. 2008 Aug;21(8):1610-21. doi: 10.1021/tx8001127. Epub 2008 Jul 15.
7
Expression and activities of several drug-metabolizing enzymes in LLC-PK1 cells.LLC-PK1细胞中几种药物代谢酶的表达及活性
Toxicol In Vitro. 2004 Dec;18(6):887-94. doi: 10.1016/j.tiv.2004.05.001.
8
Enzymes involved in the metabolism of the carcinogen 2-nitroanisole: evidence for its oxidative detoxication by human cytochromes P450.参与致癌物2-硝基苯甲醚代谢的酶:人类细胞色素P450对其进行氧化解毒的证据。
Chem Res Toxicol. 2004 May;17(5):663-71. doi: 10.1021/tx0499721.
9
Cytochrome P450-catalyzed pathways in human brain: metabolism meets pharmacology or old drugs with new mechanism of action?细胞色素P450在人脑中的催化途径:代谢与药理学的交汇,还是具有新作用机制的老药?
Pharmacol Ther. 2007 Mar;113(3):537-45. doi: 10.1016/j.pharmthera.2006.11.005. Epub 2006 Dec 20.
10
Identification of the human hepatic cytochromes P450 involved in the in vitro oxidation of antipyrine.参与安替比林体外氧化反应的人肝细胞色素P450的鉴定。
Drug Metab Dispos. 1996 Apr;24(4):487-94.

引用本文的文献

1
Flavonoids and Furanocoumarins Involved in Drug Interactions.参与药物相互作用的黄酮类化合物和呋喃香豆素。
Molecules. 2025 Apr 9;30(8):1676. doi: 10.3390/molecules30081676.
2
Pharmacokinetic optimisation of cancer chemotherapy. Effect on outcomes.癌症化疗的药代动力学优化。对治疗结果的影响。
Clin Pharmacokinet. 1997 Apr;32(4):324-43. doi: 10.2165/00003088-199732040-00005.
3
The site of absorption in the small intestine determines diltiazem bioavailability in the rabbit.
Pharm Res. 1995 Nov;12(11):1722-6. doi: 10.1023/a:1016217822770.