孕烷X受体
CYP3A型
孕烷
雄激素受体
异型生物质的
核受体
单加氧酶
CYP3A4型
细胞色素P450
药理学
转录因子
化学
生物
抄写(语言学)
芳香烃受体
戒毒(替代医学)
基因
生物化学
酶
遗传学
医学
语言学
哲学
替代医学
病理
作者
Bryan Goodwin,Matthew R. Redinbo,Steven A. Kliewer
出处
期刊:Annual Review of Pharmacology and Toxicology
[Annual Reviews]
日期:2002-04-01
卷期号:42 (1): 1-23
被引量:319
标识
DOI:10.1146/annurev.pharmtox.42.111901.111051
摘要
The pregnane X receptor (PXR) is a promiscuous nuclear receptor that has evolved to protect the body from toxic chemicals. PXR is activated by a structurally diverse collection of xenobiotics, including several widely used prescription drugs. Various lipophilic compounds produced by the body, such as bile acids and steroids, also activate PXR. PXR stimulates the transcription of cytochrome P450 3A monooxygenases and other genes involved in the detoxification and elimination of these potentially harmful chemicals. Assays that detect PXR activation have important implications for the design of future drugs in two respects. On the one hand, PXR activation assays can be used to determine whether candidate drugs are likely to induce CYP3A gene expression and interact with other medicines. On the other hand, PXR agonists may prove useful in the treatment of diseases in which toxic metabolites accumulate, such as cholestatic liver disease.
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