Aitken Alison E, Richardson Terrilyn A, Morgan Edward T
Department of Pharmacology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Annu Rev Pharmacol Toxicol. 2006;46:123-49. doi: 10.1146/annurev.pharmtox.46.120604.141059.
Inflammation and infection have long been known to downregulate the activity and expression of cytochrome P450 (CYP) enzymes involved in hepatic drug clearance. This can result in elevated plasma drug levels and increased adverse effects. Recent information on regulation of human CYP enzymes is presented, as are new developments in our understanding of the mechanisms of regulation. Experiments to study the effects of modulating CYP activities on the inflammatory response have yielded possible insights into the physiological consequences, if not the purpose, of the downregulation. Regulation of hepatic flavin monooxygenases, UDP-glucuronosyltransferases, sulfotransferases, glutathione S-transferases, as well as of hepatic transporters during the inflammatory response, exhibits similarities and differences with regulation of CYPs.
长期以来,人们一直知道炎症和感染会下调参与肝脏药物清除的细胞色素P450(CYP)酶的活性和表达。这可能导致血浆药物水平升高和不良反应增加。本文介绍了有关人类CYP酶调节的最新信息,以及我们对调节机制理解的新进展。研究调节CYP活性对炎症反应影响的实验,即使没有揭示下调的目的,也对其生理后果提供了可能的见解。炎症反应期间肝脏黄素单加氧酶、尿苷二磷酸葡萄糖醛酸转移酶、磺基转移酶、谷胱甘肽S-转移酶以及肝脏转运蛋白的调节,与CYP的调节既有相似之处,也有不同之处。