期刊文献+

多药耐药蛋白和CYP3A4介导的中草药-西药相互作用 被引量:9

MDR-and CYP3A4-mediated drug-herbal interactions
下载PDF
导出
摘要 据近年的流行病学报告,国内外越来越多的人终身服用各种中草药,包括各类疾病患者(如:癌症等)和健康人群。随着中草药与处方西药联合应用治疗疾病的日益增多,越来越多的人注意到这两者的同时使用可能引起的中草药-西药相互作用会影响到治疗药物的活性。目前已知P-糖蛋白(P-gp)和CYP3A4一起能构成许多口服吸收药物的高效屏障,然而50%以上的临床用药都会被CYP3A4代谢或被P-gp转运。本文综述了多药耐药蛋白和CYP3A4介导的中草药-西药相互作用,同时也讨论了中草药-西药相互作用的关键因素。 According to recent epidemiological reports more and more people, both healthy and ill, use all kinds of Chinese herbal medicine during their lifetime. As the increasing combined usage of Chinese herbal medicine with prescription drags, it draws lots of attentions on the therapeutic activity due to possible drug-herb interaction. It is known that P-glycoprotein (P-gp) together with cytochrome P450 3A4 (CYP3A4) leads to a highly efficient barrier for many orally absorbed drugs. Meanwhile, more than 50% of the clinical drugs are metabolized by CYP3A4 or transported by P-gp. Hence, more attention should be paid to MDR-and CYP3A4-mediated drug-herbal interactions. This survey discusses the key-factors of drug-herbal interaction as well.
出处 《中国临床药理学与治疗学》 CAS CSCD 2007年第7期728-734,共7页 Chinese Journal of Clinical Pharmacology and Therapeutics
关键词 P-糖蛋白 CYPSA4 处方西药 中草药 生物利用度 P-glycoprotein CYP3A4 prescribed drug herb bioavailability
  • 相关文献

参考文献46

  • 1Sparreboom A,Danesi R,Ando Y,et al.Pharmacogenomics of ABC transporters and its role in cancer chemotherapy[J].Drug Resist Updat,2003;6:71-84.
  • 2Thiebaut F,Tsuruo T,Hamada H,et al.Cellular localization of the multidrug resistance gene product P-glycoprotein in normal human tissues[J].Proc Natl Acad Sci USA,1987;84:7735-7738.
  • 3de Lannoy IA,Silverman M.The MDR1 gene product P-glycoprotein,mediates the transport of the cardiac glycoside,digoxin[J].Biochem Biophys Res Commun,1992;189:551-557.
  • 4Fromm MF.P-glycoprotein:a defense mechanism limiting oral bioavailability and CNS accumulation of drugs[J].Int J Clin Pharmacol Ther,2000;38:69-74.
  • 5Sakaeda T,Nakamura T,Okumura K.MDR1 genotype-related pharmacokinetics and pharmacodynamics[J].Biol Pharm Bull,2002;25:1291-1400.
  • 6Kim RB,Fromm MF,Christoph W,et al.The drug transporter P-glycoprotein limits oral absorption and brain entry of HIV21 protease inhibitors[J].J Clin Invest,1998;101:289-294.
  • 7Bosch I,Croop J.P-glycoprotein,multidrug resistance and cancer[J].Biochim Biophys Acta,1996;1288:F37-F54.
  • 8Borst P,Evers R,Kool M,et al.A family of drug transporters:the multidrug resistance-associated proteins[J].J Natl Cancer Inst,2000;92:1295-1302.
  • 9Hyde SC,Emsley P,Hartshorn MJ,et al.Structural model of ATP-binding proteins associated with cystic fibrosis,multidrug resistance and bacterial transport[J].Nature,1990;346:362-365.
  • 10Ambudkar SV,Dey S,Hrycyna CA,et al.Biochemical,cellular,and pharmacological aspects of the multidrug transporter[J].Annu Rev Pharmacol Toxicol,1999;39:361-398.

二级参考文献1

  • 1赵莉,生理科学进展,1997年,28卷,35页

共引文献7

同被引文献100

引证文献9

二级引证文献21

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部