J4 ›› 2010, Vol. 36 ›› Issue (5): 862-865.

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Effect of novel |β2 receptor |agonist trantinterol on cytochrome P450 mRNA expression in HepG2 cells

 SUN Yan-Tong1,2, GUO Ying-Jie1, ZHANG Meng-Liang1, CUI Xiang-Yong1, GU Jing-Kai1   

  1. 1. Research Center for Drug Metabolism,College of Life Science,Jilin University,Changchun 130021,China|2. Department of Pharmaceutical Analysis,School of Pharmacy,Jilin University,Changchun 130021,China
  • Received:2010-04-15 Online:2010-09-28 Published:2010-09-28

Abstract:

Abstract:Objective To study the effect of trantinterol,a potent and highly selective  β2 receptor  agonist,on the cytochrome P450 enzymes (CYP450) mRNA expression and provide a theoretical basis for clinical drug combination.Methods  The cell proliferation of HepG2 cells treated with  2.4,12,60,300,1 200 and 4 800 ng/L  trantinterol was analyzed by MTT.The mRNA expression levels of CYP1A1,CYP2E1 and CYP3A5 in HepG2 cells were examined using the real-time quantitative reverse-transcriptase polymerase chain reaction in human hepatoma HepG2 cells.Results Different concentrations of trantinterol didn’[KG-*3]t inhibit the proliferation of HepG2 cells (P>0.05).Compared with control group,the mRNA expressions of CYP2E1 and CYP3A5 in trantinterol groups had no change,while the mRNA expression of CYP1A1 was inhibited (P<0.01).Conclusion Exposure of HepG2 cells to trantinterol has no effect on the mRNA expressions of CYP2E1 and CYP3A5 but inhibit the mRNA expression of CYP1A1.

Key words: trantinterol, cytochrome P450, HepG2 cell; , real-time quantitative polymerase chain reaction

CLC Number: 

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