| Literature DB >> 19960413 |
Sang Kyu Lee1, Yoon Kim, Changbae Jin, Seung Ho Lee, Mi Jeong Kang, Tae Cheon Jeong, Seo Young Jeong, Dong-Hyun Kim, Hye Hyun Yoo.
Abstract
Deoxypodophyllotoxin (DPT) is a bioactive compound of Anthriscus sylvestris (Apiaceae). In the present study, the inhibition of cytochrome P450 (CYP) by DPT was evaluated in human liver microsomes (HLM) and the baculovirus-insect cell-expressed human CYPs using a cocktail probe assay. When a mixture of specific CYP substrates was incubated with DPT in HLM, CYP2C9-catalyzed diclofenac 4-hydroxylation and CYP3A4-catalyzed midazolam 1-hydroxylation were strongly inhibited by DPT, with IC (50) values of 6.3 and 9.2 microM, respectively. The Lineweaver-Burke plots for the inhibition of CYP2C9 and CYP3A4 in HLM and baculovirus-insect cell-expressed human CYPs were consistent with a competitive type of inhibition. From these results, DPT was characterized to be a competitive inhibitor of CYP2C9 and CYP3A4, with K(i) values of 3.5 and 10.8 microM in HLM and 24.9 and 3.5 microM in baculovirus-insect cell-expressed human CYPs, respectively. Georg Thieme Verlag KG Stuttgart. New York.Entities:
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Year: 2009 PMID: 19960413 DOI: 10.1055/s-0029-1240657
Source DB: PubMed Journal: Planta Med ISSN: 0032-0943 Impact factor: 3.352