Identification of Cytochrome P450 (CYP) Isoforms involved in the Metabolism of Corynoline, and Assessment of its Herb-Drug Interactions
Fang, Zhong-Ze1,2; Zhang, Yan-Yan1,2; Ge, Guang-Bo1,2; Liang, Si-Cheng1,2; Sun, Dong-Xue; Zhu, Liang-Liang1,2; Dong, Pei-Pei1,2; Cao, Yun-Feng3; Yang, Ling1
刊名phytotherapy research
2011-02-01
卷号25期号:2页码:256-263
关键词corynoline cytochrome P450 (CYP) drug-herb interaction time-dependent inhibition (TDI)
英文摘要corynoline, an isoquinoline alkaloid isolated from the genus corydalis, has been demonstrated to show multiple pharmacological effects including inhibition of acetylcholinesterase, inhibition of cell adhesion, fungitoxic and cytotoxic activity. the present study focused on its metabolism and metabolism-based herb drug interactions. after corynoline was incubated with human liver microsomes (hlms) in the presence of nadph, two metabolites (m-1 and m-2) were formed. chemical inhibition experiments and assays with recombinant cyp isoforms showed that cyp2c9 was mainly involved in the formation of m-1 and cyp3a4 mainly catalysed the production of m-2. among seven major cyp isoforms tested, corynoline showed strong inhibitory effects on the activities of cyp3a4 and cyp2c9, with an ic(50) of 3.3 +/- 0.9 mu m and 31.5 +/- 0.5 mu m, respectively. kinetic analysis showed that inhibition of cyp3a4 by corynoline was best fit to a noncompetitive manner with k(i) of 3.2 mu m, while inhibition of cyp2c9 by corynoline was best fit to a competitive manner with k(i) of 6.3 mu m. additionally, corynoline exhibited time-dependent inhibition (tdi) toward cyp3a4. the inactivation kinetic parameters (k(i) and k(inact)) were calculated to be 6.8 mu m and 0.07 min(-1), respectively. these data are of significance for the application of corynoline and corynoline-containing herbs. copyright (c) 2010 john wiley & sons, ltd.
WOS标题词science & technology ; life sciences & biomedicine
类目[WOS]chemistry, medicinal ; pharmacology & pharmacy
研究领域[WOS]pharmacology & pharmacy
关键词[WOS]corydalis-incisa ; aerial parts ; inhibition ; alkaloids ; p450s
收录类别SCI
语种英语
WOS记录号WOS:000287784100013
公开日期2015-11-17
内容类型期刊论文
源URL[http://159.226.238.44/handle/321008/142654]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
作者单位1.Chinese Acad Sci, Dalian Inst Chem Phys, Lab Pharmaceut Resource Discovery, Dalian 116023, Peoples R China
2.Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
3.Shenyang Pharmaceut Univ, Sch Tradit Chinese Med, Shenyang, Peoples R China
推荐引用方式
GB/T 7714
Fang, Zhong-Ze,Zhang, Yan-Yan,Ge, Guang-Bo,et al. Identification of Cytochrome P450 (CYP) Isoforms involved in the Metabolism of Corynoline, and Assessment of its Herb-Drug Interactions[J]. phytotherapy research,2011,25(2):256-263.
APA Fang, Zhong-Ze.,Zhang, Yan-Yan.,Ge, Guang-Bo.,Liang, Si-Cheng.,Sun, Dong-Xue.,...&Yang, Ling.(2011).Identification of Cytochrome P450 (CYP) Isoforms involved in the Metabolism of Corynoline, and Assessment of its Herb-Drug Interactions.phytotherapy research,25(2),256-263.
MLA Fang, Zhong-Ze,et al."Identification of Cytochrome P450 (CYP) Isoforms involved in the Metabolism of Corynoline, and Assessment of its Herb-Drug Interactions".phytotherapy research 25.2(2011):256-263.
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