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Drug-Drug Interaction between Clopidogrel and Neobavaisoflavone, Corylifolinin, and Coryfolin
被引:0
|作者:
Zhang, Yi-Qun
[1
]
Li, Qiu-Jie
[1
]
Yu, Ming-Lian
[2
]
机构:
[1] Xian 1 Hosp, Dept Cardiol, Xian 710002, Peoples R China
[2] Gen Hosp Beijing Mil Reg, Dept Pharm, Beijing, Peoples R China
来源:
关键词:
clopidogrel;
cytochrome P450 (CYP) 2C19;
Fructus Psoraleae;
human carboxyl esterase 1 (CES1);
CARBOXYLESTERASE;
1;
ACTIVE METABOLITE;
D O I:
暂无
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Clopidogrel, sold under the name Plavix by Sandi and Bristol-Myers Squibb, has been clinically utilized to inhibit blood clots in a variety of conditions such as peripheral vascular disease, coronary artery disease, and cerebrovascular disease. Fructus Psoraleae (bu-gu-zhi in China) has the therapeutic potential towards coronary artery disease. The present study aims to determine the inhibition of Fructus Psoraleae's compounds towards human carboxyl esterase 1 (CES1)-catalyzed metabolic inactivation pathway of clopidogrel. Neobavaisoflavone, corylifolinin, and coryfolin (100 FM) was utilized to screen the inhibition towards human liver microsomes (BILMs)-catalyzed hydrolysis metabolism of clopidogrel, and the results showed all the tested compounds exhibited significant inhibition towards hydrolysis metabolism of clopidogrel. Concentration -dependent inhibition behavior was furtherly found. Therefore, the co -administration of Fructus Psoraleae might increase the therapeutic function of clopidogrel through inhibiting the inactivation metabolic reaction of clopidogrel.
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页码:830 / 833
页数:4
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