芍药苷
CYP1A2
体内
CYP3A型
甲苯磺丁脲
药理学
药代动力学
细胞色素P450
非那西丁
化学
酶
生物化学
生物
内分泌学
高效液相色谱法
色谱法
生物技术
糖尿病
作者
Sicong Li,Xuting Li,Dingsheng Yuan,Bin Wang,Rui Yang,Min Zhang,Jinliang Li,Fuqiang Zeng
出处
期刊:Xenobiotica
[Informa]
日期:2017-11-21
卷期号:51 (9): 961-967
被引量:13
标识
DOI:10.1080/00498254.2017.1404659
摘要
Paeoniflorin is the major constituent in extracts of the paeony root, the purpose of the present study was to assess the effects of paeoniflorin on the activities and mRNA expression of the rat hepatic drug-metabolizing enzymes cytochrome P450 (CYP1A2), CYP2C11 and CYP3A1 in vivo.Sprague-Dawley (SD) male rats were treated with paeoniflorin at the dosage of 25, 50 and 100 mg/kg or 0.9% sodium chloride solution by intragastric administration for 7 days, then were given probe drugs phenacetin (CYP1A2), tolbutamide (CYP2C11), or midazolam (CYP3A1) orally on the eighth day. Blood samples were collected at various times, and the plasma concentrations of the probe drugs were estimated with ultra-high-performance liquid chromatography. The mRNA expression levels of rat hepatic CYP1A2, CYP2C11 and CYP3A1 were analysed with real-time PCR.The pharmacokinetic results indicated that paeoniflorin inhibits the activities of CYP1A2, CYP2C11 and CYP3A1 in vivo. The effect was most pronounced on CYP3A1, according to the United States Food and Drug Administration classification of inhibitors of CYP3A, it reached the category of moderate inhibition. The mRNA expression levels of 3 CYP enzymes were also tended to be inhibited.We conclude that paeoniflorin can inhibit the activities of CYP1A2, CYP2C11 and CYP3A1 in vivo, which may affect the metabolism of drugs that are primarily dependent on these pathways.
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