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灯盏花素对大鼠氯吡格雷代谢及药代动力学的影响。

Effect of scutellarin on the metabolism and pharmacokinetics of clopidogrel in rats.

作者信息

Chen Xinmeng, Jin Jing, Chen Yaobin, Peng Lingling, Zhong Guoping, Li Jiali, Bi Huichang, Cai Yefeng, Huang Min

机构信息

School of Pharmaceutical Science, Sun Yat-sen University, Guangzhou, 510006, PR China.

出版信息

Biopharm Drug Dispos. 2015 Jan;36(1):64-8. doi: 10.1002/bdd.1918. Epub 2014 Oct 22.

Abstract

Erigeron breviscapus (Vant.) Hand-Mazz, a traditional Chinese medicine, is often co-prescribed with clopidogrel for the treatment of ischemic vascular diseases. Scutellarin is the representative bioactive flavonoid isolated from this herb. The aim of this study was to explore the effect of scutellarin on the metabolism and pharmacokinetics of clopidogrel. The in vitro studies using rat liver microsomes showed that scutellarin significantly inhibited the metabolism of clopidogrel. The IC50 value was 2.1 µM. Ten male rats were employed to investigate the effect of scutellarin on the pharmacokinetics of clopidogrel in vivo. After pretreatment with scutellarin, there were significant increases in the AUC0-∞ (from 0.9 ± 0.4 to 1.7 ± 0.6 ng/ml h; p <0.05) and Cmax (from 0.4 ± 0.1 to 0.9 ± 0.1 ng/ml; p <0.05) of clopidogrel. The pharmacokinetic data for clopidogrel active metabolite showed significant decreases in AUC0-∞ (18.2 ± 5.6 to 11.4 ± 3.7 ng/ml h; p <0.05) and Cmax (from 8.2 ± 1.2 to 4.3 ± 0.3 ng/ml; p <0.05) after pretreatment with scutellarin. Collectively, the metabolism and pharmacokinetics of clopidogrel were significantly affected by scutellarin. This study indicated that potential herb-drug interaction between scutellarin and clopidogrel should be taken into consideration in clinical use.

摘要

灯盏细辛,一种传统中药,常与氯吡格雷联合用于治疗缺血性血管疾病。灯盏花素是从这种草药中分离出的具有代表性的生物活性黄酮类化合物。本研究的目的是探讨灯盏花素对氯吡格雷代谢和药代动力学的影响。使用大鼠肝微粒体的体外研究表明,灯盏花素显著抑制氯吡格雷的代谢。IC50值为2.1μM。选用10只雄性大鼠研究灯盏花素对氯吡格雷体内药代动力学的影响。灯盏花素预处理后,氯吡格雷的AUC0-∞(从0.9±0.4增加到1.7±0.6 ng/ml·h;p<0.05)和Cmax(从0.4±0.1增加到0.9±0.1 ng/ml;p<0.05)显著增加。氯吡格雷活性代谢物的药代动力学数据显示,灯盏花素预处理后,AUC0-∞(从18.2±5.6降至11.4±3.7 ng/ml·h;p<0.05)和Cmax(从8.2±1.2降至4.3±0.3 ng/ml;p<0.05)显著降低。总体而言,灯盏花素显著影响氯吡格雷的代谢和药代动力学。本研究表明,在临床应用中应考虑灯盏花素与氯吡格雷之间潜在的药物相互作用。

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