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作 者:王英杰[1] 沈智杰[1] 王肖龙[1] 毛玉昌 郭蔚[1] 胡卓汉
机构地区:[1]上海中医药大学附属曙光医院心血管科,上海市中医临床实验室,201203 [2]瑞德肝脏疾病研究(上海)有限公司,上海201203
出 处:《国际心血管病杂志》2013年第6期376-378,共3页International Journal of Cardiovascular Disease
基 金:上海市教育委员会科研基金(2010JW44);上海市中医药事业发展三年行动计划项目(zysnxd-cc-yjxyy);上海市自然科学基金(13ZR1462100)
摘 要:目的:在体外基于细胞色素(CYP450)酶系研究健脾化浊方对阿托伐他汀代谢的影响。方法:首先将健脾化浊方与人肝微粒体预孵育15 min后,加入CYP3A4的底物睾酮及还原型辅酶烟酰胺腺嘌呤二核苷酸,于37℃共同孵育30 min,之后加入0.5 ml预冷的甲醇终止反应,取等量上清于高效液相质谱分析仪上检测6β-羟基睾酮的生成,确立体外肝微粒体中健脾泄浊方对CYP3A4酶的作用。再将稀释好的健脾化浊方及人肝微粒体加入96深孔板中,然后加入阿托伐他汀,对照组中则加入阴性对照物,取上清用于液相色谱/质谱/质谱分析。结果:健脾化浊方对肝药酶CYP3A4有较强的抑制作用(IC50=10.5),并且能延缓阿托伐他汀在肝细胞微粒体内的代谢,使其药物浓度显著提高(P<0.01)。结论:体外健脾化浊方通过对CYP3A4酶的抑制作用而影响了阿托伐他汀的代谢,中药和西药联用存在着药物相互作用。Objective:To evaluate the effect of tonifying spleen and eliminating turbidity decoction (TSET) on atorvastatin metabolism based on CYP450 enzyme in vitro. Methods: Firstly, different concentrations of TSET were co-incubated with liver microsomes for 15 min at 37℃, then testosterone, the substrate of CYP3A4, and NADPH was added to incubate for another 30 min at 37℃. The reaction was terminated with pre-cooled 0.5 ml methanol, and then 6β-hydroxyl testosterone in the supernatant was measured by high performance liquid chromatography-mass spectrometry technology (HPLC-MS). Secondly, atorvastatin was incubated with or without TSET and liver microsomes, and concentration of atorvastatin in supernatant was determined by HPLC-MS at a series of time points. Results:With the increase of TSET concentration, the activity of liver metabolizing enzyme CYP3A4 in liver microsomes was significantly inhibited (IC50 = 10.5). TSET significantly increased the concentration of atorvastatin when incubated together with liver microsomes (P〈0.01). Conclusion:TSET reduces the metabolism of atorvastatin in liver microsomes possibly through inhibiting the activity of CYP3A4. TSET and atorvastatin may have remarkable synergy effect.
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