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化痰通络方对急性脑梗死大鼠rt-PA溶栓后MMP-9转录活化途径中AP-1与NF-κB基因表达的影响
引用本文:周震,张玉莲,张琳琳,韩文文,宋宛珊,王凯.化痰通络方对急性脑梗死大鼠rt-PA溶栓后MMP-9转录活化途径中AP-1与NF-κB基因表达的影响[J].中国实验方剂学杂志,2014,20(12):122-126.
作者姓名:周震  张玉莲  张琳琳  韩文文  宋宛珊  王凯
作者单位:中山大学药学院, 广州 510006;珠海联邦制药股份有限公司, 广东 珠海 519041;中山大学药学院, 广州 510006;中山大学药学院, 广州 510006;中山大学药学院, 广州 510006;中山大学药学院, 广州 510006;广州中医院大学中药学院, 广州 510006;广州中医院大学中药学院, 广州 510006;中山大学药学院, 广州 510006
基金项目:国家自然科学基金面上项目(81173564,81274028);中山大学青年教师培育项目(2010060)
摘    要:目的:研究天然冰片对雄性SD大鼠口服尼莫地平药代动力学的影响。方法:大鼠随机分为3组:对照组、天然冰片临床等效剂量组(90 mg·kg-1)及高剂量组(270 mg·kg-1),在灌胃给予空白溶媒或天然冰片后各组均口服尼莫地平20 mg·kg-1,于给药前和给药后不同时间点取血,样品处理后用液相色谱-串联质谱(LC-MS-MS)法测定尼莫地平含量,采用WinNonlin 5.0.1计算药代动力学参数。结果:临床等效剂量的天然冰片对尼莫地平口服吸收无显著影响,高剂量天然冰片使血浆中尼莫地平的浓度-时间曲线下面积(AUC)增大,但与对照组间的差异无统计学意义。结论:高剂量天然冰片可轻微促进尼莫地平的口服吸收,但影响较小。

关 键 词:天然冰片  尼莫地平  药代动力学
收稿时间:2013/11/16 0:00:00

Effect of Natural Borneol on Pharmacokinetics of Nimodipine in Rats after Oral Administration
ZHOU Zhen,ZHANG Yu-lian,ZHANG Lin-lin,HAN Wen-wen,SONG Wan-shan and WANG Kai.Effect of Natural Borneol on Pharmacokinetics of Nimodipine in Rats after Oral Administration[J].China Journal of Experimental Traditional Medical Formulae,2014,20(12):122-126.
Authors:ZHOU Zhen  ZHANG Yu-lian  ZHANG Lin-lin  HAN Wen-wen  SONG Wan-shan and WANG Kai
Institution:School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China;Zhuhai United Laboratories Co. Ltd, Zhuhai 519041, China;School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China;School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China;School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China;School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China;School of Chinese Materia Medica, Guangzhou University of Chinese Medicine, Guangzhou 510006, China;School of Chinese Materia Medica, Guangzhou University of Chinese Medicine, Guangzhou 510006, China;School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China
Abstract:Objective: To study the effects of natural borneol (NB) on the pharmacokinetics of nimodipine in rats after oral administration. Method: The rats were randomly divided into three groups, control group, clinically-equivalent-dose group and higher-dose group, and were gavaged with NB at doses of 0, 90, 270 mg·kg-1, respectively. After 10 min, all rats were gavaged with nimodipine at a dose of 20 mg·kg-1. The blood was obtained at different time points before and after the administration. Concentrations of nimodipine in plasma were determined by LC-MS-MS and the main pharmacokinetic parameters were calculated by WinNonlin 5.0.1. Result: Clinically equivalent dose of NB showed little influence on the pharmacokinetics of nimodipine. The mean value of AUC in higher-dose group was slightly higher than that in control group, but no significant differences were found between two groups. Conclusion: The results suggested that higher dose of NB may enhance the absorption of nimodipine in rats, but the enhancing effect is not very obvious.
Keywords:natural borneol  nimodipine  pharmacokinetics
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