首页> 外文期刊>The American journal of Chinese medicine >Study on Integrated Pharmacokinetics of Gardenia Acid and Geniposide: Time-Antioxidant Efficacy after Oral Administration of Huanglian-Zhizi Couplet Medicine from Huang-Lian-Jie-Du-Tang in MCAO Rats
【24h】

Study on Integrated Pharmacokinetics of Gardenia Acid and Geniposide: Time-Antioxidant Efficacy after Oral Administration of Huanglian-Zhizi Couplet Medicine from Huang-Lian-Jie-Du-Tang in MCAO Rats

机译:of子酸和Gen子苷的整体药代动力学研究:黄连解毒汤配黄连智联口服液对MCAO大鼠的时效抗氧化作用

获取原文
获取原文并翻译 | 示例
           

摘要

Huanglian-Zhizi couplet medicine comes from classical prescription Huang-Lian-Jie-Du-Tang (HLJDT), which has been proven by previous researches to be an effective compound for cerebral ischemia. This paper explores the integrated pharmacokinetics of gardenia acid and geniposide-time-antioxidant efficacy after the oral administration of Huanglian-Zhizi couplet medicine from HLJDT in rats with middle cerebral artery occlusion (MCAO). To investigate the differences in pharmacokinetics and antioxidant effect of Huanglian-Zhizi and HLJDT in MCAO rats, which have been scarcely reported, an oral dose, 24 crud drug g/kg, of Huanglian-Zhizi and 40 crud drug/kg of HLJDT were administered in two groups of normal rats and two groups of Sprague-Dawley (SD) MCAO rats, respectively. At different time points, concentrations of gardenia acid and geniposide were determined by high performance liquid chromatography (HPLC), and levels of superoxide dismutase (SOD) were calculated by ELIASA. Pharmacokinetic parameters including AUC, MRT, t(1/2), T-max, C-max were estimated by statistical moment analysis using a data analysis system (DAS) 2.0. An AUC based on weighting approach was used for integrating gardenia acid and geniposide. Finally, the concentration-time efficacy profiles were obtained. The integrated pharmacokinetics profiles of index components could reveal the pharmacokinetics behavior of Huanglian-Zhizi and HLJDT, corresponding to the antioxidant efficacy.
机译:黄连智联对联药源于经典处方黄连解毒汤(HLJDT),经先前的研究已证明是有效的脑缺血药物。本文探讨了HLJDT口服黄连至hi子联对大鼠大脑中动脉闭塞(MCAO)后of子酸和子苷-时间-抗氧化剂的综合药代动力学。为了研究很少报道的MCAO大鼠中黄连芝子和HLJDT的药代动力学和抗氧化作用的差异,口服黄连芝子24克/千克和HLJDT 40克/千克分别是两组正常大鼠和两组Sprague-Dawley(SD)MCAO大鼠。在不同时间点,通过高效液相色谱(HPLC)测定determined子酸和子苷的浓度,并通过ELIASA计算超氧化物歧化酶(SOD)的水平。使用数据分析系统(DAS)2.0通过统计矩分析来估算包括AUC,MRT,t(1/2),T-max,C-max在内的药代动力学参数。使用基于加权方法的AUC来整合garden子酸和gen子苷。最后,获得了浓度-时间功效曲线。指标成分的综合药代动力学特征可以揭示黄连芝子和HLJDT的药代动力学行为,与抗氧化功效相对应。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号