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首页> 外文期刊>Journal of Ethnopharmacology: An Interdisciplinary Journal Devoted to Bioscientific Research on Indigenous Drugs >Evaluation of protective effects of Chi-Zhi-Huang decoction on Phase I drug metabolism of liver injured rats by cocktail probe drugs.
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Evaluation of protective effects of Chi-Zhi-Huang decoction on Phase I drug metabolism of liver injured rats by cocktail probe drugs.

机译:鸡尾酒探针药物评价赤芝黄汤对肝损伤大鼠Ⅰ期药物代谢的保护作用。

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摘要

AIM OF THE STUDY: Chi-Zhi-Huang decoction (PGR) is one of the traditional Chinese medicine (TCM) preparations with unique effect on withdrawing jaundice and has been used to treat icteric patients in China for many years. In this research, we aim at to evaluate the potential activity of PGR in restoring hepatic drug metabolism in a damaged liver. MATERIALS AND METHODS: A cocktail approach with caffeine (10mg/kg), dapsone (10mg/kg) and chlorzoxazone (20mg/kg) respectively as probe drug of cytochrome P450 (CYP) isoform of CYP 1A2, 3A4 and 2E1 was used to evaluate its possible effects on Phase I oxidative metabolism. Pretreated with three dosages of PGR water extract (0.75, 1.5 and 3g/kg, po) for 5 days, male Wistar rats (220-240 g) were intoxicated by phenylisothiocyanate (PITC, 100mg/kg, po) 24h before probes intravenous injection. The pharmacokinetics of the probes in the blood was determined simultaneously by HPLC, and their non-compartmental parameters were used to evaluate the metabolic difference among the groups. Moreover, the levels of liver enzymes (ALT, AST, ALP) and bilirubins were also measured for insight of liver function. RESULTS: The findings in this study suggest that PGR induces CYP 3A4, does not have much effect on CYP 2E1, and inhibits CYP 1A2 at high dosage. CONCLUSION: The current pharmacokinetic approach allowed the protective effects of PGR on oxidative drug metabolism in damaged liver to be systemically examined and will certainly help in the explanation of synergistic effect of the composites formula.
机译:研究目的:赤芝黄汤(PGR)是一种对中风性黄疸有独特疗效的中药制剂,在中国已被用于治疗黄疸患者多年。在这项研究中,我们旨在评估PGR在受损肝脏中恢复肝脏药物代谢的潜在活性。材料与方法:采用鸡尾酒法,分别以咖啡因(10mg / kg),氨苯砜(10mg / kg)和氯唑沙宗(20mg / kg)作为CYP 1A2、3A4和2E1的细胞色素P450(CYP)同工型的探测药物。它可能对一期氧化代谢产生影响。用三剂PGR水提取物(0.75、1.5和3g / kg,口服)预处理5天,雄性Wistar大鼠(220-240 g)在静脉内注射探针前24小时被异硫氰酸苯酯(PITC,100mg / kg,口服)中毒。通过HPLC同时测定探针在血液中的药代动力学,并将其非房室参数用于评估各组之间的代谢差异。此外,还测量了肝酶(ALT,AST,ALP)和胆红素的水平,以了解肝功能。结果:本研究结果提示PGR高剂量诱导CYP 3A4,对CYP 2E1影响不大,抑制CYP 1A2。结论:目前的药代动力学方法可以系统地检查PGR对受损肝脏中氧化药物代谢的保护作用,并且肯定有助于解释复合物配方的协同作用。

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