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首页> 外文期刊>Journal of pharmacology & toxicology. >Assessment of Tonica, an Aqueous Herbal Haematinic, in the Modulation of Rat Hepatic Microsomal CYP-Mediated Drug Metabolizing Enzymes: Implications for Drug Interactions
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Assessment of Tonica, an Aqueous Herbal Haematinic, in the Modulation of Rat Hepatic Microsomal CYP-Mediated Drug Metabolizing Enzymes: Implications for Drug Interactions

机译:托尼卡,一种水性草药血红素,在大鼠肝微粒体CYP介导的药物代谢酶的调制中的评估:药物相互作用的影响。

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摘要

The effects of Tonica (TN), an herbal haematinic prepared from the stem barks of Khaya senegalensis, Mitragyna stipulosa and Kigelia africana, on the activities of hepatic microsomal cytochrome P450 (CYP) enzymes were investigated in Sprague-Dawley rats. TN was administered to rats, by oral gavage, at the normal human dose (28 mg/kg/day), l0x and 20x that dose for 6 weeks. Activities of certain hepatic CYP drug-metabolizing enzymes and pentobarbital-induced sleeping time were determined in control and TN-treated animals. There were insignificant (p>0.05) increases in the microsomal protein content (3.25-31 %) at all doses of TN in a non-dose-dependent fashion. However, there was a general insignificant attenuation of NADPH cytochrome c (P_450) reductase activity in TN-treated animals compared to control (8.9-26.1%). p-Nitrophenol hydroxylase (pNPH) activity was insignificantly (p>0.05) elevated (14.8-23%) in the TN-treated rats compared to control.
机译:在Sprague-Dawley大鼠中,研究了从塞内加尔海藻,米特拉草和非洲奇异果的茎皮制备的草药哈米替尼Tonica(TN)对肝微粒体细胞色素P450(CYP)酶活性的影响。通过正常人口剂量(28 mg / kg /天),10倍和20倍于该剂量的TN,通过口管法将TN给予大鼠。在对照组和经TN处理的动物中确定了某些肝CYP药物代谢酶的活性和戊巴比妥诱导的睡眠时间。在所有剂量的TN处,微粒体蛋白质含量(3.25-31%)均以非剂量依赖性方式增加(p> 0.05),无统计学意义。但是,与对照组相比,TN处理的动物中NADPH细胞色素c(P_450)还原酶的活性一般没有明显的减弱(8.9-26.1%)。与对照组相比,在用TN处理的大鼠中,对硝基苯酚羟化酶(pNPH)活性微不足道(p> 0.05)升高(14.8-23%)。

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