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首页> 外文期刊>Journal of Traditional and Complementary Medicine >Effect of Coleus forskohlii and its major constituents on cytochrome P450 induction
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Effect of Coleus forskohlii and its major constituents on cytochrome P450 induction

机译:卵石孢子素及其主要成分对细胞色素P450诱导的影响

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Coleus forskohlii Briq. has been used traditionally for the treatment of several ailments since antiquity in Ayurveda. In the present study, an approach has been made to evaluate the effect of C.?forskohlii and its major constituents on cytochrome P450 (CYP3A, CYP2B, and CYP2C) mRNA expression in rat hepatocytes. To gain better understanding of the herb–drug interaction potential of the chemical constituents present in C.?forskohlii , the extract was subjected to column chromatography followed by standardization with respect to forskolin, 1-deoxyforskolin, and 1,9-dideoxyforskolin using reversed-phase high-performance liquid chromatography (RP-HPLC). Hepatocytes were treated with extracts, fractions, and phytoconstituents, followed by extraction and purification of total mRNA. Study of mRNA expression was carried out through reverse transcription polymerase chain reaction, followed by agarose gel electrophoresis. Results revealed that the test substances did not show any significant mRNA expression compared to the control against CYP3A, CYP2B, and CYP2C. Positive controls such as dexamethasone and rifampin showed significantly high ( p ??0.001) induction potential compared to the control. It can be concluded that C.?forskohlii and its major constituents may not be involved in CYP450 induction-based drug interaction. Graphical abstract Display Omitted.
机译:柯伊斯福斯克荔枝Briq。由于Ayurveda的古代以来,传统上用于治疗几种疾病。在本研究中,已经进行了一种方法来评估C.Forskohlii及其主要成分对大鼠肝细胞中细胞色素P450(CYP3A,CYP2B和CYP2C)mRNA表达的影响。为了更好地了解C.?forskohlii中存在的化学成分的草药 - 药物相互作用电位,将提取物进行柱色谱,然后相对于Forskolin,1-脱氧芬科林和1,9-二赤氧基芬科林的标准化,使用反转 - 相高效液相色谱(RP-HPLC)。用萃取物,级分和植物试剂处理肝细胞,然后萃取和纯化总mRNA。通过逆转录聚合酶链反应进行mRNA表达的研究,然后进行琼脂糖凝胶电泳进行。结果表明,与对CYP3A,CYP2B和CYP2C的对照相比,测试物质没有显示出任何显着的mRNA表达。与对照相比,诸如地塞米松和利福平的阳性对照显着高(P?<0.001)诱导潜力。可以得出结论,C.?FORSKOHLII及其主要成分可能不参与CYP450基于诱导的药物相互作用。省略了图形抽象显示。

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