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首页> 外文期刊>Journal of biochemical and molecular toxicology >Biochanin A induction of sulfotransferases in rats.
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Biochanin A induction of sulfotransferases in rats.

机译:Biochanin A在大鼠中诱导磺基转移酶。

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Biochanin A (BCA) is a dietary isoflavone present in red clover (Trifoliumn pretense) and many herbal products. BCA has been reported to have chemopreventive actions against various cancers including prostate, breast, colon cancer, and so on. Sulfotransferases are a family of phase II drug-metabolizing enzymes, which are important for xenobiotic detoxification and regulation of biological signaling molecule biological activities. Sulfotransferase gene expressions are regulated by different hormones and xenobiotics. Improper regulation of sulfotransferases leads to improper functions of biological signaling molecules, which in turn can cause cancer or other diseases. BCA inhibits the enzyme activities of the phase I drug-metabolizing enzymes CYP1A1 and CYP1B1 in Chinese hamster ovary cells and induces the phase II drug-metabolizing enzymes UDP-glucuronosyltransferases in human prostate cancer cells. BCA induction of sulfotransferases has not been studied. This investigation evaluates the in vivo regulation of sulfotransferases at protein and mRNA levels in the liver and intestine of Sprague-Dawley rats treated with BCA (0, 2, 10, and 50 mg/kg/day) for 7 days. Our experimental results demonstrate for the first time that chronic BCA treatment can significantly induce the expression of rat sulfotransferase 1A1 (rSULT1A1, AST-IV), sulfotransferase 2A1 (rSULT2A1, STa), and rat estrogen sulfotransferase (rSULT1E1, EST) in rat liver and intestine. Our Western blot results are in good agreement with real-time RT-PCR data, suggesting that BCA induction of sulfotransferases occurs at the transcriptional level.
机译:Biochanin A(BCA)是存在于红三叶草(三叶草)和许多草药产品中的膳食异黄酮。据报道,BCA对多种癌症包括前列腺癌,乳腺癌,结肠癌等具有化学预防作用。磺基转移酶是II期药物代谢酶的一个家族,对于异生物质解毒和生物信号分子生物学活性的调节非常重要。磺基转移酶基因的表达受不同激素和异生物素的调节。磺基转移酶调节不当会导致生物信号分子功能异常,进而导致癌症或其他疾病。 BCA抑制中国仓鼠卵巢细胞中I相药物代谢酶CYP1A1和CYP1B1的酶活性,并诱导人前列腺癌细胞中II相药物代谢酶UDP-葡萄糖醛酸转移酶。尚未研究BCA诱导磺基转移酶。这项研究评估了磺胺转移酶在接受BCA(0、2、10和50 mg / kg / day)处理7天的Sprague-Dawley大鼠肝脏和肠中蛋白质和mRNA水平上的体内调节。我们的实验结果首次证明,慢性BCA治疗可以在大鼠肝脏和肝脏中显着诱导大鼠磺基转移酶1A1(rSULT1A1,AST-IV),磺基转移酶2A1(rSULT2A1,STa)和大鼠雌激素磺基转移酶(rSULT1E1,EST)的表达。肠。我们的蛋白质印迹结果与实时RT-PCR数据非常吻合,表明BCA诱导的磺基转移酶发生在转录水平。

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