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首页> 外文期刊>Chemical research in toxicology >Comparison of DNA and RNA Adduct Formation: Significantly Higher Levels of RNA than DNA Modifications in the Internal Organs of Aristolochic Acid-Dosed Rats
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Comparison of DNA and RNA Adduct Formation: Significantly Higher Levels of RNA than DNA Modifications in the Internal Organs of Aristolochic Acid-Dosed Rats

机译:DNA和RNA加合物形成的比较:在马兜铃酸给药大鼠的内脏中,RNA的水平明显高于DNA修饰的水平

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Prolonged exposure to aristolochic acid (AA) contaminated slimming drugs and food is believed to be associated with the development of endemic nephropathy in Belgian women and in farmers living alongside the Danube River. Decades of research has revealed the pathophysiology of carcinogenesis of AA, and the molecular mechanisms underlying renal interstitial fibrosis remain unclear. We hypothesized that RNA modification may have contributed to the observed toxicity of AA. Thus, a highly sensitive and selective ultra-high performance liquid chromatography-coupled tandem mass spectrometric method was developed to quantify RNA-AA adducts in target and nontarget organs of AA-dosed rats. The results revealed, for the first time, that AA forms RNA adducts in vitro and in vivo. Comparative studies on DNA revealed that RNA is modified by AA at frequencies approximately 6-fold higher than that of DNA in both kidney and liver tissue in AA-dosed rats. Results also demonstrated that guanosine is modified by AA at frequencies significantly higher than that of adenosine, 2-deoxyadenosine, and 2-deoxyguanosine in both organs of the AA-dosed. This finding suggests that guanosine is a major target for AA and that guanosine adducts of AA might be critical lesions in the pathophysiology of AA-induced toxicity. It is anticipated that the results of our study may open up a new area of investigating the nephrotoxicity and/or carcinogenicity by quantifying RNA adducts using the UPLC-MS/MS technique of high sensitivity and selectivity.
机译:据信,长时间接触受马兜铃酸(AA)污染的减肥药和食品与比利时妇女和多瑙河沿岸农民的地方性肾病的发展有关。数十年的研究揭示了AA致癌的病理生理学,而肾间质纤维化的分子机制仍不清楚。我们假设RNA修饰可能有助于观察到的AA毒性。因此,开发了一种高灵敏度和选择性的超高效液相色谱-串联质谱联用方法,用于定量AA给药大鼠的靶器官和非靶器官中的RNA-AA加合物。结果首次显示,AA在体内和体外形成RNA加合物。 DNA的比较研究表明,AA给药的大鼠肾脏和肝脏组织中,AA修饰的RNA的频率大约是DNA的6倍。结果还表明,在AA给药的两个器官中,鸟嘌呤被AA修饰的频率显着高于腺苷,2-脱氧腺苷和2-脱氧鸟苷的频率。该发现表明鸟苷是AA的主要靶标,并且AA的鸟苷加合物可能是AA诱导的毒性的病理生理学中的关键病变。可以预期,我们的研究结果可能会通过使用高灵敏度和选择性的UPLC-MS / MS技术对RNA加合物进行定量,从而开辟一个新的领域来研究肾毒性和/或致癌性。

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