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DNA和RNA加合物形成的比较:在给予马兜铃酸的大鼠内脏中,RNA修饰水平显著高于DNA修饰水平。

Comparison of DNA and RNA Adduct Formation: Significantly Higher Levels of RNA than DNA Modifications in the Internal Organs of Aristolochic Acid-Dosed Rats.

作者信息

Leung Elvis M K, Chan Wan

出版信息

Chem Res Toxicol. 2015 Feb 16;28(2):248-55. doi: 10.1021/tx500423m.

DOI:10.1021/tx500423m
PMID:25555167
Abstract

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-deoxyguanosinein 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.

摘要

长期接触受马兜铃酸(AA)污染的减肥药和食品被认为与比利时女性以及生活在多瑙河沿岸的农民中地方性肾病的发生有关。数十年的研究揭示了AA致癌的病理生理学,但肾间质纤维化的分子机制仍不清楚。我们推测RNA修饰可能导致了所观察到的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-串联质谱法,用于定量给予AA的大鼠靶器官和非靶器官中的RNA-AA加合物。结果首次表明,AA在体外和体内均能形成RNA加合物。对DNA的比较研究表明,在给予AA的大鼠的肾脏和肝脏组织中,RNA被AA修饰的频率比DNA高约6倍。结果还表明,在给予AA的大鼠的两个器官中,鸟苷被AA修饰的频率显著高于腺苷、2-脱氧腺苷和2-脱氧鸟苷。这一发现表明鸟苷是AA的主要靶点,且AA的鸟苷加合物可能是AA诱导毒性病理生理学中的关键损伤。预计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技术定量RNA加合物,开辟一个研究肾毒性和/或致癌性的新领域。

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