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纳米锐钛矿型TiO₂与小鼠肝脏DNA在体内的相互作用

Interaction Between Nano-Anatase TiO(2) and Liver DNA from Mice In Vivo.

作者信息

Li Na, Ma Linglan, Wang Jue, Zheng Lei, Liu Jie, Duan Yanmei, Liu Huiting, Zhao Xiaoyang, Wang Sisi, Wang Han, Hong Fashui, Xie Yaning

出版信息

Nanoscale Res Lett. 2009 Oct 13;5(1):108-115. doi: 10.1007/s11671-009-9451-2.

Abstract

Nano-TiO(2) was shown to cause various toxic effects in both rats and mice; however, the molecular mechanism by which TiO(2) exerts its toxicity is poorly understood. In this report, an interaction of nano-anatase TiO(2) with liver DNA from ICR mice was systematically studied in vivo using ICP-MS, various spectral methods and gel electrophoresis. We found that the liver weights of the mice treated with higher amounts of nano-anatase TiO(2) were significantly increased. Nano-anatase TiO(2) could be accumulated in liver DNA by inserting itself into DNA base pairs or binding to DNA nucleotide that bound with three oxygen or nitrogen atoms and two phosphorous atoms of DNA with the Ti-O(N) and Ti-P bond lengths of 1.87 and 2.38 A, respectively, and alter the conformation of DNA. And gel electrophoresis showed that higher dose of nano-anatase TiO(2) could cause liver DNA cleavage in mice.

摘要

纳米二氧化钛(TiO₂)已被证明会对大鼠和小鼠产生多种毒性作用;然而,TiO₂发挥其毒性的分子机制却知之甚少。在本报告中,使用电感耦合等离子体质谱法(ICP-MS)、各种光谱方法和凝胶电泳,在体内系统地研究了纳米锐钛矿型TiO₂与ICR小鼠肝脏DNA的相互作用。我们发现,用较高剂量纳米锐钛矿型TiO₂处理的小鼠肝脏重量显著增加。纳米锐钛矿型TiO₂可通过插入DNA碱基对或与与DNA的三个氧或氮原子及两个磷原子结合的DNA核苷酸结合,以Ti-O(N)和Ti-P键长分别为1.87和2.38埃的方式积累在肝脏DNA中,并改变DNA的构象。凝胶电泳显示,较高剂量的纳米锐钛矿型TiO₂可导致小鼠肝脏DNA断裂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab75/3238503/8232f3f4d0c9/1556-276X-5-108-1.jpg

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