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体内六价铬的还原及其相关自由基的产生。

In vivo reduction of chromium (VI) and its related free radical generation.

作者信息

Liu K J, Shi X

机构信息

College of Pharmacy, University of New Mexico, Albuquerque 87131, USA.

出版信息

Mol Cell Biochem. 2001 Jun;222(1-2):41-7.

Abstract

Chromium (VI) compounds are widely recognized as human carcinogens. Extensive studies in vitro and in model systems indicate that the reactive intermediate, Cr (V), generated by cellular reduction of Cr (VI), is likely the candidate for the ultimate carcinogenic form of chromium compounds. Here we review our current understanding of the in vivo reduction of Cr (VI) and its related free radical generation. Our results demonstrate that Cr (V) is indeed generated from the reduction of Cr (VI) in vivo, and that Cr (V) thus formed can mediate the generation of free radicals. Cr (V) and its related free radicals are very likely to be involved in the mechanism of Cr (VI)-induced toxicity and carcinogenesis. These studies also illustrate that in vivo EPR spectroscopy and magnetic resonance imaging can be very useful and powerful tools for studying paramagnetic metal ions in chemical and biochemical reactions occurring in intact animals.

摘要

六价铬化合物被广泛认为是人类致癌物。体外和模型系统中的大量研究表明,细胞将六价铬还原产生的反应性中间体五价铬,可能是铬化合物最终致癌形式的候选物。在此,我们综述了目前对六价铬体内还原及其相关自由基生成的理解。我们的结果表明,五价铬确实在体内由六价铬还原产生,并且这样形成的五价铬可以介导自由基的生成。五价铬及其相关自由基很可能参与六价铬诱导的毒性和致癌机制。这些研究还表明,体内电子顺磁共振光谱和磁共振成像对于研究完整动物体内发生的化学和生化反应中的顺磁性金属离子可能是非常有用和强大的工具。

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