Palladium or platinum exacerbates hydroxyl radical mediated DNA damage

Tsan Z. Liu, Ting F. Lin, Daniel T.Y. Chiu, Kan J. Tsai, Arnold Stern*

*此作品的通信作者

研究成果: 期刊稿件文章同行評審

40 引文 斯高帕斯(Scopus)

摘要

Strand breakage of supercoiled pBR322 DNA by a Fenton system is increased in the presence of palladium (Pd) or platinum (Pt) ions. Neither Pd nor Pt ions can substitute for iron in the Fenton system. We have obtained several lines of evidence that Pd and Pt ions in the presence of a Fenton system can augment the production of OH(·), as monitored by a spectrophotometric method quantifying hydroxylated salicylate or by a fluorometric method quantifying catechol production. Furthermore, the promoting effect of both metal ions on OH(·) production was substantiated by the identification of multiple hydroxylated products of salicylate [2,3- dihydroxybenzoate (A). 2,5-dihydroxybenzoate (B), and catechol (C)] using HPLC. The concentrations of A, B, and C produced in the control were 4.5, 8.0, and 2.0 μM, respectively; whereas, their respective concentrations increased to 23.6, 42.0, and 10.0 μM with the addition of Pd ions. The observed phenomenon was further confirmed by the identification of HO-DMPO spin adducts using ESR spectroscopy. Taken together, our data suggest that the mechanism of Pd or Pt ion-mediated exacerbation of DNA damage by a Fenton system is due to the promotion of OH(·) production by these metal ions.

原文英語
頁(從 - 到)155-161
頁數7
期刊Free Radical Biology and Medicine
23
發行號1
DOIs
出版狀態已出版 - 1997
對外發佈

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