Ueno Shunji, Kashimoto Takashige, Susa Nobuyuki, Shiho Kensuke, Seki Takashi, Ito Nobuhiko, Takeda-Homma Shino, Nishimura Yoshikazu, Sugiyama Masayasu
Laboratory of Veterinary Public Health, School of Veterinary Medicine, Kitasato University, Higashi 23-35-1, Towada, Japan.
Free Radic Res. 2007 Nov;41(11):1246-52. doi: 10.1080/10715760701644019.
Hydroxyl radical (*OH) generation in the kidney of mice treated with ferric nitrilotriacetate (Fe-NTA) or potassium bromate (KBrO3) in vivo was estimated by the salicylate hydroxylation method, using the optimal experimental conditions we recently reported. Induction of DNA lesions and lipid peroxidation in the kidney by these nephrotoxic compounds was also examined. The salicylate hydroxylation method revealed significant increases in the *OH generation after injection of Fe-NTA or KBrO3 in the kidneys. A significant increase in 8-hydroxy-2'-deoxyguanosine in nuclei of the kidney was detected only in the KBrO3 treated mice, while the comet assay showed that the Fe-NTA and KBrO3 treatments both resulted in significant increases in DNA breakage in the kidney. With respect to lipid peroxidation, the Fe-NTA treatment enhanced lipid peroxidation and ESR signals of the alkylperoxy radical adduct. These DNA breaks and lipid peroxidation mediated by *OH were diminished by pre-treatment with salicylate in vivo. These results clearly demonstrated the usefulness of the salicylate hydroxylation method as well as the comet assay in estimating the involvement of *OH generation in cellular injury induced by chemicals in vivo.
采用我们最近报道的最佳实验条件,通过水杨酸羟化法评估了体内经次氮基三乙酸铁(Fe-NTA)或溴酸钾(KBrO₃)处理的小鼠肾脏中羟基自由基(OH)的生成情况。还检测了这些肾毒性化合物对肾脏中DNA损伤和脂质过氧化的诱导作用。水杨酸羟化法显示,在肾脏中注射Fe-NTA或KBrO₃后,OH生成显著增加。仅在经KBrO₃处理的小鼠肾脏细胞核中检测到8-羟基-2'-脱氧鸟苷显著增加,而彗星试验表明,Fe-NTA和KBrO₃处理均导致肾脏中DNA断裂显著增加。关于脂质过氧化,Fe-NTA处理增强了脂质过氧化和烷基过氧自由基加合物的ESR信号。体内预先用水杨酸处理可减少由OH介导的这些DNA断裂和脂质过氧化。这些结果清楚地证明了水杨酸羟化法以及彗星试验在评估OH生成参与体内化学物质诱导的细胞损伤方面的有用性。