Nickel Increases Chromosomal Abnormalities by Interfering With the Initiation of DNA Repair Pathways

Q4 Pharmacology, Toxicology and Pharmaceutics
M. Ghorbani, F. Haddad, K. Shahrokhabadi
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引用次数: 0

Abstract

Background: Nickel is a carcinogenic, heavy metal released through industrial activities and via natural resources. It is able to cause DNA damages by reducing the efficiency of DNA repair mechanisms. However, the exact time point at which it is able to interfere with these mechanisms is not yet clearly understood. Methods: To find the most nickel-vulnerable time of repair mechanisms, human dermal fibroblasts (HDF) were treated with three doses of nickel before and after X-irradiation. The induced frequency of chromosomal abnormality was studied using micronucleus assay in binucleated cells. The cytotoxicity of different treatments was established using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Results: The results revealed that nickel treatment had a synergistic effect on inducing Micronucleus frequency only when cells were treated 2 hours before X-irradiation. The X-ray treatment of the cells with 5 and 10 mM nickel had a cytotoxic effect mainly when given 6 hours after the irradiation. Conclusion: The results suggest that nickel can interfere with human DNA repair mechanisms only at the start of the process, while having no significant effect on the human DNA repair mechanisms when activated.
镍通过干扰DNA修复途径的启动增加染色体异常
背景:镍是一种致癌的重金属,通过工业活动和自然资源释放。它能够通过降低DNA修复机制的效率来引起DNA损伤。然而,它能够干扰这些机制的确切时间点尚不清楚。方法:在X射线照射前后,用三种剂量的镍处理人真皮成纤维细胞(HDF),以寻找镍最易损伤的修复机制。用微核法研究了双核细胞诱发染色体异常的频率。采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑(MTT)法测定不同处理的细胞毒性。结果:只有在X射线照射前2小时对细胞进行处理时,镍处理才对诱导微核频率具有协同作用。用5mM和10mM镍对细胞的X射线处理主要在照射后6小时给予时具有细胞毒性作用。结论:研究结果表明,镍仅在人体DNA修复过程开始时才对人体DNA修复机制产生干扰,而激活后对人体DNA的修复机制没有显著影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Iranian Journal of Toxicology
Iranian Journal of Toxicology Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
1.60
自引率
0.00%
发文量
24
审稿时长
9 weeks
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