硼酸对中国仓鼠肺成纤维细胞V79氧化性DNA损伤的保护作用

Sezen Yılmaz, A. Ustundag, Ozge Cemiloglu Ulker, Y. Duydu
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引用次数: 18

摘要

目的研究硼酸(BA)和硼酸钠的体外抗氧化作用。然而,由于缺乏全面的流行病学研究,在这些体外研究中测试的硼(B)浓度没有考虑到人类血液中实际的硼浓度来选择。最近发表的在中国和土耳其进行的关于B族暴露的流行病学研究提供了日常生活中人类和职业环境中极端暴露条件下工人的血液B族浓度。这些研究结果使得在与人体相关的浓度范围内进行BA抗氧化作用的体外研究成为可能。本研究旨在探讨BA对中国仓鼠肺成纤维细胞(V79) DNA氧化损伤的保护作用。检测BA保护作用的浓度是根据先前发表的流行病学研究报告的血B浓度来选择的。因此,本研究中检测的BA浓度代表了人类在日常生活和职业环境中的暴露水平。材料与方法本实验采用彗星法和中性红吸收(NRU)法测定BA和过氧化氢(H2O2)的毒性和遗传毒性。结果NRU实验结果显示,BA在3、10、30、100和200µM浓度下均无细胞毒性。这些非细胞毒性浓度用于彗星试验。BA预处理显著降低了各BA浓度下H2O2对V79细胞的DNA损伤能力(P<0.05,单因素方差分析)。结论BA预孵育V79细胞可显著降低h2o2诱导的V79细胞DNA氧化损伤。体外实验证实了BA在5、10、50、100和200 μM(54、108、540、1080和2161 ng/ml B当量)浓度下对V79细胞DNA氧化损伤的保护作用。
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Protective Effect of Boric Acid on Oxidative DNA Damage In Chinese Hamster Lung Fibroblast V79 Cell Lines
Objective Many studies have been published on the antioxidative effects of boric acid (BA) and sodium borates in in vitro studies. However, the boron (B) concentrations tested in these in vitro studies have not been selected by taking into account the realistic blood B concentrations in humans due to the lack of comprehensive epidemiological studies. The recently published epidemiological studies on B exposure conducted in China and Turkey provided blood B concentrations for both humans in daily life and workers under extreme exposure conditions in occupational setting. The results of these studies have made it possible to test antioxidative effects of BA in in vitro studies within the concentra- tion range relevant to humans. The aim of this study was to investigate the protective ef- fects of BA against oxidative DNA damage in V79 (Chinese hamster lung fibroblast) cells. The concentrations of BA tested for its protective effect was selected by taking the blood B concentrations into account reported in previously published epidemiological studies. Therefore, the concentrations of BA tested in this study represent the exposure levels for humans in both daily life and occupational settings. Materials and Methods In this experimental study, comet assay and neutral red uptake (NRU) assay methods were used to determinacy to toxicity and genotoxicity of BA and hydrogen peroxide (H2O2). Results The results of the NRU assay showed that BA was not cytotoxic within the tested concentrations (3, 10, 30, 100 and 200 µM). These non-cytotoxic concentrations were used for comet assay. BA pre-treatment significantly reduced (P<0.05, one-way ANOVA) the DNA damaging capacity of H2O2 at each tested BA concentrations in V79 cells. Conclusion Consequently, pre-incubation of V79 cells with BA has significantly reduced the H2O2-induced oxidative DNA damage in V79 cells. The protective effect of BA against oxidative DNA damage in V79 cells at 5, 10, 50, 100 and 200 μM (54, 108, 540, 1080, and 2161 ng/ml B equivalents) concentrations was proved in this in vitro study.
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