Lack of DNA adduct formation in mice treated with benzene

M. Vijayaraj Reddy, Scott C. Schultz, G.R. Blackburn, Carl R. Mackerer
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引用次数: 24

Abstract

The potential of benzene to produce DNA adducts in B6C3F1 mice was investigated by the nuclease P1-enhanced 32P-postlabeling assay. The mice were daily treated i.p. with 500 mg/kg benzene in olive oil for 4 days, and the liver, mammary gland, and bone marrow were collected 24 h after the last treatment. Thin-layer chromatograms obtained with treated-tissue DNA specimens were qualitatively identical to those from corresponding olive oil-treated (control) tissue DNA. Quantitative evaluations revealed that there was no treatment-related increase in radioactivity on the chromatograms at or near the locations where the major in vitro adducts of phenol, hydroquinone and benzoquinone migrated. Benzene treatment, however, resulted in a decrease in the levels of certain endogenous adducts, the biological significance of which is unknown. Our results indicate that benzene treatment does not produce detectable levels of aromatic DNA adducts in mouse tissues.

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经苯处理的小鼠缺乏DNA加合物的形成
通过核酸酶p1增强32p标记后实验研究了苯在B6C3F1小鼠中产生DNA加合物的潜力。每天用橄榄油中500 mg/kg苯灌胃4 d,末次灌胃24 h后采集小鼠肝脏、乳腺、骨髓。用处理过的组织DNA标本获得的薄层色谱图与相应的橄榄油处理(对照)组织DNA的薄层色谱图在质量上相同。定量评价显示,在主要体外加合物苯酚、对苯二酚和苯醌迁移的位置或附近的色谱上,没有与处理相关的放射性增加。然而,苯处理导致某些内源性加合物水平下降,其生物学意义尚不清楚。我们的研究结果表明,苯处理不会在小鼠组织中产生可检测水平的芳香DNA加合物。
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