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2,3,7,8-四氯二苯并对二恶英(TCDD)诱导大鼠肝脏DNA单链断裂

Induction of hepatic DNA single strand breaks in rats by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD).

作者信息

Wahba Z Z, Lawson T A, Stohs S J

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center, Omaha 68105-1065.

出版信息

Cancer Lett. 1988 Apr;39(3):281-6. doi: 10.1016/0304-3835(88)90071-7.

Abstract

Previous studies have demonstrated that 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) induces lipid peroxidation in hepatic and extrahepatic tissues. DNA single strand breaks as well as other forms of DNA damage are believed to occur in conjunction with lipid peroxidation. We have therefore examined the effect of TCDD on hepatic DNA single strand breaks. Ten days after the administration of 100 micrograms TCDD/kg to female rats, a 7.5-fold increase in the DNA elution constant (single strand breaks) occurred. Similar changes were observed in the content of thiobarbituric acid reactive substances (TBARS) in the nuclei as well as the NADPH-dependent production of TBARS. The accumulation of TBARS appeared to precede the accumulation of DNA single strand breaks. The tumor promoting effects of TCDD may be associated with the enhanced formation of DNA single strand breaks.

摘要

先前的研究表明,2,3,7,8-四氯二苯并对二恶英(TCDD)可诱导肝组织和肝外组织中的脂质过氧化。DNA单链断裂以及其他形式的DNA损伤被认为与脂质过氧化同时发生。因此,我们研究了TCDD对肝脏DNA单链断裂的影响。给雌性大鼠腹腔注射100微克TCDD/千克,10天后,DNA洗脱常数(单链断裂)增加了7.5倍。在细胞核中硫代巴比妥酸反应性物质(TBARS)的含量以及NADPH依赖的TBARS生成中也观察到了类似的变化。TBARS的积累似乎先于DNA单链断裂的积累。TCDD的促肿瘤作用可能与DNA单链断裂的形成增加有关。

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