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暴露于苯并[a]芘的虹鳟肝细胞原代培养物中的DNA加合物形成及7-乙氧基异吩恶唑酮O-脱乙基酶诱导作用

DNA adduct formation and 7-ethoxyresorufin O-deethylase induction in primary culture of rainbow trout hepatocytes exposed to benzo[a]pyrene.

作者信息

Masfaraud J F, Devaux A, Pfohl-Leszkowicz A, Malaveille C, Monod G

机构信息

Laboratoire d'Ecotoxicologie, Institut National de la Recherche Agronomique, Ecole Vétérinaire de Lyon, BP 83, 69280 Marcy l'Etoile, France.

出版信息

Toxicol In Vitro. 1992 Nov;6(6):523-31. doi: 10.1016/0887-2333(92)90064-x.

Abstract

The formation of DNA adducts, using the (32)P-postlabelling assay, and induction of 7-ethoxyresorufin O-deethylase (EROD) were investigated in a primary culture of rainbow trout hepatocytes exposed to benzo[a]pyrene (B[a]P). Concentrations of 0.1 and 1 mum-B[a]P were shown to induce EROD whereas 10 mum was an inhibitory concentration. DNA adducts were detected for 12 hr to 72 hr after exposure to 1 mum-B[a]P whereas EROD activity was increased 36 hr after treatment. The pattern of adducts was shown to be identical to that obtained after B[a]P treatment of rainbow trout in vivo, as demonstrated by co-chromatography of the adducts. Pre-exposure of hepatocytes for 48 hr to beta-naphthoflavone (betaNF) and subsequent 24-hr exposure to 1 mum-B[a]P did not lead to increased DNA adduct formation although betaNF treatment led to a 3.4-fold induction of EROD activity at the time of B[a]P addition. This study suggests that primary culture of rainbow trout hepatocytes provides a suitable method for studying DNA adduct formation and its modulating factors in vitro.

摘要

利用³²P后标记分析法研究了暴露于苯并[a]芘(B[a]P)的虹鳟肝细胞原代培养物中DNA加合物的形成以及7-乙氧基异吩恶唑酮O-脱乙基酶(EROD)的诱导情况。结果显示,0.1μM和1μM的B[a]P可诱导EROD,而10μM则为抑制浓度。暴露于1μM B[a]P后12小时至72小时可检测到DNA加合物,而处理后36小时EROD活性增加。通过加合物的共色谱分析表明,加合物的模式与B[a]P对虹鳟进行体内处理后获得的模式相同。肝细胞预先暴露于β-萘黄酮(βNF)48小时,随后暴露于1μM B[a]P 24小时,虽然在添加B[a]P时βNF处理导致EROD活性诱导了3.4倍,但并未导致DNA加合物形成增加。这项研究表明,虹鳟肝细胞原代培养为体外研究DNA加合物的形成及其调节因子提供了一种合适的方法。

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