首页> 外文期刊>Toxicology and Applied Pharmacology >Comparative in vitro and in vivo benzo(a)pyrene-DNA adduct formation and its relationship to CYP1A activity in two species of ictalurid catfish.
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Comparative in vitro and in vivo benzo(a)pyrene-DNA adduct formation and its relationship to CYP1A activity in two species of ictalurid catfish.

机译:在两种卡奇多d鱼体内和体内比较苯并(a)-DNA加合物的形成及其与CYP1A活性的关系。

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We have measured the formation and persistence of benzo[a]pyrene (BaP)-DNA adducts in the liver of two closely related species of fish, the brown bullhead (Ameriurus nebulosus) and the channel catfish (Ictalurus punctatus) using the 32P-postlabeling method. Liver microsomal ethoxyresorufin-O-deethylase (EROD) activity, arylhydrocarbon hydroxylase (AHH) activity, and in vitro microsome-mediated DNA binding were all significantly higher in the channel catfish. In an in vivo time-course experiment, fish were either induced with beta NF followed by a single BaP i.p. injection (20 mg/kg) or treated with corn oil. BaP-DNA adducts and EROD activity in liver were analyzed 1, 3, 7, 14, and 45 days after the BaP dosage. As in the in vitro experiments, EROD activities in channel catfish were significantly higher at most time points than in bullhead liver (p < 0.05). However, in contrast to the in vitro data, the BaP-DNA adduct profile revealed significantly higher levels of adducts in the bullhead than the channel catfish throughout the time course (p < 0.05). Prior induction with beta NF did not significantly affect the level or type of adduct binding to DNA in either species. Further characterization of the major adduct by HPLC confirmed it to be the anti-BPDE-dGuo adduct. Analysis of tissue distribution of [14C]BaP in the two species suggested similar absorption and initial distribution, but slower elimination from the liver of bullhead than the catfish. The BaP-adduct profiles were consistent with the relative species susceptibility to polycyclic aromatic hydrocarbon-induced liver neoplasia. EROD activities, however, were negatively associated with adduct levels following in vivo exposure.
机译:我们使用32P后标记法测量了两种密切相关的鱼类,棕色bull头(Ameriurus nebulosus)和channel鱼(Ictalurus punctatus)肝脏中苯并[a] re(BaP)-DNA加合物的形成和持续存在。方法。在channel鱼中,肝微粒体乙氧基异戊二烯-O-脱乙基酶(EROD)活性,芳基烃羟化酶(AHH)活性和体外微粒体介导的DNA结合均显着较高。在体内时程实验中,用βNF诱导鱼,然后用单个BaP i.p诱导鱼。注射(20 mg / kg)或用玉米油治疗。服用BaP后1、3、7、14和45天分析肝脏中的BaP-DNA加合物和EROD活性。与体外实验一样,在大多数时间点,channel鱼的EROD活性明显高于牛头肝脏(p <0.05)。但是,与体外数据相反,整个过程中BaP-DNA加合物谱图显示,head鱼中的加合物水平明显高于the鱼(p <0.05)。事先用βNF诱导并没有显着影响两种物种中与DNA结合的加合物的水平或类型。通过HPLC对主要加合物的进一步表征证实其为抗BPDE-dGuo加合物。分析两种物种中[14C] BaP的组织分布表明吸收和初始分布相似,但从head头肝脏清除的速度比cat鱼慢。 BaP加合物的分布与对多环芳烃诱导的肝肿瘤的相对物种敏感性一致。然而,EROD活性与体内暴露后的加合物水平呈负相关。

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