首页> 外文期刊>Toxicology in vitro: an international journal published in association with BIBRA >Time-dependent modulation of cyp1a gene transcription and EROD activity by musk xylene in PLHC-1 and RTG-2 fish cell lines.
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Time-dependent modulation of cyp1a gene transcription and EROD activity by musk xylene in PLHC-1 and RTG-2 fish cell lines.

机译:麝香二甲苯在PLHC-1和RTG-2鱼细胞系中对cyp1a基因转录和EROD活性的时间依赖性调节。

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摘要

Musk xylene (MX) is a common synthetic nitromusk fragrance. Its high release in aquatic environments and evidence of bioaccumulation in biota suggest that it could have serious toxicological consequences for aquatic ecosystems. However, not much data is available on cellular pathways and mechanisms of toxicity in aquatic organisms. The aim of the present study was to investigate the interaction of MX with CYP1A by looking at gene transcription and EROD activity in two fish cell lines: PLHC-1 and RTG-2. Time-dependent (6 and 24 h) exposure experiments with three doses of MX (2, 4 and 20 muM) were performed also with co-exposure to B(a)P. Low cytotoxicity was observed in both cell lines. Reduction of cyp1a gene transcription was observed after 6 h with full dose-dependent recovery in 24 h in RTG-2 and partial recovery in PLHC-1. EROD activity was inhibited after 6 and 24 h of exposure except in PLHC-1 at 6 h at the two higher doses. MX did not alter CYP1A induction by B(a)P at gene transcription. A dose and time-dependent induction of GST activity was observed in PLHC-1 cells exposed to MX. These findings suggest that distinct signalling pathways not mediated by AhR and distinct regulatory mechanisms by CYP1A inducers are likely.
机译:麝香二甲苯(MX)是常见的合成硝基麝香香精。它在水生环境中的高释放和生物群中生物富集的证据表明,它可能对水生生态系统产生严重的毒理学后果。但是,关于水生生物的细胞途径和毒性机理的数据很少。本研究的目的是通过观察PLHC-1和RTG-2这两种鱼细胞系中的基因转录和EROD活性来研究MX与CYP1A的相互作用。还进行了三剂量MX(2、4和20μM)的时间依赖性(6和24小时)暴露实验,同时暴露于B(a)P。在两种细胞系中均观察到低细胞毒性。 6小时后观察到cyp1a基因转录的减少,RTG-2中24h完全剂量依赖性恢复,而PLHC-1中部分恢复。暴露6和24小时后,EROD活性受到抑制,但在两个较高剂量下在6小时的PLHC-1中除外。 MX不会在基因转录时改变B(a)P对CYP1A的诱导作用。在暴露于MX的PLHC-1细胞中观察到了GST活性的剂量和时间依赖性诱导。这些发现表明,可能不是由AhR介导的不同信号传导途径,还是由CYP1A诱导剂引起的不同调节机制。

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