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三硝基甲苯(TNT)诱导大型溞羰基还原酶 1(CR1)基因表达,而非其关键代谢物 2-ADNT 和 4-ADNT。

Induction of carbonyl reductase 1 (CR1) gene expression in Daphnia magna by TNT, but not its key metabolites 2-ADNT and 4-ADNT.

机构信息

Institute of Toxicology and Pharmacology for Natural Scientists, University Medical School Schleswig-Holstein, Kiel, Germany.

Institute of Toxicology and Pharmacology for Natural Scientists, University Medical School Schleswig-Holstein, Kiel, Germany.

出版信息

Chem Biol Interact. 2022 Jan 5;351:109752. doi: 10.1016/j.cbi.2021.109752. Epub 2021 Nov 19.

Abstract

2,4,6-trinitrotoluene (TNT) is a known source of reactive oxygen species (ROS), which cause oxidative stress in aquatic ecosystems. Carbonyl reductases (CRs) are one of several possible defense mechanisms induced against ROS products, especially those that result in the 'so-called' carbonyl stress. Daphnia magna, a freshwater organism living in stagnant freshwater bodies, expresses four copies of the CR gene (Dma_CR1, Dma_CR2, Dma_CR3 and Dma_CR4). In this study, induction of all four copies of Dma_CR by 2-amino-4,6-dinitrotoluene (2-ADNT) and 4-amino-2,6-dinitrotoluene (4-ADNT), was investigated. Reverse transcription polymerase chain reaction (RT-PCR) analysis of treated daphnids revealed up-regulation of Dma_CR1 alone in response to TNT, but not 2-ADNT and 4-ADNT (which are key metabolites of TNT). This concentration- and time-dependent up-regulation in mRNA-expression was observed both in the presence and absence of light, in the same magnitude. Moreover, significant change in mRNA-expression could be observed 8 h after treatment with TNT. In the presence of TNT, the antioxidant N-acetylcysteine (NAc) could not reverse TNT-induced up-regulation of Dma_CR1 mRNA-expression. On the other hand, withdrawal of TNT from the culture medium caused a significant reduction in the TNT-induced mRNA-expression of Dma_CR1 within 24 h. These findings highlight the potential of Dma_CR1 as a biomarker for biomonitoring of TNT levels in freshwater bodies.

摘要

2,4,6-三硝基甲苯(TNT)是活性氧(ROS)的已知来源,它会导致水生生态系统发生氧化应激。羰基还原酶(CRs)是几种可能的防御机制之一,用于对抗 ROS 产物,特别是那些导致“所谓”羰基应激的产物。大型溞(Daphnia magna)是一种生活在静止淡水体中的淡水生物,它表达了四个 CR 基因(Dma_CR1、Dma_CR2、Dma_CR3 和 Dma_CR4)的副本。在本研究中,研究了 2-氨基-4,6-二硝基甲苯(2-ADNT)和 4-氨基-2,6-二硝基甲苯(4-ADNT)对所有四个 Dma_CR 副本的诱导作用。用 TNT 处理的大型溞的反转录聚合酶链反应(RT-PCR)分析显示,只有 Dma_CR1 被单独上调,而 TNT 则没有被上调,2-ADNT 和 4-ADNT 也没有被上调(它们是 TNT 的关键代谢物)。这种 mRNA 表达的浓度和时间依赖性上调在有光和无光的情况下都存在,且幅度相同。此外,在 TNT 处理 8 小时后,mRNA 表达就会发生显著变化。在 TNT 的存在下,抗氧化剂 N-乙酰半胱氨酸(NAc)不能逆转 TNT 诱导的 Dma_CR1 mRNA 表达上调。另一方面,从培养基中去除 TNT 会在 24 小时内导致 TNT 诱导的 Dma_CR1 mRNA 表达显著减少。这些发现突出了 Dma_CR1 作为生物监测淡水体中 TNT 水平的生物标志物的潜力。

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