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甲基硫菌灵诱导斑马鱼产生严重的肝毒性。

Thiophanate-methyl induces severe hepatotoxicity in zebrafish.

机构信息

Department of Bioscience, College of Life Science, Nanchang University, Nanchang, 330031, China; Jiangxi Engineering Laboratory of Zebrafish Modeling and Drug Screening for Human Diseases; Jiangxi Key Laboratory of Developmental Biology of Organs, Ji'an, 343009, Jiangxi, China.

Jiangxi Engineering Laboratory of Zebrafish Modeling and Drug Screening for Human Diseases; Jiangxi Key Laboratory of Developmental Biology of Organs, Ji'an, 343009, Jiangxi, China.

出版信息

Chemosphere. 2020 Jun;248:125941. doi: 10.1016/j.chemosphere.2020.125941. Epub 2020 Jan 21.

Abstract

Thiophanate-methyl (TM) is widely used all over the world and is a typical example of pesticide residues, which can be detected in the soil, and even in vegetables and fruits. However, the molecular mechanisms underlying the hepatotoxicity of TM are not well understood. In this study, we utilized zebrafish to comprehensively evaluate the hepatotoxicity of TM and explore how the molecular mechanisms of hepatotoxicity are induced. The zebrafish larvae were exposed in 6.25, 12.5 and 25 mg/L TM from 72 to 144 hpf, while the adults were exposed in 2, 4 and 6 mg/L TM for 28 days. Here, we found that 12.5 and 25 mg/L TM induces specifically serious hepatotoxicity but not the toxicity of other organs in zebrafish larvae and adults. Moreover, it might triggered hepatotoxicity by activating the caspase-3 through apoptotic pathways and oxidative stress in zebrafish. Subsequently, this resulted in a metabolic imbalance in the zebrafish's liver. In conclusion, our results disclosed the fact that TM may induce severe hepatotoxicity by mediating activation of caspase-3 and oxidative stress in zebrafish.

摘要

甲基硫菌灵(TM)在全世界范围内被广泛使用,是农药残留的典型代表,可在土壤中检测到,甚至在蔬菜和水果中也能检测到。然而,TM 肝毒性的分子机制尚不清楚。在本研究中,我们利用斑马鱼全面评估 TM 的肝毒性,并探讨肝毒性的分子机制是如何诱导的。从 72 到 144 hpf,斑马鱼幼虫暴露于 6.25、12.5 和 25 mg/L TM 中,而成年斑马鱼暴露于 2、4 和 6 mg/L TM 中 28 天。在这里,我们发现 12.5 和 25 mg/L TM 在斑马鱼幼虫和成年鱼中特异性地引起严重的肝毒性,但对其他器官没有毒性。此外,它可能通过激活 caspase-3 并通过细胞凋亡途径和氧化应激在斑马鱼中引发肝毒性。随后,这导致了斑马鱼肝脏的代谢失衡。总之,我们的结果表明,TM 可能通过介导 caspase-3 的激活和氧化应激在斑马鱼中引起严重的肝毒性。

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