Journal
CHEMOSPHERE
Volume 248, Issue -, Pages -Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2020.125941
Keywords
Zebrafish; Thiophanate-methyl; Hepatotoxicity; Caspase-3; Oxidative stress; Glucose and lipid metabolism disorder
Categories
Funding
- National Natural Science Foundation of China [81560109, 31771606, 31900597, 81860282]
- Natural Science Foundation Project of Jiangxi Province [2018ACB21033, 20192ACB21013]
- Science and Technology Foundation of the Education Department of Jiangxi Province [GJJ150759]
- China Postdoctoral Foundation [2019M652269]
- Jinggangshan University [JZB15006, JFD1802]
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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. (C) 2020 Elsevier Ltd. All rights reserved.
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