Hepatotoxicity of tricyclazole in zebrafish (Danio rerio)

被引:64
作者
Qiu, Lingyu [1 ,2 ]
Jia, Kun [1 ,2 ,3 ]
Huang, Lirong [1 ,2 ,3 ]
Liao, Xinjun [1 ,2 ,3 ]
Guo, Xinchun [4 ]
Lu, Huiqiang [1 ,2 ,3 ]
机构
[1] Jiangxi Engn Lab Zebrafish Modeling & Drug Screen, Jian, Jiangxi, Peoples R China
[2] Jiangxi Key Lab Dev Biol Organs, Jian, Jiangxi, Peoples R China
[3] Jinggangshan Univ, Coll Life Sci, Ctr Dev Biol, Jian, Jiangxi, Peoples R China
[4] Gannan Normal Univ, Sch Geog & Environm Engn, Ganzhou, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Tricyclazole; Hepatotoxicity; Oxidative stress; Metabolism disorder; Zebrafish; CONSTITUTIVE ANDROSTANE RECEPTOR; DEVELOPMENTAL TOXICITY; LIVER HYPERTROPHY; MOUSE-LIVER; MODEL; INVOLVEMENT; ACTIVATION; PESTICIDES; TOXICOLOGY; APOPTOSIS;
D O I
10.1016/j.chemosphere.2019.05.159
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Tricyclazole is widely used in agriculture as a pesticide, but its toxicity in vertebrates is currently poorly evaluated. In this study, we used zebrafish to assess the toxicity of tricyclazole. We found that tricyclazole induces liver damage, or hepatotoxicity, in zebrafish, during both development and adulthood. In embryos, we found that tricyclazole affected the liver development rather than other endodermal tissues such as gut and pancreas. In both embryos and adult zebrafish livers, tricyclazole disrupted the relationship between oxidant and antioxidant system and resulted in reactive oxygen species (ROS) overload. Meanwhile, it triggered hepatocyte apoptosis and disturbed carbohydrate/lipid metabolism and energy demand systems. These results suggested that tricyclazole could cause severe consequences for vertebrate hepatic development and function. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:171 / 179
页数:9
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