Fenobucarb-induced developmental neurotoxicity and mechanisms in zebrafish

被引:29
|
作者
Zhu, Xiao-Yu [1 ,2 ]
Wu, Yu-Ying [2 ]
Xia, Bo [2 ]
Dai, Ming-Zhu [2 ]
Huang, Yan-Feng [2 ]
Yang, Hua [1 ]
Li, Chun-Qi [2 ]
Li, Ping [1 ]
机构
[1] China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
[2] Hunter Biotechnol Inc, F1A,Bldg 5,88 Jiangling Rd, Hangzhou 310051, Zhejiang, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Fenobucarb; BPMC; Zebrafish; Neurotoxicity; Mechanisms; ORGANOPHOSPHATE FLAME RETARDANTS; EARLY-LIFE STAGES; SONIC HEDGEHOG; LOCOMOTOR-ACTIVITY; OXIDATIVE STRESS; MEKONG DELTA; TOXICITY; EXPOSURE; PROTEIN; DRUGS;
D O I
10.1016/j.neuro.2020.03.013
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Fenobucarb (2-sec-butylphenyl methylcarbamate, BPMC) is an extensively used carbamate insecticide. Its developmental neurotoxicity and the underlying mechanisms have not been well investigated. In this study, zebrafish embryos were exposed to various concentrations of BPMC from 6 hpf (hours post fertilization, hpf) to 120 hpf. BPMC induced developmental toxicity with reduced motility in larval zebrafish. The spinal cord neutrophil infiltration, increased ROS production, caspase 3 and 9 activation, central nerve and peripheral motor neuron damage, axon and myelin degeneration were observed in zebrafish treated with BPMC generally in a dose-dependent manner. The expression of eight marker genes for nervous system function or development, namely, a1-tubulin, shha, elavl3, gap43, syn2a, gfap, mbp and manf, was significantly downregulated following BPMC exposure. AChE activity reduction and ache gene expression suppression was also found significantly in BPMC-treated zebrafish. These results indicate that BPMC is highly toxic to zebrafish and that BPMC induces zebrafish developmental neurotoxicity through pathways involved in inflammation, oxidative stress, degeneration and apoptosis.
引用
收藏
页码:11 / 19
页数:9
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