Tris (1-chloro-2-propyl) phosphate exposure to zebrafish causes neurodevelopmental toxicity and abnormal locomotor behavior

被引:46
|
作者
Xia, Min [1 ]
Wang, Xuedong [1 ]
Xu, Jiaqi [1 ]
Qian, Qiuhui [1 ]
Gao, Ming [1 ]
Wang, Huili [1 ]
机构
[1] Suzhou Univ Sci & Technol, Sch Environm Sci & Engn, Natl & Local Joint Engn Lab Municipal Sewage Reso, Suzhou 215009, Peoples R China
基金
中国国家自然科学基金;
关键词
Tris (1-chloro-2-propyl) phosphate; Neurotoxicity; Abnormal locomotor behavior; Gene expression change; Zebrafish; FLAME RETARDANTS; EXPRESSION; ORGANOPHOSPHATE; TRICLOSAN; APOPTOSIS; STRESS; TCPP;
D O I
10.1016/j.scitotenv.2020.143694
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The organophosphate flame retardant, tris (1-chloro-2-propyl) phosphate (TCPP), is ubiquitous in environmental matrices; however, there is a paucity of information concerning its systemic toxicity. Herein, we investigated the effects of TCPP exposure on zebrafish neurodevelopment and swimming behavior to elucidate the underlying molecular mechanisms of neurotoxicity. Under TCPP gradient concentration exposure, the hatching rates were declined by up to 33.3% in 72 hpf, and the malformation rates increased from 15% to 50%. Meanwhile, TCPP led to abnormal behaviors including decreased locomotive activity in the dark and slow/insensitive responses to sound and light stimulation of larvae. TCPP caused excessive apoptosis and ROS accumulation in early embryonic development, with hair cell defects and structural deformity of neuromast. Abnormal expression of neurodevelopment (pax6a, nova1, sox11b, syn2a, foxo3a and robo2) and apoptosis-related genes (baxa, bcl2a and casp8) revealed molecular mechanisms regarding abnormal behavioral and phenotypic symptoms. Chronic TCPP exposure led to anxiety-like behavior and excessive panic, lower capacity for discrimination and risk avoidance, and conditioned place preference in adults. Social interaction tests demonstrated that long-term TCPP stress resulted in unsociable, eccentric, lonely and silent behaviors in adults. Zebrafish memory and cognitive function were severely reduced as concluded fromT-maze tests. Potential mechanisms triggering behavioral abnormality were attributed to histopathological injury of diencephalon, abnormal changes in nerve-related genes at transcription and expression levels, and inhibited activity of AChE by TCPP stress. These findings provide an important reference for risk assessment and early warning to TCPP exposure, and offer insights for prevention/mitigation of pollutant-induced nervous system diseases. (C) 2020 Elsevier B.V. All rights reserved.
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页数:12
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