Literature DB >> 30612050

The adverse effect of TCIPP and TCEP on neurodevelopment of zebrafish embryos/larvae.

Ruiwen Li1, Hengqi Wang2, Chuang Mi3, Chenglian Feng4, Ling Zhang5, Lihua Yang6, Bingsheng Zhou7.   

Abstract

Tris (1-chloro-2-propyl) phosphate (TCIPP) and tris (2-chloroethyl)phosphate (TCEP) are two widely used chlorinated organophosphate flame retardants (ClOPFRs), and have been frequently detected in various environmental media. Concern is now growing whether TCIPP and TCEP can cause neurotoxicity since they have similar chemical structure with organophosphorus pesticide. Therefore, in this study, zebrafish embryos (2-120 h post-fertilization [hpf]) were exposed to TCIPP or TCEP (0, 100, 500 or 2500 μg/L) or a model neurotoxicant, chlorpyrifos (CPF, 100 μg/L) to investigate the adverse effects and possible mechanisms of TCIPP and TCEP on neurodevelopment. Our results showed that CPF exposure resulted in developmental toxicity including decreased hatching, survival rates and increased malformation rates (e.g., spinal curvature) as well as behavior changes such as decreased locomotive activity in dark stimulation. In contrast, TCIPP and TCEP showed no significant effects on developmental parameters, but caused similar effects on locomotive activity at high concentration, indicating that although not as potent as CPF, TCIPP and TCEP may still cause adverse effects on neurodevelopment. Furthermore, our results suggest that TCIPP and TCEP showed no effects on acetylcholine content or AChE activity, which were considered as the main targets of CPF. However, TCIPP and TCEP exposure can significantly down-regulate the expression of selected genes and proteins related to neurodevelopment (e.g., mbp, syn2a, and α1-tubulin) similar as CPF did. Besides that, TCIPP and TCEP can also affect the transcription of shha and gap43, which were not affected by CPF, pointing out a complex mechanism underlying TCIPP and TCEP's neurodevelopmental toxicity. Overall, our results demonstrated that TCEP and TCIPP may have adverse effect on the neurodevelopment of zebrafish embryos/larvae, but the underlying mechanism is not via the inhibition of acetyl cholinesterase activity.
Copyright © 2018. Published by Elsevier Ltd.

Entities:  

Keywords:  Acetylcholin esterase; Neurodevelopment; TCEP; TCIPP; Zebrafish

Mesh:

Substances:

Year:  2019        PMID: 30612050     DOI: 10.1016/j.chemosphere.2018.12.198

Source DB:  PubMed          Journal:  Chemosphere        ISSN: 0045-6535            Impact factor:   7.086


  4 in total

1.  Developmental Neurotoxicity and Behavioral Screening in Larval Zebrafish with a Comparison to Other Published Results.

Authors:  Kimberly A Jarema; Deborah L Hunter; Bridgett N Hill; Jeanene K Olin; Katy N Britton; Matthew R Waalkes; Stephanie Padilla
Journal:  Toxics       Date:  2022-05-17

Review 2.  COVID-19 discarded disposable gloves as a source and a vector of pollutants in the environment.

Authors:  Katarzyna Jędruchniewicz; Yong Sik Ok; Patryk Oleszczuk
Journal:  J Hazard Mater       Date:  2021-04-27       Impact factor: 10.588

3.  Organophosphate esters cause thyroid dysfunction via multiple signaling pathways in zebrafish brain.

Authors:  Zhenfei Yan; Chenglian Feng; Xiaowei Jin; Fangkun Wang; Cong Liu; Na Li; Yu Qiao; Yingchen Bai; Fengchang Wu; John P Giesy
Journal:  Environ Sci Ecotechnol       Date:  2022-06-06

4.  Toxicity testing of pesticides in zebrafish-a systematic review on chemicals and associated toxicological endpoints.

Authors:  Íris Flávia Sousa Gonçalves; Terezinha Maria Souza; Leonardo Rogério Vieira; Filipi Calbaizer Marchi; Adailton Pascoal Nascimento; Davi Felipe Farias
Journal:  Environ Sci Pollut Res Int       Date:  2020-02-15       Impact factor: 4.223

  4 in total

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