Literature DB >> 28111251

A colour preference technique to evaluate acrylamide-induced toxicity in zebrafish.

Laibing Jia1, Rakesh Kotapati Raghupathy2, Aishah Albalawi2, Zhenkai Zhao3, James Reilly2, Qing Xiao4, Xinhua Shu5.   

Abstract

The zebrafish has become a commonly used vertebrate model for toxicity assessment, of particular relevance to the study of toxic effects on the visual system because of the structural similarities shared by zebrafish and human retinae. In this article we present a colour preference-based technique that, by assessing the functionality of photoreceptors, can be used to evaluate the effects of toxicity on behaviour. A digital camera was used to record the locomotor behaviour of individual zebrafish swimming in a water tank consisting of two compartments separated by an opaque perforated wall through which the fish could pass. The colour of the lighting in each compartment could be altered independently (producing distinct but connected environments of white, red or blue) to allow association of the zebrafish's swimming behaviour with its colour preference. The functionality of the photoreceptors was evaluated based on the ability of the zebrafish to sense the different colours and to swim between the compartments. The zebrafish tracking was carried out using our algorithm developed with MATLAB. We found that zebrafish preferred blue illumination to white, and white illumination to red. Acute treatment with acrylamide (2mM for 36h) resulted in a marked reduction in locomotion and a concomitant loss of colour-preferential swimming behaviour. Histopathological examination of acrylamide-treated zebrafish eyes showed that acrylamide exposure had caused retinal damage. The colour preference tracking technique has applications in the assessment of neurodegenerative disorders, as a method for preclinical appraisal of drug efficacy and for behavioural evaluation of toxicity.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Acrylamide; Colour preference; Photoreceptors; Toxicity; Vision; Zebrafish

Mesh:

Substances:

Year:  2017        PMID: 28111251     DOI: 10.1016/j.cbpc.2017.01.004

Source DB:  PubMed          Journal:  Comp Biochem Physiol C Toxicol Pharmacol        ISSN: 1532-0456            Impact factor:   3.228


  5 in total

1.  A Novel Function of the Lysophosphatidic Acid Receptor 3 (LPAR3) Gene in Zebrafish on Modulating Anxiety, Circadian Rhythm Locomotor Activity, and Short-Term Memory.

Authors:  Yu-Nung Lin; Gilbert Audira; Nemi Malhotra; Nguyen Thi Ngoc Anh; Petrus Siregar; Jen-Her Lu; Hsinyu Lee; Chung-Der Hsiao
Journal:  Int J Mol Sci       Date:  2020-04-18       Impact factor: 5.923

2.  Quantification of the influence of drugs on zebrafish larvae swimming kinematics and energetics.

Authors:  Zhenkai Zhao; Gen Li; Qing Xiao; Hui-Rong Jiang; Gabriel Mbuta Tchivelekete; Xinhua Shu; Hao Liu
Journal:  PeerJ       Date:  2020-01-08       Impact factor: 2.984

3.  Reversal of reserpine-induced depression and cognitive disorder in zebrafish by sertraline and Traditional Chinese Medicine (TCM).

Authors:  Shuhui Zhang; Xiaodong Liu; Mingzhu Sun; Qiuping Zhang; Teng Li; Xiang Li; Jia Xu; Xin Zhao; Dongyan Chen; Xizeng Feng
Journal:  Behav Brain Funct       Date:  2018-06-14       Impact factor: 3.759

4.  Chronic Exposure to Low Concentration Lead Chloride-Induced Anxiety and Loss of Aggression and Memory in Zebrafish.

Authors:  Ngoc Hieu Bui Thi; Ngoc Anh Nguyen Thi; Gilbert Audira; Petrus Siregar; Sung-Tzu Liang; Jong-Chin Huang; Chung-Der Hsiao
Journal:  Int J Mol Sci       Date:  2020-03-07       Impact factor: 5.923

Review 5.  Neurodegeneration, Neuroprotection and Regeneration in the Zebrafish Retina.

Authors:  Salvatore L Stella; Jasmine S Geathers; Sarah R Weber; Michael A Grillo; Alistair J Barber; Jeffrey M Sundstrom; Stephanie L Grillo
Journal:  Cells       Date:  2021-03-12       Impact factor: 6.600

  5 in total

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