{"title":"From colours to cravings: Exploring conditioned colour preference to ethanol in zebrafish","authors":"Ethan V. Hagen , Yanbo Zhang , Trevor J. Hamilton","doi":"10.1016/j.pbb.2024.173909","DOIUrl":null,"url":null,"abstract":"<div><div>Conditioned preference paradigms like conditioned colour preference tests (CCP) can be used to investigate addictive drug seeking in zebrafish (<em>Danio rerio</em>), but many aspects of this procedure require further study. Conditioned preference can be tested with either biased or unbiased conditioning methods, each with their own strengths and weaknesses. The present study used unbiased stimuli to test seeking behaviour in ethanol-exposed zebrafish at different durations of drug withdrawal. Zebrafish were exposed to one of two equally preferred colours (red or yellow) while dosed with 0.8 % vol/vol ethanol or with habitat water (controls) for 1 h each day for 21 days. Next, fish experienced withdrawal for either 2-, 4-, or 8-days then were tested in a two-way red and yellow task for 10 min with their movement recorded via motion-tracking software. Fish conditioned to red showed a main effect of ethanol and a significant preference for red compared to yellow at 8-days of withdrawal but not at 2-days or 4-days of withdrawal. Fish conditioned to yellow did not show any colour preference during the 2-, 4-, or 8-days of withdrawal, but did show a main effect of withdrawal duration. This work expands our understanding of CCP paradigms in zebrafish and highlights the capacity of zebrafish to develop an association to red but not yellow under our experimental conditions.</div></div>","PeriodicalId":19893,"journal":{"name":"Pharmacology Biochemistry and Behavior","volume":"246 ","pages":"Article 173909"},"PeriodicalIF":3.3000,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmacology Biochemistry and Behavior","FirstCategoryId":"102","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S009130572400203X","RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BEHAVIORAL SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Conditioned preference paradigms like conditioned colour preference tests (CCP) can be used to investigate addictive drug seeking in zebrafish (Danio rerio), but many aspects of this procedure require further study. Conditioned preference can be tested with either biased or unbiased conditioning methods, each with their own strengths and weaknesses. The present study used unbiased stimuli to test seeking behaviour in ethanol-exposed zebrafish at different durations of drug withdrawal. Zebrafish were exposed to one of two equally preferred colours (red or yellow) while dosed with 0.8 % vol/vol ethanol or with habitat water (controls) for 1 h each day for 21 days. Next, fish experienced withdrawal for either 2-, 4-, or 8-days then were tested in a two-way red and yellow task for 10 min with their movement recorded via motion-tracking software. Fish conditioned to red showed a main effect of ethanol and a significant preference for red compared to yellow at 8-days of withdrawal but not at 2-days or 4-days of withdrawal. Fish conditioned to yellow did not show any colour preference during the 2-, 4-, or 8-days of withdrawal, but did show a main effect of withdrawal duration. This work expands our understanding of CCP paradigms in zebrafish and highlights the capacity of zebrafish to develop an association to red but not yellow under our experimental conditions.
期刊介绍:
Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely biochemical or toxicology studies will not be published. Papers describing the behavioral effects of novel drugs in models of psychiatric, neurological and cognitive disorders, and central pain must include a positive control unless the paper is on a disease where such a drug is not available yet. Papers focusing on physiological processes (e.g., peripheral pain mechanisms, body temperature regulation, seizure activity) are not accepted as we would like to retain the focus of Pharmacology Biochemistry & Behavior on behavior and its interaction with the biochemistry and neurochemistry of the central nervous system. Papers describing the effects of plant materials are generally not considered, unless the active ingredients are studied, the extraction method is well described, the doses tested are known, and clear and definite experimental evidence on the mechanism of action of the active ingredients is provided.