Behavioral and molecular analysis of nicotine-conditioned place preference in zebrafish.

Studies using mice and rats have demonstrated that nicotine induces a conditioned place preference (CPP), with more effective results obtained by using biased procedures. Zebrafish have also been used as a model system to identify factors influencing nicotine-associated reward by using an unbiased d...

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Main Authors: Ximena Kedikian, Maria Paula Faillace, Ramón Bernabeu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3722213?pdf=render
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spelling doaj-26de737bcd3844e1845d18a1ad22557b2020-11-25T01:32:06ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0187e6945310.1371/journal.pone.0069453Behavioral and molecular analysis of nicotine-conditioned place preference in zebrafish.Ximena KedikianMaria Paula FaillaceRamón BernabeuStudies using mice and rats have demonstrated that nicotine induces a conditioned place preference (CPP), with more effective results obtained by using biased procedures. Zebrafish have also been used as a model system to identify factors influencing nicotine-associated reward by using an unbiased design. Here, we report that zebrafish exhibited putative nicotine biased CPP to an initially aversive compartment (nicotine-paired group). A counterbalanced nicotine-exposed control group did not show a significant preference shift, providing evidence that the preference shift in the nicotine-paired group was not due to a reduction of aversion for this compartment. Zebrafish preference was corroborated by behavioral analysis of several indicators of drug preference, such as time spent in the drug-paired side, number of entries to the drug-paired side, and distance traveled. These results provided strong evidence that zebrafish may actually develop a preference for nicotine, although the drug was administrated in an aversive place for the fish, which was further supported by molecular studies. Reverse transcription-quantitative real-time PCR analysis depicted a significant increase in the expression of α7 and α6 but not α4 and β2 subunits of the nicotinic receptor in nicotine-paired zebrafish brains. In contrast, zebrafish brains from the counterbalanced nicotine group showed no significant changes. Moreover, CREB phosphorylation, an indicator of neural activity, accompanied the acquisition of nicotine-CPP. Our studies offered an incremental value to the drug addiction field, because they further describe behavioral features of CPP to nicotine in zebrafish. The results suggested that zebrafish exposed to nicotine in an unfriendly environment can develop a preference for that initially aversive place, which is likely due to the rewarding effect of nicotine. Therefore, this model can be used to screen exogenous and endogenous molecules involved in nicotine-associated reward in vertebrates.http://europepmc.org/articles/PMC3722213?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ximena Kedikian
Maria Paula Faillace
Ramón Bernabeu
spellingShingle Ximena Kedikian
Maria Paula Faillace
Ramón Bernabeu
Behavioral and molecular analysis of nicotine-conditioned place preference in zebrafish.
PLoS ONE
author_facet Ximena Kedikian
Maria Paula Faillace
Ramón Bernabeu
author_sort Ximena Kedikian
title Behavioral and molecular analysis of nicotine-conditioned place preference in zebrafish.
title_short Behavioral and molecular analysis of nicotine-conditioned place preference in zebrafish.
title_full Behavioral and molecular analysis of nicotine-conditioned place preference in zebrafish.
title_fullStr Behavioral and molecular analysis of nicotine-conditioned place preference in zebrafish.
title_full_unstemmed Behavioral and molecular analysis of nicotine-conditioned place preference in zebrafish.
title_sort behavioral and molecular analysis of nicotine-conditioned place preference in zebrafish.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Studies using mice and rats have demonstrated that nicotine induces a conditioned place preference (CPP), with more effective results obtained by using biased procedures. Zebrafish have also been used as a model system to identify factors influencing nicotine-associated reward by using an unbiased design. Here, we report that zebrafish exhibited putative nicotine biased CPP to an initially aversive compartment (nicotine-paired group). A counterbalanced nicotine-exposed control group did not show a significant preference shift, providing evidence that the preference shift in the nicotine-paired group was not due to a reduction of aversion for this compartment. Zebrafish preference was corroborated by behavioral analysis of several indicators of drug preference, such as time spent in the drug-paired side, number of entries to the drug-paired side, and distance traveled. These results provided strong evidence that zebrafish may actually develop a preference for nicotine, although the drug was administrated in an aversive place for the fish, which was further supported by molecular studies. Reverse transcription-quantitative real-time PCR analysis depicted a significant increase in the expression of α7 and α6 but not α4 and β2 subunits of the nicotinic receptor in nicotine-paired zebrafish brains. In contrast, zebrafish brains from the counterbalanced nicotine group showed no significant changes. Moreover, CREB phosphorylation, an indicator of neural activity, accompanied the acquisition of nicotine-CPP. Our studies offered an incremental value to the drug addiction field, because they further describe behavioral features of CPP to nicotine in zebrafish. The results suggested that zebrafish exposed to nicotine in an unfriendly environment can develop a preference for that initially aversive place, which is likely due to the rewarding effect of nicotine. Therefore, this model can be used to screen exogenous and endogenous molecules involved in nicotine-associated reward in vertebrates.
url http://europepmc.org/articles/PMC3722213?pdf=render
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