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Periodical reactivation under the effect of caffeine attenuates fear memory expression in rats

In the last decade, several studies have shown that fear memories can be attenuated by interfering with reconsolidation. However, most of the pharmacological agents used in preclinical studies cannot be administered to humans. Caffeine is one of the world’s most popular psychoactive drugs and its ef...

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Autores principales: Pedraza, Lizeth K., Sierra, Rodrigo O., Lotz, Fernanda N., de Oliveira Alvares, Lucas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5940846/
https://www.ncbi.nlm.nih.gov/pubmed/29740084
http://dx.doi.org/10.1038/s41598-018-25648-6
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author Pedraza, Lizeth K.
Sierra, Rodrigo O.
Lotz, Fernanda N.
de Oliveira Alvares, Lucas
author_facet Pedraza, Lizeth K.
Sierra, Rodrigo O.
Lotz, Fernanda N.
de Oliveira Alvares, Lucas
author_sort Pedraza, Lizeth K.
collection PubMed
description In the last decade, several studies have shown that fear memories can be attenuated by interfering with reconsolidation. However, most of the pharmacological agents used in preclinical studies cannot be administered to humans. Caffeine is one of the world’s most popular psychoactive drugs and its effects on cognitive and mood states are well documented. Nevertheless, the influence of caffeine administration on fear memory processing is not as clear. We employed contextual fear conditioning in rats and acute caffeine administration under a standard memory reconsolidation protocol or periodical memory reactivation. Additionally, potential rewarding/aversion and anxiety effects induced by caffeine were evaluated by conditioning place preference or open field, respectively. Caffeine administration was able to attenuate weak fear memories in a standard memory reconsolidation protocol; however, periodical memory reactivation under caffeine effect was necessary to attenuate strong and remote memories. Moreover, caffeine promoted conditioned place preference and anxiolytic-like behavior, suggesting that caffeine weakens the initial learning during reactivation through counterconditioning mechanisms. Thus, our study shows that rewarding and anxiolytic effects of caffeine during fear reactivation can change the emotional valence of fear memory. It brings a new promising pharmacological approach based on drugs widely used such as caffeine to treat fear-related disorders.
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spelling pubmed-59408462018-05-11 Periodical reactivation under the effect of caffeine attenuates fear memory expression in rats Pedraza, Lizeth K. Sierra, Rodrigo O. Lotz, Fernanda N. de Oliveira Alvares, Lucas Sci Rep Article In the last decade, several studies have shown that fear memories can be attenuated by interfering with reconsolidation. However, most of the pharmacological agents used in preclinical studies cannot be administered to humans. Caffeine is one of the world’s most popular psychoactive drugs and its effects on cognitive and mood states are well documented. Nevertheless, the influence of caffeine administration on fear memory processing is not as clear. We employed contextual fear conditioning in rats and acute caffeine administration under a standard memory reconsolidation protocol or periodical memory reactivation. Additionally, potential rewarding/aversion and anxiety effects induced by caffeine were evaluated by conditioning place preference or open field, respectively. Caffeine administration was able to attenuate weak fear memories in a standard memory reconsolidation protocol; however, periodical memory reactivation under caffeine effect was necessary to attenuate strong and remote memories. Moreover, caffeine promoted conditioned place preference and anxiolytic-like behavior, suggesting that caffeine weakens the initial learning during reactivation through counterconditioning mechanisms. Thus, our study shows that rewarding and anxiolytic effects of caffeine during fear reactivation can change the emotional valence of fear memory. It brings a new promising pharmacological approach based on drugs widely used such as caffeine to treat fear-related disorders. Nature Publishing Group UK 2018-05-08 /pmc/articles/PMC5940846/ /pubmed/29740084 http://dx.doi.org/10.1038/s41598-018-25648-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pedraza, Lizeth K.
Sierra, Rodrigo O.
Lotz, Fernanda N.
de Oliveira Alvares, Lucas
Periodical reactivation under the effect of caffeine attenuates fear memory expression in rats
title Periodical reactivation under the effect of caffeine attenuates fear memory expression in rats
title_full Periodical reactivation under the effect of caffeine attenuates fear memory expression in rats
title_fullStr Periodical reactivation under the effect of caffeine attenuates fear memory expression in rats
title_full_unstemmed Periodical reactivation under the effect of caffeine attenuates fear memory expression in rats
title_short Periodical reactivation under the effect of caffeine attenuates fear memory expression in rats
title_sort periodical reactivation under the effect of caffeine attenuates fear memory expression in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5940846/
https://www.ncbi.nlm.nih.gov/pubmed/29740084
http://dx.doi.org/10.1038/s41598-018-25648-6
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