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Cocaine Directly Impairs Memory Extinction and Alters Brain DNA Methylation Dynamics in Honey Bees
Drug addiction is a chronic relapsing behavioral disorder. The high relapse rate has often been attributed to the perseverance of drug-associated memories due to high incentive salience of stimuli learnt under the influence of drugs. Drug addiction has also been interpreted as a memory disorder sinc...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816933/ https://www.ncbi.nlm.nih.gov/pubmed/29487536 http://dx.doi.org/10.3389/fphys.2018.00079 |
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author | Søvik, Eirik Berthier, Pauline Klare, William P. Helliwell, Paul Buckle, Edwina L. S. Plath, Jenny A. Barron, Andrew B. Maleszka, Ryszard |
author_facet | Søvik, Eirik Berthier, Pauline Klare, William P. Helliwell, Paul Buckle, Edwina L. S. Plath, Jenny A. Barron, Andrew B. Maleszka, Ryszard |
author_sort | Søvik, Eirik |
collection | PubMed |
description | Drug addiction is a chronic relapsing behavioral disorder. The high relapse rate has often been attributed to the perseverance of drug-associated memories due to high incentive salience of stimuli learnt under the influence of drugs. Drug addiction has also been interpreted as a memory disorder since drug associated memories are unusually enduring and some drugs, such as cocaine, interfere with neuroepigenetic machinery known to be involved in memory processing. Here we used the honey bee (an established invertebrate model for epigenomics and behavioral studies) to examine whether or not cocaine affects memory processing independently of its effect on incentive salience. Using the proboscis extension reflex training paradigm we found that cocaine strongly impairs consolidation of extinction memory. Based on correlation between the observed effect of cocaine on learning and expression of epigenetic processes, we propose that cocaine interferes with memory processing independently of incentive salience by directly altering DNA methylation dynamics. Our findings emphasize the impact of cocaine on memory systems, with relevance for understanding how cocaine can have such an enduring impact on behavior. |
format | Online Article Text |
id | pubmed-5816933 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58169332018-02-27 Cocaine Directly Impairs Memory Extinction and Alters Brain DNA Methylation Dynamics in Honey Bees Søvik, Eirik Berthier, Pauline Klare, William P. Helliwell, Paul Buckle, Edwina L. S. Plath, Jenny A. Barron, Andrew B. Maleszka, Ryszard Front Physiol Physiology Drug addiction is a chronic relapsing behavioral disorder. The high relapse rate has often been attributed to the perseverance of drug-associated memories due to high incentive salience of stimuli learnt under the influence of drugs. Drug addiction has also been interpreted as a memory disorder since drug associated memories are unusually enduring and some drugs, such as cocaine, interfere with neuroepigenetic machinery known to be involved in memory processing. Here we used the honey bee (an established invertebrate model for epigenomics and behavioral studies) to examine whether or not cocaine affects memory processing independently of its effect on incentive salience. Using the proboscis extension reflex training paradigm we found that cocaine strongly impairs consolidation of extinction memory. Based on correlation between the observed effect of cocaine on learning and expression of epigenetic processes, we propose that cocaine interferes with memory processing independently of incentive salience by directly altering DNA methylation dynamics. Our findings emphasize the impact of cocaine on memory systems, with relevance for understanding how cocaine can have such an enduring impact on behavior. Frontiers Media S.A. 2018-02-13 /pmc/articles/PMC5816933/ /pubmed/29487536 http://dx.doi.org/10.3389/fphys.2018.00079 Text en Copyright © 2018 Søvik, Berthier, Klare, Helliwell, Buckle, Plath, Barron and Maleszka. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Søvik, Eirik Berthier, Pauline Klare, William P. Helliwell, Paul Buckle, Edwina L. S. Plath, Jenny A. Barron, Andrew B. Maleszka, Ryszard Cocaine Directly Impairs Memory Extinction and Alters Brain DNA Methylation Dynamics in Honey Bees |
title | Cocaine Directly Impairs Memory Extinction and Alters Brain DNA Methylation Dynamics in Honey Bees |
title_full | Cocaine Directly Impairs Memory Extinction and Alters Brain DNA Methylation Dynamics in Honey Bees |
title_fullStr | Cocaine Directly Impairs Memory Extinction and Alters Brain DNA Methylation Dynamics in Honey Bees |
title_full_unstemmed | Cocaine Directly Impairs Memory Extinction and Alters Brain DNA Methylation Dynamics in Honey Bees |
title_short | Cocaine Directly Impairs Memory Extinction and Alters Brain DNA Methylation Dynamics in Honey Bees |
title_sort | cocaine directly impairs memory extinction and alters brain dna methylation dynamics in honey bees |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816933/ https://www.ncbi.nlm.nih.gov/pubmed/29487536 http://dx.doi.org/10.3389/fphys.2018.00079 |
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