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Knockdown of zif268 in the Posterior Dorsolateral Striatum Does Not Enduringly Disrupt a Response Memory of a Rewarded T-Maze Task

Under certain conditions pavlovian memories undergo reconsolidation, whereby the reactivated memory can be disrupted by manipulations such as knockdown of zif268. For instrumental memories, reconsolidation disruption is less well established. Our previous, preliminary data identified that there was...

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Autores principales: Cahill, Emma N., Vousden, George H., Exton-McGuinness, Marc T.J., Beh, Ian R.C., Swerner, Casey B., Macak, Matej, Abas, Sameera, Cole, Cameron C., Kelleher, Brian F., Everitt, Barry J., Milton, Amy L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800740/
https://www.ncbi.nlm.nih.gov/pubmed/28736133
http://dx.doi.org/10.1016/j.neuroscience.2017.07.014
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author Cahill, Emma N.
Vousden, George H.
Exton-McGuinness, Marc T.J.
Beh, Ian R.C.
Swerner, Casey B.
Macak, Matej
Abas, Sameera
Cole, Cameron C.
Kelleher, Brian F.
Everitt, Barry J.
Milton, Amy L.
author_facet Cahill, Emma N.
Vousden, George H.
Exton-McGuinness, Marc T.J.
Beh, Ian R.C.
Swerner, Casey B.
Macak, Matej
Abas, Sameera
Cole, Cameron C.
Kelleher, Brian F.
Everitt, Barry J.
Milton, Amy L.
author_sort Cahill, Emma N.
collection PubMed
description Under certain conditions pavlovian memories undergo reconsolidation, whereby the reactivated memory can be disrupted by manipulations such as knockdown of zif268. For instrumental memories, reconsolidation disruption is less well established. Our previous, preliminary data identified that there was an increase in Zif268 in the posterior dorsolateral striatum (pDLS) after expression of an instrumental habit-like 'response' memory, but not an instrumental goal-directed 'place' memory on a T-maze task. Here, the requirement for Zif268 in the reconsolidation of a response memory was tested by knockdown of Zif268, using antisense oligodeoxynucleotide infusion into the pDLS, at memory reactivation. Zif268 knockdown reduced response memory expression 72H, but not 7d later. Western blotting revealed a non-significant increase in Zif268 in the pDLS in rats using response memories, but there was no change in Zif268 expression in the hippocampus following retrieval of a place memory. Zif268 expression increased in the basolateral amygdala after memory reactivation whether a response or place strategy was used during reactivation. We propose that Zif268 expression in the basolateral amygdala may be linked to prediction error, generated by the absence of reward at reactivation. Taken together, these results suggest a complex role for Zif268 in the maintenance of instrumental memories.
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spelling pubmed-58007402018-02-09 Knockdown of zif268 in the Posterior Dorsolateral Striatum Does Not Enduringly Disrupt a Response Memory of a Rewarded T-Maze Task Cahill, Emma N. Vousden, George H. Exton-McGuinness, Marc T.J. Beh, Ian R.C. Swerner, Casey B. Macak, Matej Abas, Sameera Cole, Cameron C. Kelleher, Brian F. Everitt, Barry J. Milton, Amy L. Neuroscience Article Under certain conditions pavlovian memories undergo reconsolidation, whereby the reactivated memory can be disrupted by manipulations such as knockdown of zif268. For instrumental memories, reconsolidation disruption is less well established. Our previous, preliminary data identified that there was an increase in Zif268 in the posterior dorsolateral striatum (pDLS) after expression of an instrumental habit-like 'response' memory, but not an instrumental goal-directed 'place' memory on a T-maze task. Here, the requirement for Zif268 in the reconsolidation of a response memory was tested by knockdown of Zif268, using antisense oligodeoxynucleotide infusion into the pDLS, at memory reactivation. Zif268 knockdown reduced response memory expression 72H, but not 7d later. Western blotting revealed a non-significant increase in Zif268 in the pDLS in rats using response memories, but there was no change in Zif268 expression in the hippocampus following retrieval of a place memory. Zif268 expression increased in the basolateral amygdala after memory reactivation whether a response or place strategy was used during reactivation. We propose that Zif268 expression in the basolateral amygdala may be linked to prediction error, generated by the absence of reward at reactivation. Taken together, these results suggest a complex role for Zif268 in the maintenance of instrumental memories. Elsevier Science 2018-02-01 /pmc/articles/PMC5800740/ /pubmed/28736133 http://dx.doi.org/10.1016/j.neuroscience.2017.07.014 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cahill, Emma N.
Vousden, George H.
Exton-McGuinness, Marc T.J.
Beh, Ian R.C.
Swerner, Casey B.
Macak, Matej
Abas, Sameera
Cole, Cameron C.
Kelleher, Brian F.
Everitt, Barry J.
Milton, Amy L.
Knockdown of zif268 in the Posterior Dorsolateral Striatum Does Not Enduringly Disrupt a Response Memory of a Rewarded T-Maze Task
title Knockdown of zif268 in the Posterior Dorsolateral Striatum Does Not Enduringly Disrupt a Response Memory of a Rewarded T-Maze Task
title_full Knockdown of zif268 in the Posterior Dorsolateral Striatum Does Not Enduringly Disrupt a Response Memory of a Rewarded T-Maze Task
title_fullStr Knockdown of zif268 in the Posterior Dorsolateral Striatum Does Not Enduringly Disrupt a Response Memory of a Rewarded T-Maze Task
title_full_unstemmed Knockdown of zif268 in the Posterior Dorsolateral Striatum Does Not Enduringly Disrupt a Response Memory of a Rewarded T-Maze Task
title_short Knockdown of zif268 in the Posterior Dorsolateral Striatum Does Not Enduringly Disrupt a Response Memory of a Rewarded T-Maze Task
title_sort knockdown of zif268 in the posterior dorsolateral striatum does not enduringly disrupt a response memory of a rewarded t-maze task
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800740/
https://www.ncbi.nlm.nih.gov/pubmed/28736133
http://dx.doi.org/10.1016/j.neuroscience.2017.07.014
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