Cargando…

Ventromedial prefrontal cortex drives hippocampal theta oscillations induced by mismatch computations

Detecting environmental change is fundamental for adaptive behavior in an uncertain world. Previous work indicates the hippocampus supports the generation of novelty signals via implementation of a match–mismatch detector that signals when an incoming sensory input violates expectations based on pas...

Descripción completa

Detalles Bibliográficos
Autores principales: Garrido, Marta I., Barnes, Gareth R., Kumaran, Dharshan, Maguire, Eleanor A., Dolan, Raymond J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4594308/
https://www.ncbi.nlm.nih.gov/pubmed/26187453
http://dx.doi.org/10.1016/j.neuroimage.2015.07.016
_version_ 1782393431912349696
author Garrido, Marta I.
Barnes, Gareth R.
Kumaran, Dharshan
Maguire, Eleanor A.
Dolan, Raymond J.
author_facet Garrido, Marta I.
Barnes, Gareth R.
Kumaran, Dharshan
Maguire, Eleanor A.
Dolan, Raymond J.
author_sort Garrido, Marta I.
collection PubMed
description Detecting environmental change is fundamental for adaptive behavior in an uncertain world. Previous work indicates the hippocampus supports the generation of novelty signals via implementation of a match–mismatch detector that signals when an incoming sensory input violates expectations based on past experience. While existing work has emphasized the particular contribution of the hippocampus, here we ask which other brain structures also contribute to match–mismatch detection. Furthermore, we leverage the fine-grained temporal resolution of magnetoencephalography (MEG) to investigate whether mismatch computations are spectrally confined to the theta range, based on the prominence of this range of oscillations in models of hippocampal function. By recording MEG activity while human subjects perform a task that incorporates conditions of match–mismatch novelty we show that mismatch signals are confined to the theta band and are expressed in both the hippocampus and ventromedial prefrontal cortex (vmPFC). Effective connectivity analyses (dynamic causal modeling) show that the hippocampus and vmPFC work as a functional circuit during mismatch detection. Surprisingly, our results suggest that the vmPFC drives the hippocampus during the generation and processing of mismatch signals. Our findings provide new evidence that the hippocampal–vmPFC circuit is engaged during novelty processing, which has implications for emerging theories regarding the role of vmPFC in memory.
format Online
Article
Text
id pubmed-4594308
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Academic Press
record_format MEDLINE/PubMed
spelling pubmed-45943082015-10-28 Ventromedial prefrontal cortex drives hippocampal theta oscillations induced by mismatch computations Garrido, Marta I. Barnes, Gareth R. Kumaran, Dharshan Maguire, Eleanor A. Dolan, Raymond J. Neuroimage Article Detecting environmental change is fundamental for adaptive behavior in an uncertain world. Previous work indicates the hippocampus supports the generation of novelty signals via implementation of a match–mismatch detector that signals when an incoming sensory input violates expectations based on past experience. While existing work has emphasized the particular contribution of the hippocampus, here we ask which other brain structures also contribute to match–mismatch detection. Furthermore, we leverage the fine-grained temporal resolution of magnetoencephalography (MEG) to investigate whether mismatch computations are spectrally confined to the theta range, based on the prominence of this range of oscillations in models of hippocampal function. By recording MEG activity while human subjects perform a task that incorporates conditions of match–mismatch novelty we show that mismatch signals are confined to the theta band and are expressed in both the hippocampus and ventromedial prefrontal cortex (vmPFC). Effective connectivity analyses (dynamic causal modeling) show that the hippocampus and vmPFC work as a functional circuit during mismatch detection. Surprisingly, our results suggest that the vmPFC drives the hippocampus during the generation and processing of mismatch signals. Our findings provide new evidence that the hippocampal–vmPFC circuit is engaged during novelty processing, which has implications for emerging theories regarding the role of vmPFC in memory. Academic Press 2015-10-15 /pmc/articles/PMC4594308/ /pubmed/26187453 http://dx.doi.org/10.1016/j.neuroimage.2015.07.016 Text en © 2015 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Garrido, Marta I.
Barnes, Gareth R.
Kumaran, Dharshan
Maguire, Eleanor A.
Dolan, Raymond J.
Ventromedial prefrontal cortex drives hippocampal theta oscillations induced by mismatch computations
title Ventromedial prefrontal cortex drives hippocampal theta oscillations induced by mismatch computations
title_full Ventromedial prefrontal cortex drives hippocampal theta oscillations induced by mismatch computations
title_fullStr Ventromedial prefrontal cortex drives hippocampal theta oscillations induced by mismatch computations
title_full_unstemmed Ventromedial prefrontal cortex drives hippocampal theta oscillations induced by mismatch computations
title_short Ventromedial prefrontal cortex drives hippocampal theta oscillations induced by mismatch computations
title_sort ventromedial prefrontal cortex drives hippocampal theta oscillations induced by mismatch computations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4594308/
https://www.ncbi.nlm.nih.gov/pubmed/26187453
http://dx.doi.org/10.1016/j.neuroimage.2015.07.016
work_keys_str_mv AT garridomartai ventromedialprefrontalcortexdriveshippocampalthetaoscillationsinducedbymismatchcomputations
AT barnesgarethr ventromedialprefrontalcortexdriveshippocampalthetaoscillationsinducedbymismatchcomputations
AT kumarandharshan ventromedialprefrontalcortexdriveshippocampalthetaoscillationsinducedbymismatchcomputations
AT maguireeleanora ventromedialprefrontalcortexdriveshippocampalthetaoscillationsinducedbymismatchcomputations
AT dolanraymondj ventromedialprefrontalcortexdriveshippocampalthetaoscillationsinducedbymismatchcomputations