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Disrupting neural activity related to awake-state sharp wave-ripple complexes prevents hippocampal learning

Oscillations in hippocampal local-field potentials (LFPs) reflect the crucial involvement of the hippocampus in memory trace formation: theta (4–8 Hz) oscillations and ripples (~200 Hz) occurring during sharp waves are thought to mediate encoding and consolidation, respectively. During sharp wave-ri...

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Autores principales: Nokia, Miriam S., Mikkonen, Jarno E., Penttonen, Markku, Wikgren, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3540934/
https://www.ncbi.nlm.nih.gov/pubmed/23316148
http://dx.doi.org/10.3389/fnbeh.2012.00084
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author Nokia, Miriam S.
Mikkonen, Jarno E.
Penttonen, Markku
Wikgren, Jan
author_facet Nokia, Miriam S.
Mikkonen, Jarno E.
Penttonen, Markku
Wikgren, Jan
author_sort Nokia, Miriam S.
collection PubMed
description Oscillations in hippocampal local-field potentials (LFPs) reflect the crucial involvement of the hippocampus in memory trace formation: theta (4–8 Hz) oscillations and ripples (~200 Hz) occurring during sharp waves are thought to mediate encoding and consolidation, respectively. During sharp wave-ripple complexes (SPW-Rs), hippocampal cell firing closely follows the pattern that took place during the initial experience, most likely reflecting replay of that event. Disrupting hippocampal ripples using electrical stimulation either during training in awake animals or during sleep after training retards spatial learning. Here, adult rabbits were trained in trace eyeblink conditioning, a hippocampus-dependent associative learning task. A bright light was presented to the animals during the inter-trial interval (ITI), when awake, either during SPW-Rs or irrespective of their neural state. Learning was particularly poor when the light was presented following SPW-Rs. While the light did not disrupt the ripple itself, it elicited a theta-band oscillation, a state that does not usually coincide with SPW-Rs. Thus, it seems that consolidation depends on neuronal activity within and beyond the hippocampus taking place immediately after, but by no means limited to, hippocampal SPW-Rs.
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spelling pubmed-35409342013-01-11 Disrupting neural activity related to awake-state sharp wave-ripple complexes prevents hippocampal learning Nokia, Miriam S. Mikkonen, Jarno E. Penttonen, Markku Wikgren, Jan Front Behav Neurosci Neuroscience Oscillations in hippocampal local-field potentials (LFPs) reflect the crucial involvement of the hippocampus in memory trace formation: theta (4–8 Hz) oscillations and ripples (~200 Hz) occurring during sharp waves are thought to mediate encoding and consolidation, respectively. During sharp wave-ripple complexes (SPW-Rs), hippocampal cell firing closely follows the pattern that took place during the initial experience, most likely reflecting replay of that event. Disrupting hippocampal ripples using electrical stimulation either during training in awake animals or during sleep after training retards spatial learning. Here, adult rabbits were trained in trace eyeblink conditioning, a hippocampus-dependent associative learning task. A bright light was presented to the animals during the inter-trial interval (ITI), when awake, either during SPW-Rs or irrespective of their neural state. Learning was particularly poor when the light was presented following SPW-Rs. While the light did not disrupt the ripple itself, it elicited a theta-band oscillation, a state that does not usually coincide with SPW-Rs. Thus, it seems that consolidation depends on neuronal activity within and beyond the hippocampus taking place immediately after, but by no means limited to, hippocampal SPW-Rs. Frontiers Media S.A. 2012-12-04 /pmc/articles/PMC3540934/ /pubmed/23316148 http://dx.doi.org/10.3389/fnbeh.2012.00084 Text en Copyright © 2012 Nokia, Mikkonen, Penttonen and Wikgren. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Nokia, Miriam S.
Mikkonen, Jarno E.
Penttonen, Markku
Wikgren, Jan
Disrupting neural activity related to awake-state sharp wave-ripple complexes prevents hippocampal learning
title Disrupting neural activity related to awake-state sharp wave-ripple complexes prevents hippocampal learning
title_full Disrupting neural activity related to awake-state sharp wave-ripple complexes prevents hippocampal learning
title_fullStr Disrupting neural activity related to awake-state sharp wave-ripple complexes prevents hippocampal learning
title_full_unstemmed Disrupting neural activity related to awake-state sharp wave-ripple complexes prevents hippocampal learning
title_short Disrupting neural activity related to awake-state sharp wave-ripple complexes prevents hippocampal learning
title_sort disrupting neural activity related to awake-state sharp wave-ripple complexes prevents hippocampal learning
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3540934/
https://www.ncbi.nlm.nih.gov/pubmed/23316148
http://dx.doi.org/10.3389/fnbeh.2012.00084
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