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Hippocampal sharp wave‐ripple: A cognitive biomarker for episodic memory and planning
Sharp wave ripples (SPW‐Rs) represent the most synchronous population pattern in the mammalian brain. Their excitatory output affects a wide area of the cortex and several subcortical nuclei. SPW‐Rs occur during “off‐line” states of the brain, associated with consummatory behaviors and non‐REM sleep...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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John Wiley and Sons Inc.
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4648295/ https://www.ncbi.nlm.nih.gov/pubmed/26135716 http://dx.doi.org/10.1002/hipo.22488 |
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author | Buzsáki, György |
author_facet | Buzsáki, György |
author_sort | Buzsáki, György |
collection | PubMed |
description | Sharp wave ripples (SPW‐Rs) represent the most synchronous population pattern in the mammalian brain. Their excitatory output affects a wide area of the cortex and several subcortical nuclei. SPW‐Rs occur during “off‐line” states of the brain, associated with consummatory behaviors and non‐REM sleep, and are influenced by numerous neurotransmitters and neuromodulators. They arise from the excitatory recurrent system of the CA3 region and the SPW‐induced excitation brings about a fast network oscillation (ripple) in CA1. The spike content of SPW‐Rs is temporally and spatially coordinated by a consortium of interneurons to replay fragments of waking neuronal sequences in a compressed format. SPW‐Rs assist in transferring this compressed hippocampal representation to distributed circuits to support memory consolidation; selective disruption of SPW‐Rs interferes with memory. Recently acquired and pre‐existing information are combined during SPW‐R replay to influence decisions, plan actions and, potentially, allow for creative thoughts. In addition to the widely studied contribution to memory, SPW‐Rs may also affect endocrine function via activation of hypothalamic circuits. Alteration of the physiological mechanisms supporting SPW‐Rs leads to their pathological conversion, “p‐ripples,” which are a marker of epileptogenic tissue and can be observed in rodent models of schizophrenia and Alzheimer's Disease. Mechanisms for SPW‐R genesis and function are discussed in this review. © 2015 The Authors Hippocampus Published by Wiley Periodicals, Inc. |
format | Online Article Text |
id | pubmed-4648295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-46482952016-09-23 Hippocampal sharp wave‐ripple: A cognitive biomarker for episodic memory and planning Buzsáki, György Hippocampus Research Articles Sharp wave ripples (SPW‐Rs) represent the most synchronous population pattern in the mammalian brain. Their excitatory output affects a wide area of the cortex and several subcortical nuclei. SPW‐Rs occur during “off‐line” states of the brain, associated with consummatory behaviors and non‐REM sleep, and are influenced by numerous neurotransmitters and neuromodulators. They arise from the excitatory recurrent system of the CA3 region and the SPW‐induced excitation brings about a fast network oscillation (ripple) in CA1. The spike content of SPW‐Rs is temporally and spatially coordinated by a consortium of interneurons to replay fragments of waking neuronal sequences in a compressed format. SPW‐Rs assist in transferring this compressed hippocampal representation to distributed circuits to support memory consolidation; selective disruption of SPW‐Rs interferes with memory. Recently acquired and pre‐existing information are combined during SPW‐R replay to influence decisions, plan actions and, potentially, allow for creative thoughts. In addition to the widely studied contribution to memory, SPW‐Rs may also affect endocrine function via activation of hypothalamic circuits. Alteration of the physiological mechanisms supporting SPW‐Rs leads to their pathological conversion, “p‐ripples,” which are a marker of epileptogenic tissue and can be observed in rodent models of schizophrenia and Alzheimer's Disease. Mechanisms for SPW‐R genesis and function are discussed in this review. © 2015 The Authors Hippocampus Published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2015-09-26 2015-10 /pmc/articles/PMC4648295/ /pubmed/26135716 http://dx.doi.org/10.1002/hipo.22488 Text en © 2015 The Authors Hippocampus Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Buzsáki, György Hippocampal sharp wave‐ripple: A cognitive biomarker for episodic memory and planning |
title | Hippocampal sharp wave‐ripple: A cognitive biomarker for episodic memory and planning |
title_full | Hippocampal sharp wave‐ripple: A cognitive biomarker for episodic memory and planning |
title_fullStr | Hippocampal sharp wave‐ripple: A cognitive biomarker for episodic memory and planning |
title_full_unstemmed | Hippocampal sharp wave‐ripple: A cognitive biomarker for episodic memory and planning |
title_short | Hippocampal sharp wave‐ripple: A cognitive biomarker for episodic memory and planning |
title_sort | hippocampal sharp wave‐ripple: a cognitive biomarker for episodic memory and planning |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4648295/ https://www.ncbi.nlm.nih.gov/pubmed/26135716 http://dx.doi.org/10.1002/hipo.22488 |
work_keys_str_mv | AT buzsakigyorgy hippocampalsharpwaverippleacognitivebiomarkerforepisodicmemoryandplanning |