Cargando…
NREM sleep in the rodent neocortex and hippocampus reflects excitable dynamics
During non-rapid eye movement (NREM) sleep, neuronal populations in the mammalian forebrain alternate between periods of spiking and inactivity. Termed the slow oscillation in the neocortex and sharp wave-ripples in the hippocampus, these alternations are often considered separately but are both cru...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6554409/ https://www.ncbi.nlm.nih.gov/pubmed/31171779 http://dx.doi.org/10.1038/s41467-019-10327-5 |
_version_ | 1783424964185030656 |
---|---|
author | Levenstein, Daniel Buzsáki, György Rinzel, John |
author_facet | Levenstein, Daniel Buzsáki, György Rinzel, John |
author_sort | Levenstein, Daniel |
collection | PubMed |
description | During non-rapid eye movement (NREM) sleep, neuronal populations in the mammalian forebrain alternate between periods of spiking and inactivity. Termed the slow oscillation in the neocortex and sharp wave-ripples in the hippocampus, these alternations are often considered separately but are both crucial for NREM functions. By directly comparing experimental observations of naturally-sleeping rats with a mean field model of an adapting, recurrent neuronal population, we find that the neocortical alternations reflect a dynamical regime in which a stable active state is interrupted by transient inactive states (slow waves) while the hippocampal alternations reflect a stable inactive state interrupted by transient active states (sharp waves). We propose that during NREM sleep in the rodent, hippocampal and neocortical populations are excitable: each in a stable state from which internal fluctuations or external perturbation can evoke the stereotyped population events that mediate NREM functions. |
format | Online Article Text |
id | pubmed-6554409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65544092019-06-17 NREM sleep in the rodent neocortex and hippocampus reflects excitable dynamics Levenstein, Daniel Buzsáki, György Rinzel, John Nat Commun Article During non-rapid eye movement (NREM) sleep, neuronal populations in the mammalian forebrain alternate between periods of spiking and inactivity. Termed the slow oscillation in the neocortex and sharp wave-ripples in the hippocampus, these alternations are often considered separately but are both crucial for NREM functions. By directly comparing experimental observations of naturally-sleeping rats with a mean field model of an adapting, recurrent neuronal population, we find that the neocortical alternations reflect a dynamical regime in which a stable active state is interrupted by transient inactive states (slow waves) while the hippocampal alternations reflect a stable inactive state interrupted by transient active states (sharp waves). We propose that during NREM sleep in the rodent, hippocampal and neocortical populations are excitable: each in a stable state from which internal fluctuations or external perturbation can evoke the stereotyped population events that mediate NREM functions. Nature Publishing Group UK 2019-06-06 /pmc/articles/PMC6554409/ /pubmed/31171779 http://dx.doi.org/10.1038/s41467-019-10327-5 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Levenstein, Daniel Buzsáki, György Rinzel, John NREM sleep in the rodent neocortex and hippocampus reflects excitable dynamics |
title | NREM sleep in the rodent neocortex and hippocampus reflects excitable dynamics |
title_full | NREM sleep in the rodent neocortex and hippocampus reflects excitable dynamics |
title_fullStr | NREM sleep in the rodent neocortex and hippocampus reflects excitable dynamics |
title_full_unstemmed | NREM sleep in the rodent neocortex and hippocampus reflects excitable dynamics |
title_short | NREM sleep in the rodent neocortex and hippocampus reflects excitable dynamics |
title_sort | nrem sleep in the rodent neocortex and hippocampus reflects excitable dynamics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6554409/ https://www.ncbi.nlm.nih.gov/pubmed/31171779 http://dx.doi.org/10.1038/s41467-019-10327-5 |
work_keys_str_mv | AT levensteindaniel nremsleepintherodentneocortexandhippocampusreflectsexcitabledynamics AT buzsakigyorgy nremsleepintherodentneocortexandhippocampusreflectsexcitabledynamics AT rinzeljohn nremsleepintherodentneocortexandhippocampusreflectsexcitabledynamics |