Cargando…

ATP-Dependent Infra-Slow (<0.1 Hz) Oscillations in Thalamic Networks

An increasing number of EEG and resting state fMRI studies in both humans and animals indicate that spontaneous low frequency fluctuations in cerebral activity at <0.1 Hz (infra-slow oscillations, ISOs) represent a fundamental component of brain functioning, being known to correlate with faster n...

Descripción completa

Detalles Bibliográficos
Autores principales: Lőrincz, Magor L., Geall, Freya, Bao, Ying, Crunelli, Vincenzo, Hughes, Stuart W.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2637539/
https://www.ncbi.nlm.nih.gov/pubmed/19212445
http://dx.doi.org/10.1371/journal.pone.0004447
_version_ 1782164359102857216
author Lőrincz, Magor L.
Geall, Freya
Bao, Ying
Crunelli, Vincenzo
Hughes, Stuart W.
author_facet Lőrincz, Magor L.
Geall, Freya
Bao, Ying
Crunelli, Vincenzo
Hughes, Stuart W.
author_sort Lőrincz, Magor L.
collection PubMed
description An increasing number of EEG and resting state fMRI studies in both humans and animals indicate that spontaneous low frequency fluctuations in cerebral activity at <0.1 Hz (infra-slow oscillations, ISOs) represent a fundamental component of brain functioning, being known to correlate with faster neuronal ensemble oscillations, regulate behavioural performance and influence seizure susceptibility. Although these oscillations have been commonly indicated to involve the thalamus their basic cellular mechanisms remain poorly understood. Here we show that various nuclei in the dorsal thalamus in vitro can express a robust ISO at ∼0.005–0.1 Hz that is greatly facilitated by activating metabotropic glutamate receptors (mGluRs) and/or Ach receptors (AchRs). This ISO is a neuronal population phenomenon which modulates faster gap junction (GJ)-dependent network oscillations, and can underlie epileptic activity when AchRs or mGluRs are stimulated excessively. In individual thalamocortical neurons the ISO is primarily shaped by rhythmic, long-lasting hyperpolarizing potentials which reflect the activation of A1 receptors, by ATP-derived adenosine, and subsequent opening of Ba(2+)-sensitive K(+) channels. We argue that this ISO has a likely non-neuronal origin and may contribute to shaping ISOs in the intact brain.
format Text
id pubmed-2637539
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-26375392009-02-12 ATP-Dependent Infra-Slow (<0.1 Hz) Oscillations in Thalamic Networks Lőrincz, Magor L. Geall, Freya Bao, Ying Crunelli, Vincenzo Hughes, Stuart W. PLoS One Research Article An increasing number of EEG and resting state fMRI studies in both humans and animals indicate that spontaneous low frequency fluctuations in cerebral activity at <0.1 Hz (infra-slow oscillations, ISOs) represent a fundamental component of brain functioning, being known to correlate with faster neuronal ensemble oscillations, regulate behavioural performance and influence seizure susceptibility. Although these oscillations have been commonly indicated to involve the thalamus their basic cellular mechanisms remain poorly understood. Here we show that various nuclei in the dorsal thalamus in vitro can express a robust ISO at ∼0.005–0.1 Hz that is greatly facilitated by activating metabotropic glutamate receptors (mGluRs) and/or Ach receptors (AchRs). This ISO is a neuronal population phenomenon which modulates faster gap junction (GJ)-dependent network oscillations, and can underlie epileptic activity when AchRs or mGluRs are stimulated excessively. In individual thalamocortical neurons the ISO is primarily shaped by rhythmic, long-lasting hyperpolarizing potentials which reflect the activation of A1 receptors, by ATP-derived adenosine, and subsequent opening of Ba(2+)-sensitive K(+) channels. We argue that this ISO has a likely non-neuronal origin and may contribute to shaping ISOs in the intact brain. Public Library of Science 2009-02-12 /pmc/articles/PMC2637539/ /pubmed/19212445 http://dx.doi.org/10.1371/journal.pone.0004447 Text en Lőrincz et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lőrincz, Magor L.
Geall, Freya
Bao, Ying
Crunelli, Vincenzo
Hughes, Stuart W.
ATP-Dependent Infra-Slow (<0.1 Hz) Oscillations in Thalamic Networks
title ATP-Dependent Infra-Slow (<0.1 Hz) Oscillations in Thalamic Networks
title_full ATP-Dependent Infra-Slow (<0.1 Hz) Oscillations in Thalamic Networks
title_fullStr ATP-Dependent Infra-Slow (<0.1 Hz) Oscillations in Thalamic Networks
title_full_unstemmed ATP-Dependent Infra-Slow (<0.1 Hz) Oscillations in Thalamic Networks
title_short ATP-Dependent Infra-Slow (<0.1 Hz) Oscillations in Thalamic Networks
title_sort atp-dependent infra-slow (<0.1 hz) oscillations in thalamic networks
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2637539/
https://www.ncbi.nlm.nih.gov/pubmed/19212445
http://dx.doi.org/10.1371/journal.pone.0004447
work_keys_str_mv AT lorinczmagorl atpdependentinfraslow01hzoscillationsinthalamicnetworks
AT geallfreya atpdependentinfraslow01hzoscillationsinthalamicnetworks
AT baoying atpdependentinfraslow01hzoscillationsinthalamicnetworks
AT crunellivincenzo atpdependentinfraslow01hzoscillationsinthalamicnetworks
AT hughesstuartw atpdependentinfraslow01hzoscillationsinthalamicnetworks