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Olivary subthreshold oscillations and burst activity revisited
The inferior olive (IO) forms one of the major gateways for information that travels to the cerebellar cortex. Olivary neurons process sensory and motor signals that are subsequently relayed to Purkinje cells. The intrinsic subthreshold membrane potential oscillations of the olivary neurons are thou...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504313/ https://www.ncbi.nlm.nih.gov/pubmed/23189043 http://dx.doi.org/10.3389/fncir.2012.00091 |
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author | Bazzigaluppi, Paolo De Gruijl, Jornt R. van der Giessen, Ruben S. Khosrovani, Sara De Zeeuw, Chris I. de Jeu, Marcel T. G. |
author_facet | Bazzigaluppi, Paolo De Gruijl, Jornt R. van der Giessen, Ruben S. Khosrovani, Sara De Zeeuw, Chris I. de Jeu, Marcel T. G. |
author_sort | Bazzigaluppi, Paolo |
collection | PubMed |
description | The inferior olive (IO) forms one of the major gateways for information that travels to the cerebellar cortex. Olivary neurons process sensory and motor signals that are subsequently relayed to Purkinje cells. The intrinsic subthreshold membrane potential oscillations of the olivary neurons are thought to be important for gating this flow of information. In vitro studies have revealed that the phase of the subthreshold oscillation determines the size of the olivary burst and may gate the information flow or encode the temporal state of the olivary network. Here, we investigated whether the same phenomenon occurred in murine olivary cells in an intact olivocerebellar system using the in vivo whole-cell recording technique. Our in vivo findings revealed that the number of wavelets within the olivary burst did not encode the timing of the spike relative to the phase of the oscillation but was related to the amplitude of the oscillation. Manipulating the oscillation amplitude by applying Harmaline confirmed the inverse relationship between the amplitude of oscillation and the number of wavelets within the olivary burst. Furthermore, we demonstrated that electrotonic coupling between olivary neurons affect this modulation of the olivary burst size. Based on these results, we suggest that the olivary burst size might reflect the “expectancy” of a spike to occur rather than the spike timing, and that this process requires the presence of gap junction coupling. |
format | Online Article Text |
id | pubmed-3504313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-35043132012-11-27 Olivary subthreshold oscillations and burst activity revisited Bazzigaluppi, Paolo De Gruijl, Jornt R. van der Giessen, Ruben S. Khosrovani, Sara De Zeeuw, Chris I. de Jeu, Marcel T. G. Front Neural Circuits Neuroscience The inferior olive (IO) forms one of the major gateways for information that travels to the cerebellar cortex. Olivary neurons process sensory and motor signals that are subsequently relayed to Purkinje cells. The intrinsic subthreshold membrane potential oscillations of the olivary neurons are thought to be important for gating this flow of information. In vitro studies have revealed that the phase of the subthreshold oscillation determines the size of the olivary burst and may gate the information flow or encode the temporal state of the olivary network. Here, we investigated whether the same phenomenon occurred in murine olivary cells in an intact olivocerebellar system using the in vivo whole-cell recording technique. Our in vivo findings revealed that the number of wavelets within the olivary burst did not encode the timing of the spike relative to the phase of the oscillation but was related to the amplitude of the oscillation. Manipulating the oscillation amplitude by applying Harmaline confirmed the inverse relationship between the amplitude of oscillation and the number of wavelets within the olivary burst. Furthermore, we demonstrated that electrotonic coupling between olivary neurons affect this modulation of the olivary burst size. Based on these results, we suggest that the olivary burst size might reflect the “expectancy” of a spike to occur rather than the spike timing, and that this process requires the presence of gap junction coupling. Frontiers Media S.A. 2012-11-22 /pmc/articles/PMC3504313/ /pubmed/23189043 http://dx.doi.org/10.3389/fncir.2012.00091 Text en Copyright © 2012 Bazzigaluppi, De Gruijl, van der Giessen, Khosrovani, De Zeeuw and de Jeu. http://www.frontiersin.org/licenseagreement 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 Bazzigaluppi, Paolo De Gruijl, Jornt R. van der Giessen, Ruben S. Khosrovani, Sara De Zeeuw, Chris I. de Jeu, Marcel T. G. Olivary subthreshold oscillations and burst activity revisited |
title | Olivary subthreshold oscillations and burst activity revisited |
title_full | Olivary subthreshold oscillations and burst activity revisited |
title_fullStr | Olivary subthreshold oscillations and burst activity revisited |
title_full_unstemmed | Olivary subthreshold oscillations and burst activity revisited |
title_short | Olivary subthreshold oscillations and burst activity revisited |
title_sort | olivary subthreshold oscillations and burst activity revisited |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504313/ https://www.ncbi.nlm.nih.gov/pubmed/23189043 http://dx.doi.org/10.3389/fncir.2012.00091 |
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