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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...

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Autores principales: Bazzigaluppi, Paolo, De Gruijl, Jornt R., van der Giessen, Ruben S., Khosrovani, Sara, De Zeeuw, Chris I., de Jeu, Marcel T. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
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.
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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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