Cargando…

Adaptation to prolonged neuromodulation in cortical cultures: an invariable return to network synchrony

BACKGROUND: Prolonged neuromodulatory regimes, such as those critically involved in promoting arousal and suppressing sleep-associated synchronous activity patterns, might be expected to trigger adaptation processes and, consequently, a decline in neuromodulator-driven effects. This possibility, how...

Descripción completa

Detalles Bibliográficos
Autores principales: Kaufman, Maya, Reinartz, Sebastian, Ziv, Noam E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237737/
https://www.ncbi.nlm.nih.gov/pubmed/25339462
http://dx.doi.org/10.1186/s12915-014-0083-3
_version_ 1782345384247427072
author Kaufman, Maya
Reinartz, Sebastian
Ziv, Noam E
author_facet Kaufman, Maya
Reinartz, Sebastian
Ziv, Noam E
author_sort Kaufman, Maya
collection PubMed
description BACKGROUND: Prolonged neuromodulatory regimes, such as those critically involved in promoting arousal and suppressing sleep-associated synchronous activity patterns, might be expected to trigger adaptation processes and, consequently, a decline in neuromodulator-driven effects. This possibility, however, has rarely been addressed. RESULTS: Using networks of cultured cortical neurons, acetylcholine microinjections and a novel closed-loop ‘synchrony-clamp’ system, we found that acetylcholine pulses strongly suppressed network synchrony. Over the course of many hours, however, synchrony invariably reemerged, even when feedback was used to compensate for declining cholinergic efficacy. Network synchrony also reemerged following its initial suppression by noradrenaline, but this did not occlude the suppression of synchrony or its gradual reemergence following subsequent cholinergic input. Importantly, cholinergic efficacy could be restored and preserved over extended time scales by periodically withdrawing cholinergic input. CONCLUSIONS: These findings indicate that the capacity of neuromodulators to suppress network synchrony is constrained by slow-acting, reactive processes. A multiplicity of neuromodulators and ultimately neuromodulator withdrawal periods might thus be necessary to cope with an inevitable reemergence of network synchrony. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-014-0083-3) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4237737
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-42377372014-11-24 Adaptation to prolonged neuromodulation in cortical cultures: an invariable return to network synchrony Kaufman, Maya Reinartz, Sebastian Ziv, Noam E BMC Biol Research Article BACKGROUND: Prolonged neuromodulatory regimes, such as those critically involved in promoting arousal and suppressing sleep-associated synchronous activity patterns, might be expected to trigger adaptation processes and, consequently, a decline in neuromodulator-driven effects. This possibility, however, has rarely been addressed. RESULTS: Using networks of cultured cortical neurons, acetylcholine microinjections and a novel closed-loop ‘synchrony-clamp’ system, we found that acetylcholine pulses strongly suppressed network synchrony. Over the course of many hours, however, synchrony invariably reemerged, even when feedback was used to compensate for declining cholinergic efficacy. Network synchrony also reemerged following its initial suppression by noradrenaline, but this did not occlude the suppression of synchrony or its gradual reemergence following subsequent cholinergic input. Importantly, cholinergic efficacy could be restored and preserved over extended time scales by periodically withdrawing cholinergic input. CONCLUSIONS: These findings indicate that the capacity of neuromodulators to suppress network synchrony is constrained by slow-acting, reactive processes. A multiplicity of neuromodulators and ultimately neuromodulator withdrawal periods might thus be necessary to cope with an inevitable reemergence of network synchrony. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-014-0083-3) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-23 /pmc/articles/PMC4237737/ /pubmed/25339462 http://dx.doi.org/10.1186/s12915-014-0083-3 Text en © Kaufman et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kaufman, Maya
Reinartz, Sebastian
Ziv, Noam E
Adaptation to prolonged neuromodulation in cortical cultures: an invariable return to network synchrony
title Adaptation to prolonged neuromodulation in cortical cultures: an invariable return to network synchrony
title_full Adaptation to prolonged neuromodulation in cortical cultures: an invariable return to network synchrony
title_fullStr Adaptation to prolonged neuromodulation in cortical cultures: an invariable return to network synchrony
title_full_unstemmed Adaptation to prolonged neuromodulation in cortical cultures: an invariable return to network synchrony
title_short Adaptation to prolonged neuromodulation in cortical cultures: an invariable return to network synchrony
title_sort adaptation to prolonged neuromodulation in cortical cultures: an invariable return to network synchrony
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237737/
https://www.ncbi.nlm.nih.gov/pubmed/25339462
http://dx.doi.org/10.1186/s12915-014-0083-3
work_keys_str_mv AT kaufmanmaya adaptationtoprolongedneuromodulationincorticalculturesaninvariablereturntonetworksynchrony
AT reinartzsebastian adaptationtoprolongedneuromodulationincorticalculturesaninvariablereturntonetworksynchrony
AT zivnoame adaptationtoprolongedneuromodulationincorticalculturesaninvariablereturntonetworksynchrony