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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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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 |
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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 |
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