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Synaptic up-scaling preserves motor circuit output after chronic, natural inactivity
Neural systems use homeostatic plasticity to maintain normal brain functions and to prevent abnormal activity. Surprisingly, homeostatic mechanisms that regulate circuit output have mainly been demonstrated during artificial and/or pathological perturbations. Natural, physiological scenarios that ac...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5636609/ https://www.ncbi.nlm.nih.gov/pubmed/28914603 http://dx.doi.org/10.7554/eLife.30005 |
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author | Santin, Joseph M Vallejo, Mauricio Hartzler, Lynn K |
author_facet | Santin, Joseph M Vallejo, Mauricio Hartzler, Lynn K |
author_sort | Santin, Joseph M |
collection | PubMed |
description | Neural systems use homeostatic plasticity to maintain normal brain functions and to prevent abnormal activity. Surprisingly, homeostatic mechanisms that regulate circuit output have mainly been demonstrated during artificial and/or pathological perturbations. Natural, physiological scenarios that activate these stabilizing mechanisms in neural networks of mature animals remain elusive. To establish the extent to which a naturally inactive circuit engages mechanisms of homeostatic plasticity, we utilized the respiratory motor circuit in bullfrogs that normally remains inactive for several months during the winter. We found that inactive respiratory motoneurons exhibit a classic form of homeostatic plasticity, up-scaling of AMPA-glutamate receptors. Up-scaling increased the synaptic strength of respiratory motoneurons and acted to boost motor amplitude from the respiratory network following months of inactivity. Our results show that synaptic scaling sustains strength of the respiratory motor output following months of inactivity, thereby supporting a major neuroscience hypothesis in a normal context for an adult animal. |
format | Online Article Text |
id | pubmed-5636609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56366092017-10-12 Synaptic up-scaling preserves motor circuit output after chronic, natural inactivity Santin, Joseph M Vallejo, Mauricio Hartzler, Lynn K eLife Neuroscience Neural systems use homeostatic plasticity to maintain normal brain functions and to prevent abnormal activity. Surprisingly, homeostatic mechanisms that regulate circuit output have mainly been demonstrated during artificial and/or pathological perturbations. Natural, physiological scenarios that activate these stabilizing mechanisms in neural networks of mature animals remain elusive. To establish the extent to which a naturally inactive circuit engages mechanisms of homeostatic plasticity, we utilized the respiratory motor circuit in bullfrogs that normally remains inactive for several months during the winter. We found that inactive respiratory motoneurons exhibit a classic form of homeostatic plasticity, up-scaling of AMPA-glutamate receptors. Up-scaling increased the synaptic strength of respiratory motoneurons and acted to boost motor amplitude from the respiratory network following months of inactivity. Our results show that synaptic scaling sustains strength of the respiratory motor output following months of inactivity, thereby supporting a major neuroscience hypothesis in a normal context for an adult animal. eLife Sciences Publications, Ltd 2017-09-15 /pmc/articles/PMC5636609/ /pubmed/28914603 http://dx.doi.org/10.7554/eLife.30005 Text en © 2017, Santin et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Santin, Joseph M Vallejo, Mauricio Hartzler, Lynn K Synaptic up-scaling preserves motor circuit output after chronic, natural inactivity |
title | Synaptic up-scaling preserves motor circuit output after chronic, natural inactivity |
title_full | Synaptic up-scaling preserves motor circuit output after chronic, natural inactivity |
title_fullStr | Synaptic up-scaling preserves motor circuit output after chronic, natural inactivity |
title_full_unstemmed | Synaptic up-scaling preserves motor circuit output after chronic, natural inactivity |
title_short | Synaptic up-scaling preserves motor circuit output after chronic, natural inactivity |
title_sort | synaptic up-scaling preserves motor circuit output after chronic, natural inactivity |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5636609/ https://www.ncbi.nlm.nih.gov/pubmed/28914603 http://dx.doi.org/10.7554/eLife.30005 |
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