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Stretch induced hyperexcitability of mice callosal pathway
Memory and learning are thought to result from changes in synaptic strength. Previous studies on synaptic physiology in brain slices have traditionally been focused on biochemical processes. Here, we demonstrate with experiments on mouse brain slices that central nervous system plasticity is also se...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4525056/ https://www.ncbi.nlm.nih.gov/pubmed/26300729 http://dx.doi.org/10.3389/fncel.2015.00292 |
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author | Fan, Anthony Stebbings, Kevin A. Llano, Daniel A. Saif, Taher |
author_facet | Fan, Anthony Stebbings, Kevin A. Llano, Daniel A. Saif, Taher |
author_sort | Fan, Anthony |
collection | PubMed |
description | Memory and learning are thought to result from changes in synaptic strength. Previous studies on synaptic physiology in brain slices have traditionally been focused on biochemical processes. Here, we demonstrate with experiments on mouse brain slices that central nervous system plasticity is also sensitive to mechanical stretch. This is important, given the host of clinical conditions involving changes in mechanical tension on the brain, and the normal role that mechanical tension plays in brain development. A novel platform is developed to investigate neural responses to mechanical stretching. Flavoprotein autofluoresence (FA) imaging was employed for measuring neural activity. We observed that synaptic excitability substantially increases after a small (2.5%) stretch was held for 10 min and released. The increase is accumulative, i.e., multiple stretch cycles further increase the excitability. We also developed analytical tools to quantify the spatial spread and response strength. Results show that the spatial spread is less stable in slices undergoing the stretch-unstretch cycle. FA amplitude and activation rate decrease as excitability increases in stretch cases but not in electrically enhanced cases. These results collectively demonstrate that a small stretch in physiological range can modulate neural activities significantly, suggesting that mechanical events can be employed as a novel tool for the modulation of neural plasticity. |
format | Online Article Text |
id | pubmed-4525056 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-45250562015-08-21 Stretch induced hyperexcitability of mice callosal pathway Fan, Anthony Stebbings, Kevin A. Llano, Daniel A. Saif, Taher Front Cell Neurosci Neuroscience Memory and learning are thought to result from changes in synaptic strength. Previous studies on synaptic physiology in brain slices have traditionally been focused on biochemical processes. Here, we demonstrate with experiments on mouse brain slices that central nervous system plasticity is also sensitive to mechanical stretch. This is important, given the host of clinical conditions involving changes in mechanical tension on the brain, and the normal role that mechanical tension plays in brain development. A novel platform is developed to investigate neural responses to mechanical stretching. Flavoprotein autofluoresence (FA) imaging was employed for measuring neural activity. We observed that synaptic excitability substantially increases after a small (2.5%) stretch was held for 10 min and released. The increase is accumulative, i.e., multiple stretch cycles further increase the excitability. We also developed analytical tools to quantify the spatial spread and response strength. Results show that the spatial spread is less stable in slices undergoing the stretch-unstretch cycle. FA amplitude and activation rate decrease as excitability increases in stretch cases but not in electrically enhanced cases. These results collectively demonstrate that a small stretch in physiological range can modulate neural activities significantly, suggesting that mechanical events can be employed as a novel tool for the modulation of neural plasticity. Frontiers Media S.A. 2015-08-05 /pmc/articles/PMC4525056/ /pubmed/26300729 http://dx.doi.org/10.3389/fncel.2015.00292 Text en Copyright © 2015 Fan, Stebbings, Llano and Saif. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Fan, Anthony Stebbings, Kevin A. Llano, Daniel A. Saif, Taher Stretch induced hyperexcitability of mice callosal pathway |
title | Stretch induced hyperexcitability of mice callosal pathway |
title_full | Stretch induced hyperexcitability of mice callosal pathway |
title_fullStr | Stretch induced hyperexcitability of mice callosal pathway |
title_full_unstemmed | Stretch induced hyperexcitability of mice callosal pathway |
title_short | Stretch induced hyperexcitability of mice callosal pathway |
title_sort | stretch induced hyperexcitability of mice callosal pathway |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4525056/ https://www.ncbi.nlm.nih.gov/pubmed/26300729 http://dx.doi.org/10.3389/fncel.2015.00292 |
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