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In Vivo Mesoscopic Voltage-Sensitive Dye Imaging of Brain Activation
Functional mapping of brain activity is important in elucidating how neural networks operate in the living brain. The whisker sensory system of rodents is an excellent model to study peripherally evoked neural activity in the central nervous system. Each facial whisker is represented by discrete mod...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4850485/ https://www.ncbi.nlm.nih.gov/pubmed/27125318 http://dx.doi.org/10.1038/srep25269 |
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author | Tang, Qinggong Tsytsarev, Vassiliy Frank, Aaron Wu, Yalun Chen, Chao-wei Erzurumlu, Reha S. Chen, Yu |
author_facet | Tang, Qinggong Tsytsarev, Vassiliy Frank, Aaron Wu, Yalun Chen, Chao-wei Erzurumlu, Reha S. Chen, Yu |
author_sort | Tang, Qinggong |
collection | PubMed |
description | Functional mapping of brain activity is important in elucidating how neural networks operate in the living brain. The whisker sensory system of rodents is an excellent model to study peripherally evoked neural activity in the central nervous system. Each facial whisker is represented by discrete modules of neurons all along the pathway leading to the neocortex. These modules are called “barrels” in layer 4 of the primary somatosensory cortex. Their location (approximately 300–500 μm below cortical surface) allows for convenient imaging of whisker-evoked neural activity in vivo. Fluorescence laminar optical tomography (FLOT) provides depth-resolved fluorescence molecular information with an imaging depth of a few millimeters. Angled illumination and detection configurations can improve both resolution and penetration depth. We applied angled FLOT (aFLOT) to record 3D neural activities evoked in the whisker system of mice by deflection of a single whisker in vivo. A 100 μm capillary and a pair of microelectrodes were inserted to the mouse brain to test the capability of the imaging system. The results show that it is possible to obtain 3D functional maps of the sensory periphery in the brain. This approach can be broadly applicable to functional imaging of other brain structures. |
format | Online Article Text |
id | pubmed-4850485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48504852016-05-16 In Vivo Mesoscopic Voltage-Sensitive Dye Imaging of Brain Activation Tang, Qinggong Tsytsarev, Vassiliy Frank, Aaron Wu, Yalun Chen, Chao-wei Erzurumlu, Reha S. Chen, Yu Sci Rep Article Functional mapping of brain activity is important in elucidating how neural networks operate in the living brain. The whisker sensory system of rodents is an excellent model to study peripherally evoked neural activity in the central nervous system. Each facial whisker is represented by discrete modules of neurons all along the pathway leading to the neocortex. These modules are called “barrels” in layer 4 of the primary somatosensory cortex. Their location (approximately 300–500 μm below cortical surface) allows for convenient imaging of whisker-evoked neural activity in vivo. Fluorescence laminar optical tomography (FLOT) provides depth-resolved fluorescence molecular information with an imaging depth of a few millimeters. Angled illumination and detection configurations can improve both resolution and penetration depth. We applied angled FLOT (aFLOT) to record 3D neural activities evoked in the whisker system of mice by deflection of a single whisker in vivo. A 100 μm capillary and a pair of microelectrodes were inserted to the mouse brain to test the capability of the imaging system. The results show that it is possible to obtain 3D functional maps of the sensory periphery in the brain. This approach can be broadly applicable to functional imaging of other brain structures. Nature Publishing Group 2016-04-29 /pmc/articles/PMC4850485/ /pubmed/27125318 http://dx.doi.org/10.1038/srep25269 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Tang, Qinggong Tsytsarev, Vassiliy Frank, Aaron Wu, Yalun Chen, Chao-wei Erzurumlu, Reha S. Chen, Yu In Vivo Mesoscopic Voltage-Sensitive Dye Imaging of Brain Activation |
title | In Vivo Mesoscopic Voltage-Sensitive Dye Imaging of Brain Activation |
title_full | In Vivo Mesoscopic Voltage-Sensitive Dye Imaging of Brain Activation |
title_fullStr | In Vivo Mesoscopic Voltage-Sensitive Dye Imaging of Brain Activation |
title_full_unstemmed | In Vivo Mesoscopic Voltage-Sensitive Dye Imaging of Brain Activation |
title_short | In Vivo Mesoscopic Voltage-Sensitive Dye Imaging of Brain Activation |
title_sort | in vivo mesoscopic voltage-sensitive dye imaging of brain activation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4850485/ https://www.ncbi.nlm.nih.gov/pubmed/27125318 http://dx.doi.org/10.1038/srep25269 |
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