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Light controls cerebral blood flow in naive animals

Optogenetics is increasingly used to map brain activation using techniques that rely on functional hyperaemia, such as opto-fMRI. Here we test whether light stimulation protocols similar to those commonly used in opto-fMRI or to study neurovascular coupling modulate blood flow in mice that do not ex...

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Autores principales: Rungta, Ravi L, Osmanski, Bruno-Félix, Boido, Davide, Tanter, Mickael, Charpak, Serge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5290324/
https://www.ncbi.nlm.nih.gov/pubmed/28139643
http://dx.doi.org/10.1038/ncomms14191
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author Rungta, Ravi L
Osmanski, Bruno-Félix
Boido, Davide
Tanter, Mickael
Charpak, Serge
author_facet Rungta, Ravi L
Osmanski, Bruno-Félix
Boido, Davide
Tanter, Mickael
Charpak, Serge
author_sort Rungta, Ravi L
collection PubMed
description Optogenetics is increasingly used to map brain activation using techniques that rely on functional hyperaemia, such as opto-fMRI. Here we test whether light stimulation protocols similar to those commonly used in opto-fMRI or to study neurovascular coupling modulate blood flow in mice that do not express light sensitive proteins. Combining two-photon laser scanning microscopy and ultrafast functional ultrasound imaging, we report that in the naive mouse brain, light per se causes a calcium decrease in arteriolar smooth muscle cells, leading to pronounced vasodilation, without excitation of neurons and astrocytes. This photodilation is reversible, reproducible and energy-dependent, appearing at about 0.5 mJ. These results impose careful consideration on the use of photo-activation in studies involving blood flow regulation, as well as in studies requiring prolonged and repetitive stimulations to correct cellular defects in pathological models. They also suggest that light could be used to locally increase blood flow in a controlled fashion.
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spelling pubmed-52903242017-02-07 Light controls cerebral blood flow in naive animals Rungta, Ravi L Osmanski, Bruno-Félix Boido, Davide Tanter, Mickael Charpak, Serge Nat Commun Article Optogenetics is increasingly used to map brain activation using techniques that rely on functional hyperaemia, such as opto-fMRI. Here we test whether light stimulation protocols similar to those commonly used in opto-fMRI or to study neurovascular coupling modulate blood flow in mice that do not express light sensitive proteins. Combining two-photon laser scanning microscopy and ultrafast functional ultrasound imaging, we report that in the naive mouse brain, light per se causes a calcium decrease in arteriolar smooth muscle cells, leading to pronounced vasodilation, without excitation of neurons and astrocytes. This photodilation is reversible, reproducible and energy-dependent, appearing at about 0.5 mJ. These results impose careful consideration on the use of photo-activation in studies involving blood flow regulation, as well as in studies requiring prolonged and repetitive stimulations to correct cellular defects in pathological models. They also suggest that light could be used to locally increase blood flow in a controlled fashion. Nature Publishing Group 2017-01-31 /pmc/articles/PMC5290324/ /pubmed/28139643 http://dx.doi.org/10.1038/ncomms14191 Text en Copyright © 2017, The Author(s) 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
Rungta, Ravi L
Osmanski, Bruno-Félix
Boido, Davide
Tanter, Mickael
Charpak, Serge
Light controls cerebral blood flow in naive animals
title Light controls cerebral blood flow in naive animals
title_full Light controls cerebral blood flow in naive animals
title_fullStr Light controls cerebral blood flow in naive animals
title_full_unstemmed Light controls cerebral blood flow in naive animals
title_short Light controls cerebral blood flow in naive animals
title_sort light controls cerebral blood flow in naive animals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5290324/
https://www.ncbi.nlm.nih.gov/pubmed/28139643
http://dx.doi.org/10.1038/ncomms14191
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