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Simultaneous recording of neuronal and vascular activity in the rodent brain using fiber-photometry

Coupling of hemodynamic responses to neuronal activity is the foundation of several functional neuroimaging techniques. Here, we provide three fiber-photometry approaches to simultaneously measure neuronal and vascular signals in the rodent brain using a spectrometer-based system. Two out of these t...

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Detalles Bibliográficos
Autores principales: Zhang, Wei-Ting, Chao, Tzu-Hao Harry, Cui, Guohong, Shih, Yen-Yu Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9243291/
https://www.ncbi.nlm.nih.gov/pubmed/35776651
http://dx.doi.org/10.1016/j.xpro.2022.101497
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author Zhang, Wei-Ting
Chao, Tzu-Hao Harry
Cui, Guohong
Shih, Yen-Yu Ian
author_facet Zhang, Wei-Ting
Chao, Tzu-Hao Harry
Cui, Guohong
Shih, Yen-Yu Ian
author_sort Zhang, Wei-Ting
collection PubMed
description Coupling of hemodynamic responses to neuronal activity is the foundation of several functional neuroimaging techniques. Here, we provide three fiber-photometry approaches to simultaneously measure neuronal and vascular signals in the rodent brain using a spectrometer-based system. Two out of these three approaches allow the removal of hemoglobin (Hb)-absorption artifacts and restore the underlying neuronal activity. This technique is applicable to different fluorescent sensors and provides a more accurate measurement of hemodynamic response function in any location of the rodent brain. For complete details on the use and execution of this protocol, please refer to Zhang et al. (2022).
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spelling pubmed-92432912022-07-01 Simultaneous recording of neuronal and vascular activity in the rodent brain using fiber-photometry Zhang, Wei-Ting Chao, Tzu-Hao Harry Cui, Guohong Shih, Yen-Yu Ian STAR Protoc Protocol Coupling of hemodynamic responses to neuronal activity is the foundation of several functional neuroimaging techniques. Here, we provide three fiber-photometry approaches to simultaneously measure neuronal and vascular signals in the rodent brain using a spectrometer-based system. Two out of these three approaches allow the removal of hemoglobin (Hb)-absorption artifacts and restore the underlying neuronal activity. This technique is applicable to different fluorescent sensors and provides a more accurate measurement of hemodynamic response function in any location of the rodent brain. For complete details on the use and execution of this protocol, please refer to Zhang et al. (2022). Elsevier 2022-06-23 /pmc/articles/PMC9243291/ /pubmed/35776651 http://dx.doi.org/10.1016/j.xpro.2022.101497 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Zhang, Wei-Ting
Chao, Tzu-Hao Harry
Cui, Guohong
Shih, Yen-Yu Ian
Simultaneous recording of neuronal and vascular activity in the rodent brain using fiber-photometry
title Simultaneous recording of neuronal and vascular activity in the rodent brain using fiber-photometry
title_full Simultaneous recording of neuronal and vascular activity in the rodent brain using fiber-photometry
title_fullStr Simultaneous recording of neuronal and vascular activity in the rodent brain using fiber-photometry
title_full_unstemmed Simultaneous recording of neuronal and vascular activity in the rodent brain using fiber-photometry
title_short Simultaneous recording of neuronal and vascular activity in the rodent brain using fiber-photometry
title_sort simultaneous recording of neuronal and vascular activity in the rodent brain using fiber-photometry
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9243291/
https://www.ncbi.nlm.nih.gov/pubmed/35776651
http://dx.doi.org/10.1016/j.xpro.2022.101497
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