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Comparison of stimulus-evoked cerebral hemodynamics in the awake mouse and under a novel anesthetic regime

Neural activity is closely followed by a localised change in cerebral blood flow, a process termed neurovascular coupling. These hemodynamic changes form the basis of contrast in functional magnetic resonance imaging (fMRI) and are used as a correlate for neural activity. Anesthesia is widely employ...

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Autores principales: Sharp, Paul S., Shaw, Kira, Boorman, Luke, Harris, Samuel, Kennerley, Aneurin J., Azzouz, Mimoun, Berwick, Jason
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517464/
https://www.ncbi.nlm.nih.gov/pubmed/26218081
http://dx.doi.org/10.1038/srep12621
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author Sharp, Paul S.
Shaw, Kira
Boorman, Luke
Harris, Samuel
Kennerley, Aneurin J.
Azzouz, Mimoun
Berwick, Jason
author_facet Sharp, Paul S.
Shaw, Kira
Boorman, Luke
Harris, Samuel
Kennerley, Aneurin J.
Azzouz, Mimoun
Berwick, Jason
author_sort Sharp, Paul S.
collection PubMed
description Neural activity is closely followed by a localised change in cerebral blood flow, a process termed neurovascular coupling. These hemodynamic changes form the basis of contrast in functional magnetic resonance imaging (fMRI) and are used as a correlate for neural activity. Anesthesia is widely employed in animal fMRI and neurovascular studies, however anesthetics are known to profoundly affect neural and vascular physiology, particularly in mice. Therefore, we investigated the efficacy of a novel ‘modular’ anesthesia that combined injectable (fentanyl-fluanisone/midazolam) and volatile (isoflurane) anesthetics in mice. To characterize sensory-evoked cortical hemodynamic responses, we used optical imaging spectroscopy to produce functional maps of changes in tissue oxygenation and blood volume in response to mechanical whisker stimulation. Following fine-tuning of the anesthetic regime, stimulation elicited large and robust hemodynamic responses in the somatosensory cortex, characterized by fast arterial activation, increases in total and oxygenated hemoglobin, and decreases in deoxygenated hemoglobin. Overall, the magnitude and speed of evoked hemodynamic responses under anesthesia resembled those in the awake state, indicating that the novel anesthetic combination significantly minimizes the impact of anesthesia. Our findings have broad implications for both neurovascular research and longitudinal fMRI studies that increasingly require the use of genetically engineered mice.
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spelling pubmed-45174642015-07-30 Comparison of stimulus-evoked cerebral hemodynamics in the awake mouse and under a novel anesthetic regime Sharp, Paul S. Shaw, Kira Boorman, Luke Harris, Samuel Kennerley, Aneurin J. Azzouz, Mimoun Berwick, Jason Sci Rep Article Neural activity is closely followed by a localised change in cerebral blood flow, a process termed neurovascular coupling. These hemodynamic changes form the basis of contrast in functional magnetic resonance imaging (fMRI) and are used as a correlate for neural activity. Anesthesia is widely employed in animal fMRI and neurovascular studies, however anesthetics are known to profoundly affect neural and vascular physiology, particularly in mice. Therefore, we investigated the efficacy of a novel ‘modular’ anesthesia that combined injectable (fentanyl-fluanisone/midazolam) and volatile (isoflurane) anesthetics in mice. To characterize sensory-evoked cortical hemodynamic responses, we used optical imaging spectroscopy to produce functional maps of changes in tissue oxygenation and blood volume in response to mechanical whisker stimulation. Following fine-tuning of the anesthetic regime, stimulation elicited large and robust hemodynamic responses in the somatosensory cortex, characterized by fast arterial activation, increases in total and oxygenated hemoglobin, and decreases in deoxygenated hemoglobin. Overall, the magnitude and speed of evoked hemodynamic responses under anesthesia resembled those in the awake state, indicating that the novel anesthetic combination significantly minimizes the impact of anesthesia. Our findings have broad implications for both neurovascular research and longitudinal fMRI studies that increasingly require the use of genetically engineered mice. Nature Publishing Group 2015-07-28 /pmc/articles/PMC4517464/ /pubmed/26218081 http://dx.doi.org/10.1038/srep12621 Text en Copyright © 2015, 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
Sharp, Paul S.
Shaw, Kira
Boorman, Luke
Harris, Samuel
Kennerley, Aneurin J.
Azzouz, Mimoun
Berwick, Jason
Comparison of stimulus-evoked cerebral hemodynamics in the awake mouse and under a novel anesthetic regime
title Comparison of stimulus-evoked cerebral hemodynamics in the awake mouse and under a novel anesthetic regime
title_full Comparison of stimulus-evoked cerebral hemodynamics in the awake mouse and under a novel anesthetic regime
title_fullStr Comparison of stimulus-evoked cerebral hemodynamics in the awake mouse and under a novel anesthetic regime
title_full_unstemmed Comparison of stimulus-evoked cerebral hemodynamics in the awake mouse and under a novel anesthetic regime
title_short Comparison of stimulus-evoked cerebral hemodynamics in the awake mouse and under a novel anesthetic regime
title_sort comparison of stimulus-evoked cerebral hemodynamics in the awake mouse and under a novel anesthetic regime
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517464/
https://www.ncbi.nlm.nih.gov/pubmed/26218081
http://dx.doi.org/10.1038/srep12621
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