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A novel anesthesia regime enables neurofunctional studies and imaging genetics across mouse strains
Functional magnetic resonance imaging (fMRI) has revolutionized neuroscience by opening a unique window that allows neurocircuitry function and pathological alterations to be probed non-invasively across brain disorders. Here we report a novel sustainable anesthesia procedure for small animal neuroi...
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/PMC4832200/ https://www.ncbi.nlm.nih.gov/pubmed/27080031 http://dx.doi.org/10.1038/srep24523 |
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author | Petrinovic, Marija M. Hankov, Georges Schroeter, Aileen Bruns, Andreas Rudin, Markus von Kienlin, Markus Künnecke, Basil Mueggler, Thomas |
author_facet | Petrinovic, Marija M. Hankov, Georges Schroeter, Aileen Bruns, Andreas Rudin, Markus von Kienlin, Markus Künnecke, Basil Mueggler, Thomas |
author_sort | Petrinovic, Marija M. |
collection | PubMed |
description | Functional magnetic resonance imaging (fMRI) has revolutionized neuroscience by opening a unique window that allows neurocircuitry function and pathological alterations to be probed non-invasively across brain disorders. Here we report a novel sustainable anesthesia procedure for small animal neuroimaging that overcomes shortcomings of anesthetics commonly used in rodent fMRI. The significantly improved preservation of cerebrovascular dynamics enhances sensitivity to neural activity changes for which it serves as a proxy in fMRI readouts. Excellent cross-species/strain applicability provides coherence among preclinical findings and is expected to improve translation to clinical fMRI investigations. The novel anesthesia procedure based on the GABAergic anesthetic etomidate was extensively validated in fMRI studies conducted in a range of genetically engineered rodent models of autism and strains commonly used for transgenic manipulations. Etomidate proved effective, yielded long-term stable physiology with basal cerebral blood flow of ~0.5 ml/g/min and full recovery. Cerebrovascular responsiveness of up to 180% was maintained as demonstrated with perfusion- and BOLD-based fMRI upon hypercapnic, pharmacological and sensory stimulation. Hence, etomidate lends itself as an anesthetic-of-choice for translational neuroimaging studies across rodent models of brain disorders. |
format | Online Article Text |
id | pubmed-4832200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48322002016-04-20 A novel anesthesia regime enables neurofunctional studies and imaging genetics across mouse strains Petrinovic, Marija M. Hankov, Georges Schroeter, Aileen Bruns, Andreas Rudin, Markus von Kienlin, Markus Künnecke, Basil Mueggler, Thomas Sci Rep Article Functional magnetic resonance imaging (fMRI) has revolutionized neuroscience by opening a unique window that allows neurocircuitry function and pathological alterations to be probed non-invasively across brain disorders. Here we report a novel sustainable anesthesia procedure for small animal neuroimaging that overcomes shortcomings of anesthetics commonly used in rodent fMRI. The significantly improved preservation of cerebrovascular dynamics enhances sensitivity to neural activity changes for which it serves as a proxy in fMRI readouts. Excellent cross-species/strain applicability provides coherence among preclinical findings and is expected to improve translation to clinical fMRI investigations. The novel anesthesia procedure based on the GABAergic anesthetic etomidate was extensively validated in fMRI studies conducted in a range of genetically engineered rodent models of autism and strains commonly used for transgenic manipulations. Etomidate proved effective, yielded long-term stable physiology with basal cerebral blood flow of ~0.5 ml/g/min and full recovery. Cerebrovascular responsiveness of up to 180% was maintained as demonstrated with perfusion- and BOLD-based fMRI upon hypercapnic, pharmacological and sensory stimulation. Hence, etomidate lends itself as an anesthetic-of-choice for translational neuroimaging studies across rodent models of brain disorders. Nature Publishing Group 2016-04-15 /pmc/articles/PMC4832200/ /pubmed/27080031 http://dx.doi.org/10.1038/srep24523 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 Petrinovic, Marija M. Hankov, Georges Schroeter, Aileen Bruns, Andreas Rudin, Markus von Kienlin, Markus Künnecke, Basil Mueggler, Thomas A novel anesthesia regime enables neurofunctional studies and imaging genetics across mouse strains |
title | A novel anesthesia regime enables neurofunctional studies and imaging genetics across mouse strains |
title_full | A novel anesthesia regime enables neurofunctional studies and imaging genetics across mouse strains |
title_fullStr | A novel anesthesia regime enables neurofunctional studies and imaging genetics across mouse strains |
title_full_unstemmed | A novel anesthesia regime enables neurofunctional studies and imaging genetics across mouse strains |
title_short | A novel anesthesia regime enables neurofunctional studies and imaging genetics across mouse strains |
title_sort | novel anesthesia regime enables neurofunctional studies and imaging genetics across mouse strains |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832200/ https://www.ncbi.nlm.nih.gov/pubmed/27080031 http://dx.doi.org/10.1038/srep24523 |
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