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The effects of locomotion on sensory-evoked haemodynamic responses in the cortex of awake mice

Investigating neurovascular coupling in awake rodents is becoming ever more popular due, in part, to our increasing knowledge of the profound impacts that anaesthesia can have upon brain physiology. Although awake imaging brings with it many advantages, we still do not fully understand how voluntary...

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Autores principales: Eyre, Beth, Shaw, Kira, Sharp, Paul, Boorman, Luke, Lee, Llywelyn, Shabir, Osman, Berwick, Jason, Howarth, Clare
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010417/
https://www.ncbi.nlm.nih.gov/pubmed/35422473
http://dx.doi.org/10.1038/s41598-022-10195-y
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author Eyre, Beth
Shaw, Kira
Sharp, Paul
Boorman, Luke
Lee, Llywelyn
Shabir, Osman
Berwick, Jason
Howarth, Clare
author_facet Eyre, Beth
Shaw, Kira
Sharp, Paul
Boorman, Luke
Lee, Llywelyn
Shabir, Osman
Berwick, Jason
Howarth, Clare
author_sort Eyre, Beth
collection PubMed
description Investigating neurovascular coupling in awake rodents is becoming ever more popular due, in part, to our increasing knowledge of the profound impacts that anaesthesia can have upon brain physiology. Although awake imaging brings with it many advantages, we still do not fully understand how voluntary locomotion during imaging affects sensory-evoked haemodynamic responses. In this study we investigated how evoked haemodynamic responses can be affected by the amount and timing of locomotion. Using an awake imaging set up, we used 2D-Optical Imaging Spectroscopy (2D-OIS) to measure changes in cerebral haemodynamics within the sensory cortex of the brain during either 2 s whisker stimulation or spontaneous (no whisker stimulation) experiments, whilst animals could walk on a spherical treadmill. We show that locomotion alters haemodynamic responses. The amount and timing of locomotion relative to whisker stimulation is important, and can significantly impact sensory-evoked haemodynamic responses. If locomotion occurred before or during whisker stimulation, the amplitude of the stimulus-evoked haemodynamic response was significantly altered. Therefore, monitoring of locomotion during awake imaging is necessary to ensure that conclusions based on comparisons of evoked haemodynamic responses (e.g., between control and disease groups) are not confounded by the effects of locomotion.
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spelling pubmed-90104172022-04-15 The effects of locomotion on sensory-evoked haemodynamic responses in the cortex of awake mice Eyre, Beth Shaw, Kira Sharp, Paul Boorman, Luke Lee, Llywelyn Shabir, Osman Berwick, Jason Howarth, Clare Sci Rep Article Investigating neurovascular coupling in awake rodents is becoming ever more popular due, in part, to our increasing knowledge of the profound impacts that anaesthesia can have upon brain physiology. Although awake imaging brings with it many advantages, we still do not fully understand how voluntary locomotion during imaging affects sensory-evoked haemodynamic responses. In this study we investigated how evoked haemodynamic responses can be affected by the amount and timing of locomotion. Using an awake imaging set up, we used 2D-Optical Imaging Spectroscopy (2D-OIS) to measure changes in cerebral haemodynamics within the sensory cortex of the brain during either 2 s whisker stimulation or spontaneous (no whisker stimulation) experiments, whilst animals could walk on a spherical treadmill. We show that locomotion alters haemodynamic responses. The amount and timing of locomotion relative to whisker stimulation is important, and can significantly impact sensory-evoked haemodynamic responses. If locomotion occurred before or during whisker stimulation, the amplitude of the stimulus-evoked haemodynamic response was significantly altered. Therefore, monitoring of locomotion during awake imaging is necessary to ensure that conclusions based on comparisons of evoked haemodynamic responses (e.g., between control and disease groups) are not confounded by the effects of locomotion. Nature Publishing Group UK 2022-04-14 /pmc/articles/PMC9010417/ /pubmed/35422473 http://dx.doi.org/10.1038/s41598-022-10195-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Eyre, Beth
Shaw, Kira
Sharp, Paul
Boorman, Luke
Lee, Llywelyn
Shabir, Osman
Berwick, Jason
Howarth, Clare
The effects of locomotion on sensory-evoked haemodynamic responses in the cortex of awake mice
title The effects of locomotion on sensory-evoked haemodynamic responses in the cortex of awake mice
title_full The effects of locomotion on sensory-evoked haemodynamic responses in the cortex of awake mice
title_fullStr The effects of locomotion on sensory-evoked haemodynamic responses in the cortex of awake mice
title_full_unstemmed The effects of locomotion on sensory-evoked haemodynamic responses in the cortex of awake mice
title_short The effects of locomotion on sensory-evoked haemodynamic responses in the cortex of awake mice
title_sort effects of locomotion on sensory-evoked haemodynamic responses in the cortex of awake mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010417/
https://www.ncbi.nlm.nih.gov/pubmed/35422473
http://dx.doi.org/10.1038/s41598-022-10195-y
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