Cargando…

Functional ultrasound imaging of intrinsic connectivity in the living rat brain with high spatiotemporal resolution

Long-range coherences in spontaneous brain activity reflect functional connectivity. Here we propose a novel, highly resolved connectivity mapping approach, using ultrafast functional ultrasound (fUS), which enables imaging of cerebral microvascular haemodynamics deep in the anaesthetized rodent bra...

Descripción completa

Detalles Bibliográficos
Autores principales: Osmanski, Bruno-Félix, Pezet, Sophie, Ricobaraza, Ana, Lenkei, Zsolt, Tanter, Mickael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4205893/
https://www.ncbi.nlm.nih.gov/pubmed/25277668
http://dx.doi.org/10.1038/ncomms6023
_version_ 1782340735970836480
author Osmanski, Bruno-Félix
Pezet, Sophie
Ricobaraza, Ana
Lenkei, Zsolt
Tanter, Mickael
author_facet Osmanski, Bruno-Félix
Pezet, Sophie
Ricobaraza, Ana
Lenkei, Zsolt
Tanter, Mickael
author_sort Osmanski, Bruno-Félix
collection PubMed
description Long-range coherences in spontaneous brain activity reflect functional connectivity. Here we propose a novel, highly resolved connectivity mapping approach, using ultrafast functional ultrasound (fUS), which enables imaging of cerebral microvascular haemodynamics deep in the anaesthetized rodent brain, through a large thinned-skull cranial window, with pixel dimensions of 100 μm × 100 μm in-plane. The millisecond-range temporal resolution allows unambiguous cancellation of low-frequency cardio-respiratory noise. Both seed-based and singular value decomposition analysis of spatial coherences in the low-frequency (<0.1 Hz) spontaneous fUS signal fluctuations reproducibly report, at different coronal planes, overlapping high-contrast, intrinsic functional connectivity patterns. These patterns are similar to major functional networks described in humans by resting-state fMRI, such as the lateral task-dependent network putatively anticorrelated with the midline default-mode network. These results introduce fUS as a powerful novel neuroimaging method, which could be extended to portable systems for three-dimensional functional connectivity imaging in awake and freely moving rodents.
format Online
Article
Text
id pubmed-4205893
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Nature Pub. Group
record_format MEDLINE/PubMed
spelling pubmed-42058932014-10-27 Functional ultrasound imaging of intrinsic connectivity in the living rat brain with high spatiotemporal resolution Osmanski, Bruno-Félix Pezet, Sophie Ricobaraza, Ana Lenkei, Zsolt Tanter, Mickael Nat Commun Article Long-range coherences in spontaneous brain activity reflect functional connectivity. Here we propose a novel, highly resolved connectivity mapping approach, using ultrafast functional ultrasound (fUS), which enables imaging of cerebral microvascular haemodynamics deep in the anaesthetized rodent brain, through a large thinned-skull cranial window, with pixel dimensions of 100 μm × 100 μm in-plane. The millisecond-range temporal resolution allows unambiguous cancellation of low-frequency cardio-respiratory noise. Both seed-based and singular value decomposition analysis of spatial coherences in the low-frequency (<0.1 Hz) spontaneous fUS signal fluctuations reproducibly report, at different coronal planes, overlapping high-contrast, intrinsic functional connectivity patterns. These patterns are similar to major functional networks described in humans by resting-state fMRI, such as the lateral task-dependent network putatively anticorrelated with the midline default-mode network. These results introduce fUS as a powerful novel neuroimaging method, which could be extended to portable systems for three-dimensional functional connectivity imaging in awake and freely moving rodents. Nature Pub. Group 2014-10-03 /pmc/articles/PMC4205893/ /pubmed/25277668 http://dx.doi.org/10.1038/ncomms6023 Text en Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 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
Osmanski, Bruno-Félix
Pezet, Sophie
Ricobaraza, Ana
Lenkei, Zsolt
Tanter, Mickael
Functional ultrasound imaging of intrinsic connectivity in the living rat brain with high spatiotemporal resolution
title Functional ultrasound imaging of intrinsic connectivity in the living rat brain with high spatiotemporal resolution
title_full Functional ultrasound imaging of intrinsic connectivity in the living rat brain with high spatiotemporal resolution
title_fullStr Functional ultrasound imaging of intrinsic connectivity in the living rat brain with high spatiotemporal resolution
title_full_unstemmed Functional ultrasound imaging of intrinsic connectivity in the living rat brain with high spatiotemporal resolution
title_short Functional ultrasound imaging of intrinsic connectivity in the living rat brain with high spatiotemporal resolution
title_sort functional ultrasound imaging of intrinsic connectivity in the living rat brain with high spatiotemporal resolution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4205893/
https://www.ncbi.nlm.nih.gov/pubmed/25277668
http://dx.doi.org/10.1038/ncomms6023
work_keys_str_mv AT osmanskibrunofelix functionalultrasoundimagingofintrinsicconnectivityinthelivingratbrainwithhighspatiotemporalresolution
AT pezetsophie functionalultrasoundimagingofintrinsicconnectivityinthelivingratbrainwithhighspatiotemporalresolution
AT ricobarazaana functionalultrasoundimagingofintrinsicconnectivityinthelivingratbrainwithhighspatiotemporalresolution
AT lenkeizsolt functionalultrasoundimagingofintrinsicconnectivityinthelivingratbrainwithhighspatiotemporalresolution
AT tantermickael functionalultrasoundimagingofintrinsicconnectivityinthelivingratbrainwithhighspatiotemporalresolution