Cargando…
Intrinsic functional architecture of the non-human primate spinal cord derived from fMRI and electrophysiology
Resting-state functional MRI (rsfMRI) has recently revealed correlated signals in the spinal cord horns of monkeys and humans. However, the interpretation of these rsfMRI correlations as indicators of functional connectivity in the spinal cord remains unclear. Here, we recorded stimulus-evoked and s...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6440970/ https://www.ncbi.nlm.nih.gov/pubmed/30926817 http://dx.doi.org/10.1038/s41467-019-09485-3 |
_version_ | 1783407461350244352 |
---|---|
author | Wu, Tung-Lin Yang, Pai-Feng Wang, Feng Shi, Zhaoyue Mishra, Arabinda Wu, Ruiqi Chen, Li Min Gore, John C. |
author_facet | Wu, Tung-Lin Yang, Pai-Feng Wang, Feng Shi, Zhaoyue Mishra, Arabinda Wu, Ruiqi Chen, Li Min Gore, John C. |
author_sort | Wu, Tung-Lin |
collection | PubMed |
description | Resting-state functional MRI (rsfMRI) has recently revealed correlated signals in the spinal cord horns of monkeys and humans. However, the interpretation of these rsfMRI correlations as indicators of functional connectivity in the spinal cord remains unclear. Here, we recorded stimulus-evoked and spontaneous spiking activity and local field potentials (LFPs) from monkey spinal cord in order to validate fMRI measures. We found that both BOLD and electrophysiological signals elicited by tactile stimulation co-localized to the ipsilateral dorsal horn. Temporal profiles of stimulus-evoked BOLD signals covaried with LFP and multiunit spiking in a similar way to those observed in the brain. Functional connectivity of dorsal horns exhibited a U-shaped profile along the dorsal-intermediate-ventral axis. Overall, these results suggest that there is an intrinsic functional architecture within the gray matter of a single spinal segment, and that rsfMRI signals at high field directly reflect this underlying spontaneous neuronal activity. |
format | Online Article Text |
id | pubmed-6440970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64409702019-04-01 Intrinsic functional architecture of the non-human primate spinal cord derived from fMRI and electrophysiology Wu, Tung-Lin Yang, Pai-Feng Wang, Feng Shi, Zhaoyue Mishra, Arabinda Wu, Ruiqi Chen, Li Min Gore, John C. Nat Commun Article Resting-state functional MRI (rsfMRI) has recently revealed correlated signals in the spinal cord horns of monkeys and humans. However, the interpretation of these rsfMRI correlations as indicators of functional connectivity in the spinal cord remains unclear. Here, we recorded stimulus-evoked and spontaneous spiking activity and local field potentials (LFPs) from monkey spinal cord in order to validate fMRI measures. We found that both BOLD and electrophysiological signals elicited by tactile stimulation co-localized to the ipsilateral dorsal horn. Temporal profiles of stimulus-evoked BOLD signals covaried with LFP and multiunit spiking in a similar way to those observed in the brain. Functional connectivity of dorsal horns exhibited a U-shaped profile along the dorsal-intermediate-ventral axis. Overall, these results suggest that there is an intrinsic functional architecture within the gray matter of a single spinal segment, and that rsfMRI signals at high field directly reflect this underlying spontaneous neuronal activity. Nature Publishing Group UK 2019-03-29 /pmc/articles/PMC6440970/ /pubmed/30926817 http://dx.doi.org/10.1038/s41467-019-09485-3 Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2019 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wu, Tung-Lin Yang, Pai-Feng Wang, Feng Shi, Zhaoyue Mishra, Arabinda Wu, Ruiqi Chen, Li Min Gore, John C. Intrinsic functional architecture of the non-human primate spinal cord derived from fMRI and electrophysiology |
title | Intrinsic functional architecture of the non-human primate spinal cord derived from fMRI and electrophysiology |
title_full | Intrinsic functional architecture of the non-human primate spinal cord derived from fMRI and electrophysiology |
title_fullStr | Intrinsic functional architecture of the non-human primate spinal cord derived from fMRI and electrophysiology |
title_full_unstemmed | Intrinsic functional architecture of the non-human primate spinal cord derived from fMRI and electrophysiology |
title_short | Intrinsic functional architecture of the non-human primate spinal cord derived from fMRI and electrophysiology |
title_sort | intrinsic functional architecture of the non-human primate spinal cord derived from fmri and electrophysiology |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6440970/ https://www.ncbi.nlm.nih.gov/pubmed/30926817 http://dx.doi.org/10.1038/s41467-019-09485-3 |
work_keys_str_mv | AT wutunglin intrinsicfunctionalarchitectureofthenonhumanprimatespinalcordderivedfromfmriandelectrophysiology AT yangpaifeng intrinsicfunctionalarchitectureofthenonhumanprimatespinalcordderivedfromfmriandelectrophysiology AT wangfeng intrinsicfunctionalarchitectureofthenonhumanprimatespinalcordderivedfromfmriandelectrophysiology AT shizhaoyue intrinsicfunctionalarchitectureofthenonhumanprimatespinalcordderivedfromfmriandelectrophysiology AT mishraarabinda intrinsicfunctionalarchitectureofthenonhumanprimatespinalcordderivedfromfmriandelectrophysiology AT wuruiqi intrinsicfunctionalarchitectureofthenonhumanprimatespinalcordderivedfromfmriandelectrophysiology AT chenlimin intrinsicfunctionalarchitectureofthenonhumanprimatespinalcordderivedfromfmriandelectrophysiology AT gorejohnc intrinsicfunctionalarchitectureofthenonhumanprimatespinalcordderivedfromfmriandelectrophysiology |