High-resolution MEMRI characterizes laminar specific ascending and descending spinal cord pathways in rats.

Manganese enhanced magnetic resonance imaging Motor neurons Non-Invasive Spinal cord

Journal

Journal of neuroscience methods
ISSN: 1872-678X
Titre abrégé: J Neurosci Methods
Pays: Netherlands
ID NLM: 7905558

Informations de publication

Date de publication:
01 07 2020
Historique:
received: 06 01 2020
revised: 19 04 2020
accepted: 19 04 2020
pubmed: 27 4 2020
medline: 22 6 2021
entrez: 27 4 2020
Statut: ppublish

Résumé

The spinal cord is composed of nine distinct cellular laminae that currently can only be visualized by histological methods. Developing imaging methods that can visualize laminar architecture in-vivo is of significant interest. Manganese enhanced magnetic resonance imaging (MEMRI) yields valuable architectural and functional information about the brain and has great potential in characterizing neural pathways in the spinal cord. Here we apply MEMRI to visualize laminae architecture in the thoracic region of the spinal cord with ultra-high resolution. Manganese chloride (MnCl Here we demonstrate laminar specific signal enhancement in the spinal cord of rats administered with MnCl This is the first study to demonstrate that MEMRI is capable of identifying spinal laminae at a high resolution of 69 μm in a living animal. This would enable the visualization of architecture and function of distinct regions with improved resolution, in healthy and diseased animal models. The regions with the largest T1 enhancements were observed to correspond to laminae that contain either high cell density or large motor neurons, making MEMRI an excellent tool for studying spinal cord architecture, physiology and function in different animal models.

Sections du résumé

BACKGROUND
The spinal cord is composed of nine distinct cellular laminae that currently can only be visualized by histological methods. Developing imaging methods that can visualize laminar architecture in-vivo is of significant interest. Manganese enhanced magnetic resonance imaging (MEMRI) yields valuable architectural and functional information about the brain and has great potential in characterizing neural pathways in the spinal cord. Here we apply MEMRI to visualize laminae architecture in the thoracic region of the spinal cord with ultra-high resolution.
NEW METHOD
Manganese chloride (MnCl
RESULTS
Here we demonstrate laminar specific signal enhancement in the spinal cord of rats administered with MnCl
COMPARISONS WITH EXISTING METHODS
This is the first study to demonstrate that MEMRI is capable of identifying spinal laminae at a high resolution of 69 μm in a living animal. This would enable the visualization of architecture and function of distinct regions with improved resolution, in healthy and diseased animal models.
CONCLUSIONS
The regions with the largest T1 enhancements were observed to correspond to laminae that contain either high cell density or large motor neurons, making MEMRI an excellent tool for studying spinal cord architecture, physiology and function in different animal models.

Identifiants

pubmed: 32335077
pii: S0165-0270(20)30171-0
doi: 10.1016/j.jneumeth.2020.108748
pmc: PMC7281828
mid: NIHMS1590970
pii:
doi:

Substances chimiques

Manganese 42Z2K6ZL8P

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, N.I.H., Intramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

108748

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS072171
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS098231
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest There is no conflict of interest for any of the authors.

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Auteurs

Vijai Krishnan (V)

Department of Biomedical Engineering, Michigan State University, East Lansing, MI, United States; The Institute for Quantitative Health Science and Engineering, Michigan State University, East Lansing, MI, United States.

Jiadi Xu (J)

Johns Hopkins Medicine Department of Radiology and Radiological Science, Baltimore, MD, United States.

Albert German Mendoza (AG)

Johns Hopkins Medicine Department of Radiology and Radiological Science, Baltimore, MD, United States.

Alan Koretsky (A)

Laboratory of Functional and Molecular Imaging, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, United States.

Stasia A Anderson (SA)

National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD, United States.

Galit Pelled (G)

Department of Biomedical Engineering, Michigan State University, East Lansing, MI, United States; The Institute for Quantitative Health Science and Engineering, Michigan State University, East Lansing, MI, United States; Department of Radiology, Michigan State University, East Lansing, MI, United States; Johns Hopkins Medicine Department of Radiology and Radiological Science, Baltimore, MD, United States. Electronic address: pelledga@msu.edu.

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