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Imaging functional neuroplasticity in human white matter tracts

Magnetic resonance imaging (MRI) studies are sensitive to biological mechanisms of neuroplasticity in white matter (WM). In particular, diffusion tensor imaging (DTI) has been used to investigate structural changes. Historically, functional MRI (fMRI) neuroplasticity studies have been restricted to...

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Autores principales: Frizzell, Tory O., Phull, Elisha, Khan, Mishaa, Song, Xiaowei, Grajauskas, Lukas A., Gawryluk, Jodie, D’Arcy, Ryan C. N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741691/
https://www.ncbi.nlm.nih.gov/pubmed/34812936
http://dx.doi.org/10.1007/s00429-021-02407-4
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author Frizzell, Tory O.
Phull, Elisha
Khan, Mishaa
Song, Xiaowei
Grajauskas, Lukas A.
Gawryluk, Jodie
D’Arcy, Ryan C. N.
author_facet Frizzell, Tory O.
Phull, Elisha
Khan, Mishaa
Song, Xiaowei
Grajauskas, Lukas A.
Gawryluk, Jodie
D’Arcy, Ryan C. N.
author_sort Frizzell, Tory O.
collection PubMed
description Magnetic resonance imaging (MRI) studies are sensitive to biological mechanisms of neuroplasticity in white matter (WM). In particular, diffusion tensor imaging (DTI) has been used to investigate structural changes. Historically, functional MRI (fMRI) neuroplasticity studies have been restricted to gray matter, as fMRI studies have only recently expanded to WM. The current study evaluated WM neuroplasticity pre–post motor training in healthy adults, focusing on motor learning in the non-dominant hand. Neuroplasticity changes were evaluated in two established WM regions-of-interest: the internal capsule and the corpus callosum. Behavioral improvements following training were greater for the non-dominant hand, which corresponded with MRI-based neuroplasticity changes in the internal capsule for DTI fractional anisotropy, fMRI hemodynamic response functions, and low-frequency oscillations (LFOs). In the corpus callosum, MRI-based neuroplasticity changes were detected in LFOs, DTI, and functional correlation tensors (FCT). Taken together, the LFO results converged as significant amplitude reductions, implicating a common underlying mechanism of optimized transmission through altered myelination. The structural and functional neuroplasticity findings open new avenues for direct WM investigations into mapping connectomes and advancing MRI clinical applications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00429-021-02407-4.
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spelling pubmed-87416912022-01-20 Imaging functional neuroplasticity in human white matter tracts Frizzell, Tory O. Phull, Elisha Khan, Mishaa Song, Xiaowei Grajauskas, Lukas A. Gawryluk, Jodie D’Arcy, Ryan C. N. Brain Struct Funct Original Article Magnetic resonance imaging (MRI) studies are sensitive to biological mechanisms of neuroplasticity in white matter (WM). In particular, diffusion tensor imaging (DTI) has been used to investigate structural changes. Historically, functional MRI (fMRI) neuroplasticity studies have been restricted to gray matter, as fMRI studies have only recently expanded to WM. The current study evaluated WM neuroplasticity pre–post motor training in healthy adults, focusing on motor learning in the non-dominant hand. Neuroplasticity changes were evaluated in two established WM regions-of-interest: the internal capsule and the corpus callosum. Behavioral improvements following training were greater for the non-dominant hand, which corresponded with MRI-based neuroplasticity changes in the internal capsule for DTI fractional anisotropy, fMRI hemodynamic response functions, and low-frequency oscillations (LFOs). In the corpus callosum, MRI-based neuroplasticity changes were detected in LFOs, DTI, and functional correlation tensors (FCT). Taken together, the LFO results converged as significant amplitude reductions, implicating a common underlying mechanism of optimized transmission through altered myelination. The structural and functional neuroplasticity findings open new avenues for direct WM investigations into mapping connectomes and advancing MRI clinical applications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00429-021-02407-4. Springer Berlin Heidelberg 2021-11-23 2022 /pmc/articles/PMC8741691/ /pubmed/34812936 http://dx.doi.org/10.1007/s00429-021-02407-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Original Article
Frizzell, Tory O.
Phull, Elisha
Khan, Mishaa
Song, Xiaowei
Grajauskas, Lukas A.
Gawryluk, Jodie
D’Arcy, Ryan C. N.
Imaging functional neuroplasticity in human white matter tracts
title Imaging functional neuroplasticity in human white matter tracts
title_full Imaging functional neuroplasticity in human white matter tracts
title_fullStr Imaging functional neuroplasticity in human white matter tracts
title_full_unstemmed Imaging functional neuroplasticity in human white matter tracts
title_short Imaging functional neuroplasticity in human white matter tracts
title_sort imaging functional neuroplasticity in human white matter tracts
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741691/
https://www.ncbi.nlm.nih.gov/pubmed/34812936
http://dx.doi.org/10.1007/s00429-021-02407-4
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