Efficient neural transmission is crucial for optimal brain function, yet the plastic potential of white matter (WM) has long been overlooked. Growing evidence now shows that modifications to axons and myelin occur not only as a result of long-term learning, but also after short training periods. Motor sequence learning (MSL), a common paradigm used to study neuroplasticity, occurs in overlapping learning stages and different neural circuits are involved in each stage. However, most studies investigating short-term WM plasticity have used a pre-post design, in which the temporal dynamics of changes across learning stages cannot be assessed. In this study, we used multiple magnetic resonance imaging (MRI) scans at 7 T to investigate changes in WM in a group learning a complex visuomotor sequence (LRN) and in a control group (SMP) performing a simple sequence, for five consecutive days. Consistent with behavioral results, where most improvements occurred between the two first days, structural changes in WM were observed only in the early phase of learning (d1-d2), and in overall learning (d1-d5). In LRNs, WM microstructure was altered in the tracts underlying the primary motor and sensorimotor cortices. Moreover, our structural findings in WM were related to changes in functional connectivity, assessed with resting-state functional MRI data in the same cohort, through analyses in regions of interest (ROIs). Significant changes in WM microstructure were found in a ROI underlying the right supplementary motor area. Together, our findings provide evidence for highly dynamic WM plasticity in the sensorimotor network during short-term MSL.
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http://dx.doi.org/10.1007/s00429-021-02267-y | DOI Listing |
Phys Eng Sci Med
December 2024
Department of Mathematics, IIT Roorkee, Roorkee, Uttarakhand, 247667, India.
This article introduces an innovative methodology to unveil the intricacies of white matter fiber pathways in the brain using diffusion MRI. Relying on the rationale that traditional methods observe a significant decrease in signal intensity values in the direction of higher diffusivity, our novel approach strategically selects for diffusion-sensitizing gradient directions (dSGDs, representing the directions along which signals are generated) aligned with reduced signal intensities. By treating these selected directions as maximum diffusivity directions, we generate uniformly distributed gradient directions (GDs) around them, which are subsequently employed in the reconstruction process.
View Article and Find Full Text PDFAge Ageing
November 2024
Department of Neurology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, People's Republic of China.
Background: Immunity and inflammation may be essential to the pathogenesis of dementia. However, the association of immune-mediated diseases with the risk of incident dementia has not been well characterised.
Objectives: We aimed to investigate the prospective association of 27 immune-mediated diseases and incident dementia risk and to explore the underlying mechanisms driven by brain structures.
Ann Neurol
December 2024
Department of Neurology, Washington University School of Medicine, St. Louis, MO.
Objective: Despite treatments which reduce relapses in multiple sclerosis (MS), many patients continue to experience progressive disability accumulation. MS is associated with metabolic disruptions and cerebral metabolic stress predisposes to tissue injury and possibly impaired remyelination. Additionally, myelin homeostasis is metabolically expensive and reliant on glycolysis.
View Article and Find Full Text PDFJ Neurosci Res
December 2024
Department of Pharmacology and Clinical Pharmacology, Faculty of Medical and Health Sciences, School of Medical Science, Centre for Brain Research, University of Auckland, Auckland, New Zealand.
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder traditionally characterized by the selective loss of medium spiny neurons in the basal ganglia. However, it has become apparent that white matter injury and oligodendrocyte dysfunction precede the degeneration of medium spiny neurons, garnering interest as a key pathogenic mechanism of HD. Oligodendrocytes are glial cells found within the central nervous system involved in the production of myelin and the myelination of axons.
View Article and Find Full Text PDFWe developed a new sodium magnetic resonance fingerprinting ($^\text{23}\text{Na}$ MRF) method for the simultaneous mapping of $\text{T}_\text{1}$, $\text{T}_\text{2,long}^{*}$, $\text{T}_\text{2,short}^{*}$ and sodium density with built-in $\Delta\text{B}_{1}^{+}$ (radiofrequency transmission inhomogeneities) and $\Delta\text{f}_\text{0}$ corrections (frequency offsets). We based our $^\text{23}\text{Na}$ MRF implementation on a 3D FLORET sequence with 23 radiofrequency pulses. To capture the complex spin ${\frac{\text{3}}{\text{2}}}$ dynamics of the $^\text{23}\text{Na}$ nucleus, the fingerprint dictionary was simulated using the irreducible spherical tensor operators formalism.
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