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Motor adaptation is crucial for performing accurate movements in a changing environment and relies on the cerebellum. Although cerebellar involvement has been well characterized, the neurochemical changes in the cerebellum underpinning human motor adaptation remain unknown. We used a novel magnetic resonance spectroscopic imaging (MRSI) technique to measure changes in the inhibitory neurotransmitter GABA in the human cerebellum during visuomotor adaptation. Participants ( = 17, six female) used their right hand to adapt to a rotated cursor in the scanner, compared with a control task requiring no adaptation. We spatially resolved adaptation-driven GABA changes at the cerebellar nuclei and cerebellar cortex in the left and the right cerebellar hemisphere independently and found that simple right-hand movements increase GABA in the right cerebellar nuclei and decreases GABA in the left. When isolating adaptation-driven GABA changes, we found that GABA in the left cerebellar nuclei and the right cerebellar nuclei diverged, although GABA change from baseline at the right cerebellar nuclei was not different from zero at the group level. Early adaptation-driven GABA fluctuations in the right cerebellar nuclei correlated with adaptation performance. Participants showing greater GABA decrease adapted better, suggesting early GABA change is behaviorally relevant. Early GABA change also correlated with functional connectivity change in a cerebellar network. Participants showing greater decreases in GABA showed greater strength increases in cerebellar network connectivity. Results were specific to GABA, to adaptation, and to the cerebellar network. This study provides first evidence for plastic changes in cerebellar neurochemistry during motor adaptation. Characterizing these naturally occurring neurochemical changes may provide a basis for developing therapeutic interventions to facilitate human motor adaptation. Despite motor adaptation being fundamental to maintaining accurate movements, its neurochemical basis remains poorly understood, perhaps because measuring neurochemicals in the human cerebellum is technically challenging. Using a novel magnetic resonance spectroscopic imaging method, this study provides evidence for GABA changes in the left compared with the right cerebellar nuclei driven by both simple movement and motor adaptation. Although right cerebellar GABA changes were not significantly different from zero at the group level, the adaptation-driven GABA fluctuations in the right cerebellar nuclei correlated with adaptation performance and with functional connectivity change in a cerebellar network. These results show the first evidence for plastic changes in cerebellar neurochemistry during a cerebellar learning task. This provides the basis for developing therapeutic interventions that facilitate these naturally occurring changes to amplify cerebellar-dependent learning.
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http://dx.doi.org/10.1523/JNEUROSCI.0096-22.2022 | DOI Listing |
Mov Disord
September 2025
Movement Investigation and Therapeutics Team, Sorbonne Université, INSERM U1127, CNRS UMR 7225, Paris Brain Institute, Paris, France.
Background: Cervical dystonia is characterized by abnormal neck and head movements, possibly related to a dysfunction of the interstitial nucleus of Cajal (INC) and the head neural integrator, a system responsible for the control of head and eye movements. However, neuroanatomical evidence of alterations in the head neural integrator in cervical dystonia is sparse.
Objectives: We investigated structural and functional integrity of the INC and its connections in cervical dystonia.
Sci Rep
August 2025
Department of Pharmacology, Nippon Medical School, Tokyo, 113-8602, Japan.
Modulation of synaptic transmission in the deep cerebellar nuclei, a major output region of the cerebellum, is essential for regulating motor and non-motor functions by controlling information flow from the cerebellar cortex. In this study, we aimed to investigate the effects of dopamine (DA) and noradrenaline (NA) on glutamatergic synaptic transmission using cerebellar slices from both male and female Wistar rats. Stimulation-evoked excitatory postsynaptic currents (eEPSCs) were recorded from deep cerebellar nuclei neurons using whole-cell patch-clamp technique.
View Article and Find Full Text PDFDiagn Cytopathol
August 2025
Department of Pathology and Division of Pathology, Osaka Medical and Pharmaceutical University, Osaka, Japan.
Solitary fibrous tumors (SFTs) are rare neoplasms characterized by spindle neoplastic cell proliferation within collagenous stroma and prominent dilated vasculature. They present a wide histopathological spectrum, ranging from hypocellular lesions with a rich collagenous stroma to hypercellular lesions with scant stroma. Meningeal SFTs are usually hypercellular, and their cytological features remain poorly characterized.
View Article and Find Full Text PDFRadiographics
September 2025
From the Department of Diagnostic and Interventional Radiology, The Hospital for Sick Children, 170 Elizabeth St, Toronto, ON, Canada M5G 1X8 (S.K.G., O.M.N.); Department of Medical Imaging, University of Toronto, Toronto, ON, Canada (S.K.G., O.M.N.); Department of Radiology, Stollery Children's Hos
Head US is the mainstay of initial neuroimaging in preterm and term neonates and young infants. Echogenic lesions are a commonly encountered finding on US images, with a wide spectrum of underlying causes. These include normal structures and normal variants such as the choroid plexus and cerebellar vermis, normal transmantle white matter tracts, and benign entities that should not be mistaken for disease, such as hyperechoic caudate nuclei and thalamostriate mineralizing vasculopathy.
View Article and Find Full Text PDFAJNR Am J Neuroradiol
August 2025
From the Neuroradiology Unit, Department of Diagnostic and Interventional Radiology, A.O.U. Città della Salute e della Scienza di Torino, Turin, Italy (F.C., G.M.); Department of Radiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK (S.P., F.D'A., U.L., P.G., P.V., K
Background And Purpose: GM1 gangliosidosis is a rare lysosomal storage disorder caused by pathogenic variants in the gene, leading to deficient β-galactosidase activity and accumulation of gangliosides. This multi-institutional retrospective study aims to systematically characterize neuroimaging features across all clinical subtypes of GM1 gangliosidosis.
Materials And Methods: Patients were retrospectively identified from 4 centers based on confirmed variants or βgalactosidase deficiency.