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The neural plasticity underlying language learning is a process rather than a single event. However, the dynamics of training-induced brain reorganization have rarely been examined, especially using a multimodal magnetic resonance imaging approach, which allows us to study the relationship between functional and structural changes. We focus on sign language acquisition in hearing adults who underwent an 8-month long course and five neuroimaging sessions. We assessed what neural changes occurred as participants learned a new language in a different modality-as reflected by task-based activity, connectivity changes, and co-occurring structural alterations. Major changes in the activity pattern appeared after just 3 months of learning, as indicated by increases in activation within the modality-independent perisylvian language network, together with increased activation in modality-dependent parieto-occipital, visuospatial and motion-sensitive regions. Despite further learning, no alterations in activation were detected during the following months. However, enhanced coupling between left-lateralized occipital and inferior frontal regions was observed as the proficiency increased. Furthermore, an increase in gray matter volume was detected in the left inferior frontal gyrus which peaked at the end of learning. Overall, these results showed complexity and temporal distinctiveness of various aspects of brain reorganization associated with learning of new language in different sensory modality.
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http://dx.doi.org/10.1002/hbm.25229 | DOI Listing |
Epilepsy Behav
September 2025
Department of Neurology, Yale University, 333 Cedar Street, New Haven, CT 06520, United States. Electronic address:
Temporal lobe epilepsy (TLE) is frequently associated with language impairment. This meta-analysis quantitatively synthesized data from 12 functional neuroimaging studies, including 390 TLE patients and 356 healthy controls (age range: 8.1-70 years; 57.
View Article and Find Full Text PDFCNS Neurosci Ther
September 2025
Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Objectives: Unruptured brain arteriovenous malformations (AVMs) typically do not cause aphasia, even when the traditional language areas are affected by the nidus. We attempted to elucidate its language reorganization mechanism by analyzing the alterations in functional connectivity using functional connectivity (FC) and track-weighted static functional connectivity (TW-sFC) approaches.
Methods: This cross-sectional study prospectively enrolled patients with AVMs involving left-hemisphere language areas and healthy controls.
Neurobiol Dis
September 2025
Mudanjiang Collaborative Innovation Center for development and application of Northern Medicine Resources, Mudanjiang, PR China; Institute of Neural Tissue Engineering, Mudanjiang Medical University, Mudanjiang, Heilongjiang, PR China. Electronic address:
Spinal cord injury (SCI) causes irreversible motor deficits due to disrupted lumbar circuitry. However, transcriptional mechanisms in distal lumbar circuits are poorly understood. We identify POU6F1 as a critical transcriptional regulator in spinal lumbar segment (SLS, L3-L5) motor circuit regeneration.
View Article and Find Full Text PDFFront Microbiol
August 2025
Department of Biology, College of Science, Qassim University, Buraydah, Saudi Arabia.
Neuroplasticity, the brain's ability to reorganize and adapt, has traditionally been attributed to external stimuli, learning, and experience. However, emerging research highlights the gut microbiota as a key modulator of neuroplasticity through the gut-brain axis. This review examines the mechanisms by which intestinal microorganisms influence brain function, including microbial metabolite production, immune system modulation, neurotransmitter synthesis, and hormonal regulation.
View Article and Find Full Text PDFbioRxiv
August 2025
Department of Pharmacology and Cancer Biology, Duke University, Durham, NC 27710.
In the brain, G protein-coupled receptors (GPCRs) regulate neuronal excitability, synaptic transmission, and behavior by engaging transcriptional and translational programs that produce enduring changes in cellular function and architecture. However, the molecular mechanisms that couple GPCR activation to these adaptations remain poorly understood. Here, we demonstrate that the beta-adrenergic receptor (β2AR), a mediator of noradrenaline in the central nervous system, remodels neuronal morphology through compartmentalized signaling pathways that orchestrate distinct layers of gene regulation.
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