Early Alterations of Motor Learning and Corticostriatal Network Activity in a Huntington's Disease Mouse Model
Year: 2025
Type: article
Abstract: ABSTRACT Huntington's disease (HD) is a neurodegenerative disorder that presents motor, cognitive, and psychiatric symptoms as it progresses. Prior to motor symptoms onset, alterations, and dysfunctions in the corticostriatal projections have been described along with cognitive deficits, but the sequence of early alterations of brain circuits is largely unknown. There is thus a crucial need to identify early alterations that precede symptoms and that could be used as potential early disease markers. Using an HD knock‐in mouse model (Hdh CAG140/+ ) that recapitulates the human genetic alterations and that shows a late and progressive appearance of anatomical and behavioral deficits, we identified early alterations in the motor learning abilities of young mice, long before any motor coordination dysfunctions. In parallel, ex vivo two‐photon calcium recordings revealed that young HD mice have altered basal activity patterns in both the dorsomedial and dorsolateral parts of the striatum. In addition, although wild‐type mice display specific reorganization of the activity upon motor training, network alterations present in the basal state of non‐trained mice are not affected by motor training of HD mice. Our results thus identify early behavioral deficits and network alterations that could serve as early markers of the disease.
Source: European Journal of Neuroscience
DOI: 10.1111/ejn.70056
Institutions: Centre National de la Recherche Scientifique, Inserm, Aix-Marseille Université, Institut de Neurobiologie de la Méditerranée, Grenoble Institute of Neurosciences, Institut pour l'avancée des biosciences, Université Grenoble Alpes, Institut polytechnique de Grenoble, GIPSA-Lab, Laboratoire Jean Kuntzmann
Language: English
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: bronze
OpenAlex ID: W4408419701
