bioRxivNeurosciencePreprint
Differential contribution of direct and indirect pathways from dorsolateral and dorsomedial striatum to motor symptoms in Huntington's disease mice
Sara Conde-BerriozabaliD, Laia Sitjà‐Roqueta, Esther García-GarcíaiD, Lia García-Gilabert, Anna Sancho‐BalsellsiD, Sara Fernández‐GarcíaiD, Ened Rodríguez-Urgellés, Albert GiraltiD, Javier López-Gil, Emma Muñoz‐MorenoiD, Anna CastañéiD, Guadalupe SòriaiD, Manuel José RodrígueziD, Jordi AlberchiD, Mercè MasanaiD
Abstract
The alterations in the basal ganglia circuitry associated with motor symptoms in Huntingtons Disease (HD) have been extensively investigated. Yet, the specific contribution of the direct and indirect striatal output pathways from the dorsolateral (DLS) and dorsomedial striatum (DMS) to the motor dysfunction is still not fully understood. Here, using the symptomatic R6/1 male mouse model of HD, strong functional connectivity alterations between DMS and DLS regions with the rest of brain were observed by fMRI, particularly pronounced in the DLS. Then, we systematically evaluated how the selective optogenetic stimulation of the direct and indirect pathways from DLS and DMS influences locomotion, exploratory behavior, and motor learning. In wild type (WT) mice, optogenetic stimulation of the direct pathway from DLS and the indirect pathway from DMS elicited subtle locomotor enhancements, while exploratory behavior remained unaltered. Additionally, stimulation of the indirect pathway from DLS improved the performance in the accelerated rotarod task. In contrast, in HD mice, optogenetic stimulation of the distinct striatal pathways did not modulate these behaviors. Overall, this study points to deficits in the integration of neuronal activity in HD mice, while it contributes to deeper understanding of the complexity of motor control by the diverse striatal subcircuits.
- Citations
- 1
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- M2 Cortex-Dorsolateral striatum stimulation reverses motor symptoms and synaptic deficits in Huntington's Disease
Sara Fernández‐García, Sara Conde-Berriozabal, … Mercè Masana·eLifePeer-reviewed·Oct 5, 2020
- Deficit in motor skill learning-dependent synaptic plasticity at motor cortex to Dorso Lateral Striatum synapses in a mouse model of Huntington's disease
Christelle Glangetas, Pedro Espinosa, Camilla Bellone·eNeuroPeer-reviewed·Mar 1, 2020
- Dysregulation of the basal ganglia indirect pathway prior to cell loss in the Q175 mouse model of Huntington's disease
Joshua W. Callahan, David L. Wokosin, Mark D. Bevan·bioRxiv·Jan 6, 2021
- Early alterations of motor learning and corticostriatal network activity in a Huntington's disease mouse model
Nagham Badreddine, Florence Appaix, … Élodie Fino·European Journal of NeurosciencePeer-reviewed·Mar 1, 2025
- Mutant huntingtin expression in the hypothalamus promotes ventral striatal neuropathology
Rana Soylu-Kucharz, Natalie Adlesic, … Åsa Petersén·bioRxiv·Mar 4, 2023
- Altered M2 Cortex - Superior Colliculus visual perception circuit in Huntington's Disease
Sara Conde-Berriozabal, Lia García-Gilabert, … Mercè Masana·Journal of NeurosciencePeer-reviewed·Mar 31, 2023