Journal
BRAIN
Volume 145, Issue 7, Pages 2378-2393Publisher
OXFORD UNIV PRESS
DOI: 10.1093/brain/awac103
Keywords
stroke; corticospinal tract; gabapentinoids; structural plasticity; functional recovery
Categories
Funding
- National Institute of Neurological Disorders and Stroke [R01NS110681, R21NS109787]
- Chronic Brain Injury Discovery Theme at The Ohio State University [202001]
- NIH [P30NS104177]
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The daily administration of gabapentin promotes structural and functional cortical plasticity in adult mice after a stroke. Gabapentin increases neuroplasticity and reduces maladaptive plasticity, leading to functional recovery. The findings suggest that repurposing gabapentinoids could be a promising treatment strategy for stroke repair.
Stroke causes devastating sensory-motor deficits and long-term disability due to disruption of descending motor pathways. Restoration of these functions enables independent living and therefore represents a high priority for those afflicted by stroke. Here, we report that daily administration of gabapentin, a clinically approved drug already used to treat various neurological disorders, promotes structural and functional plasticity of the corticospinal pathway after photothrombotic cortical stroke in adult mice. We found that gabapentin administration had no effects on vascular occlusion, haemodynamic changes nor survival of corticospinal neurons within the ipsilateral sensory-motor cortex in the acute stages of stroke. Instead, using a combination of tract tracing, electrical stimulation and functional connectivity mapping, we demonstrated that corticospinal axons originating from the contralateral side of the brain in mice administered gabapentin extend numerous collaterals, form new synaptic contacts and better integrate within spinal circuits that control forelimb muscles. Not only does gabapentin daily administration promote neuroplasticity, but it also dampens maladaptive plasticity by reducing the excitability of spinal motor circuitry. In turn, mice administered gabapentin starting 1 h or 1 day after stroke recovered skilled upper extremity function. Functional recovery persists even after stopping the treatment at 6 weeks following a stroke. Finally, chemogenetic silencing of cortical projections originating from the contralateral side of the brain transiently abrogated recovery in mice administered gabapentin, further supporting the conclusion that gabapentin-dependent reorganization of spared cortical pathways drives functional recovery after stroke. These observations highlight the strong potential for repurposing gabapentinoids as a promising treatment strategy for stroke repair. Tedeschi et al. report that daily administration of gabapentin, a clinically approved drug already used to treat various neurological disorders, promotes structural and functional cortical plasticity after photothrombotic cortical stroke in adult mice.
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