<p>Ischemic stroke frequently results in persistent motor impairment, which highlights the need for effective strategies for neural repair. Functional recovery relies fundamentally on neurobehavioral remodeling, yet traditional physical and electrical stimulation therapies often lack the necessary cell-type and spatial specificity. Optogenetics overcomes these limitations by enabling the selective activation or inhibition of specific neuronal subpopulations with millisecond-level spatiotemporal precision, offering a powerful approach to modulate post-injury plasticity. This review synthesizes recent evidence regarding optogenetic interventions for motor rehabilitation in rodent models of ischemic stroke. We detail the multi-level neurobiological mechanisms that drive functional recovery. At the molecular and cellular levels, targeted optical stimulation enhances neurotrophic factor secretion, regulates neurovascular coupling, and modulates glial cell plasticity to create a reparative microenvironment. Circuit-level analysis demonstrates that specific stimulation protocols promote corticospinal tract remodeling and restore the balance of interhemispheric inhibition. Furthermore, modulation of whole-brain network dynamics, particularly the restoration of gamma oscillation rhythmicity, plays a critical role in coordinating motor output and reducing secondary injury. Optogenetics provides crucial mechanistic insights into the neural substrates of stroke recovery. These findings offer a theoretical basis for optimizing parameter selection in existing brain stimulation therapies. While clinical translation faces challenges related to viral vector safety and deep-brain light delivery, precise neuromodulation represents a promising frontier for restoring motor function after cerebral ischemia.</p>