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These studies suggest that understanding the complex interactions between the immune system, brain networks, and cellular changes is crucial for developing new stroke therapies and improving recovery outcomes.
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Multiple strokes in the brain result from complex interactions of various damaging pathways. These include excitotoxicity, acidotoxicity, ionic imbalance, peri-infarct depolarization, oxidative and nitrative stress, inflammation, and apoptosis. Each of these mechanisms contributes to neuronal death and brain injury, making stroke a leading cause of disability and death worldwide .
The immune system plays a dual role in stroke pathophysiology. Initially, innate immune cells invade the brain and meninges, contributing to ischemic damage. However, these cells can also offer protective effects . The damaged brain releases danger signals that activate systemic immunity, followed by immunodepression, which increases the risk of infections . Understanding these immune responses is crucial for developing therapeutic interventions .
Strokes not only cause localized brain damage but also disrupt the brain's global network organization. This disruption affects the brain's modularity, which is the degree of integration within and segregation between networks . Studies using neuroimaging have shown that stroke impacts both local and remote cortical areas, leading to changes in white-matter tracts and neural interactions . These network disturbances are not confined to the lesion site but extend to remote cortical areas in both hemispheres.
The brain exhibits a remarkable capacity for reorganization and plasticity following a stroke. This period of enhanced plasticity involves the sprouting of new axons, formation of new synapses, and remapping of sensory-motor functions, which are associated with motor recovery. Recovery of brain networks, particularly the restoration of interhemispheric functional coherence, is crucial for regaining lost functions . Changes in neuronal excitability and the reformation of neural circuits are driven by molecular systems similar to those involved in learning and memory.
Modulating the immune system offers a promising avenue for stroke therapy. Immune interventions aim to restrict brain inflammation, vascular permeability, and tissue edema to reduce acute immune-mediated destruction and prevent subsequent immunosuppression. Drugs used in multiple sclerosis are being explored for their potential to achieve these goals in stroke patients.
Innovative treatment approaches are targeting specific network patterns to enhance recovery. Assessing network changes can help predict treatment responses and individualize rehabilitation strategies, thereby improving overall outcomes. The normalization of large-scale modular brain systems is essential for successful recovery, particularly in cognitive functions such as language, spatial memory, and attention .
Multiple strokes in the brain involve complex mechanisms of damage and recovery, significantly impacting brain networks and overall function. Understanding the interplay between immune responses, brain network disruptions, and plasticity is crucial for developing effective therapeutic interventions. Advances in neuroimaging and network analysis are paving the way for personalized rehabilitation strategies, offering hope for better recovery outcomes in stroke patients.
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