Disentangling neuroplasticity mechanisms in post-stroke language recovery

被引:0
|
作者
Billot, Anne [1 ,2 ,3 ]
Kiran, Swathi [1 ]
机构
[1] Boston Univ, Ctr Brain Recovery, Boston, MA 02118 USA
[2] Harvard Univ, Dept Psychol, Ctr Brain Sci, Cambridge, MA USA
[3] Massachusetts Gen Hosp, Dept Neurol, Boston, MA USA
基金
美国国家卫生研究院;
关键词
Neuroplasticity; Control; Aphasia; Recovery; Stroke; fMRI; Rehabilitation; Hebbian plasticity; Homeostatic plasticity; TRANSCRANIAL MAGNETIC STIMULATION; STATE FUNCTIONAL CONNECTIVITY; TIMING-DEPENDENT PLASTICITY; COMPUTED TOMOGRAPHIC SCAN; MULTIPLE-DEMAND CORTEX; INFERIOR FRONTAL GYRUS; LONG-TERM POTENTIATION; CORTICAL EXCITABILITY; STRUCTURAL PLASTICITY; SYNAPTIC PLASTICITY;
D O I
10.1016/j.bandl.2024.105381
中图分类号
R36 [病理学]; R76 [耳鼻咽喉科学];
学科分类号
100104 ; 100213 ;
摘要
A major objective in post -stroke aphasia research is to gain a deeper understanding of neuroplastic mechanisms that drive language recovery, with the ultimate goal of enhancing treatment outcomes. Subsequent to recent advances in neuroimaging techniques, we now have the ability to examine more closely how neural activity patterns change after a stroke. However, the way these neural activity changes relate to language impairments and language recovery is still debated. The aim of this review is to provide a theoretical framework to better investigate and interpret neuroplasticity mechanisms underlying language recovery in post -stroke aphasia. We detail two sets of neuroplasticity mechanisms observed at the synaptic level that may explain functional neuroimaging findings in post -stroke aphasia recovery at the network level: feedback -based homeostatic plasticity and associative Hebbian plasticity. In conjunction with these plasticity mechanisms, higher -order cognitive control processes dynamically modulate neural activity in other regions to meet communication demands, despite reduced neural resources. This work provides a network -level neurobiological framework for understanding neural changes observed in post -stroke aphasia and can be used to define guidelines for personalized treatment development.
引用
收藏
页数:17
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