Abstract

Objective: Short intracortical inhibition (SICI) is a GABAA-mediated phenomenon, argued to mediate selective muscle activation during coordinated motor activity. Markedly reduced SICI has been observed in the acute period following stroke and, based on findings in animal models, it has been posited this disinhibitory phenomenon may facilitate neural plasticity and contribute to early motor recovery. However, it remains unresolved whether SICI normalizes over time, as part of the natural course of stroke recovery. Whether intracortical inhibition contributes to motor recovery in chronic stroke also remains unclear. Notably, SICI is typically measured at rest, which may not fully reveal its role in motor control. Here we investigated SICI at rest and during voluntary motor activity to determine: (1) whether GABAA-mediated inhibition recovers, and (2) how GABAA-mediated inhibition is related to motor function, in the chronic phase post-stroke.Methods: We studied 16 chronic stroke survivors (age: 64.6 ± 9.3 years; chronicity: 74.3 ± 52.9 months) and 12 age-matched healthy controls. We used paired-pulse transcranial magnetic stimulation (TMS) to induce SICI during three conditions: rest, submaximal grip, and performance of box-and-blocks. Upper-extremity Fugl-Meyer Assessment and Box-and-Blocks tests were used to evaluate motor impairment in stroke survivors and manual dexterity in all participants, respectively.Results: At rest, SICI revealed no differences between ipsilesional and contralesional hemispheres of either cortical or subcortical stroke survivors, or healthy controls (P's > 0.05). During box-and-blocks, however, ipsilesional hemisphere SICI was significantly reduced (P = 0.025), especially following cortical stroke (P < 0.001). SICI in the ipsilesional hemisphere during box-and-blocks task was significantly related to paretic hand dexterity (r = 0.56, P = 0.039) and motor impairment (r = 0.56, P = 0.037).Conclusions: SICI during motor activity, but not rest, reveals persistent impairment in chronic stroke survivors indicating that inhibitory brain circuits responsible for motor coordination do not fully normalize as part of the natural history of stroke recovery. Observation that reduced SICI (i.e., disinhibition) is associated with greater motor impairment and worse dexterity in chronic hemiparetic individuals suggests the response considered to promote neuroplasticity and recovery in the acute phase could be maladaptive in the chronic phase post-stroke.

Highlights

  • GABAergic inhibitory brain circuits are important to motor control [1,2,3,4,5,6]

  • Using data from stroke survivors’ ipsilesional hemisphere (IH) and healthy controls we found SICIB&B was positively correlated with Box and Blocks Test (BBT) score (r = 0.57, P = 0.005) (Figure 3)

  • Our primary findings are: [1] when measured at rest, IH Short intracortical inhibition (SICI) appears to be normalized in chronic stroke; but [2] when measured during motor activity, IH SICI is reduced, reflecting motor disinhibition, especially following cortical stroke or in the presence of severe motor impairment; [3] when S1 intensity is adjusted to induce maximal inhibition, SICIrest and SICIactive are similar in healthy individuals

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Summary

Introduction

Reduced GABAergic activity, or disinhibition, is considered relevant to early motor recovery following stroke [7,8,9,10]. This argument stems from observations in a mouse model of acute stroke that excessive GABAA-mediated tonic inhibition is reduced by blockage of extrasynaptic GABAA receptors [11]. As a result, reduced GABAergic activity, or disinhibition, is believed to be relevant to early motor recovery following stroke in humans [7,8,9,10]. Due to differences in both the underlying biology and measurement of GABAergic activity, it remains unclear how well results from animals models can be generalized to humans

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