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Decrease in short‐latency afferent inhibition during corticomotor postexercise depression following repetitive finger movement
INTRODUCTION: This study aimed to clarify cortical circuit mechanisms contributing to corticomotor excitability during postexercise depression (PED) following repetitive nonfatiguing movement. We investigated changes in short‐latency afferent inhibition (SAI) and short‐interval intracortical inhibit...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516614/ https://www.ncbi.nlm.nih.gov/pubmed/28729946 http://dx.doi.org/10.1002/brb3.744 |
Sumario: | INTRODUCTION: This study aimed to clarify cortical circuit mechanisms contributing to corticomotor excitability during postexercise depression (PED) following repetitive nonfatiguing movement. We investigated changes in short‐latency afferent inhibition (SAI) and short‐interval intracortical inhibition (SICI) by paired‐pulse transcranial magnetic stimulation (TMS) during PED. METHODS: A total of 16 healthy subjects performed repetitive abduction movements of the right index finger at 2.0 Hz for 6 min at 10% maximum voluntary contraction. We measured SAI evoked by pairing ulnar nerve stimulation with TMS (interstimulus interval, 22 ms) before and during PED (n = 10, experiment 1). We also measured SICI evoked by paired TMS (interstimulus interval, 2 ms) at 80% resting motor threshold (n = 10, experiment 2), and at 80% active motor threshold (n = 8, experiment 3) before and during PED. RESULTS: Single motor evoked potential amplitude significantly decreased 1–2 min after the movement task in all experiments, indicating reliable PED induction. In experiment 1, SAI significantly decreased (disinhibited) 1–2 min during PED, whereas in experiments 2 and 3, SICI showed no significant change during PED. CONCLUSION: This study suggests that cholinergic inhibitory circuit activity decreases during PED following repetitive nonfatiguing movement, whereas GABA(A) circuit activity remains stable. |
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