Intermittent theta burst stimulation facilitates functional connectivity from the dorsal premotor cortex to primary motor cortex

Motor information in the brain is transmitted from the dorsal premotor cortex (PMd) to the primary motor cortex (M1), where it is further processed and relayed to the spinal cord to eventually generate muscle movement. However, how information from the PMd affects M1 processing and the final output...

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Veröffentlicht in:PeerJ (San Francisco, CA) CA), 2020-07, Vol.8, p.e9253-e9253, Article e9253
Hauptverfasser: Meng, Hai-Jiang, Cao, Na, Zhang, Jian, Pi, Yan-Ling
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Sprache:eng
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Zusammenfassung:Motor information in the brain is transmitted from the dorsal premotor cortex (PMd) to the primary motor cortex (M1), where it is further processed and relayed to the spinal cord to eventually generate muscle movement. However, how information from the PMd affects M1 processing and the final output is unclear. Here, we applied intermittent theta burst stimulation (iTBS) to the PMd to alter cortical excitability not only at the application site but also at the PMd projection site of M1. We aimed to determine how PMd iTBS-altered information changed M1 processing and the corticospinal output. In total, 16 young, healthy participants underwent PMd iTBS with 600 pulses (iTBS600) or sham-iTBS600. Corticospinal excitability, short-interval intracortical inhibition (SICI), and intracortical facilitation (ICF) were measured using transcranial magnetic stimulation before and up to 60 min after stimulation. Corticospinal excitability in M1 was significantly greater 15 min after PMd iTBS600 than that after sham-iTBS600 ( = 0.012). Compared with that after sham-iTBS600, at 0 ( = 0.014) and 15 ( = 0.037) min after iTBS600, SICI in M1 was significantly decreased, whereas 15 min after iTBS600, ICF in M1 was significantly increased ( = 0.033). Our results suggested that projections from the PMd to M1 facilitated M1 corticospinal output and that this facilitation may be attributable in part to decreased intracortical inhibition and increased intracortical facilitation in M1. Such a facilitatory network may inform future understanding of the allocation of resources to achieve optimal motion output.
ISSN:2167-8359
2167-8359
DOI:10.7717/peerj.9253