Training of a discrete motor skill in humans is accompanied by increased excitability of the fastest corticospinal connections at movement onset

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Training of a discrete motor skill in humans is accompanied by increased excitability of the fastest corticospinal connections at movement onset. / Wiegel, Patrick; Leukel, Christian.

I: Journal of Physiology, Bind 598, Nr. 16, 2020, s. 3485-3500.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Wiegel, P & Leukel, C 2020, 'Training of a discrete motor skill in humans is accompanied by increased excitability of the fastest corticospinal connections at movement onset', Journal of Physiology, bind 598, nr. 16, s. 3485-3500. https://doi.org/10.1113/JP279879

APA

Wiegel, P., & Leukel, C. (2020). Training of a discrete motor skill in humans is accompanied by increased excitability of the fastest corticospinal connections at movement onset. Journal of Physiology, 598(16), 3485-3500. https://doi.org/10.1113/JP279879

Vancouver

Wiegel P, Leukel C. Training of a discrete motor skill in humans is accompanied by increased excitability of the fastest corticospinal connections at movement onset. Journal of Physiology. 2020;598(16):3485-3500. https://doi.org/10.1113/JP279879

Author

Wiegel, Patrick ; Leukel, Christian. / Training of a discrete motor skill in humans is accompanied by increased excitability of the fastest corticospinal connections at movement onset. I: Journal of Physiology. 2020 ; Bind 598, Nr. 16. s. 3485-3500.

Bibtex

@article{8d231307205344658012294fc9a419be,
title = "Training of a discrete motor skill in humans is accompanied by increased excitability of the fastest corticospinal connections at movement onset",
abstract = "The primary motor cortex (M1) is fundamentally important for the acquisition of skilled motor behaviours. Recent advances in imaging and electrophysiological techniques have improved our understanding of M1 neural circuit modulation in rodents and non-human primates during motor learning. However, little remains known about the learning-related changes of distinct elements in the human brain. In this study, we tested excitability changes of different neural circuits (infragranular and supragranular layers) in the M1 of human subjects who underwent training in a discrete spatiotemporal motor skill. Excitability modulations were assessed by recording H-reflex facilitation from transcranial magnetic stimulation at movement onset. Motor practice improved the consistency of movements and was accompanied by an excitability increase of the fastest corticospinal connections during the initial stages of motor practice. No such excitability changes were observed for training in a simple motor skill and circuits at supragranular layers of M1. Notably, changes in excitability were not associated with changes in motor performance. Our findings could reflect learning-related increases in the recruitment and/or reorganisation of the fastest corticospinal connections.",
keywords = "Corticospinal, Motor cortex, Motor learning, Neural circuits, Sensorimotor control",
author = "Patrick Wiegel and Christian Leukel",
note = "(Ekstern)",
year = "2020",
doi = "10.1113/JP279879",
language = "English",
volume = "598",
pages = "3485--3500",
journal = "The Journal of Physiology",
issn = "0022-3751",
publisher = "Wiley-Blackwell",
number = "16",

}

RIS

TY - JOUR

T1 - Training of a discrete motor skill in humans is accompanied by increased excitability of the fastest corticospinal connections at movement onset

AU - Wiegel, Patrick

AU - Leukel, Christian

N1 - (Ekstern)

PY - 2020

Y1 - 2020

N2 - The primary motor cortex (M1) is fundamentally important for the acquisition of skilled motor behaviours. Recent advances in imaging and electrophysiological techniques have improved our understanding of M1 neural circuit modulation in rodents and non-human primates during motor learning. However, little remains known about the learning-related changes of distinct elements in the human brain. In this study, we tested excitability changes of different neural circuits (infragranular and supragranular layers) in the M1 of human subjects who underwent training in a discrete spatiotemporal motor skill. Excitability modulations were assessed by recording H-reflex facilitation from transcranial magnetic stimulation at movement onset. Motor practice improved the consistency of movements and was accompanied by an excitability increase of the fastest corticospinal connections during the initial stages of motor practice. No such excitability changes were observed for training in a simple motor skill and circuits at supragranular layers of M1. Notably, changes in excitability were not associated with changes in motor performance. Our findings could reflect learning-related increases in the recruitment and/or reorganisation of the fastest corticospinal connections.

AB - The primary motor cortex (M1) is fundamentally important for the acquisition of skilled motor behaviours. Recent advances in imaging and electrophysiological techniques have improved our understanding of M1 neural circuit modulation in rodents and non-human primates during motor learning. However, little remains known about the learning-related changes of distinct elements in the human brain. In this study, we tested excitability changes of different neural circuits (infragranular and supragranular layers) in the M1 of human subjects who underwent training in a discrete spatiotemporal motor skill. Excitability modulations were assessed by recording H-reflex facilitation from transcranial magnetic stimulation at movement onset. Motor practice improved the consistency of movements and was accompanied by an excitability increase of the fastest corticospinal connections during the initial stages of motor practice. No such excitability changes were observed for training in a simple motor skill and circuits at supragranular layers of M1. Notably, changes in excitability were not associated with changes in motor performance. Our findings could reflect learning-related increases in the recruitment and/or reorganisation of the fastest corticospinal connections.

KW - Corticospinal

KW - Motor cortex

KW - Motor learning

KW - Neural circuits

KW - Sensorimotor control

UR - http://www.scopus.com/inward/record.url?scp=85086003808&partnerID=8YFLogxK

U2 - 10.1113/JP279879

DO - 10.1113/JP279879

M3 - Journal article

C2 - 32452030

AN - SCOPUS:85086003808

VL - 598

SP - 3485

EP - 3500

JO - The Journal of Physiology

JF - The Journal of Physiology

SN - 0022-3751

IS - 16

ER -

ID: 243345565