Hebbian priming of human motor learning

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Standard

Hebbian priming of human motor learning. / Bjørndal, Jonas Rud; Beck, Mikkel Malling; Jespersen, Lasse; Christiansen, Lasse; Lundbye-jensen, Jesper.

I: Nature Communications, Bind 15, Nr. 1, 5126, 2024.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Bjørndal, JR, Beck, MM, Jespersen, L, Christiansen, L & Lundbye-jensen, J 2024, 'Hebbian priming of human motor learning', Nature Communications, bind 15, nr. 1, 5126. https://doi.org/10.1038/s41467-024-49478-5

APA

Bjørndal, J. R., Beck, M. M., Jespersen, L., Christiansen, L., & Lundbye-jensen, J. (2024). Hebbian priming of human motor learning. Nature Communications, 15(1), [5126]. https://doi.org/10.1038/s41467-024-49478-5

Vancouver

Bjørndal JR, Beck MM, Jespersen L, Christiansen L, Lundbye-jensen J. Hebbian priming of human motor learning. Nature Communications. 2024;15(1). 5126. https://doi.org/10.1038/s41467-024-49478-5

Author

Bjørndal, Jonas Rud ; Beck, Mikkel Malling ; Jespersen, Lasse ; Christiansen, Lasse ; Lundbye-jensen, Jesper. / Hebbian priming of human motor learning. I: Nature Communications. 2024 ; Bind 15, Nr. 1.

Bibtex

@article{311a38ed189841b9bbc64fdcde6e2190,
title = "Hebbian priming of human motor learning",
abstract = "Motor learning relies on experience-dependent plasticity in relevant neural circuits. In four experiments, we provide initial evidence and a double-blinded, sham-controlled replication (Experiment I-II) demonstrating that motor learning involving ballistic index finger movements is improved by preceding paired corticospinal-motoneuronal stimulation (PCMS), a human model for exogenous induction of spike-timing-dependent plasticity. Behavioral effects of PCMS targeting corticomotoneuronal (CM) synapses are order- and timing-specific and partially bidirectional (Experiment III). PCMS with a 2 ms inter-arrival interval at CM-synapses enhances learning and increases corticospinal excitability compared to control protocols. Unpaired stimulations did not increase corticospinal excitability (Experiment IV). Our findings demonstrate that non-invasively induced plasticity interacts positively with experience-dependent plasticity to promote motor learning. The effects of PCMS on motor learning approximate Hebbian learning rules, while the effects on corticospinal excitability demonstrate timing-specificity but not bidirectionality. These findings offer a mechanistic rationale to enhance motor practice effects by priming sensorimotor training with individualized PCMS.",
author = "Bj{\o}rndal, {Jonas Rud} and Beck, {Mikkel Malling} and Lasse Jespersen and Lasse Christiansen and Jesper Lundbye-jensen",
year = "2024",
doi = "10.1038/s41467-024-49478-5",
language = "English",
volume = "15",
journal = "Nature Communications",
issn = "2041-1723",
publisher = "nature publishing group",
number = "1",

}

RIS

TY - JOUR

T1 - Hebbian priming of human motor learning

AU - Bjørndal, Jonas Rud

AU - Beck, Mikkel Malling

AU - Jespersen, Lasse

AU - Christiansen, Lasse

AU - Lundbye-jensen, Jesper

PY - 2024

Y1 - 2024

N2 - Motor learning relies on experience-dependent plasticity in relevant neural circuits. In four experiments, we provide initial evidence and a double-blinded, sham-controlled replication (Experiment I-II) demonstrating that motor learning involving ballistic index finger movements is improved by preceding paired corticospinal-motoneuronal stimulation (PCMS), a human model for exogenous induction of spike-timing-dependent plasticity. Behavioral effects of PCMS targeting corticomotoneuronal (CM) synapses are order- and timing-specific and partially bidirectional (Experiment III). PCMS with a 2 ms inter-arrival interval at CM-synapses enhances learning and increases corticospinal excitability compared to control protocols. Unpaired stimulations did not increase corticospinal excitability (Experiment IV). Our findings demonstrate that non-invasively induced plasticity interacts positively with experience-dependent plasticity to promote motor learning. The effects of PCMS on motor learning approximate Hebbian learning rules, while the effects on corticospinal excitability demonstrate timing-specificity but not bidirectionality. These findings offer a mechanistic rationale to enhance motor practice effects by priming sensorimotor training with individualized PCMS.

AB - Motor learning relies on experience-dependent plasticity in relevant neural circuits. In four experiments, we provide initial evidence and a double-blinded, sham-controlled replication (Experiment I-II) demonstrating that motor learning involving ballistic index finger movements is improved by preceding paired corticospinal-motoneuronal stimulation (PCMS), a human model for exogenous induction of spike-timing-dependent plasticity. Behavioral effects of PCMS targeting corticomotoneuronal (CM) synapses are order- and timing-specific and partially bidirectional (Experiment III). PCMS with a 2 ms inter-arrival interval at CM-synapses enhances learning and increases corticospinal excitability compared to control protocols. Unpaired stimulations did not increase corticospinal excitability (Experiment IV). Our findings demonstrate that non-invasively induced plasticity interacts positively with experience-dependent plasticity to promote motor learning. The effects of PCMS on motor learning approximate Hebbian learning rules, while the effects on corticospinal excitability demonstrate timing-specificity but not bidirectionality. These findings offer a mechanistic rationale to enhance motor practice effects by priming sensorimotor training with individualized PCMS.

U2 - 10.1038/s41467-024-49478-5

DO - 10.1038/s41467-024-49478-5

M3 - Journal article

VL - 15

JO - Nature Communications

JF - Nature Communications

SN - 2041-1723

IS - 1

M1 - 5126

ER -

ID: 394979740