Double-Sine-Wave Quadri-Pulse Theta Burst Stimulation of Precentral Motor Hand Representation Induces Bidirectional Changes in Corticomotor Excitability

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Double-Sine-Wave Quadri-Pulse Theta Burst Stimulation of Precentral Motor Hand Representation Induces Bidirectional Changes in Corticomotor Excitability. / Jung, Nikolai H.; Gleich, Bernhard; Gattinger, Norbert; Kalb, Anke; Fritsch, Julia; Asenbauer, Elisabeth; Siebner, Hartwig R.; Mall, Volker.

In: Frontiers in Neurology, Vol. 12, 673560, 2021.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Jung, NH, Gleich, B, Gattinger, N, Kalb, A, Fritsch, J, Asenbauer, E, Siebner, HR & Mall, V 2021, 'Double-Sine-Wave Quadri-Pulse Theta Burst Stimulation of Precentral Motor Hand Representation Induces Bidirectional Changes in Corticomotor Excitability', Frontiers in Neurology, vol. 12, 673560. https://doi.org/10.3389/fneur.2021.673560

APA

Jung, N. H., Gleich, B., Gattinger, N., Kalb, A., Fritsch, J., Asenbauer, E., Siebner, H. R., & Mall, V. (2021). Double-Sine-Wave Quadri-Pulse Theta Burst Stimulation of Precentral Motor Hand Representation Induces Bidirectional Changes in Corticomotor Excitability. Frontiers in Neurology, 12, [673560]. https://doi.org/10.3389/fneur.2021.673560

Vancouver

Jung NH, Gleich B, Gattinger N, Kalb A, Fritsch J, Asenbauer E et al. Double-Sine-Wave Quadri-Pulse Theta Burst Stimulation of Precentral Motor Hand Representation Induces Bidirectional Changes in Corticomotor Excitability. Frontiers in Neurology. 2021;12. 673560. https://doi.org/10.3389/fneur.2021.673560

Author

Jung, Nikolai H. ; Gleich, Bernhard ; Gattinger, Norbert ; Kalb, Anke ; Fritsch, Julia ; Asenbauer, Elisabeth ; Siebner, Hartwig R. ; Mall, Volker. / Double-Sine-Wave Quadri-Pulse Theta Burst Stimulation of Precentral Motor Hand Representation Induces Bidirectional Changes in Corticomotor Excitability. In: Frontiers in Neurology. 2021 ; Vol. 12.

Bibtex

@article{fab9fe0b44f5459d8365e0ef0b821cc6,
title = "Double-Sine-Wave Quadri-Pulse Theta Burst Stimulation of Precentral Motor Hand Representation Induces Bidirectional Changes in Corticomotor Excitability",
abstract = "Neuronal plasticity is considered to be the neurophysiological correlate of learning and memory and changes in corticospinal excitability play a key role in the normal development of the central nervous system as well as in developmental disorders. In a previous study, it was shown that quadri-pulse theta burst stimulation (qTBS) can induce bidirectional changes in corticospinal excitability (1). There, a quadruple burst consisted of four single-sine-wave (SSW) pulses with a duration of 160 μs and inter-pulse intervals of 1.5 ms to match I-wave periodicity (666 Hz). In the present study, the pulse shape was modified applying double-sine-waves (DSW) rather than SSW pulses, while keeping the pulse duration at 160 μs. In two separate sessions, we reversed the current direction of the DSW pulse, so that its second component elicited either a mainly posterior-to-anterior (DSW PA-qTBS) or anterior-to-posterior (DSW AP-qTBS) directed current in the precentral gyrus. The after-effects of DSW qTBS on corticospinal excitability were examined in healthy individuals (n = 10) with single SSW TMS pulses. For single-pulse SSW TMS, the second component produced the same preferential current direction as DSW qTBS but had a suprathreshold intensity, thus eliciting motor evoked potentials (PA-MEP or AP-MEP). Single-pulse SSW TMS revealed bidirectional changes in corticospinal excitability after DSW qTBS, which depended on the preferentially induced current direction. DSW PA-qTBS at 666 Hz caused a stable increase in PA-MEP, whereas AP-qTBS at 666 Hz induced a transient decrease in AP-MEP. The sign of excitability following DSW qTBS at I-wave periodicity was opposite to the bidirectional changes after SSW qTBS. The results show that the pulse configuration and induced current direction determine the plasticity-effects of ultra-high frequency SSW and DSW qTBS at I-wave periodicity. These findings may offer new opportunities for short non-invasive brain stimulation protocols that are especially suited for stimulation in children and patients with neurological or neurodevelopmental disorders.",
keywords = "corticospinal excitability, double-sine pulses, human primary motor cortex, long-term depression, long-term potentiation, neuronal plasticity, non-invasive brain stimulation, transcranial magnetic stimulation",
author = "Jung, {Nikolai H.} and Bernhard Gleich and Norbert Gattinger and Anke Kalb and Julia Fritsch and Elisabeth Asenbauer and Siebner, {Hartwig R.} and Volker Mall",
note = "Publisher Copyright: {\textcopyright} Copyright {\textcopyright} 2021 Jung, Gleich, Gattinger, Kalb, Fritsch, Asenbauer, Siebner and Mall.",
year = "2021",
doi = "10.3389/fneur.2021.673560",
language = "English",
volume = "12",
journal = "Frontiers in Neurology",
issn = "1664-2295",
publisher = "Frontiers Research Foundation",

}

RIS

TY - JOUR

T1 - Double-Sine-Wave Quadri-Pulse Theta Burst Stimulation of Precentral Motor Hand Representation Induces Bidirectional Changes in Corticomotor Excitability

AU - Jung, Nikolai H.

AU - Gleich, Bernhard

AU - Gattinger, Norbert

AU - Kalb, Anke

AU - Fritsch, Julia

AU - Asenbauer, Elisabeth

AU - Siebner, Hartwig R.

AU - Mall, Volker

N1 - Publisher Copyright: © Copyright © 2021 Jung, Gleich, Gattinger, Kalb, Fritsch, Asenbauer, Siebner and Mall.

PY - 2021

Y1 - 2021

N2 - Neuronal plasticity is considered to be the neurophysiological correlate of learning and memory and changes in corticospinal excitability play a key role in the normal development of the central nervous system as well as in developmental disorders. In a previous study, it was shown that quadri-pulse theta burst stimulation (qTBS) can induce bidirectional changes in corticospinal excitability (1). There, a quadruple burst consisted of four single-sine-wave (SSW) pulses with a duration of 160 μs and inter-pulse intervals of 1.5 ms to match I-wave periodicity (666 Hz). In the present study, the pulse shape was modified applying double-sine-waves (DSW) rather than SSW pulses, while keeping the pulse duration at 160 μs. In two separate sessions, we reversed the current direction of the DSW pulse, so that its second component elicited either a mainly posterior-to-anterior (DSW PA-qTBS) or anterior-to-posterior (DSW AP-qTBS) directed current in the precentral gyrus. The after-effects of DSW qTBS on corticospinal excitability were examined in healthy individuals (n = 10) with single SSW TMS pulses. For single-pulse SSW TMS, the second component produced the same preferential current direction as DSW qTBS but had a suprathreshold intensity, thus eliciting motor evoked potentials (PA-MEP or AP-MEP). Single-pulse SSW TMS revealed bidirectional changes in corticospinal excitability after DSW qTBS, which depended on the preferentially induced current direction. DSW PA-qTBS at 666 Hz caused a stable increase in PA-MEP, whereas AP-qTBS at 666 Hz induced a transient decrease in AP-MEP. The sign of excitability following DSW qTBS at I-wave periodicity was opposite to the bidirectional changes after SSW qTBS. The results show that the pulse configuration and induced current direction determine the plasticity-effects of ultra-high frequency SSW and DSW qTBS at I-wave periodicity. These findings may offer new opportunities for short non-invasive brain stimulation protocols that are especially suited for stimulation in children and patients with neurological or neurodevelopmental disorders.

AB - Neuronal plasticity is considered to be the neurophysiological correlate of learning and memory and changes in corticospinal excitability play a key role in the normal development of the central nervous system as well as in developmental disorders. In a previous study, it was shown that quadri-pulse theta burst stimulation (qTBS) can induce bidirectional changes in corticospinal excitability (1). There, a quadruple burst consisted of four single-sine-wave (SSW) pulses with a duration of 160 μs and inter-pulse intervals of 1.5 ms to match I-wave periodicity (666 Hz). In the present study, the pulse shape was modified applying double-sine-waves (DSW) rather than SSW pulses, while keeping the pulse duration at 160 μs. In two separate sessions, we reversed the current direction of the DSW pulse, so that its second component elicited either a mainly posterior-to-anterior (DSW PA-qTBS) or anterior-to-posterior (DSW AP-qTBS) directed current in the precentral gyrus. The after-effects of DSW qTBS on corticospinal excitability were examined in healthy individuals (n = 10) with single SSW TMS pulses. For single-pulse SSW TMS, the second component produced the same preferential current direction as DSW qTBS but had a suprathreshold intensity, thus eliciting motor evoked potentials (PA-MEP or AP-MEP). Single-pulse SSW TMS revealed bidirectional changes in corticospinal excitability after DSW qTBS, which depended on the preferentially induced current direction. DSW PA-qTBS at 666 Hz caused a stable increase in PA-MEP, whereas AP-qTBS at 666 Hz induced a transient decrease in AP-MEP. The sign of excitability following DSW qTBS at I-wave periodicity was opposite to the bidirectional changes after SSW qTBS. The results show that the pulse configuration and induced current direction determine the plasticity-effects of ultra-high frequency SSW and DSW qTBS at I-wave periodicity. These findings may offer new opportunities for short non-invasive brain stimulation protocols that are especially suited for stimulation in children and patients with neurological or neurodevelopmental disorders.

KW - corticospinal excitability

KW - double-sine pulses

KW - human primary motor cortex

KW - long-term depression

KW - long-term potentiation

KW - neuronal plasticity

KW - non-invasive brain stimulation

KW - transcranial magnetic stimulation

U2 - 10.3389/fneur.2021.673560

DO - 10.3389/fneur.2021.673560

M3 - Journal article

C2 - 34262522

AN - SCOPUS:85109780175

VL - 12

JO - Frontiers in Neurology

JF - Frontiers in Neurology

SN - 1664-2295

M1 - 673560

ER -

ID: 275014977