» Articles » PMID: 8566198

Programming the Duration of a Motor Sequence: Role of the Primary and Supplementary Motor Areas in Man

Overview
Journal Exp Brain Res
Specialty Neurology
Date 1995 Jan 1
PMID 8566198
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Event-related potentials were recorded in a reaction time (RT) paradigm, where the duration of a learned interval (either 0.7 s or 2.5 s) delimited by two brief button-presses was to be accurately controlled. A preparatory signal (PS) either did not give or gave prior information concerning the duration of the following response (neutral condition or primed conditions, respectively). In the latter case, the information was either validated (valid condition) or invalidated (invalid condition) by the response signal (RS). When duration was not known in advance (invalid and neutral conditions), RTs were longer before a response of short than long duration. This difference was not found under the valid condition. During the preparatory period (PP), the amplitude of the contingent negative variation (CNV) was larger when the duration was primed than when it was not. A larger CNV appeared when the PS primed a short rather than a long duration. This effect occurred in the early part of the PP over the supplementary motor area (SMA) and in its latest part over the primary motor area (MI). The RT and the electrophysiological pattern were interpreted as revealing the occurrence of programming operations regarding the temporal dimension of the response. The time course of the CNV over the SMA and MI suggested that these two areas were hierarchically organized. Between the RS and the onset of the response, differences probably related to programming effects were still found over MI: the activities were larger under the valid than under the neutral condition. However, no sign of deprogramming (expected in the invalid condition) was observed: similar amplitudes were found under the neutral and invalid conditions. Deprogramming operations seemed to be postponed during response execution where the invalid condition evoked larger activities than the two other conditions over the SMA. Finally, MI but not the SMA yielded a Bereitschaftpotential before the second press ending the response (i.e., during response execution). These results suggest that the duration of a motor response can be a part of the motor program and that the SMA plays a major role in programming processes but not in response execution, contrary to MI.

Citing Articles

Online Movement Correction in Response to the Unexpectedly Perturbed Initial or Final Action Goals: An ERP and sLORETA Study.

Yu L, Schack T, Koester D Brain Sci. 2021; 11(5).

PMID: 34063437 PMC: 8156469. DOI: 10.3390/brainsci11050641.


The Way We Do the Things We Do: How Cognitive Contexts Shape the Neural Dynamics of Motor Areas in Humans.

Vidal F, Burle B, Hasbroucq T Front Psychol. 2018; 9:1296.

PMID: 30100890 PMC: 6073480. DOI: 10.3389/fpsyg.2018.01296.


Stimulus-dependent deliberation process leading to a specific motor action demonstrated via a multi-channel EEG analysis.

Henz S, Kutz D, Werner J, Hurster W, Kolb F, Nida-Ruemelin J Front Hum Neurosci. 2015; 9:355.

PMID: 26190987 PMC: 4488757. DOI: 10.3389/fnhum.2015.00355.


Basics for sensorimotor information processing: some implications for learning.

Vidal F, Meckler C, Hasbroucq T Front Psychol. 2015; 6:33.

PMID: 25762944 PMC: 4329794. DOI: 10.3389/fpsyg.2015.00033.


The influence of an acute bout of aerobic exercise on cortical contributions to motor preparation and execution.

Thacker J, Middleton L, McIlroy W, Staines W Physiol Rep. 2014; 2(10).

PMID: 25355852 PMC: 4254103. DOI: 10.14814/phy2.12178.


References
1.
Toleikis J, Sloan T, Ronai A . Optimal transcranial magnetic stimulation sites for the assessment of motor function. Electroencephalogr Clin Neurophysiol. 1991; 81(6):443-9. DOI: 10.1016/0013-4694(91)90006-p. View

2.
WIESENDANGER M . Recent developments in studies of the supplementary motor area of primates. Rev Physiol Biochem Pharmacol. 1986; 103:1-59. DOI: 10.1007/3540153330_1. View

3.
Perrin F, Bertrand O, Pernier J . Scalp current density mapping: value and estimation from potential data. IEEE Trans Biomed Eng. 1987; 34(4):283-8. DOI: 10.1109/tbme.1987.326089. View

4.
Goodman D, Kelso J . Are movements prepared in parts? Not under compatible (naturalized) conditions. J Exp Psychol Gen. 1980; 109(4):475-95. DOI: 10.1037//0096-3445.109.4.475. View

5.
Cheyne D, WEINBERG H . Neuromagnetic fields accompanying unilateral finger movements: pre-movement and movement-evoked fields. Exp Brain Res. 1989; 78(3):604-12. DOI: 10.1007/BF00230248. View