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Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-47143

Naranjo, J R; Wang, X; Schulte-Mönting, J; Huethe, F; Maurer, C; Hepp-Reymond, M C; Kristeva, R (2010). Corticospinal interaction during isometric compensation for modulated forces with different frequencies. BMC Neuroscience, 11:157.

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Abstract

BACKGROUND: During isometric compensation of modulated low-level forces corticomuscular coherence (CMC) has been shown to occur in high-beta or gamma-range. The influence of the frequency of force modulation on CMC has up to now remained unexplored. We addressed this question by investigating CMC, motor performance, and cortical spectral power during a visuomotor task in which subjects had to compensate a modulated force of 8% of the maximum voluntary contraction exerted on their right index finger. The effect of three frequencies of force modulation (0.6, 1.0 and 1.6 Hz) was tested. EEG, EMG from first dorsal interosseus, hand flexor and extensor muscles, and finger position were recorded in eight right-handed women.

RESULTS: Five subjects showed CMC in gamma- (28-45 Hz) and three in beta-range (15-30 Hz). Beta- and gamma-range CMC and cortical motor spectral power were not modulated by the various frequencies. However, a sharp bilateral CMC peak at 1.6 Hz was observed, but only in the five gamma-range CMC subjects. The performance error increased linearly with the frequency.

CONCLUSIONS: Our findings suggest that the frequency of force modulation has no effect on the beta- and gamma-range CMC during isometric compensation for modulated forces at 8% MVC. The beta- and gamma-range CMC may be related to interindividual differences and possibly to strategy differences.

Item Type:Journal Article, refereed, original work
Communities & Collections:07 Faculty of Science > Institute of Neuroinformatics
DDC:570 Life sciences; biology
Language:English
Date:01 January 2010
Deposited On:04 Mar 2011 16:23
Last Modified:28 Nov 2013 02:13
Publisher:BioMed Central
Series Name:BMC neuroscience
Number of Pages:-157
ISSN:1471-2202
Publisher DOI:10.1186/1471-2202-11-157
PubMed ID:21194447
Citations:Web of Science®. Times Cited: 3
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