Literature DB >> 15826863

Temporal activation pattern of parietal and premotor areas related to praxis movements.

Lewis A Wheaton1, Hiroshi Shibasaki, Mark Hallett.   

Abstract

OBJECTIVE: We sought to determine the cortical physiology underlying praxis movements in normal subjects using electroencephalography (EEG).
METHODS: Eight normal subjects were instructed to perform six types of self-paced tool-use pantomime and communicative gesture movements with the right hand. We recorded 64-channel EEG using a linked ear reference and electromyogram (EMG) from right thumb and forearm flexors.
RESULTS: Data revealed early slow wave components of the movement-related cortical potential (MRCP) beginning over the left parietal area about 3s before movement onset, similarly for both movement types. At movement onset, maximal amplitude was present over central and bilateral sensorimotor areas. Event-related desynchronization (ERD) in the beta band was seen over the left parietal and sensorimotor cortices during preparation, later spreading to the homologous area of the right hemisphere. Alpha ERD was mainly in the left sensorimotor cortex about 1.5s before movement onset. Beta ERD in mesial frontal areas was greater during preparation for tool use compared to communicative gesture movements. Mesial frontal beta event-related synchronization (ERS) developed more rapidly after communicative gestures than tool-use.
CONCLUSIONS: The dynamics of parietal and frontal activities indicates the timing of these areas in the production of praxis. The posterior parietal cortex contributes to the early slow wave negativity of the MRCP. SIGNIFICANCE: Planning self-paced praxis movements begins as early as 3s before movement in the left parietal area and subsequently engages frontal cortical regions.

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Year:  2005        PMID: 15826863     DOI: 10.1016/j.clinph.2005.01.001

Source DB:  PubMed          Journal:  Clin Neurophysiol        ISSN: 1388-2457            Impact factor:   3.708


  32 in total

1.  Posterior parietal negativity preceding self-paced praxis movements.

Authors:  Lewis A Wheaton; Satoshi Yakota; Mark Hallett
Journal:  Exp Brain Res       Date:  2005-05-10       Impact factor: 1.972

2.  Preparatory band specific premotor cortical activity differentiates upper and lower extremity movement.

Authors:  Lewis A Wheaton; Mackenzie Carpenter; J C Mizelle; Larry Forrester
Journal:  Exp Brain Res       Date:  2007-10-23       Impact factor: 1.972

3.  Cortico-cortical networks in patients with ideomotor apraxia as revealed by EEG coherence analysis.

Authors:  Lewis A Wheaton; Stephan Bohlhalter; Guido Nolte; Hiroshi Shibasaki; Noriaki Hattori; Esteban Fridman; Sherry Vorbach; Jordan Grafman; Mark Hallett
Journal:  Neurosci Lett       Date:  2008-01-12       Impact factor: 3.046

4.  Evaluating Model Misspecification in Independent Component Analysis.

Authors:  Seonjoo Lee; Brian S Caffo; Balaji Lakshmanan; Dzung L Pham
Journal:  J Stat Comput Simul       Date:  2015-04       Impact factor: 1.424

5.  Gesture subtype-dependent left lateralization of praxis planning: an event-related fMRI study.

Authors:  S Bohlhalter; N Hattori; L Wheaton; E Fridman; E A Shamim; G Garraux; M Hallett
Journal:  Cereb Cortex       Date:  2008-09-16       Impact factor: 5.357

6.  Modulating conscious movement intention by noninvasive brain stimulation and the underlying neural mechanisms.

Authors:  Zachary H Douglas; Brian Maniscalco; Mark Hallett; Eric M Wassermann; Biyu J He
Journal:  J Neurosci       Date:  2015-05-06       Impact factor: 6.167

7.  I know what I will see: action-specific motor preparation activity in a passive observation task.

Authors:  Chiara Bozzacchi; Donatella Spinelli; Sabrina Pitzalis; Maria Assunta Giusti; Francesco Di Russo
Journal:  Soc Cogn Affect Neurosci       Date:  2014-09-26       Impact factor: 3.436

8.  Cerebral preparation of spontaneous movements: An EEG study.

Authors:  Elise Houdayer; Sae-Jin Lee; Mark Hallett
Journal:  Clin Neurophysiol       Date:  2020-08-25       Impact factor: 3.708

9.  Remodeling of cortical activity for motor control following upper limb loss.

Authors:  Laura Williams; Nikta Pirouz; J C Mizelle; William Cusack; Rob Kistenberg; Lewis A Wheaton
Journal:  Clin Neurophysiol       Date:  2016-07-16       Impact factor: 3.708

10.  Deficient supplementary motor area at rest: Neural basis of limb kinetic deficits in Parkinson's disease.

Authors:  Stefanie Kübel; Katharina Stegmayer; Tim Vanbellingen; Sebastian Walther; Stephan Bohlhalter
Journal:  Hum Brain Mapp       Date:  2018-05-02       Impact factor: 5.038

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