Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Correspondence:
Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Correspondence are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Samuel, M.
Right arrow Articles by Brooks, D. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Samuel, M.
Right arrow Articles by Brooks, D. J.
NEUROLOGY 1998;51:1567-1575
© 1998 American Academy of Neurology

Exploring the temporal nature of hemodynamic responses of cortical motor areas using functional MRI

M. Samuel, MRCP, S.C.R. Williams, PhD, P. N. Leigh, FRCP, A. Simmons, PhD, S. Chakraborti, BSc, C. M. Andrew, K. J. Friston, MRCPsych, L. H. Goldstein, PhD and D. J. Brooks, FRCP

From the MRC Cyclotron Unit (Dr. Samuel, S. Chakraborti, and Dr. Brooks), Hammersmith Hospital; Department of Clinical Neurosciences and MR Research Institute (Drs. Williams, Leigh, and Simmons, C.M. Andrew, and Dr. Goldstein), Institute of Psychiatry; Institute of Neurology (Drs. Friston and Brooks), Queen Square; and Department of Psychology (Dr. Goldstein), Institute of Psychiatry, London, UK.

Address correspondence and reprint requests to Dr. M. Samuel, MRC Cyclotron Unit, Hammersmith Hospital, Du Cane Road, London, W12 ONN, UK.

Objective: To use functional MRI (fMRI) to study grouped patterns of cerebral activation and the course of hemodynamic responses during performance of two activation tasks (paradigms) using a hand-held joystick to perform movements in a repetitively fixed direction and movements in freely selected random directions.

Background: Evidence from lesion, electrophysiologic, and functional imaging studies implicates prefrontal and mesial frontal cortex in motor preparation and primary motor cortex in motor execution. fMRI can be used to study cerebral activation and has practical advantages over other methods of functional neuroimaging.

Methods: We acquired 100 multislice T2* -weighted data sets from five healthy volunteers during performance of each paradigm using conventional fMRI. For each paradigm, rest and movement epochs were alternated every 30 seconds. After coregistration and spatial normalization, we combined the data for group studies. We used statistical parametric mapping to compare the early (first 15 seconds) components of the movement epochs with rest as well as the late (last 15 seconds) components of the movement epochs with rest.

Results: During the early phase of both paradigms, significant activation was present in rostral and caudal mesial premotor cortex. Right prefrontal cortex was significantly activated during the early component of freely selected joystick movements. Activation of rostral supplementary motor area was maintained during the late component of freely selected movements but decreased during repetitively fixed movements. In contrast, significant activation in contralateral sensorimotor cortex was maintained during both early and late components of both paradigms.

Conclusions: fMRI can detect cortical activation. The temporal resolution of fMRI also allows adaptation of blood oxygenation level-dependent (BOLD) contrast signal to be detected in association cortex. However, the level of BOLD contrast signal in primary motor cortex remained significantly elevated throughout task performance.


Supported by the Medical Research Council (M.S.), London, and the Wellcome Trust (K.J.F.), London, UK.

Received July 14, 1997. Accepted in final form August 21, 1998.




This article has been cited by other articles:


Home page
Cereb CortexHome page
R. B. Postuma and A. Dagher
Basal Ganglia Functional Connectivity Based on a Meta-Analysis of 126 Positron Emission Tomography and Functional Magnetic Resonance Imaging Publications
Cereb Cortex, October 1, 2006; 16(10): 1508 - 1521.
[Abstract] [Full Text] [PDF]


Home page
Cereb CortexHome page
D. M. Barch, T. S. Braver, E. Akbudak, T. Conturo, J. Ollinger, and A. Snyder
Anterior Cingulate Cortex and Response Conflict: Effects of Response Modality and Processing Domain
Cereb Cortex, September 1, 2001; 11(9): 837 - 848.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Neuroradiol.Home page
C. H. Moritz, M. E. Meyerand, D. Cordes, and V. M. Haughton
Functional MR Imaging Activation after Finger Tapping Has a Shorter Duration in the Basal Ganglia Than in the Sensorimotor Cortex
AJNR Am. J. Neuroradiol., July 1, 2000; 21(7): 1228 - 1234.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
J. Moll, R. de Oliveira-Souza, L. J. Passman, F. C. Cunha, F. Souza-Lima, and P. A. Andreiuolo
Functional MRI correlates of real and imagined tool-use pantomimes
Neurology, March 28, 2000; 54(6): 1331 - 1336.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Neuroradiol.Home page
M. Marquart, R. Birn, and V. Haughton
Single- and Multiple-Event Paradigms for Identification of Motor Cortex Activation
AJNR Am. J. Neuroradiol., January 1, 2000; 21(1): 94 - 98.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1998 by AAN Enterprises, Inc.