Brain Advance Access originally published online on August 22, 2003
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Brain, Vol. 126, No. 12, 2609-2615,
December 2003
© 2003 Guarantors of Brain
doi: 10.1093/brain/awg268
Striatal dopamine release induced by repetitive transcranial magnetic stimulation of the human motor cortex
PausMcConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, Montréal, Québec, Canada
Correspondence to: Alain Dagher, Montreal Neurological Institute, 3801 University Street, Montreal, Québec, Canada H3A 2134E-mail: alain{at}bic.mni.mcgill.ca
Brain dopamine is implicated in the regulation of movement, attention, reward and learning. Dysfunction of dopamine plays a role in Parkinsons disease, schizophrenia and drug addiction. It is released in the striatum when dopamine neurons in the midbrain undergo burst firing. Several animal studies have shown that dopamine can also be released under direct control of glutamatergic corticostriatal efferents. However, the existence and physiological significance of this mode of action remain controversial. We have shown previously that repetitive transcranial magnetic stimulation (rTMS) of the human prefrontal cortex led to focal dopamine release in the ipsilateral caudate nucleus, supporting the corticostriatal mode of dopamine release. Using the same experimental approach, we sought to confirm this hypothesis. We used [11C]raclopride and PET to measure changes in extracellular dopamine concentration following rTMS of the motor cortex in six healthy human subjects. rTMS of the left primary motor cortex caused a reduction in [11C]raclopride binding in the left putamen compared with rTMS of the left occipital cortex. There were no changes in binding in the right putamen, caudate nucleus or nucleus accumbens. The area of statistically significant change in binding corresponded closely to the known projection zone of corticostriatal efferents originating in monkey motor cortex. This finding has implications for the functional role of subcortical dopamine.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
H. Rothkegel, M. Sommer, T. Rammsayer, C. Trenkwalder, and W. Paulus Training Effects Outweigh Effects of Single-Session Conventional rTMS and Theta Burst Stimulation in PD Patients Neurorehabil Neural Repair, May 1, 2009; 23(4): 373 - 381. [Abstract] [PDF] |
||||
![]() |
G. Garraux, P. Peigneux, R. E. Carson, and M. Hallett Task-Related Interaction between Basal Ganglia and Cortical Dopamine Release J. Neurosci., December 26, 2007; 27(52): 14434 - 14441. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. W. Dunlop and C. B. Nemeroff The Role of Dopamine in the Pathophysiology of Depression Arch Gen Psychiatry, March 1, 2007; 64(3): 327 - 337. [Full Text] [PDF] |
||||
![]() |
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] |
||||
![]() |
E. M. Khedr, M. A. Ahmed, N. Fathy, and J. C. Rothwell Therapeutic trial of repetitive transcranial magnetic stimulation after acute ischemic stroke Neurology, August 9, 2005; 65(3): 466 - 468. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Terao, T. Furubayashi, S. Okabe, N. Arai, H. Mochizuki, S. Kobayashi, M. Yumoto, M. Nishikawa, N. K. Iwata, and Y. Ugawa Interhemispheric Transmission of Visuomotor Information for Motor Implementation Cereb Cortex, July 1, 2005; 15(7): 1025 - 1036. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Paus Inferring causality in brain images: a perturbation approach Phil Trans R Soc B, May 29, 2005; 360(1457): 1109 - 1114. [Abstract] [Full Text] [PDF] |
||||





