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Brain, Vol. 122, No. 3, 497-512, March 1999
© 1999 Oxford University Press


Article

The neural consequences of conflict between intention and the senses

Gereon R. Fink1,6,7, John C. Marshall4, Peter W. Halligan5, Chris D. Frith1, Jon Driver2, Richard S. J. Frackowiak1 and Raymond J. Dolan1,3

1 Wellcome Department of Cognitive Neurology, Institute of Neurology, 2 University College London, 3 Royal Free Hospital School of Medicine, London, 4 Neuropsychology Unit, University Department of Clinical Neurology, The Radcliffe Infirmary, 5 Department of Experimental Psychology, Oxford, UK, 6 Neurologische Klinik, Heinrich-Heine-Universität Düsseldorf, Düsseldorf and 7 Institut für Medizin, Forschungszentrum Jülich, Germany

Correspondence to: Dr G. R. Fink, Neurologische Klinik, Heinrich-Heine-Universität, Postfach 10 10 07, 40001 Düsseldorf, Germany E-mail: gereon.fink{at}uni-duesseldorf.de

Normal sensorimotor states involve integration of intention, action and sensory feedback. An example is the congruence between motor intention and sensory experience (both proprioceptive and visual) when we move a limb through space. Such goal-directed action necessitates a mechanism that monitors sensorimotor inputs to ensure that motor outputs are congruent with current intentions. Monitoring in this sense is usually implicit and automatic but becomes conscious whenever there is a mismatch between expected and realized sensorimotor states. To investigate how the latter type of monitoring is achieved we conducted three fully factorial functional neuroimaging experiments using PET measures of relative regional cerebral blood flow with healthy volunteers. In the first experiment subjects were asked to perform Luria's bimanual co-ordination task which involves either in-phase (conditions 1 and 3) or out-of-phase (conditions 2 and 4) bimanual movements (factor one), while looking towards their left hand. In half of the conditions (conditions 3 and 4) a mirror was used that altered visual feedback (factor two) by replacing their left hand with the mirror image of their right hand. Hence (in the critical condition 4) subjects saw in-phase movements despite performing out-of-phase movements. This mismatch between intention, proprioception and visual feedback engendered cognitive conflict. The main effect of out-of-phase movements was associated with increased neural activity in posterior parietal cortex (PPC) bilaterally [Brodmann area (BA) 40, extending into BA 7] and dorsolateral prefrontal cortex (DLPFC) bilaterally (BA 9/46). The main effect of the mirror showed increased neural activity in right DLPFC (BA 9/46) and right superior PPC (BA 7) only. Analysis of the critical interaction revealed that the mismatch condition led to a specific activation in the right DLPFC alone (BA 9/46). Study 2, using an identical experimental set-up but manipulating visual feedback from the right hand (instead of the left), subsequently demonstrated that this right DLPFC activation was independent of the hand attended. Finally, study 3 removed the motor intentional component by moving the subjects' hand passively, thus engendering a mismatch between proprioception and vision only. Activation in the right lateral prefrontal cortex was now more ventral than in studies 1 or 2 (BA 44/45). A direct comparison of studies 1 and 3 (which both manipulated visual feedback from the left hand) confirmed that a ventral right lateral prefrontal region is primarily activated by discrepancies between signals from sensory systems, while a more dorsal area in right lateral prefrontal cortex is activated when actions must be maintained in the face of a conflict between intention and sensory outcome.

prefrontal cortex; sensorimotor integration; PET; monitoring; Luria's bimanual co-ordination task

BA = Brodmann area; DLPFC = dorsolateral prefrontal cortex; PPC = posterior parietal cortex; rCBF = regional cerebral blood flow; SPM = statistical parametric map


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