Changing plans: neural correlates of executive control in monkey and human frontal cortex

Changing plans depends on executive control, the orchestration of behavior based on knowledge of both goal and context. Dorsolateral prefrontal (DLPFC) and anterior cingulate (ACC) cortices are clearly involved in these processes. Intracranial recordings in these regions were obtained from a monkey performing an executive control-challenging task that is widely used in clinic and laboratory to assess the integrity of cognitive function, the AX version of the continuous performance task (AX-CPT), and directly compared to scalp-recorded evoked potentials in humans. In this task the subject presses a button when detecting a frequent cue–target probe sequence in a stream of letters presented on a computer screen, and withholds response following incorrect sequences. Thus correct performance requires correct encoding of cue and probe instruction and inhibitory control. Intracranial recordings showed that DLPFC in the monkey was primarily activated by conditions that required inhibition of imminent action, as had been shown in human event-related potential (ERP) recordings. Different subregions of monkey ACC were activated primarily by either initiating or inhibiting action, whereas human ERP had shown ACC activation in both situations. We suggest that simultaneous activation of both types of subregions in conflict conditions may account the ubiquitous ACC activation observed with fMRI and ERP in those conditions.

[1]  P. Strick,et al.  Motor areas of the medial wall: a review of their location and functional activation. , 1996, Cerebral cortex.

[2]  J. Cohen,et al.  Dissociating the role of the dorsolateral prefrontal and anterior cingulate cortex in cognitive control. , 2000, Science.

[3]  P. Stratta,et al.  Schizophrenic deficits in the processing of context. , 1998, Archives of general psychiatry.

[4]  Joshua W. Brown,et al.  Performance Monitoring by the Anterior Cingulate Cortex During Saccade Countermanding , 2003, Science.

[5]  John J. Foxe,et al.  The Spatiotemporal Dynamics of Illusory Contour Processing: Combined High-Density Electrical Mapping, Source Analysis, and Functional Magnetic Resonance Imaging , 2002, The Journal of Neuroscience.

[6]  J. Cohen,et al.  Schizophrenic deficits in the processing of context. A test of a theoretical model. , 1996, Archives of general psychiatry.

[7]  M. Casanova,et al.  Functional and anatomical aspects of prefrontal pathology in schizophrenia. , 1997, Schizophrenia bulletin.

[8]  J. Schall,et al.  Performance monitoring by the supplementary eye ® eld , 2000 .

[9]  M. Scherg,et al.  Two bilateral sources of the late AEP as identified by a spatio-temporal dipole model. , 1985, Electroencephalography and clinical neurophysiology.

[10]  Jonathan D. Cohen,et al.  Anterior Cingulate Cortex, Conflict Monitoring, and Levels of Processing , 2001, NeuroImage.

[11]  J. Cohen,et al.  Functional hypofrontality and working memory dysfunction in schizophrenia. , 1998, The American journal of psychiatry.

[12]  J. Lieberman,et al.  Deficits in auditory and visual context-dependent processing in schizophrenia: defining the pattern. , 2000, Archives of general psychiatry.

[13]  T. Paus Primate anterior cingulate cortex: Where motor control, drive and cognition interface , 2001, Nature Reviews Neuroscience.

[14]  H E ROSVOLD,et al.  A continuous performance test of brain damage. , 1956, Journal of consulting psychology.

[15]  J. Hohnsbein,et al.  Late ERP components in visual and auditory Go/Nogo tasks. , 1995, Electroencephalography and clinical neurophysiology.

[16]  M. Botvinick,et al.  Anterior cingulate cortex, error detection, and the online monitoring of performance. , 1998, Science.

[17]  Hisae Gemba,et al.  Potential related to no-go reaction in go/no-go hand movement with discrimination between tone stimuli of different frequencies in the monkey , 1990, Brain Research.

[18]  John J. Foxe,et al.  Multisensory visual-auditory object recognition in humans: a high-density electrical mapping study. , 2004, Cerebral cortex.

[19]  T. Braver,et al.  Sensitivity of prefrontal cortex to changes in target probability: A functional MRI study , 2001, Human brain mapping.

[20]  D. Javitt,et al.  Ketamine-induced deficits in auditory and visual context-dependent processing in healthy volunteers: implications for models of cognitive deficits in schizophrenia. , 2000, Archives of general psychiatry.

[21]  J. Tanji,et al.  Role for cingulate motor area cells in voluntary movement selection based on reward. , 1998, Science.

[22]  John J. Foxe,et al.  Predicting Success: Patterns of Cortical Activation and Deactivation Prior to Response Inhibition , 2004, Journal of Cognitive Neuroscience.

[23]  J. Cohen,et al.  Context-processing deficits in schizophrenia: converging evidence from three theoretically motivated cognitive tasks. , 1999, Journal of abnormal psychology.

[24]  M. Raichle,et al.  The anterior cingulate cortex mediates processing selection in the Stroop attentional conflict paradigm. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[25]  Masataka Watanabe,et al.  Prefrontal and cingulate unit activity during timing behavior in the monkey , 1979, Brain Research.

[26]  M. Mishkin,et al.  Perseverative interference in monkeys following selective lesions of the inferior prefrontal convexity , 1970, Experimental Brain Research.

[27]  C. Schroeder,et al.  Striate cortical contribution to the surface-recorded pattern-reversal vep in the alert monkey , 1991, Vision Research.

[28]  N. Logothetis,et al.  Neurophysiological investigation of the basis of the fMRI signal , 2001, Nature.

[29]  C E Schroeder,et al.  Defining the neural bases of visual selective attention: conceptual and empirical issues. , 1995, The International journal of neuroscience.

[30]  A. Mirsky,et al.  Attention-related unit activity in the frontal association cortex during a go/no-go visual discrimination task , 1987, Experimental Neurology.

[31]  M. Botvinick,et al.  Conflict monitoring and cognitive control. , 2001, Psychological review.

[32]  J. Cohen,et al.  Context, cortex, and dopamine: a connectionist approach to behavior and biology in schizophrenia. , 1992, Psychological review.

[33]  Cameron S. Carter,et al.  Prefrontal functioning during context processing in schizophrenia and major depression: An event-related fMRI study , 2005, Schizophrenia Research.

[34]  P. Stratta,et al.  Processing of context information in schizophrenia: relation to clinical symptoms and WCST performance , 2000, Schizophrenia Research.

[35]  K. Kiehl,et al.  Event‐related fMRI study of response inhibition , 2001, Human brain mapping.

[36]  J. Hohnsbein,et al.  ERP components in Go/Nogo tasks and their relation to inhibition. , 1999, Acta psychologica.

[37]  M Spitzer,et al.  The time course of brain activations during response inhibition: evidence from event‐related potentials in a go/no go task , 1998, Neuroreport.

[38]  Thomas E. Nichols,et al.  Anterior cingulate gyrus dysfunction and selective attention deficits in schizophrenia: [15O]H2O PET study during single-trial Stroop task performance. , 1997, The American journal of psychiatry.

[39]  J. Cohen,et al.  Selective deficits in prefrontal cortex function in medication-naive patients with schizophrenia. , 2001, Archives of general psychiatry.

[40]  D. Javitt,et al.  Panmodal processing imprecision as a basis for dysfunction of transient memory storage systems in schizophrenia. , 1999, Schizophrenia bulletin.

[41]  M. Botvinick,et al.  Parsing executive processes: strategic vs. evaluative functions of the anterior cingulate cortex. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[42]  John J. Foxe,et al.  Don't think of a white bear: An fMRI investigation of the effects of sequential instructional sets on cortical activity in a task‐switching paradigm , 2004, Human brain mapping.

[43]  A. Nambu,et al.  No-go activity in the frontal association cortex of human subjects , 1993, Neuroscience Research.

[44]  C. Schroeder,et al.  A spatiotemporal profile of visual system activation revealed by current source density analysis in the awake macaque. , 1998, Cerebral cortex.

[45]  R. Knight,et al.  Prefrontal–cingulate interactions in action monitoring , 2000, Nature Neuroscience.

[46]  A. Dale,et al.  Dorsal anterior cingulate cortex: A role in reward-based decision making , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[47]  Jonathan D. Cohen,et al.  Prefrontal cortex dysfunction mediates deficits in working memory and prepotent responding in schizophrenia , 2003, Biological Psychiatry.

[48]  B. J. Casey,et al.  The Effect of Preceding Context on Inhibition: An Event-Related fMRI Study , 2002, NeuroImage.

[49]  B. Vogt,et al.  Contributions of anterior cingulate cortex to behaviour. , 1995, Brain : a journal of neurology.

[50]  John J. Foxe,et al.  Changing plans: a high density electrical mapping study of cortical control. , 2003, Cerebral cortex.

[51]  K. R. Ridderinkhof,et al.  The Role of the Medial Frontal Cortex in Cognitive Control , 2004, Science.