Brain, Vol. 118, No. 1, 279-306, 1995
© 1995 Oxford University Press
review-article |
REVIEW ARTICLE
Contributions of anterior cingulate cortex to behaviour
1Department of Neurology, New York University School of Medicine New York 2Department of Neurology and Neurological Sciences, Stanford University School of Medicine Stanford 3Department of Physiology and Pharmacology Bowman Gray School of Medicine, Wake Forest University, Medical Center Boulevard Winston-Salem, USA
Correspondence to:
Orrin Devinsky, MD, Department of Neurology, Hospital for Joint Diseases, 301 East 17th Street, New York, NY 10003, USA
Assessments of anterior cingulate cortex in experimental animals and humans have led to unifying theories of its structural organization and contributions to mammalian behaviour. The anterior cingulate cortex forms a large region around the rostrum of the corpus callosum that is termed the anterior executive region. This region has numerous projections into motor systems, however, since these projections originate from different parts of anterior cingulate cortex and because functional studies have shown that it does not have a uniform contribution to brain functions, the anterior executive region is further subdivided into ‘affect’ and ‘cognition’ components. The affect division includes areas 25, 33 and rostral area 24, and has extensive connections with the amygdala and periaqueductal grey, and parts of it project to autonomic brainstem motor nuclei. In addition to regulating autonomic and endocrine functions, it is involved in conditioned emotional learning, vocalizations associated with expressing internal states, assessments of motivational content and assigning emotional valence to internal and external stimuli, and maternal—infant interactions. The cognition division includes caudal areas 24' and 32', the cingulate motor areas in the cingulate sulcus and nociceptive cortex. The cingulate motor areas project to the spinal cord and red nucleus and have premotor functions, while the nociceptive area is engaged in both response selection and cognitively demanding information processing. The cingulate epilepsy syndrome provides important support of experimental animal and human functional imaging studies for the role of anterior cingulate cortex in movement, affect and social behaviours. Excessive cingulate activity in cases with seizures confirmed in anterior cingulate cortex with subdural electrode recordings, can impair consciousness, alter affective state and expression, and influence skeletomotor and autonomic activity. Interictally, patients with anterior cingulate cortex epilepsy often display psychopathic or sociopathic behaviours. In other clinical examples of elevated anterior cingulate cortex activity it may contribute to tics, obsessive—compulsive behaviours, and aberrent social behaviour. Conversely, reduced cingulate activity following infarcts or surgery can contribute to behavioural disorders including akinetic mutism, diminished self-awareness and depression, motor neglect and impaired motor initiation, reduced responses to pain, and aberrent social behaviour. The role of anterior cingulate cortex in pain responsiveness is suggested by cingulumotomy results and functional imaging studies during noxious somatic stimulation. The affect division of anterior cingulate cortex modulates autonomic activity and internal emotional responses, while the cognition division is engaged in response selection associated with skeletomotor activity and responses to noxious stimuli. Overall, anterior cingulate cortex appears to play a crucial role in initiation, motivation, and goal-directed behaviours. The anterior cingulate cortex is part of a larger matrix of structures that are engaged in similar functions. These structures form the rostral limbic system and include the amygdala, periaqueductal grey, ventral striatum, orbitofrontal and anterior insular cortices. The system formed by these interconnected areas assesses the motivational content of internal and external stimuli and regulates context-dependent behaviours.
limbic system; premotor function; epilepsy; visceromotor control; affect; cognition; nociception; akinetic mutism; schizophrenia
Received July 8, 1994. Revised September 22, 1994. Accepted October 6, 1994.
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N. Abe, M. Suzuki, T. Tsukiura, E. Mori, K. Yamaguchi, M. Itoh, and T. Fujii Dissociable Roles of Prefrontal and Anterior Cingulate Cortices in Deception Cereb Cortex, February 1, 2006; 16(2): 192 - 199. [Abstract] [Full Text] [PDF]
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C. N. Vidal, J. L. Rapoport, K. M. Hayashi, J. A. Geaga, Y. Sui, L. E. McLemore, Y. Alaghband, J. N. Giedd, P. Gochman, J. Blumenthal, et al. Dynamically Spreading Frontal and Cingulate Deficits Mapped in Adolescents With Schizophrenia Arch Gen Psychiatry, January 1, 2006; 63(1): 25 - 34. [Abstract] [Full Text] [PDF]
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B. Simon, B. Knuckley, J. Churchwell, and D. A. Powell Post-Training Lesions of the Medial Prefrontal Cortex Interfere with Subsequent Performance of Trace Eyeblink Conditioning J. Neurosci., November 16, 2005; 25(46): 10740 - 10746. [Abstract] [Full Text] [PDF]
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T. F. D. FARROW, M. D. HUNTER, I. D. WILKINSON, R. D. J. GREEN, and S. A. SPENCE Structural brain correlates of unconstrained motor activity in people with schizophrenia The British Journal of Psychiatry, November 1, 2005; 187(5): 481 - 482. [Abstract] [Full Text] [PDF]
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H. J. Rosen, S. C. Allison, G. F. Schauer, M. L. Gorno-Tempini, M. W. Weiner, and B. L. Miller Neuroanatomical correlates of behavioural disorders in dementia Brain, November 1, 2005; 128(11): 2612 - 2625. [Abstract] [Full Text] [PDF]
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F. E. Polli, J. J. S. Barton, M. S. Cain, K. N. Thakkar, S. L. Rauch, and D. S. Manoach Rostral and dorsal anterior cingulate cortex make dissociable contributions during antisaccade error commission PNAS, October 25, 2005; 102(43): 15700 - 15705. [Abstract] [Full Text] [PDF]
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