The functional organization of human extrastriate cortex: a PET-rCBF study of selective attention to faces and locations

The functional dissociation of human extrastriate cortical processing streams for the perception of face identity and location was investigated in healthy men by measuring visual task-related changes in regional cerebral blood flow (rCBF) with positron emission tomography (PET) and H2(15)O. Separate scans were obtained while subjects performed face matching, location matching, or sensorimotor control tasks. The matching tasks used identical stimuli for some scans and stimuli of equivalent visual complexity for others. Face matching was associated with selective rCBF increases in the fusiform gyrus in occipital and occipitotemporal cortex bilaterally and in a right prefrontal area in the inferior frontal gyrus. Location matching was associated with selective rCBF increases in dorsal occipital, superior parietal, and intraparietal sulcus cortex bilaterally and in dorsal right premotor cortex. Decreases in rCBF, relative to the sensorimotor control task, were observed for both matching tasks in auditory, auditory association, somatosensory, and midcingulate cortex. These results suggest that, within a sensory modality, selective attention is associated with increased activity in those cortical areas that process the attended information but is not associated with decreased activity in areas that process unattended visual information. Selective attention to one sensory modality, on the other hand, is associated with decreased activity in cortical areas dedicated to processing input from other sensory modalities. Direct comparison of our results with those from other PET-rCBF studies of extrastriate cortex demonstrates agreement in the localization of cortical areas mediating face and location perception and dissociations between these areas and those mediating the perception of color and motion.

[1]  a.R.V.,et al.  Human Neuroanatomy , 1954, Neurology.

[2]  R. Hernández-Peón,et al.  Modification of electric activity in cochlear nucleus during attention in unanesthetized cats. , 1956, Science.

[3]  John A. Nelder,et al.  A Simplex Method for Function Minimization , 1965, Comput. J..

[4]  L. C. Oatman Effects of visual attention on the intensity of auditory evoked potentials , 1976, Experimental Neurology.

[5]  Deepak N. Pandya,et al.  Further observations on corticofrontal connections in the rhesus monkey , 1976, Brain Research.

[6]  M. H. Goldstein,et al.  Evoked unit activity in auditory cortex of monkeys performing a selective attention task , 1976, Brain Research.

[7]  J. Mazziotta,et al.  Tomographic mapping of human cerebral metabolism , 1981, Neurology.

[8]  Leslie G. Ungerleider Two cortical visual systems , 1982 .

[9]  W. Krieg Functional Neuroanatomy , 1953, Springer Series in Experimental Entomology.

[10]  M. Raichle,et al.  The role of cerebral cortex in the generation of voluntary saccades: a positron emission tomographic study. , 1985, Journal of neurophysiology.

[11]  J. Allman,et al.  Mapping human visual cortex with positron emission tomography , 1986, Nature.

[12]  D. V. van Essen,et al.  Retinotopic organization of human visual cortex mapped with positron- emission tomography , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[13]  M. Mintun,et al.  Enhanced Detection of Focal Brain Responses Using Intersubject Averaging and Change-Distribution Analysis of Subtracted PET Images , 1988, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[14]  J. Talairach,et al.  Co-Planar Stereotaxic Atlas of the Human Brain: 3-Dimensional Proportional System: An Approach to Cerebral Imaging , 1988 .

[15]  P. Goldman-Rakic,et al.  Posterior parietal cortex in rhesus monkey: II. Evidence for segregated corticocortical networks linking sensory and limbic areas with the frontal lobe , 1989, The Journal of comparative neurology.

[16]  P. Goldman-Rakic,et al.  Posterior parietal cortex in rhesus monkey: I. Parcellation of areas based on distinctive limbic and sensory corticocortical connections , 1989, The Journal of comparative neurology.

[17]  Karl J. Friston,et al.  Localisation in PET Images: Direct Fitting of the Intercommissural (AC—PC) Line , 1989, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[18]  Karl J. Friston,et al.  The Relationship between Global and Local Changes in PET Scans , 1990, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[19]  S. Hillyard,et al.  Cross-modal selective attention effects on retinal, myogenic, brainstem, and cerebral evoked potentials. , 1990, Psychophysiology.

[20]  S. Clarke,et al.  Occipital cortex in man: Organization of callosal connections, related myelo‐ and cytoarchitecture, and putative boundaries of functional visual areas , 1990, The Journal of comparative neurology.

[21]  Karl J. Friston,et al.  Comparing Functional (PET) Images: The Assessment of Significant Change , 1991, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[22]  Karl J. Friston,et al.  A direct demonstration of functional specialization in human visual cortex , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[23]  Leslie G. Ungerleider,et al.  Dissociation of object and spatial visual processing pathways in human extrastriate cortex. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[24]  D. J. Felleman,et al.  Distributed hierarchical processing in the primate cerebral cortex. , 1991, Cerebral cortex.

[25]  M. Corbetta,et al.  Selective and divided attention during visual discriminations of shape, color, and speed: functional anatomy by positron emission tomography , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[26]  Karl J. Friston,et al.  Plastic transformation of PET images. , 1991, Journal of computer assisted tomography.

[27]  S Minoshima,et al.  An automated method for rotational correction and centering of three-dimensional functional brain images. , 1992, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[28]  C. Olson,et al.  Functional heterogeneity in cingulate cortex: the anterior executive and posterior evaluative regions. , 1992, Cerebral cortex.

[29]  J. Sergent,et al.  Functional neuroanatomy of face and object processing. A positron emission tomography study. , 1992, Brain : a journal of neurology.

[30]  Cheryl L. Grady,et al.  Functional Associations among Human Posterior Extrastriate Brain Regions during Object and Spatial Vision , 1992, Journal of Cognitive Neuroscience.

[31]  T. Allison,et al.  Electrophysiological studies of color processing in human visual cortex. , 1993, Electroencephalography and clinical neurophysiology.

[32]  M. Corbetta,et al.  A PET study of visuospatial attention , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[33]  Richard S. J. Frackowiak,et al.  Area V5 of the human brain: evidence from a combined study using positron emission tomography and magnetic resonance imaging. , 1993, Cerebral cortex.

[34]  Jonathan D. Cohen,et al.  Functional topographic mapping of the cortical ribbon in human vision with conventional MRI scanners , 1993, Nature.

[35]  A. Berthoz,et al.  PET study of voluntary saccadic eye movements in humans: basal ganglia-thalamocortical system and cingulate cortex involvement. , 1993, Journal of neurophysiology.

[36]  Edward E. Smith,et al.  Spatial working memory in humans as revealed by PET , 1993, Nature.

[37]  T. Allison,et al.  Face recognition in human extrastriate cortex. , 1994, Journal of neurophysiology.