I. Functional properties of neurons in lateral part of associative area 7 in awake monkeys

SummaryThe lateral part of area 7, area 7b, of alert, behaving macaque monkeys was investigated using transdural microelectrode recording technique. Two hundred twenty-eight cells from five hemispheres of four monkeys were isolated and studied. The functional properties of 2% of the cells isolated remained unidentified. Functions of the identified cells were prominently related to the spatial control of arm movements.Of the cells 70% responded to somatosensory (40%) or visual (16%) or both somatosensory and visual (14%) stimulation. The receptive fields of these passively drivable cells were large, covering, e.g., the arm or leg or chest or even the skin of the whole body. Most of the visually drivable cells responded to stimuli in both halves of the visual field.Of the cells responding to sensory stimulation 80% were activated by stimuli moving in a certain direction. Of the directionally selective cells 25% received information through more than one sensory channel. The complex stimulus-response relationships of these “convergence” cells revealed the existence of an integrative system which analyzes the direction of a stimulus moving in one sensory system using an other sensory system as a reference.Of all the cells isolated 28% discharged only during active movements of the arms (25%) or eyes (3%). Firing of these neurons was related to contraction of a functionally uniform group of muscles and not individual muscles.Some previous investigations of the parietal association cortex, conducted mainly in area 7a, have shown that most cells are active only when the monkey himself moves his eyes or arms. In our study on area 7b most cells responded to passive stimulation. The discrepancy between the results indicates functional differentiation within area 7.

[1]  K H PRIBRAM,et al.  A behavioral analysis of the organization of the parieto‐temporo‐preoccipital cortex , 1950, The Journal of comparative neurology.

[2]  D. Pandya,et al.  Limbic and sensory connections of the inferior parietal lobule (area PG) in the rhesus monkey: A study with a new method for horseradish peroxidase histochemistry , 1977, Brain Research.

[3]  C. G. Phillips,et al.  Projection from low-threshold muscle afferents of hand and forearm to area 3a of baboon's cortex. , 1971, The Journal of physiology.

[4]  M. O'connor,et al.  Motor areas of the cerebral cortex , 1987 .

[5]  R. A. Chambers,et al.  The parietal lobe and behavior. , 1958, Research publications - Association for Research in Nervous and Mental Disease.

[6]  E. Crosby,et al.  The parietal lobe as an additional motor area. The motor effects of electrical stimulation and ablation of cortical areas 5 and 7 in monkeys , 1955, The Journal of comparative neurology.

[7]  F H Duffy,et al.  Muscle afferent input to single cells in primate somatosensory cortex. , 1972, Brain research.

[8]  G. Bonin,et al.  The neocortex of Macaca mulatta , 1947 .

[9]  D. Pandya,et al.  Cortico-cortical connections in the rhesus monkey. , 1969, Brain research.

[10]  V. Mountcastle,et al.  Parietal lobe mechanisms for directed visual attention. , 1977, Journal of neurophysiology.

[11]  J. Kaas,et al.  Some cortical projections of the dorsomedial visual area (DM) of association cortex in the owl monkey, Aotus trivirgatus , 1975, The Journal of comparative neurology.

[12]  J. Kaas,et al.  Cortical projections of posterior parietal cortex in owl monkeys , 1977, The Journal of comparative neurology.

[13]  M. Mishkin,et al.  OCCIPITOTEMPORAL CORTICOCORTICAL CONNECTIONS IN THE RHESUS MONKEY. , 1965, Experimental neurology.

[14]  G. Werner,et al.  Symmetry and connectivity in the map of the body surface in somatosensory area II of primates. , 1969, Journal of neurophysiology.

[15]  D. Robinson,et al.  Parietal association cortex in the primate: sensory mechanisms and behavioral modulations. , 1978, Journal of neurophysiology.

[16]  ACUTE AND CHRONIC PARIETAL LOBE ABLATIONS IN MONKEYS , 1945 .

[17]  D. Pandya,et al.  Cortico‐cortical connections of somatic sensory cortex (areas 3, 1 and 2) in the rhesus monkey , 1978, The Journal of comparative neurology.

[18]  K. Chow,et al.  A retrograde cell degeneration study of the cortical projection field of the pulvinar in the monkey , 1950, The Journal of comparative neurology.

[19]  W. R. Levick,et al.  Another tungsten microelectrode , 1972, Medical and biological engineering.

[20]  G. Ettlinger,et al.  Posterior biparietal ablations in the monkey. Changes to neurological and behavioral testing. , 1960, Archives of neurology.

[21]  P. Rakić,et al.  Heterogeneous afferents to the inferior parietal lobule of the rhesus monkey revealed by the retrograde transport method , 1977, Brain Research.

[22]  W. Pohl,et al.  Dissociation of spatial discrimination deficits following frontal and parietal lesions in monkeys. , 1973, Journal of comparative and physiological psychology.

[23]  F. Duffy,et al.  Somatosensory System: Organizational Hierarchy from Single Units in Monkey Area 5 , 1971, Science.

[24]  T. Powell,et al.  An anatomical study of converging sensory pathways within the cerebral cortex of the monkey. , 1970, Brain : a journal of neurology.

[25]  D. Pandya,et al.  The topographical distribution of interhemispheric projections in the corpus callosum of the rhesus monkey. , 1971, Brain research.

[26]  V. Mountcastle,et al.  Visual input to the visuomotor mechanisms of the monkey's parietal lobe. , 1977, Science.

[27]  A R Friendlich,et al.  Primate head restrainer using a nonsurgical technique. , 1973, Journal of applied physiology.

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

[29]  G. Ettlinger,et al.  Changes in tactile discrimination and in visual reaching after successive and simultaneous bilateral posterior parietal ablations in the monkey , 1962, Journal of neurology, neurosurgery, and psychiatry.

[30]  M. Critchley The parietal lobes , 1966 .

[31]  T. Ruch,et al.  SENSORY DISCRIMINATION IN MONKEY, CHIMPANZEE AND MAN AFTER LESIONS OF THE PARIETAL LOBE , 1938 .

[32]  H. Kuypers,et al.  Basal forebrain and hypothalamic connection to frontal and parietal cortex in the Rhesus monkey. , 1975, Science.

[33]  J. Trojanowski,et al.  Areal and laminar distribution of some pulvinar cortical efferents in rhesus monkey , 1976, The Journal of comparative neurology.

[34]  J. Hyvärinen,et al.  Function of the parietal associative area 7 as revealed from cellular discharges in alert monkeys. , 1974, Brain : a journal of neurology.

[35]  V. Mountcastle,et al.  Posterior parietal association cortex of the monkey: command functions for operations within extrapersonal space. , 1975, Journal of neurophysiology.

[36]  H. Sakata,et al.  Somatosensory properties of neurons in the superior parietal cortex (area 5) of the rhesus monkey. , 1973, Brain research.

[37]  D. Schwarz,et al.  Rhesus Monkey Vestibular Cortex: A Bimodal Primary Projection Field , 1971, Science.

[38]  G. Werner,et al.  Cortical information processing of stimulus motion on primate skin. , 1972, Journal of neurophysiology.

[39]  H. W. Bond,et al.  Solid miniature silver-silver chloride electrodes for chronic implantation. , 1970, Electroencephalography and clinical neurophysiology.

[40]  Leslie G. Ungerleider,et al.  Extrapersonal spatial orientation: The role of posterior parietal, anterior frontal, and inferotemporal cortex , 1977, Experimental Neurology.

[41]  J. M. Fredrickson,et al.  Cortical projection of group I muscle afferents to areas 2, 3a, and the vestibular field in the rhesus monkey , 1973, Experimental Brain Research.

[42]  W. Nauta THE PROBLEM OF THE FRONTAL LOBE: A REINTERPRETATION , 1972 .

[43]  J Hyvärinen,et al.  Movement‐sensitive and direction and orientation‐selective cutaneous receptive fields in the hand area of the post‐central gyrus in monkeys. , 1978, The Journal of physiology.

[44]  J. Hyvärinen,et al.  Cortical neuronal mechanisms in flutter-vibration studied in unanesthetized monkeys. Neuronal periodicity and frequency discrimination. , 1969, Journal of neurophysiology.