Summary
Seven cats were trained to press a lever that moved in front of them at an adjustable speed and at random from left to right or from right to left. Efficient presses were reinforced by food. After measuring accuracy and latency of pressing the lever, the animals underwent bilateral ablation of the suprasylvian (SS) cortex; in three animals the lesions involved its anterior aspect; in two animals, they were restricted to its middle portion; two others cats had lesions of both anterior and the middle SS cortex. No long-lasting postoperative deficits were observed in any group when the lever remained immobile. On the other hand, the scores after anterior SS lesions were severely deteriorated, when presses had to be performed on the moving lever. No such deficits were noticed when the ablations were restricted to the middle SS. These results suggest that the cat anterior suprasylvian cortex (that includes parts of areas 5 and 7) plays a determinant role in the spatial adjustment of a visually guided (or visually triggered) forelimb movement.
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References
Albe-Fessard D, Besson JM (1973) Convergent thalamic and cortical projections. The non-specific system. In: Iggo A (ed) Handbook of sensory physiology, vol II. Springer, Berlin Heidelberg New York, pp 489–560
Baumann TP, Spear PD (1977) Role of the lateral suprasylvian visual area in behavioral recovery from effects of visual cortex damage in cats. Brain Res 138: 445–468
Buser P, Bignall KE (1967) Non-primary sensory projections onto the cat neocortex. Int Rev Neurobiol 10: 111–165
Buser P, Borenstein P, Bruner J (1959) Etude des systèmes “associatifs” visuels et auditifs chez le chat anesthésié au chloralose. Electroencephalogr Clin Neurophysiol 11: 305–324
Clare MH, Bishop GH (1954) Responses from an association area secondarily activated from optic cortex. J Neurophysiol 17: 271–277
Darian-Smith I, Isbister J, Mok H, Yokota T (1966) Somatic sensory cortical projection areas excited by tactile stimulation of the cat. A triple representation. J Physiol (Lond) 183: 671–689
Fabre M, André C, Buser P (1979) Testing visually guided forepaw movements in the cat. Physiol Behav 23: 263–266
Fabre M, Buser P (1979) Guidage visuo-moteur chez le chat. Différence d'effets d'une lésion bilatérale du noyau ventral latéral du thalamus effectuée soit avant, soit après apprentissage. CR Acad Sci [D] (Paris) 288: 417–420
Fabre M, Buser P (1980) Structures involved in acquisition and performance of visually guided movements. Acta Biol Exp 40: 95–116
Faugier S, Frenois C, Stein DG (1978) Effects of posterior parietal lesions on visually guided behavior in monkeys. Neuropsychologia 16: 151–158
Graybiel AM (1970) Some ascending connections of the pulvinar and nucleus lateralis posterior of the thalamus in the cat. Brain Res 22: 131–136
Hara K (1962) Visual defects resulting from prestriate cortical lesions in cats. J Comp Physiol Psychol 55: 293–298
Hartje W, Ettlinger G (1974) Reaching in light and dark after unilateral posterior parietal ablations in the monkey. Cortex 9: 346–354
Hassler R, Muhs-Clement K (1964) Architektonischer Aufbau des sensomotorischen und parietalen Cortex der Katze. J Hirnforsch 6: 377–420
Heath CJ, Jones EG (1971) The anatomical organization of the suprasylvian gyrus of the cat. Ergeb Anat Entwicklungsgesch 45: 5–64
Hyvärinen J, Poranen A (1974) Function of the parietal associative area 7 as revealed from cellular discharges in alert monkeys. Brain 97: 673–692
Iwamura Y, Tanaka M (1978) Functional organization of receptive fields in the cat somatosensory cortex. II. Second representation of the forepaw in the ansate region. Brain Res 151: 61–72
Jasper HH, Ajmone-Marsan C (1954) A stereotaxic atlas of the diencephalon of the cat. Nat Res Council Canada, Ottawa
Jones EG, Powell IPS (1968) The ipsilateral cortical connections of the somatic sensory areas in the cat. Brain Res 9: 71–94
Lamotte RH, Acuna C (1978) Defects in accuracy of reaching after removal of posterior parietal cortex in monkeys. Brain Res 139: 309–326
Landgren S, Silfvenius H (1968) Projections of the eye and the neck region on the anterior suprasylvian cerebral cortex of the cat. Acta Physiol Scand 74: 340–347
Landgren S, Silfvenius H, Wolsk D (1967a) Somato-sensory paths to the second cortical projection area of the group I muscle afferents. J Physiol (Lond) 191: 543–559
Landgren S, Silfvenius H, Wolsk D (1967b) Vestibular, cochlear, and trigeminal projections to the cortex in the anterior suprasylvian sulcus of the cat. J Physiol (Lond) 191: 561–573
Lynch JC, Mountcastle VB, Talbot WH, Yin TCT (1977) Parietal lobe mechanisms for directed visual attention. J Neurophysiol 40: 362–389
Meulders M (1970) Intégration centrale des afférences visuelles. J Physiol (Paris) [Suppl 1] 62: 61–109
Milner AD, Ockleford EM, Dewar W (1977) Visuo-spatial performance following posterior parietal and lateral frontal lesions in stumptail macaques. Cortex 13: 350–360
Mountcastle VB (1975) The view from within. Pathways to the study of perception. Johns Hopkins Med J 136: 109–131
Mountcastle VB, Lynch JC, Georgopoulos A, Sakata H, Acuna C (1975) Posterior parietal association cortex of the monkey. Command functions for operations within the extrapersonal space. J Neurophysiol 38: 875–908
Niimi K, Kadota M, Matsushita Y (1974) Cortical projections of the pulvinar nuclear group of the thalamus in the cat. Brain Behav Evol 9: 422–457
Oscarsson O, Rosen I (1966) Short-latency projections to the cat's cerebral cortex from skin and muscle afferents in the contralateral forelimb. J Physiol (Lond) 182: 164–184
Petrides M, Iversen SD (1979) Restricted posterior parietal lesions in the rhesus monkey and performance on visuo-spatial tasks. Brain Res 161: 63
Reinoso-Suarez F (1961) Topographischer Hirnatlas der Katze für experimentelle physiologische Untersuchungen. Merck, Darmstadt
Robertson RT, Mayers KS, Teyler JJ, Bettinger LA, Birch H, Davis JL, Phillips DS, Thompson RF (1975) Unit activity in posterior association cortex of cat. J Neurophysiol 38: 780–794
Robinson DL, Goldberg ME, Stanton GB (1978) Parietal association cortex in the primate. Sensory mechanisms and behavioral modulations. J Neurophysiol 41: 910
Sakata H, Takaoka Y, Kawarasaki A, Shibutani H (1973) Somatosensory properties of neurons in the superior parietal cortex (area 5) of the rhesus monkey. Brain Res 64: 85–102
Sasaki K, Matsuda Y, Kawaguchi S, Mizuno N (1972) On the cerebello-thalamo-cerebral pathway for the parietal cortex. Exp Brain Res 16: 89–103
Sasaki K, Oka H, Malsuda Y, Shimono T, Mizuno N (1975) Electrophysiological studies of the projections from the parietal association area to the cerebellar cortex. Exp Brain Res 23: 91–102
Silfvenius H (1972) Properties of cortical group I neurones located in the lower bank of the anterior suprasylvian sulcus of the cat. Acta Physiol Scand 84: 555–576
Thompson RF, Johnson RH, Hoopes JJ (1963) Organization of auditory, somatic sensory, and visual projection to association fields of cerebral cortex in the cat. J Neurophysiol 26: 343–364
Warren JM, Warren HB, Akert K (1961) “Umweg” learning by cats with lesions in the prestriate association cortex. J Comp Physiol Psychol 54: 629–632
Wood CC, Spear PD, Braun JJ (1974) Effects of sequential lesions of suprasylvian gyri and visual cortex on pattern discrimination in the cat. Brain Res 66: 443–466
Woolsey CN (1961) Organization of cortical auditory system. In: Rosenblith WA (ed) Sensory communication. Wiley, New York London, pp 235–257
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This work was supported by the following grants: ERA - CNRS 411; ATP 36-22; Fondation pour la Recherche Medicale Française
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Fabre, M., Buser, P. Effects of lesioning the anterior suprasylvian cortex on visuo-motor guidance performance in the cat. Exp Brain Res 41, 81–88 (1981). https://doi.org/10.1007/BF00236597
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DOI: https://doi.org/10.1007/BF00236597