Cortical potentials reflecting motion processing in humans

Visual Neuroscience - Tập 11 Số 6 - Trang 1135-1147 - 1994
Dieter R. Patzwahl1, Johannes M. Zanker2, Eckart Altenmüller1
1Neurologische Universitätsklinik, Hoppe-Seyler-Str. 3, D-72076 Tübingen, Germany
2Max-Planck-Institut für biologische Kybernetik, Spemannstr. 38, D-72076 Tübingen, Germany

Tóm tắt

AbstractMotion processing is a fundamental task of visual systems, and in the monkey cortical areas can be identified which appear to be functionally specialized for motion processing. The human visual system is expected to be organized in a similar way. A noninvasive method to study the functional organization of the visual cortex is the recording of scalp potentials generated by neural activity of the underlying cortical areas. In the present study, we recorded slow cortical potentials from normal subjects in order to investigate how motion stimuli are processed. Three classes of object motion were realized as random dot kinematograms, namely Fourier motion, drift-balanced motion, and theta motion, because they require mechanisms of increasing complexity in order to be extracted. Large-field motion and counterphase flicker were used as control stimuli. Three basic results were obtained: (1) The responses evoked by the three classes of object motion do not differ significantly in their time course and distribution of activation. (2) The distributions of cortical activation evoked by object motion, and the control stimuli are different. During object motion the maximum activation occurs over the superior parietal cortex. Large-field motion activates occipital and parietal locations to the same extent, and during counterphase flicker the activity is maximum over the occipital lobe. Thus, the parietal slow potentials are interpreted to specifically reflect the cortical processing of object motion. (3) The time course of the activation reflects changes in the spatial position of the object: the amplitude of a transient negative component (TNC) which occurs 240 ms after motion onset decreases with increasing eccentricity of motion onset. The consecutive sustained negative component (SNC), which persists until the movement stops, decreases during centrifugal and increases during centripetal object motion. These results can be understood on the basis of physiological and anatomical knowledge about the mapping of the visual field on the cortex.

Từ khóa


Tài liệu tham khảo

10.1016/0013-4694(89)90232-0

10.1163/156856889X00112

Speckmann, 1979, Origin of Cerebral Field Potentials

10.1007/BF00337434

Jasper, 1958, Report of committee on methods of clinical examination in electroencephalography, Electroencephalography and Clinical Neurophysiology, 10, 370, 10.1016/0013-4694(58)90053-1

10.1016/0166-2236(89)90010-6

10.1007/BF01138495

10.1016/0042-6989(93)90258-X

10.1126/science.3283936

Nuñez, 1981, Electric Fields of the Brain. The Neurophysics of EEG.

10.1007/BF00603660

10.1126/science.1546317

10.3109/00207458208985920

Clarke, 1973, Comparison of visual evoked potentials to stationary and to moving patterns, Experimental Brain Research, 18, 156

10.1007/BF00161234

10.1007/BF00237163

10.1068/p080125

10.1163/156856889X00077

Clarke, 1973, Visual evoked potentials to changes in the motion of a patterned field, Experimental Brain Research, 18, 145

10.1146/annurev.ne.12.030189.002113

10.1002/cne.902320403

10.1364/JOSAA.5.001986

10.1523/JNEUROSCI.11-08-02383.1991

Cunningham, 1990, The motion area (area V5) of human visual cortex, Journal of Physiology, 423, 101P

10.1113/jphysiol.1961.sp006803

Heilman, 1987, Handbook of Physiology: Higher Cortical Functions of the Brain, 5, 461

10.1016/0013-4694(75)90056-5

10.1016/0013-4694(87)90206-9

10.1016/0168-5597(85)90015-2

10.1146/annurev.ne.16.030193.002101

10.1038/349061a0

10.1097/00001756-199304000-00009

10.1038/scientificamerican0686-102

10.1016/0042-6989(89)90194-6

Reichardt, 1961, Sensory Communication, 303

10.1016/0926-6410(93)90024-Y

Speckmann, 1993, Electroencephalography, 15

10.1016/0042-6989(85)90045-8

Sperling, 1994, Immunity to pedestrals distinguishes motion-energy from feature-tracking motion-perception mechanisms, Investigative Ophthalmology and Visual Science, 35, 1390

10.1016/0166-2236(83)90081-4

Ungerleider, 1982, The Analysis of Visual Behaviour, 549

10.1017/S0952523800009573

10.1016/0042-6989(91)90119-P

Zanker, 1994, What is the elementary mechanism underlying secondary motion perception, Investigative Ophthalmology and Visual Science, 35, 1405

10.1523/JNEUROSCI.11-03-00641.1991

10.1001/archopht.1991.01080060080030