Contingent negative variation (CNV) topography, hemispheric asymmetry and time-course were investigated in healthy subjects and non-medicated paranoid schizophrenic patients in two antisaccade paradigms with the short (800-1000 ms) and long (1200-1400 ms) durations of the fixation period. EEG and electrooculogram (EOG) were recorded. Saccade characteristics and mean amplitudes of slow cortical potentials time-locked to peripheral target were analyzed in 23 healthy volunteers and 19 schizophrenic patients. Compared to healthy control subjects, schizophrenic patients had significantly slower antisaccades and committed significantly more erroneous saccades in the both antisaccade tasks. The prolongation of the fixation period resulted in noticeable decrease of error percent in patients group. The analysis of CNV time-course has revealed two distinct stages in both groups. The early CNV stage was represented by a negative wave with the maximal amplitude over midline fronto-central area, and the late stage was characterized by increased CNV amplitude at the midline and left parietal electrode sites. In healthy subjects the simultaneous activation of frontal and parietal areas was observed in the paradigm with the shorter fixation interval; the increase of the fixation period produced consecutive activation of these areas. Schizophrenic patients' CNV amplitude was generally smaller than that of healthy subjects. The most pronounced between-group differences of the negative shift amplitude were revealed at frontal electrode sites during the early CNV stage in both modifications of the antisaccade task. The deficit of frontal activation revealed in patients at the early stage of antisaccade preparatory set in both antisaccadic paradigms may be related to pathogenesis of paranoid schizophrenia.

Motion 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.

The topography of the postimperative negative variation (PINV) was analyzed in participants with high and low scores on the German version of the Schizotypal Personality Questionnaire. Scalp amplitude and Laplacian maps of the terminal contingent negative variation (tCNV) and PINV and the time course of the PINV were compared between the two groups. CNV and PINV were induced with a delayed matching-to-sample task, in which the pattern of the imperative stimulus was either clearly or ambiguous matched to one of the two diamonds simultaneously presented as a warning stimulus 4.0 s earlier. Electroencephalograms were recorded with a DC amplifier (32 channels). Negativity increased from tCNV to PINV, especially at frontal sites, and the PINV was larger under ambiguous than under clear matching conditions. Low-scoring participants showed a right-sided predominance of the PINV, which was absent in high-scoring participants. These results resemble differences in the topography of the PINV between healthy control participants and those with schizophrenia under identical experimental conditions and suggest functional differences between tCNV and PINV.