Studies in 47 right-handed subjects with right and left leading eyes addressed the latent periods of visually-evoked saccades in the horizontal, vertical, and diagonal directions within the field of vision. Visual environments with three levels of temporospatial complexity and two standard time protocols of visual stimulation, with "gap" and "overlap," were used. In subjects with left leading eyes, saccades were more often performed with shorter latent periods in the direction ipsilateral to the leading eye than in the contralateral direction (53% versus 20%); among subjects with right leading eyes, the proportions with decreases in the latent periods in the ipsi- and contralateral directions were different (25% and 22%, respectively). Thus, there was a relationship between eye dominance and the spatial asymmetry of the latent periods of saccades.

The saccadic eye movements declining given the development of Parkinson's disease (PD) still deserves thorough analysis. Recent studies confirmed that PD patients show poor saccadic control in visuomotor tasks. The purpose of this study was to investigate the dynamics of saccades parameters at the development of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) model of PD. The gradual decline of saccadic control was studied in two monkeys that executed the visuomotor task with low doses of MPTP being injected at a prolonged period of time. The experiment included investigating the horizontal, vertical, oblique visually guided saccades as well as the corrective saccades triggered by stimuli onset in various loci within a two-dimensional visual field in the Gap-Step-Overlap paradigm. Our study revealed that the execution of visually guided saccades with small amplitude and corrective saccades changed dramatically with MPTP-model progressing. These changes are also confirmed statistically at the presymptomatic stage of MPTP syndrome. Not only our study gives a robust report of PD dynamics development and saccadic control but the obtained data could also be helpful in developing methods for the early diagnosis of PD.

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