Abstract

Spike-responses of single binocular neurons were recorded from a distinct part of primary visual cortex, the parastriate cortex (cytoarchitectonic area 18) of anaesthetized and immobilized domestic cats. Functional identification of neurons was based on the ratios of phase-variant (F1) component to the mean firing rate (F0) of their spike-responses to optimized (orientation, direction, spatial and temporal frequencies and size) sine-wave-luminance-modulated drifting grating patches presented separately via each eye. In over 95% of neurons, the interocular differences in the phase-sensitivities (differences in F1/F0 spike-response ratios) were small (≤0.3) and in over 80% of neurons, the interocular differences in preferred orientations were ≤10°. The interocular correlations of the direction selectivity indices and optimal spatial frequencies, like those of the phase sensitivies and optimal orientations, were also strong (coefficients of correlation r ≥0.7005). By contrast, the interocular correlations of the optimal temporal frequencies, the diameters of summation areas of the excitatory responses and suppression indices were weak (coefficients of correlation r ≤0.4585). In cells with high eye dominance indices (HEDI cells), the mean magnitudes of suppressions evoked by stimulation of silent, extra-classical receptive fields via the non-dominant eyes, were significantly greater than those when the stimuli were presented via the dominant eyes. We argue that the well documented ‘eye-origin specific’ segregation of the lateral geniculate inputs underpinning distinct eye dominance columns in primary visual cortices of mammals with frontally positioned eyes (distinct eye dominance columns), combined with significant interocular differences in the strength of silent suppressive fields, putatively contribute to binocular stereoscopic vision.

Highlights

  • In mammals with frontally positioned eyes such as domestic cats or macaque monkeys, the great majority (,90%) of neurons in the dorsal lateral geniculate nucleus (LGNd) are reported to be monocular, that is, they generate action potentials only when appropriate visual stimuli are presented via a particular eye [1,2,3,4,5,6]

  • (20/37; 54%) or complex (17/37; 46%) on the basis of their phase sensitivities expressed as F1/F0 spike-response ratios to high-contrast, optimized, summation receptive fields (sRF)-confined grating patches presented via the dominant eye (Figs 1Ai and 1Aii)

  • The slope of the linear regression line of Direction selectivity indices (DSI) for stimuli presented via dominant eyes vs. DSI for stimuli presented via the non-dominant eyes was relatively low (Fig. 2D)

Read more

Summary

Introduction

In mammals with frontally positioned eyes such as domestic cats or macaque monkeys, the great majority (,90%) of neurons in the dorsal lateral geniculate nucleus (LGNd) are reported to be monocular, that is, they generate action potentials (spikes) only when appropriate visual stimuli are presented via a particular eye [1,2,3,4,5,6]. In the striate cortices (cytoarchitectonic areas 17, areas V1) of those species, within topographic representation of a given part of the contralateral visual hemifield, there is very little overlap between the subregions of the geniculo-recipient layers which receive inputs from the LGNd neurons relaying signals from either the contralateral or the ipsilateral eyes [7,8,9,10,11]. This ‘eye-originspecific’ spatial segregation of the geniculo-cortical terminals constitutes a putative basis for the so-called ‘eye dominance columns’ [7]. It has been argued that both stereoscopic single vision and binocular depth discrimination are derivatives of binocular interactions (facilitatory and/or suppressive) at the single neuron level in the primary visual cortices [13,14,22,23,24,25,26]

Methods
Results
Discussion
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.