August 2023
Volume 23, Issue 9
Open Access
Vision Sciences Society Annual Meeting Abstract  |   August 2023
MEG Reveals Distinct Dorsal and Ventral Streams for Binocular Rivalry Dominance and Suppression
Author Affiliations & Notes
  • Janine Mendola
    Department of Ophthalmology and Vision Sciences, McGill University, Montreal, QC H9G 1A4
  • Elizabeth Bock
    Department of Neurology and Neurosurgery and the McConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University
  • Jeremy Fesi
    Department of Ophthalmology and Vision Sciences, McGill University, Montreal, QC H9G 1A4
  • Jason Da Silve Castenheira
    Department of Neurology and Neurosurgery and the McConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University
  • Sylvain Baillet
    Department of Neurology and Neurosurgery and the McConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University
  • Footnotes
    Acknowledgements  This work was supported by a Discovery Grant from NSERC to J.M.; S.B. was supported by an NSERC Discovery Grant, Canada Research Chair of Neural Dynamics of Brain Systems, NIH, Healthy Brains for Healthy Lives Canada Excellence Research Fund, and Brain Canada Foundation Platform Support Grant.
Journal of Vision August 2023, Vol.23, 5122. doi:https://doi.org/10.1167/jov.23.9.5122
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      Janine Mendola, Elizabeth Bock, Jeremy Fesi, Jason Da Silve Castenheira, Sylvain Baillet; MEG Reveals Distinct Dorsal and Ventral Streams for Binocular Rivalry Dominance and Suppression. Journal of Vision 2023;23(9):5122. https://doi.org/10.1167/jov.23.9.5122.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Binocular rivalry is an example of bistable visual perception extensively examined in neuroimaging. Magneto-encephalography (MEG) can track brain responses to phasic visual stimulations of pre-determined frequency and phase to advance our understanding of perceptual dominance and suppression in binocular rivalry. We used left and right eye stimuli (red and green orthogonal gratings) that flickered at two tagging frequencies (5 and 7.5 Hz) to track their respective oscillatory cortical evoked responses. We computed time-resolved measures of coherence to track the brain responses phase-locked with stimulus frequencies, and with respect to the participants’ indications of alternations of visual rivalry they experienced. Using Brainstorm software, we compared the brain maps obtained to those from a non-rivalrous control replay condition that used physically changing stimuli to mimic rivalry. We found stronger coherence within a posterior cortical network of visual areas during rivalry dominance compared to rivalry suppression and replay control. This network extended beyond the primary visual cortex (V1) to several retinotopic visual areas. In addition, network coherence with dominant percepts in V1 peaked at least 50 ms prior to the suppressed percept nadir; consistent with Wilson’s (2003) escape theory of alternations. Moreover, individual alternation rates were correlated with the rate of change (slope) in dominant evoked peaks, but not for the slope of response to suppressed percepts. This further supports the (escape) theory that a perceptual switch occurs when the suppressed-to-dominant tag increases sufficiently. Finally, an effective connectivity measure (Phase Transfer Entropy) revealed that dominant or suppressed percepts were preferentially expressed in dorsal or ventral stream streams, respectively. We thus demonstrate that binocular rivalry dominance and suppression engage distinct mechanisms and brain networks. These findings advance neural models of rivalry and may relate to more general aspects of selection and suppression in natural vision.

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