August 2012
Volume 12, Issue 9
Free
Vision Sciences Society Annual Meeting Abstract  |   August 2012
Population receptive field measurements in macaque visual cortex.
Author Affiliations
  • Stelios M. Smirnakis
    Departments of Neurosci. and Neurol., Baylor Col. of Med., Houston, TX
  • G.A. Keliris
    Max Planck Inst. For Biol. Cybernetics, Tuebingen, Germany
  • Y. Shao
    Max Planck Inst. For Biol. Cybernetics, Tuebingen, Germany
  • A. Papanikolaou
    Max Planck Inst. For Biol. Cybernetics, Tuebingen, Germany
  • N.K. Logothetis
    Max Planck Inst. For Biol. Cybernetics, Tuebingen, Germany, Div. of Imaging Sci. and Biomed. Engin., Univ. of Manchester, United Kingdom
Journal of Vision August 2012, Vol.12, 1397. doi:https://doi.org/10.1167/12.9.1397
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      Stelios M. Smirnakis, G.A. Keliris, Y. Shao, A. Papanikolaou, N.K. Logothetis; Population receptive field measurements in macaque visual cortex.. Journal of Vision 2012;12(9):1397. https://doi.org/10.1167/12.9.1397.

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

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Abstract

Visual receptive fields have dynamic properties that may change with the conditions of visual stimulation or with the state of chronic visual deprivation. We used 4.7 Tesla functional magnetic resonance imaging (fMRI) to study the visual cortex of two normal adult macaque monkeys and one macaque with binocular central retinal lesions due to a form of juvenile macular degeneration (MD). FMRI experiments were performed under light remifentanyl induced anesthesia (Logothetis et al. Nat. Neurosci. 1999). Standard moving horizontal/vertical bar stimuli were presented to the subjects and the population receptive field (pRF) method (Dumoulin and Wandell, Neuroimage 2008) was used to measure retinotopic maps and pRF sizes in early visual areas. FMRI measurements of normal monkeys agree with published electrophysiological results, with pRF sizes and electrophysiology measurements showing similar trends. For the MD monkey, the size and location of the lesion projection zone (LPZ) was consistent with the retinotopic projection of the retinal lesion in early visual areas. No significant BOLD activity was seen within the V1 LPZ, and the retinotopic organization of the non-deafferented V1 periphery was regular without distortion. Interestingly, area V5/MT of the MD monkey showed more extensive activation than area V5/MT of control monkeys which had part of their visual field obscured (artificial scotoma) to match the scotoma of the MD monkey. V5/MT PRF sizes of the MD monkey were on average smaller than controls. PRF estimation methods allow us to measure and follow in vivo how the properties of visual areas change as a function of cortical reorganization. Finally, if there is time, we will discuss a different method of pRF estimation that yields additional information.

Meeting abstract presented at VSS 2012

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