Noisy Spiking in Visual Area V2 of Amblyopic Monkeys

Interocular decorrelation of input signals in developing visual cortex can cause impaired binocular vision and amblyopia. Although increased intrinsic noise is thought to be responsible for a range of perceptual deficits in amblyopic humans, the neural basis for the elevated perceptual noise in ambl...

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Veröffentlicht in:The Journal of neuroscience 2017-01, Vol.37 (4), p.922-935
Hauptverfasser: Wang, Ye, Zhang, Bin, Tao, Xiaofeng, Wensveen, Janice M, Smith 3rd, Earl L, Chino, Yuzo M
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container_issue 4
container_start_page 922
container_title The Journal of neuroscience
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creator Wang, Ye
Zhang, Bin
Tao, Xiaofeng
Wensveen, Janice M
Smith 3rd, Earl L
Chino, Yuzo M
description Interocular decorrelation of input signals in developing visual cortex can cause impaired binocular vision and amblyopia. Although increased intrinsic noise is thought to be responsible for a range of perceptual deficits in amblyopic humans, the neural basis for the elevated perceptual noise in amblyopic primates is not known. Here, we tested the idea that perceptual noise is linked to the neuronal spiking noise (variability) resulting from developmental alterations in cortical circuitry. To assess spiking noise, we analyzed the contrast-dependent dynamics of spike counts and spiking irregularity by calculating the square of the coefficient of variation in interspike intervals (CV super(2)) and the trial-to-trial fluctuations in spiking, or mean matched Fano factor (m-FF) in visual area V2 of monkeys reared with chronic monocular defocus. In amblyopic neurons, the contrast versus response functions and the spike count dynamics exhibited significant deviations from comparable data for normal monkeys. The CV super(2) was pronounced in amblyopic neurons for high-contrast stimuli and the m-FF was abnormally high in amblyopic neurons for low-contrast gratings. The spike count, CV super(2), and m-FF of spontaneous activity were also elevated in amblyopic neurons. These contrast-dependent spiking irregularities were correlated with the level of binocular suppression in these V2 neurons and with the severity of perceptual loss for individual monkeys. Our results suggest that the developmental alterations in normalization mechanisms resulting from early binocular suppression can explain much of these contrast-dependent spiking abnormalities in V2 neurons and the perceptual performance of our amblyopic monkeys.
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title Noisy Spiking in Visual Area V2 of Amblyopic Monkeys
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