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J Neurophysiol 92: 1023-1033, 2004. First published April 7, 2004; doi:10.1152/jn.01089.2003
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Impact of Noise on Retinal Coding of Visual Signals

Christopher L. Passaglia1,2 and John B. Troy1

1Biomedical Engineering Department and Neuroscience Institute, Northwestern University, Evanston, Illinois 60208; and 2Biomedical Engineering Department, Boston University, Boston, Massachusetts 02215

Submitted 10 November 2003; accepted in final form 31 March 2004

Neural noise introduces uncertainty about the signals encoded in neural spike trains. Because of the uncertainty neurons can reliably transmit a limited amount of information. This amount is difficult to quantify for neurons that combine signals and noise in a complex manner, as many trials would be needed to estimate the joint probability distribution of stimulus and neural response accurately. The task is experimentally tractable, however, for neurons that combine signals with additive Gaussian noise. For such neurons, the joint probability distribution is well defined and information transmission rates can be computed from estimates of signal-to-noise ratio. Here we use power spectral analysis to specify the contributions of signal and noise to retinal coding of visual information. We show that in the spike trains of cat ganglion cells noise power is minimal and constant at temporal frequencies from 0.3 to 20 Hz and that it increases at higher frequencies to a plateau level that generally depends on stimulus contrast. We also show that trial-to-trial fluctuations in noise amplitude at different frequencies are uncorrelated and normally distributed. Although the contrast dependence indicates that noise at high temporal frequencies contributes nonlinearly to ganglion cell spike trains, cells in the primary visual cortex are not known to respond to stimulus modulations >20 Hz. Hence, noise in the retinal output would appear additive, white, and Gaussian from their perspective. This greatly simplifies analysis of information transmission from the eye to the primary visual cortex and perhaps other regions of the brain.


Address for reprint requests and other correspondence: C. L. Passaglia, Boston University, Biomedical Engineering Department, 44 Cummington St., Boston, MA 02215 (E-mail: psagls{at}bu.edu).







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