The variable discharge of cortical neurons: implications for connectivity, computation, and information coding

MN Shadlen, WT Newsome - Journal of neuroscience, 1998 - Soc Neuroscience
Journal of neuroscience, 1998Soc Neuroscience
Cortical neurons exhibit tremendous variability in the number and temporal distribution of
spikes in their discharge patterns. Furthermore, this variability appears to be conserved over
large regions of the cerebral cortex, suggesting that it is neither reduced nor expanded from
stage to stage within a processing pathway. To investigate the principles underlying such
statistical homogeneity, we have analyzed a model of synaptic integration incorporating a
highly simplified integrate and fire mechanism with decay. We analyzed a “high-input …
Cortical neurons exhibit tremendous variability in the number and temporal distribution of spikes in their discharge patterns. Furthermore, this variability appears to be conserved over large regions of the cerebral cortex, suggesting that it is neither reduced nor expanded from stage to stage within a processing pathway. To investigate the principles underlying such statistical homogeneity, we have analyzed a model of synaptic integration incorporating a highly simplified integrate and fire mechanism with decay. We analyzed a “high-input regime” in which neurons receive hundreds of excitatory synaptic inputs during each interspike interval. To produce a graded response in this regime, the neuron must balance excitation with inhibition. We find that a simple integrate and fire mechanism with balanced excitation and inhibition produces a highly variable interspike interval, consistent with experimental data. Detailed information about the temporal pattern of synaptic inputs cannot be recovered from the pattern of output spikes, and we infer that cortical neurons are unlikely to transmit information in the temporal pattern of spike discharge. Rather, we suggest that quantities are represented as rate codes in ensembles of 50–100 neurons. These column-like ensembles tolerate large fractions of common synaptic input and yet covary only weakly in their spike discharge. We find that an ensemble of 100 neurons provides a reliable estimate of rate in just one interspike interval (10–50 msec). Finally, we derived an expression for the variance of the neural spike count that leads to a stable propagation of signal and noise in networks of neurons—that is, conditions that do not impose an accumulation or diminution of noise. The solution implies that single neurons perform simple algebra resembling averaging, and that more sophisticated computations arise by virtue of the anatomical convergence of novel combinations of inputs to the cortical column from external sources.
Soc Neuroscience
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