Synaptic background activity controls spike transfer from thalamus to
cortex
Jakob Wolfart, Damien Debay, Gwen Le Masson, Alain Destexhe and Thierry Bal
Nature Neuroscience 8: 1760-1767, 2005.
Abstract
Characterizing the responsiveness of thalamic neurons is crucial to understanding
the flow of sensory information. Typically, thalamocortical neurons possess two
distinct firing modes. At depolarized membrane potentials, thalamic cells fire
single action potentials and faithfully relay synaptic inputs to the cortex. At
hyperpolarized potentials, the activation of T-type calcium channels promotes
burst firing, and the transfer is less accurate. Our results suggest that this
duality no longer holds if synaptic background activity is taken into account. By
injecting stochastic conductances into guinea-pig thalamocortical neurons in
slices, we show that the transfer function of these neurons is strongly
influenced by conductance noise. The combination of synaptic noise with intrinsic
properties gives a global responsiveness that is more linear, mixing single-spike
and burst responses at all membrane potentials. Because in thalamic neurons,
background synaptic input originates mainly from cortex, these results support a
determinant role of corticothalamic feedback during sensory information
processing.
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