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The Journal of Neurophysiology Vol. 85 No. 1 January 2001, pp. 43-53
Copyright ©2001 by the American Physiological Society
1Department of Physiology, Emory University, Atlanta, Georgia 30322; and 2Department of Physiology and Biophysics, University of Washington, Seattle, Washington 98195
Prather, Jonathan F.,
Randall K. Powers, and
Timothy C. Cope.
Amplification and Linear Summation of Synaptic Effects on
Motoneuron Firing Rate. J. Neurophysiol. 85: 43-53, 2001. The aim of this study was to measure
the effects of synaptic input on motoneuron firing rate in an
unanesthetized cat preparation, where activation of voltage-sensitive
dendritic conductances may influence synaptic integration and
repetitive firing. In anesthetized cats, the change in firing rate
produced by a steady synaptic input is approximately equal to the
product of the effective synaptic current measured at the resting
potential (IN) and the slope of the
linear relation between somatically injected current and motoneuron discharge rate (f-I slope). However, previous
studies in the unanesthetized decerebrate cat indicate that firing rate
modulation may be strongly influenced by voltage-dependent dendritic
conductances. To quantify the effects of these conductances on
motoneuron firing behavior, we injected suprathreshold current steps
into medial gastrocnemius motoneurons of decerebrate cats and measured
the changes in firing rate produced by superimposed excitatory synaptic
input. In the same cells, we measured
IN and the f-I slope to
determine the predicted change in firing rate (
F = IN * f-I slope).
In contrast to previous results in anesthetized cats, synaptically
induced changes in motoneuron firing rate were greater-than-predicted. This enhanced effect indicates that additional inward current was
present during repetitive firing. This additional inward current amplified the effective synaptic currents produced by two different excitatory sources, group Ia muscle spindle afferents and caudal cutaneous sural nerve afferents. There was a trend toward more prevalent amplification of the Ia input (14/16 cells) than the sural
input (11/16 cells). However, in those cells where both inputs were
amplified (10/16 cells), amplification was similar in magnitude for
each source. When these two synaptic inputs were simultaneously
activated, their combined effect was generally very close to the linear
sum of their amplified individual effects. Linear summation is also
observed in medial gastrocnemius motoneurons of anesthetized cats,
where amplification is not present. This similarity suggests that
amplification does not disturb the processes of synaptic integration.
Linear summation of amplified input was evident for the two segmental
inputs studied here. If these phenomena also hold for other synaptic
sources, then the presence of active dendritic conductances underlying
amplification might enable motoneurons to integrate multiple synaptic
inputs and drive motoneuron firing rates throughout the entire
physiological range in a relatively simple fashion.
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