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The Journal of Neuroscience, April 15, 2000, 20(8):3006-3016
The Control of Rate and Timing of Spikes in the Deep Cerebellar
Nuclei by Inhibition
Volker
Gauck and
Dieter
Jaeger
Department of Biology, Emory University, Atlanta, Georgia 30322
Cerebellar nucleus neurons were recorded in vitro,
and dynamic clamping was used to simulate inhibitory synaptic input
from Purkinje cells likely to occur in vivo. Inhibitory
input patterns with varying synaptic amplitudes and synchronicity were
applied to determine how spike rate and spike timing can be controlled by inhibition. The excitatory input conductance was held constant to
isolate the effect of dynamic inhibitory inputs on spiking. We found
that the timing of individual spikes was controlled precisely by short
decreases in the inhibitory conductance that were the consequence of
synchronization between many inputs. The spike rate of nucleus neurons
was controlled in a linear way by the rate of inhibitory inputs. The
spike rate, however, also depended strongly on the amount of
synchronicity present in the inhibitory inputs. An irregular spike
train similar to in vivo data resulted from applied
synaptic conductances when the conductance was large enough to overcome
intrinsic pacemaker currents. In this situation subthreshold
fluctuations in membrane potential closely followed the time course of
the combined reversal potential of excitation and inhibition. This
indicates that the net synaptic driving force for realistic input
levels in vivo may be small and that synaptic input may
operate primarily by shunting. The accurate temporal control of output
spiking by inhibitory input that can be achieved in this way in the
deep cerebellar nuclei may be particularly important to allow fine
temporal control of movement via inhibitory output from cerebellar cortex.
Key words:
cerebellum; Purkinje cell; synaptic; coding; inhibition; dynamic clamp; in vitro; whole cell; synchronization
Copyright © 2000 Society for Neuroscience 0270-6474/00/2083006-11$05.00/0
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