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The Journal of Neurophysiology Vol. 87 No. 1 January 2002, pp. 149-156
Copyright ©2002 by the American Physiological Society
Department of Neurobiology, Institute of Life Sciences and the Interdisciplinary Center for Neuronal Computation, Hebrew University, Jerusalem 91904, Israel
Mann-Metzer, Puah and
Yosef Yarom.
Jittery Trains Induced by Synaptic-Like Currents in Cerebellar
Inhibitory Interneurons. J. Neurophysiol. 87: 149-156, 2002. Cerebellar inhibitory interneurons
respond to parallel fiber input with a characteristic train of action
potentials. Here we show that the characteristics of these trains
reflect the intrinsic properties of the interneurons. In in vitro
cerebellar slices, the response of these neurons to synaptic-like
current resembles their in vivo response to parallel fiber input
a
train of action potentials characterized by a gradual increase in
interspike interval and spike amplitude. A large variability in spike
timing, or jitter, was observed, the last action potential emerging
from a slow depolarizing wave that lasted beyond the synaptic current
and was prevented by either TTX or membrane hyperpolarization. While
response duration was weakly dependent on current intensity, the
variability of the overall duration was closely related to the
variability of the timing of the last action potential. Blocking the
Ca2+ currents or partial blockade of the delayed
rectifier (TEA 2 mM) decreased the excitability, leading to a decrease
in the duration and variability of the response and increasing its
dependence on stimulus intensity. Increased duration and variability
was observed in the presence of Cs+ ions (5 mM)
that blocked an h-like current. We conclude that a persistent
Na+ current governs the duration of the response,
whereas the synaptic current and the spiking mechanism shape its
pattern. The large variability between trials is due to the stochastic
nature of the persistent Na+ current. Thus unless
precise timing is achieved by a network of interconnected neurons,
these results vote against temporal coding as a player in the
cerebellar computational processing.
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