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The Journal of Neurophysiology Vol. 81 No. 2 February 1999, pp. 535-543
Copyright ©1999 by the American Physiological Society
Division of Neuroscience, Baylor College of Medicine, Houston, Texas 77030
Voltage-dependent properties of dendrites that eliminate
location-dependent variability of synaptic input. We examined
the hypothesis that voltage-dependent properties of dendrites allow for
the accurate transfer of synaptic information to the soma independent
of synapse location. This hypothesis is motivated by experimental
evidence that dendrites contain a complex array of voltage-gated
channels. How these channels affect synaptic integration is unknown.
One hypothesized role for dendritic voltage-gated channels is to
counteract passive cable properties, rendering all synapses
electrotonically equidistant from the soma. With dendrites modeled as
passive cables, the effect a synapse exerts at the soma depends on
dendritic location (referred to as location-dependent variability of
the synaptic input). In this theoretical study we used a simplified
three-compartment model of a neuron to determine the dendritic
voltage-dependent properties required for accurate transfer of synaptic
information to the soma independent of synapse location. A dendrite
that eliminates location-dependent variability requires three
components: 1) a steady-state, voltage-dependent inward
current that together with the passive leak current provides a net
outward current and a zero slope conductance at depolarized potentials,
2) a fast, transient, inward current that compensates for
dendritic membrane capacitance, and 3) both
amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid- and
N-methyl-D-aspartate-like synaptic conductances
that together permit synapses to behave as ideal current sources. These components are consistent with the known properties of dendrites. In
addition, these results indicate that a dendrite designed to eliminate
location-dependent variability also actively back-propagates somatic
action potentials.
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