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Journal of Neuroscience, Vol 13, 5301-5311, Copyright © 1993 by Society for Neuroscience
Apical dendrites of the neocortex: correlation between sodium- and calcium-dependent spiking and pyramidal cell morphology
HG Kim and BW Connors
Department of Neuroscience, Brown University, Providence, Rhode Island 02192.
Apical dendrites and somata of layer V pyramidal neurons were recorded with
tight-seal patch electrodes in a slice preparation of rat somatosensory
cortex. Recording sites were confirmed by measurements of the electrode
location and by staining with biocytin. Dendritic recordings were made
along the main trunk of the apical dendrite, usually within layer IV, at
distances from 100 to 500 microns from the soma. Most cells recorded
through the dendrite had a distinct enlargement of the apical trunk around
the presumed recording site. The electrical properties of apical dendrites
were readily distinguishable from those of somata. Dendrites generated two
types of response when injected with depolarizing current. Group I
responses were relatively small and broad Na(+)-dependent action potentials
whose amplitude and rate-of-rise were negatively correlated with recording
distance from the soma. Group II responses were complex, clustered firing
patterns of Na(+)-dependent spikes together with higher-threshold slow
spikes or plateaus; in these dendrites spike parameters were not correlated
with distance from the soma. These two response groups were correlated with
dendritic morphology: group I had significantly fewer oblique branches on
the apical dendrite (5.5 vs 12.0) and a thinner apical trunk (2.0 vs 2.5
microns) than group II. TTX (1-2 microM) selectively blocked fast dendritic
spikes, but not slow spikes and plateaus. Blocking Ca2+ currents reduced
complex firing patterns and suppressed high-threshold slow spikes.
Physiological and pharmacological studies imply that slow spikes and
plateau potentials were primarily generated by high- threshold Ca2+
channels in the apical dendrite. Stimulating axons of layer I elicited
EPSPs on distal apical dendrites of layer V cells. Recordings from both
groups of apical dendrites revealed that EPSPs triggered a variety of
distally generated, all-or-nothing depolarizations. The results show that
voltage-dependent Na+ and Ca2+ currents are present in distal apical
dendrites, in variable densities. These currents significantly modify
distal synaptic events. The prevalence and character of active dendritic
spiking (and presumably of Na+ and Ca2+ channel densities) correlate with
the morphology of the apical dendritic tree.
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