APICAL DENDRITES OF THE NEOCORTEX - CORRELATION BETWEEN SODIUM-DEPENDENT AND CALCIUM-DEPENDENT SPIKING AND PYRAMIDAL CELL MORPHOLOGY

Authors
Citation
Hg. Kim et Bw. Connors, APICAL DENDRITES OF THE NEOCORTEX - CORRELATION BETWEEN SODIUM-DEPENDENT AND CALCIUM-DEPENDENT SPIKING AND PYRAMIDAL CELL MORPHOLOGY, The Journal of neuroscience, 13(12), 1993, pp. 5301-5311
Citations number
64
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
02706474
Volume
13
Issue
12
Year of publication
1993
Pages
5301 - 5311
Database
ISI
SICI code
0270-6474(1993)13:12<5301:ADOTN->2.0.ZU;2-4
Abstract
Apical dendrites and somata of layer V pyramidal neurons were recorded with tight-seal patch electrodes in a slice preparation of rat somato sensory 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 1 00 to 500 mum f rom the soma. Most cell s recorded through the dendrite had a distinct enlargement of the apic al 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 depolar izing current. Group I responses were relatively small and broad Na+-d ependent action potentials whose amplitude and rate-of-rise were negat ively correlated with recording distance from the soma. Group II respo nses were complex, clustered firing patterns of Na+-dependent spikes t ogether with higher-threshold slow spikes or plateaus; in these dendri tes spike parameters were not correlated with distance from the soma. These two response groups were correlated with dendritic morphology: g roup 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 mum) than group II. TTX (1-2 mum) selectively blocked fast dendritic spikes, but not s low 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 apica l dendrite. Stimulating axons of layer I elicited EPSPs on distal apic al dendrites of layer V cells. Recordings from both groups of apical d endrites revealed that EPSPs triggered a variety of distally generated , all-or-nothing depolarizations. The results show that voltage-depend ent Na+ and Ca2+ currents are present in distal apical dendrites, in v ariable 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 morp hology of the apical dendritic tree.