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J Neurophysiol (June 4, 2003). doi:10.1152/jn.00310.2003
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00310.2003v1
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Submitted on March 28, 2003
Accepted on May 25, 2003

Dendritic Initiation and Propagation of Spikes and Spike Bursts in a Multimodal Sensory Interneuron: the Crustacean Parasol Cell

DeForest Mellon1*

1 Biology, University of Virginia, Charlottesville, Virginia, USA

* To whom correspondence should be addressed. E-mail: dm6d{at}virginia.edu.

Abstract Invasion of dendrites by spikes and spike bursts can play a critical role in regulating the output of central neurons by modifying their dynamic input-output relationships. Back-propagating bursts can modulate voltage-gated channels in the short term and can also modify long-term responses to synaptic input. Determining the morphological site of spike initiation and the mode of propagation through the dendritic arbor is therefore crucial to an understanding of a neuron's functional properties. I used electrophysiological methods to study parasol cells in isolated, perfused head preparations of the freshwater crayfish Procambarus clarkii to determine the compartment of origin of orthodromically activated action potentials and bursts that propagate within the dendritic arbor, and to examine the identity of low-amplitude, electrotonically recorded spike events that are present in more than half of the intracellular recordings obtained from dendrites in these neurons. Experiments using antidromic activation of parasol cell axons indicated that electrotonically recorded spikes probably are generated in neighboring parasol cells, to which the impaled neurons are electrically coupled. Both paired intracellular recordings and extracellular field potential measurements, were used to compare arrival times of antidromic and orthodromic spikes at loci in the vicinity of the trunk and the basal branch compartments of parasol cell dendrites. These methods provided consistent results indicating that synaptically-evoked action potentials are initiated at a site on the trunk, from which point they back-propagate into the basal branches within the hemiellipsoid body and, presumably, also orthodromically to the axon. Data are presented suggesting that bursts also arise at a trunk locus, but one that is different from the initiation point of single spikes evoked by EPSPs. Morphological specializations between the dendritic trunk and basal branches may facilitate backpropagation of spikes and spike bursts into the basal branches.







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