JN Journal of Applied Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 69: 261-281, 1993;
0022-3077/93 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ketchum, K. L.
Right arrow Articles by Haberly, L. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ketchum, K. L.
Right arrow Articles by Haberly, L. B.

Journal of Neurophysiology, Vol 69, Issue 1 261-281, Copyright © 1993 by APS


ARTICLES

Membrane currents evoked by afferent fiber stimulation in rat piriform cortex. II. Analysis with a system model

K. L. Ketchum and L. B. Haberly
Department of Anatomy, University of Wisconsin, Madison 53706.

1. The detailed visualization of membrane currents over time and depth provided by current source-density (CSD) analysis was used as the basis for development of a system model that reproduces the response of piriform cortex to afferent fiber stimulation. This model has allowed the testing and substantial revision of previous hypotheses concerning the sequence of neuronal events underlying this response, has enabled net membrane currents visualized by CSD analysis to be separated into active and passive components, and has generated predictions for important axonal and synaptic parameters as well as for the behavior of piriform cortex as a system. 2. The model was developed in three steps. Activity in excitatory fiber systems was first represented with continuous distributions. The "population conductances" due to the activation of excitatory fiber systems were then computed from the distribution of action-potential arrival times and the conductance waveform for excitatory synapses. Finally, these temporally dispersed excitatory conductances and locally mediated inhibitory conductances were introduced at appropriate locations on a compartmentalized cable that simulated the passive response of the pyramidal cell population. 3. After the simulation of membrane currents at one site, all parameters in the model were fixed so that it could be used to predict the variation in the time course of membrane currents at additional recording sites; comparison with the results of CSD analysis at these sites provided the primary validation of the model. Additional validation included the simulation of membrane potentials derived by intracellular recording, including the effects of manipulating somatic potential with current injection. 4. Several conclusions have emerged from the mathematical description of activity in fiber systems. Propagation of activity in both afferent and association (corticocortical) fiber systems is "dispersive" as a result of a wide spectrum of axon conduction velocities. The characteristically different time courses of afferent and association fiber-mediated responses are largely determined by the focal, shock-evoked origin of the volley in afferent fibers as opposed to the spatially distributed disynaptic origin of activity in association fibers. Conduction velocity distributions for afferent and association fiber systems are skewed and can be approximated with lognormal distributions. 5. General solutions, which relate an arbitrary conduction velocity distribution to arrival time and spatial distributions of action potentials, were used to generate specific solutions describing the effects of dispersive propagation.(ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
Chem SensesHome page
A.M. McNamara, T.A. Cleland, and C. Linster
Characterization of the Synaptic Properties of Olfactory Bulb Projections
Chem Senses, March 1, 2004; 29(3): 225 - 233.
[Abstract] [Full Text] [PDF]


Home page
Chem SensesHome page
L. B. Haberly
Parallel-distributed Processing in Olfactory Cortex: New Insights from Morphological and Physiological Analysis of Neuronal Circuitry
Chem Senses, June 1, 2001; 26(5): 551 - 576.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. Kapur and L. B. Haberly
Duration of NMDA-Dependent Synaptic Potentiation in Piriform Cortex In Vivo Is Increased After Epileptiform Bursting
J Neurophysiol, October 1, 1998; 80(4): 1623 - 1629.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. Kapur, W. W. Lytton, K. L. Ketchum, and L. B. Haberly
Regulation of the NMDA Component of EPSPs by Different Components of Postsynaptic GABAergic Inhibition: Computer Simulation Analysis in Piriform Cortex
J Neurophysiol, November 1, 1997; 78(5): 2546 - 2559.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online