Literature DB >> 11139041

An ionic current model for medullary respiratory neurons.

A Athanasiades1, J W Clark, F Ghorbel, A Bidani.   

Abstract

Neurons of the mammalian medullary respiratory center have complex patterns of electrophysiological behavior. Three typical phenomena associated with these patterns are spike frequency adaptation (SFA), delayed excitation (DE), and postinhibitory rebound (PIR). Although several nuclei are associated with the medullary-pontine respiratory center, we focused on neurons from two nuclei: (1) the ventral subnucleus of the nucleus tractus solitarius (vNTS) of the dorsal respiratory group and (2) the nucleus ambiguus (NA) of the ventral respiratory group. We developed a Hodgkin-Huxley (HH) type model of the typical medullary neuron that is capable of mimicking the discharge pattern of real neurons to a very high degree. Closer examination of typical data revealed, however, that there was not one type of medullary respiratory neuron, but at least three (types A, B1, and B2). We classified these neurons based on the electrophysiologic phenomena that they exhibited (type A exhibits DE but not PIR; types B1 and B2 exhibit PIR but not DE; all types are adapting). Our objective was to relate each of these well-known phenomena to specific ionic current mechanisms. In the model, three currents directly affect the phenomena investigated: the Ca2+-activated K+ current, I(K,Ca), controls peak and steady-state firing rates and the time constant of adaptation; the transient outward K+ current, I(A), is responsible for all aspects of DE, including the dependence of delay on the magnitude and duration of conditioning hyperpolarization; and the hyperpolarization-activated current, Ih, elicits PIR and dictates its dependencies. We consider that our HH model represents a unifying structure, whereby different electrophysiological phenomena or discharge patterns can be emulated using different strengths of the component ionic membrane currents (particularly I(K,Ca), I(A), and Ih). Moreover, its predictions suggest that the electrophysiological characteristics of medullary respiratory neurons, from different areas of the brainstem and even from different species, can be modeled using the same structural framework, wherein the specific properties of individual neurons are emulated by adjusting the strengths of key ionic membrane currents in the model.

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Year:  2000        PMID: 11139041     DOI: 10.1023/a:1026583620467

Source DB:  PubMed          Journal:  J Comput Neurosci        ISSN: 0929-5313            Impact factor:   1.621


  31 in total

1.  Driving respiration: the respiratory central pattern generator.

Authors:  M C Bellingham
Journal:  Clin Exp Pharmacol Physiol       Date:  1998-10       Impact factor: 2.557

Review 2.  Synaptic connections between medullary respiratory neurons and considerations on the genesis of respiratory rhythm.

Authors:  K Ezure
Journal:  Prog Neurobiol       Date:  1990       Impact factor: 11.685

Review 3.  PreBötzinger complex and pacemaker neurons: hypothesized site and kernel for respiratory rhythm generation.

Authors:  J C Rekling; J L Feldman
Journal:  Annu Rev Physiol       Date:  1998       Impact factor: 19.318

4.  In vitro characterization of neurons in the ventral part of the nucleus tractus solitarius. II. Ionic basis for repetitive firing patterns.

Authors:  M S Dekin; P A Getting
Journal:  J Neurophysiol       Date:  1987-07       Impact factor: 2.714

5.  Experimentally induced postinhibitory rebound in rat nucleus ambiguus is dependent on hyperpolarization parameters and membrane potential.

Authors:  J B Dean; M Czyzyk-Krzeska; D E Millhorn
Journal:  Neurosci Res       Date:  1989-06       Impact factor: 3.304

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Authors:  M S Dekin; P A Getting
Journal:  Brain Res       Date:  1984-12-17       Impact factor: 3.252

7.  Interactions between brainstem respiratory neurons.

Authors:  J L Feldman
Journal:  Fed Proc       Date:  1981-07

8.  Afferent synaptic drive of rat medial nucleus tractus solitarius neurons: dynamic simulation of graded vesicular mobilization, release, and non-NMDA receptor kinetics.

Authors:  J H Schild; J W Clark; C C Canavier; D L Kunze; M C Andresen
Journal:  J Neurophysiol       Date:  1995-10       Impact factor: 2.714

9.  Potassium currents of neurons isolated from medical nucleus tractus solitarius.

Authors:  J P Moak; D L Kunze
Journal:  Am J Physiol       Date:  1993-11

10.  Inward rectification and its effects on the repetitive firing properties of bulbospinal neurons located in the ventral part of the nucleus tractus solitarius.

Authors:  M S Dekin
Journal:  J Neurophysiol       Date:  1993-08       Impact factor: 2.714

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  4 in total

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4.  Theoretical perspectives on central chemosensitivity: CO2/H+-sensitive neurons in the locus coeruleus.

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Journal:  PLoS Comput Biol       Date:  2017-12-21       Impact factor: 4.475

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