Literature DB >> 15826856

Differences in potentials and excitability properties in simulated cases of demyelinating neuropathies. Part I.

D I Stephanova1, M Daskalova, A S Alexandrov.   

Abstract

OBJECTIVE: The aim of this study is to investigate the potentials (intracellular, extracellular, electrotonic) and excitability properties (strength-duration and charge-duration curves, strength-duration time constants, rheobases, recovery cycles) in three cases of uniform myelin wrap reduction (20, 50 and 70%) along the fibre length.
METHODS: The internodally systematically demyelinated cases (termed as ISD1, ISD2 and ISD3) are simulated using our previous double cable model of human motor fibres.
RESULTS: In the more severely demyelinated cases, the intracellular potentials are with significantly reduced amplitude, prolonged duration and slowed conduction velocity, whereas the electrotonic potentials show greater increase in the early part of the hyperpolarizing responses. The radial decline of the extracellular potential amplitudes depends on the radial distance of the field point and increases with the increase of the distance and demyelination. The time constants and rheobasic currents increase with the increase of the degree of demyelination. In the recovery cycles, the more severely demyelinated cases have greater refractoriness (the increase in threshold current during the relative refractory period), supernormality and less late subnormality than the normal case.
CONCLUSIONS: The myelin thickness has significant effects on the potentials and axonal excitability properties of the simulated demyelinated human motor fibres. The obtained abnormalities in the potentials and excitability properties can be observed in Charcot-Marie-Tooth disease type 1A (CMT1A). SIGNIFICANCE: The study provides new information about the pathophysiology of human demyelinating neuropathies.

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Year:  2005        PMID: 15826856     DOI: 10.1016/j.clinph.2004.12.011

Source DB:  PubMed          Journal:  Clin Neurophysiol        ISSN: 1388-2457            Impact factor:   3.708


  6 in total

1.  Primary paranode demyelination modulates slowly developing axonal depolarization in a model of axonal injury.

Authors:  Vladislav Volman; Laurel J Ng
Journal:  J Comput Neurosci       Date:  2014-07-03       Impact factor: 1.621

2.  Differences in membrane properties in simulated cases of demyelinating neuropathies: internodal focal demyelinations without conduction block.

Authors:  D I Stephanova; M S Daskalova; A S Alexandrov
Journal:  J Biol Phys       Date:  2006-04-20       Impact factor: 1.365

3.  Differences in membrane properties in simulated cases of demyelinating neuropathies: internodal focal demyelinations with conduction block.

Authors:  D I Stephanova; M S Daskalova; A S Alexandrov
Journal:  J Biol Phys       Date:  2006-06-14       Impact factor: 1.365

4.  Differences between the channels, currents and mechanisms of conduction slowing/block and accommodative processes in simulated cases of focal demyelinating neuropathies.

Authors:  Diana I Stephanova; Mariya S Daskalova
Journal:  Eur Biophys J       Date:  2008-02-20       Impact factor: 1.733

5.  Membrane property abnormalities in simulated cases of mild systematic and severe focal demyelinating neuropathies.

Authors:  Diana Stephanova; Mariya Daskalova
Journal:  Eur Biophys J       Date:  2007-09-05       Impact factor: 1.733

6.  Linking demyelination to compound action potential dispersion with a spike-diffuse-spike approach.

Authors:  Richard Naud; André Longtin
Journal:  J Math Neurosci       Date:  2019-05-30       Impact factor: 1.300

  6 in total

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