Strength-duration properties of human peripheral nerve

The strength—duration time constant (τSD) is a property of nodal membrane and, while it depends on a number of factors, its measurement may shed light on axonal properties when taken in conjunction with measurements of axonal excitability. For example, τSD increases with demyelination as the exposed...

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Bibliographic Details
Published inBrain (London, England : 1878) Vol. 119; no. 2; pp. 439 - 447
Main Authors Mogyoros, Ilona, Kiernan, Matthew C., Burke, David
Format Journal Article
LanguageEnglish
Published Oxford Oxford University Press 01.04.1996
Oxford Publishing Limited (England)
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Summary:The strength—duration time constant (τSD) is a property of nodal membrane and, while it depends on a number of factors, its measurement may shed light on axonal properties when taken in conjunction with measurements of axonal excitability. For example, τSD increases with demyelination as the exposed membrane is enlarged by inclusion of paranodal and internodal membrane, it decreases with hyperpolarization and it increases with depolarization. The present study was undertaken in 20 normal volunteers to compare strength—duration curves for compound sensory and muscle action potentials, to determine the most appropriate curve fitting equation for the data, and to examine the reproducibility of the calculated time constant on different days, for potentials of different amplitude and at different sites along the nerve. Using a computerized threshold-tracking system, stimulus intensity was adjusted to produce an antidromic compound sensory action potential (CSAP) or an orthodromic muscle action potential of 30% of maximum. Stimulus duration was increased every minute in 20 μs steps from 20 μs to 1 ms. The time constant for compound sensory potentials (665±182 μs) was longer than that for compound EMG potentials (459±126 μs). Weiss's formula, which relates threshold charge to stimulus duration, provided an accurate fit for the experimental data, and the study validated that, using it, relatively few experimental measurements were required to calculate the time constant. In repeated studies on the same subject, time constants usually differed by <400 μs for sensory axons and <250 μs for motor axons. They were identical at different sites along the nerve and did not alter with the size of the compound action potential. These characteristics suggest that the determinations of strength-duration time constant could be suitable for clinical usage.
Bibliography:ArticleID:119.2.439
Correspondence to: Dr Ilona Mogyoros, Prince of Wales Medical Research Institute, High Street, Randwick, Sydney, NSW 2031, Australia
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ISSN:0006-8950
1460-2156
DOI:10.1093/brain/119.2.439