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Somatotopy of perceptual threshold to cutaneous electrical stimulation in man

Published online by Cambridge University Press:  31 July 2001

Nick J. Davey
Affiliation:
Division of Neuroscience and Psychological Medicine, Imperial College School of Medicine, Charing Cross Hospital, London W6 8RF and Department of Sport Sciences, Brunel University, Isleworth, London TW7 5DU, UK
Alex V. Nowicky
Affiliation:
Division of Neuroscience and Psychological Medicine, Imperial College School of Medicine, Charing Cross Hospital, London W6 8RF and Department of Sport Sciences, Brunel University, Isleworth, London TW7 5DU, UK
Rashid Zaman
Affiliation:
Division of Neuroscience and Psychological Medicine, Imperial College School of Medicine, Charing Cross Hospital, London W6 8RF and Department of Sport Sciences, Brunel University, Isleworth, London TW7 5DU, UK
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Abstract

Neurological testing tools for measuring and monitoring somatosensory function lack resolution and are often dependent on the clinician testing. In this study we have measured perceptual threshold (PT) to electrical stimulation of the skin and compared it with two-point discriminative ability (TPDA) in 12 control subjects. Tests were made on both sides of the body at American Spinal Injury Association (ASIA) key points on seven spinal dermatomes (C3 (neck), C4 (shoulder), C5 (upper arm), C6 (thumb), T8 (abdomen), L3 (knee), L5 (foot)) and in the mandibular (chin) and maxillary (cheek) fields of the trigeminal (V) nerve. Electrical stimulation (0·5 ms pulse width; 3 Hz) was applied via a self-adhesive cathode and an anode strapped to the wrist or ankle. The stimulus intensity was adjusted and PT was recorded as the lowest current at which the subject reported sensation. Sites were tested in random order. Indices for both TPDA and PT differed according to the dermatome tested but there was no correlation between TPDA and PT for any dermatome. There was good correlation between results from equivalent dermatomes on left and right sides for both PT and TPDA. Women frequently had lower mean (± s.e.) PTs and better TPDA than men; differences were significant (P < 0·05) for PT on the knee (women, 1·31 ± 0·15 mA; men, 2·05 ± 0·26 mA) and the foot (women, 2·90 ± 0·19 mA; men, 4·13 ± 0·28 mA) and for TPDA on the thumb (women, 3·8 ± 0·2 mm; men, 7·8 ± 1·3 mm) and the knee (women, 17·8 ± 1·6 mm; men, 27·1 ± 4·0 mm). Four subjects repeated the experiment on another day and the results correlated well with the first test for PT (r2, 0·62) and TPDA (r2, 0·48). PT differs between dermatomes in a predictable way but does not relate to TPDA. PT is easy to measure and may be a useful assessment tool with which to monitor recovery or deterioration in neuropathies, neurotrauma or after surgery. Experimental Physiology (2001) 86.1, 127-130.

Type
Research Article
Copyright
© The Physiological Society 2001

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