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Axonal changes in spinal cord injured patients distal to the site of injury.

Journal article
Authors Cindy Shin-Yi Lin
Vaughan G Macefield
Mikael Elam
Gunnar B Wallin
Stella Engel
Matthew C Kiernan
Published in Brain : a journal of neurology
Volume 130
Issue Pt 4
Pages 985-94
ISSN 1460-2156
Publication year 2007
Published at Institute of Neuroscience and Physiology, Department of Clinical Neuroscience and Rehabilitation
Pages 985-94
Language en
Links dx.doi.org/10.1093/brain/awl339
Keywords Action Potentials, physiology, Adolescent, Adult, Axons, physiology, Electric Stimulation, methods, Female, Humans, Male, Median Nerve, physiopathology, Middle Aged, Motor Neurons, physiology, Muscle, Skeletal, physiopathology, Neurons, Afferent, physiology, Peroneal Nerve, physiopathology, Reaction Time, physiology, Refractory Period, Electrophysiological, physiology, Spinal Cord, physiopathology, Spinal Cord Injuries, physiopathology
Subject categories Medical and Health Sciences

Abstract

It is generally assumed that the peripheral nervous system remains intact following a spinal injury. Accordingly, the electrical thresholds of motor axons in a peripheral nerve below the lesion should be similar to those in intact subjects. Yet in attempts to enter the common peroneal nerve with microelectrodes in 24 quadriplegic or paraplegic individuals it was often found that electrical stimulation over or within the nerve failed to elicit contractions in the pre-tibial flexors. To investigate whether consistent changes in axonal physiology occurred distal to the site of injury in patients with spinal cord injury (SCI), motor nerve excitability was formally tested in 15 of these patients. Threshold tracking techniques were used to measure axonal excitability parameters (stimulus-response curves, strength-duration properties, threshold electrotonus, a current-threshold relationship and the recovery cycle) of motor axons in the median and common peroneal nerves. In these patients motor axons were uniformly of high threshold and consequently, stimulus-response curves were shifted to the right. In some SCI patients, axons were completely inexcitable. Amplitudes of compound motor action potentials were reduced, consistent with axonal loss and strength-duration time constant was significantly reduced in SCI patients (SCI 0.13 +/- 0.02 ms, controls 0.43 +/- 0.02 ms, mean +/- SE, P < 0.0001). Excitability changes were more prominent the more clinically severe the injury, with progressive deterioration over time since the original injury. While compression and traction sustained during the original injury or subsequent hospital rehabilitation may contribute in part to some of these changes, it is difficult to attribute these findings solely to such processes. Changes in axonal structure and ion channel function, but perhaps more critically decentralization and consequent inactivity, are likely to underlie the complex changes observed in axonal excitability in SCI patients.

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