A magnetic evaluation of peripheral nerve regeneration: I. The discrepancy between magnetic and histologic data from the proximal segment

Histologic techniques can quantify the number of axons in a nerve, but give no information about electrical conductibility. The number of functional myelinated neuronal units in a nerve can be quantified based on a magnetic recording technique. When studying reconstructed peripheral nerves a signifi...

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Veröffentlicht in:Muscle & nerve 1998-06, Vol.21 (6), p.739-749
Hauptverfasser: Kuypers, Paul D.L., van Egeraat, Jan M., Dudok v Heel, Michiel, van Briemen, Lourens J., Godschalk, Moshe, Hovius, Steven E.R.
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Sprache:eng
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Zusammenfassung:Histologic techniques can quantify the number of axons in a nerve, but give no information about electrical conductibility. The number of functional myelinated neuronal units in a nerve can be quantified based on a magnetic recording technique. When studying reconstructed peripheral nerves a significant difference between the results found with these two techniques can be observed. A comparison was made between the long‐term changes in the number of histologically and magnetoneurophysiologically measured neuronal units proximal to a nerve reconstruction. This study was performed on 6 New Zealand White rabbits, 20 weeks after the peroneal nerve had been reconstructed. The contralateral nerves were used as a control. Histologic examination demonstrates a statistically significant decrease of approximately 5% in the number of myelinated fibers. The magnetoneurophysiological results demonstrate a decrease which is estimated to be caused by the loss of approximately 50% of the functional myelinated neuronal units in the nerve. Therefore we conclude that of the initially available myelinated neuronal units, 5% degenerate completely, 45% are vital but lose their signal conducting capability, and the remaining 50% are vital and continue to conduct signals. Apparently, only this latter group of 50% of the initially available functional neuronal units appears to remain available for functional recovery. © 1998 John Wiley & Sons, Inc. Muscle Nerve 21:739–749, 1998.
ISSN:0148-639X
1097-4598
DOI:10.1002/(SICI)1097-4598(199806)21:6<739::AID-MUS5>3.0.CO;2-8