Original Article
Unilateral nerve injury produces bilateral loss of distal innervation
Article first published online: 12 APR 2004
DOI: 10.1002/ana.20048
Copyright © 2003 American Neurological Association
Additional Information
How to Cite
Oaklander, A. L. and Brown, J. M. (2004), Unilateral nerve injury produces bilateral loss of distal innervation. Annals of Neurology, 55: 639–644. doi: 10.1002/ana.20048
Publication History
- Issue published online: 21 APR 2004
- Article first published online: 12 APR 2004
- Manuscript Received: 14 AUG 2003
- Manuscript Accepted: 3 JAN 2003
Funded by
- NIH, NINDS. Grant Number: R01NS42866
- Paul Beeson Scholarship from the American Federation for Aging Research
- Abstract
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- Cited By
Abstract
There are no known anatomical connections between neurons that innervate homologous right and left body parts. Nevertheless, some patients develop bilateral abnormalities after unilateral injury, a phenomenon often unrecognized and not yet characterized. Therefore, we examined in rats the effects of ligating and cutting one tibial nerve on sensory function and on density of innervation in hind paws contralaterally as well as ipsilaterally to the injury, at times between 1 day and 5 months after surgery. Punches removed from tibial- or sural-innervated planter paw skin were immunolabeled to quantitate epidermal nerve endings. Naive and sham-operated rats provided controls. Axotomized rats had near-total loss of PGP9.5+ innervation within ipsilateral tibial-innervated skin at all time-points. Adjacent ipsilateral sural-innervated skin had persistent hyperalgesia without denervation, and robust axonal sprouting at 5 months after surgery. Contralesional hind paws lost 54% of innervation in tibial-innervated epidermis starting 1 week after surgery and persisting throughout. Contralesional sural-innervated skin had neither neurite loss nor sprouting. These results imply that unilateral nerve injury can cause profound, long lasting, nerve–branch–specific loss of distal innervation contralaterally as well as ipsilaterally. They discredit the practice of using tissues contralateral to an injury to provide normative controls and suggest the possibility of rapid, transmedian postinjury signals between homologous mirror-image neurons.

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