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Transected dorsal column axons within the guinea pig spinal cord regenerate in the presence of an applied electric field
Author(s) -
Borgens Richard B.,
Blight Andrew R.,
Murphy D. J.,
Stewart Lygia
Publication year - 1986
Publication title -
journal of comparative neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.855
H-Index - 209
eISSN - 1096-9861
pISSN - 0021-9967
DOI - 10.1002/cne.902500204
Subject(s) - spinal cord , anatomy , axon , biology , regeneration (biology) , axoplasmic transport , horseradish peroxidase , neuroscience , lesion , dorsum , guinea pig , pathology , medicine , microbiology and biotechnology , biochemistry , enzyme , endocrinology
Using an implanted battery and electrodes, we have imposed a weak, steady electrical field across partially severed guinea pig spinal cords. We have analyzed regeneration of dorsal column axons in experimental animals and sham‐treated controls at 50‐60 days postirjury by anterograde filling of these axons with the intracellular marker horseradish peroxidase and by employing a marking device to identify precisely the original plane of transection ( J. Comp. Neurol. 250 : 157‐167, '86). In response to electric field applications, axons grew into the glial scar, as far as the plane of transection in most experimental animals. In a few animals axons could be traced around the margins of the lesion (but never through it). Moreover, these fibers returned to their approximate positions within the rostral spinal cord before turning toward the brain. In sham‐treatede controls, ascending axons were found to terminate caudal to the glial scar, and rarely were any fibers found within the scar itself. Axons were never observed to cross into the rostral cord segment. These findings suggest that an imposed electrical field promotes growth of axons within the partially severed mammalian spinal cord, that a steady voltage gradient may e an environmental component necessary for axonal development and regeneration, and that some component(s) of the scar impede or deflect axonal growth and projection.