Ensheathing glia transplants promote dorsal root regeneration and spinal reflex restitution after multiple lumbar rhizotomy

Citation
X. Navarro et al., Ensheathing glia transplants promote dorsal root regeneration and spinal reflex restitution after multiple lumbar rhizotomy, ANN NEUROL, 45(2), 1999, pp. 207-215
Citations number
43
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
ANNALS OF NEUROLOGY
ISSN journal
03645134 → ACNP
Volume
45
Issue
2
Year of publication
1999
Pages
207 - 215
Database
ISI
SICI code
0364-5134(199902)45:2<207:EGTPDR>2.0.ZU;2-L
Abstract
Previously, we have shown that transplants of olfactory bulb ensheathing ce lls promoted regeneration of transected dorsal roots into the spinal cord. In this study, we assessed the ability of regenerating axons to make functi onal connections in the cord. Dorsal roots L3 to L6 were sectioned close to their entrance into the spinal cord and reapposed after injecting a suspen sion of ensheathing cells into each dorsal root entry zone (Group G). Affer ent regeneration into the cord and recovery of spinal reflexes were compare d with animals that received no injection (Group S) or culture medium witho ut cells (Group C). Electrophysiological tests, to measure nerve conduction and spinal reflexes (H response and withdrawal reflex) evoked by stimulati on of afferents of the sciatic nerve, were performed. At 14 days after surg ery, H response was found in only 1 of 7 rats of Group G, and withdrawal re flexes were absent from all animals. At 60 days, the H response reappeared in 7 of 10 rats of Group G, and 1 of 5 of each of Groups C and S. The withd rawal reflex recovered in 4 of 10 rats of Group G, but in none of Groups C and S. Immunohistochemical labeling for calcitonin gene-related peptide (CG RP) in rats of Group G showed immunoreabive fibers entering the dorsal horn from sectioned roots, although at lower density than in the contralateral side. In conclusion, transplanted ensheathing cells promoted central regene ration and functional reconnection of regenerating sensory afferents.