Journal of Neuroscience, Vol 6, 3205-3217, Copyright © 1986 by Society for Neuroscience
Replacement of synaptic terminals in lamina II and Clarke's nucleus after unilateral lumbosacral dorsal rhizotomy in adult cats
M Murray and ME Goldberger
Evidence from previous light-microscopic studies suggested that lumbosacral
dorsal rhizotomy in cats elicits sprouting of converging undamaged systems
into partially deafferented Clarke's nucleus and lamina II. We therefore
applied quantitative electron-microscopic methods to determine whether this
sprouting is associated with replacement of synaptic terminals (reactive
reinnervation). We used stereological and morphometric methods to estimate
terminal number per cross section in right and left lamina II and Clarke's
nucleus in adult cats after acute and chronic unilateral (right-sided)
lumbosacral deafferentation. Planimetric measurements of area indicated no
significant shrinkage of either region as a result of the deafferentation;
an increase in area occupied by glial cytoplasm (gliosis) equaled the
decrease occupied by axonal components. The gliosis appears to persist
indefinitely, although the degenerative debris stainable with conventional
light-microscopic methods does not persist. Analysis of the synaptic
population of lamina II reveals that the large central or "scalloped"
terminals comprise a substantial fraction (greater than 40%) of the total
area occupied by terminals in control material and that this population is
largely lost upon deafferentation, leaving a large population of small
terminals with spherical vesicles. Nevertheless, estimates of total
terminal number indicate no difference between control and deafferented
lamina II, suggesting a rapid and virtually complete replacement of lost
dorsal root terminals by small terminals containing spherical vesicles.
Terminal number in Clarke's nucleus also remains constant despite the loss
of the dorsal root input. We conclude that there is also a virtually
complete and rapid replacement of lost terminals in Clarke's nucleus by
terminals containing spherical vesicles. These data provide an example of a
case in which axonal sprouting demonstrated with light- microscopic methods
is associated with electron-microscopic evidence of reactive reinnervation.