Premium
Origin and ultrastructural identification of dorsal column nuclear synaptic terminals in the basilar pontine gray of rats
Author(s) -
Kosinski R. J.,
Azizi S. A.,
Border B. G.,
Mihailoff B. G. A.
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.902530108
Subject(s) - dorsal column nuclei , biology , anatomy , reticular formation , pons , axon , synaptic vesicle , ultrastructure , pontine nuclei , thalamic reticular nucleus , reticular connective tissue , axoplasmic transport , neuroscience , vesicle , nucleus , dorsum , genetics , membrane
The ultrastructural characteristics of HRP‐WGA‐labeled or degenerating axon terminals arising from neurons in the dorsal column nuclei (DCN) were identified within the contralateral basilar pontine nuclei (BPN) following unilateral HRP‐WGA injections or ablations of the DCN. The cells of origin of these projections were also identified through the application of the retrograde tracer HRP‐WGA. Two groups of degenerating DCN‐pontine terminals were identified. Both formed asymmetrical synaptic contacts with dendritic shafts and/or dendritic appendages of pontine neurons. One group of degenerating terminals contained small, round synaptic vesicles, while the other exhibited a mixture of dense core and pleomorphic vesicles. The former group, which clearly represented the majority of degenerating terminals observed, was interpreted to progress from an early filamentous form of degeneration to a later electron‐dense variety and to originate from dorsally located DCN cells distributed primarily at the level of and just caudal to the area postrema. Other DCN‐labeled neurons were more ventrally located and were postulated to give rise to those degenerative boutons that contained a mixture of dense core and pleomorphic‐shaped vesicles. The present study also identified the cells of origin of two additional projections to the basilar pons: one from cells in the external cuneate nucleus and another from neurons of the medullary reticular formation.