SYNAPTIC PLASTICITY OF 5-HYDROXYTRYPTAMINE-IMMUNOREACTIVE TERMINALS IN THE PHRENIC NUCLEUS FOLLOWING SPINAL-CORD INJURY - A QUANTITATIVE ELECTRON-MICROSCOPIC ANALYSIS
Q. Tai et al., SYNAPTIC PLASTICITY OF 5-HYDROXYTRYPTAMINE-IMMUNOREACTIVE TERMINALS IN THE PHRENIC NUCLEUS FOLLOWING SPINAL-CORD INJURY - A QUANTITATIVE ELECTRON-MICROSCOPIC ANALYSIS, Journal of comparative neurology, 386(4), 1997, pp. 613-624
The present study was conducted to examine the plasticity of 5-hydroxy
tryptamine (5-HT)-immunoreactive terminals in the rat phrenic nucleus
following an ipsilateral C2 spinal cord hemisection and 30-day surviva
l period. A retrograde horseradish peroxidase (HRP) labeling technique
was used to identify the phrenic motoneurons at the electron microsco
pic (EM) level. After employing a pre-embedding immunocytochemical tec
hnique, the ultrastructural characteristics of 5-HT-immunoreactive ter
minals were qualitatively and then quantitatively analyzed with a comp
uterized morphometric system before and after injury in separate group
s of rats. The results indicated that the majority of the 5-HT-labeled
terminals formed axodendritic contacts, but some 5-HT-labeled termina
ls made axosomatic contacts. 5-HT terminals were associated with eithe
r asymmetrical or symmetrical synapses, and some displayed postsynapti
c dense bodies. Approximately 2% of the 5-HT terminals had dense-core
vesicles. Although the total number of labeled and unlabeled terminals
in the phrenic nucleus was reduced after hemisection, the number of 5
-HT terminals in the hemisected group was greater than that of the con
trol group. Moreover, the total number and length of asymmetrical and
symmetrical synaptic active zones per 5-HT terminal were significantly
greater after injury. Finally, the total number of 5-HT terminals wit
h multiple synapses was significantly greater in the hemisected group
as compared to controls. It is possible that 5-HT synaptic plasticity
may be part of the morphological substrate for the unmasking of the la
tent crossed phrenic pathway which mediates recovery of the ipsilatera
l hemidiaphragm paralyzed by C2 spinal cord hemisection. (C) 1997 Wile
y-Liss, Inc.