PERIPHERAL AXOTOMY INFLUENCES THE IN-VIVO RELEASE OF CHOLECYSTOKININ IN THE SPINAL-CORD DORSAL HORN - POSSIBLE INVOLVEMENT OF CHOLECYSTOKININ-B RECEPTORS
H. Gustafsson et al., PERIPHERAL AXOTOMY INFLUENCES THE IN-VIVO RELEASE OF CHOLECYSTOKININ IN THE SPINAL-CORD DORSAL HORN - POSSIBLE INVOLVEMENT OF CHOLECYSTOKININ-B RECEPTORS, Brain research, 790(1-2), 1998, pp. 141-150
An increased expression of cholecystokinin (CCK) messenger RNA (mRNA)
as well as CCK-B receptor mRNA in dorsal root ganglion (DRG) cells fol
lowing peripheral axotomy has previously been demonstrated. In the pre
sent in vivo microdialysis study, the effect of unilateral sciatic ner
ve section on basal and potassium-induced release of CCK-like (CCK-LI)
immunoreactivity in the rat dorsal horn was investigated. We also com
pared the effects of the CCK-B receptor antagonist CI988 on basal and
potassium-stimulated CCK-LI release in intact animals and in chronical
ly axotomized rats. Perfusion of the microdialysis probe with KCl (100
mM) induced a more than 6-fold increase of the extracellular level of
CCK-LI in control animals. In contrast, following unilateral sciatic
nerve section the same KCl stimulation failed to evoke a release of CC
K-LI ipsilaterally. However, after systemic administration of CI988 (1
mg kg(-1), i.v.), 100 mM KCl induced a significant increase of the ex
tracellular CCK-LI level in axotomized rats, similar to that observed
in control animals. In control animals no effect of CI988 on KCl-stimu
lated CCK-LI release could be detected. CI988 by itself had no influen
ce on the extracellular CCK-LI level in either nerve injured or contro
l animals. The present data suggest that axotomy reduces the release o
f CCK-Like immunoreactivity in the spinal cord by a mechanism involvin
g the CCK-B receptor binding site. (C) 1998 Elsevier Science B.V.