PERIPHERAL AXOTOMY INFLUENCES THE IN-VIVO RELEASE OF CHOLECYSTOKININ IN THE SPINAL-CORD DORSAL HORN - POSSIBLE INVOLVEMENT OF CHOLECYSTOKININ-B RECEPTORS

Citation
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
Citations number
66
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
00068993
Volume
790
Issue
1-2
Year of publication
1998
Pages
141 - 150
Database
ISI
SICI code
0006-8993(1998)790:1-2<141:PAITIR>2.0.ZU;2-O
Abstract
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.