MODULATION OF STRIATAL ASPARTATE AND DYNORPHIN-B RELEASE BY CHOLECYSTOKININ (CCK-8) STUDIED IN-VIVO WITH MICRODIALYSIS

Citation
Zb. You et al., MODULATION OF STRIATAL ASPARTATE AND DYNORPHIN-B RELEASE BY CHOLECYSTOKININ (CCK-8) STUDIED IN-VIVO WITH MICRODIALYSIS, NeuroReport, 5(17), 1994, pp. 2301-2304
Citations number
25
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
09594965
Volume
5
Issue
17
Year of publication
1994
Pages
2301 - 2304
Database
ISI
SICI code
0959-4965(1994)5:17<2301:MOSAAD>2.0.ZU;2-W
Abstract
SULPHATED cholecystokinin-8 (CCK-8) given into the neostriatum of the rat by in vivo microdialysis produced a concentration-dependent (1-100 mu M) increase in extracellular aspartate (Asp) and dynorphin B (Dyn B), but not in glutamate, GABA or dopamine levels. The increase in Asp levels produced by 10 mu M CCK-8 was similar to 10 fold and was inhib ited (similar to 50%) by the CCKB antagonist L-365,260 (20 mg kg(-1) i .p.), while the increase in Dyn B (similar to 2 fold) was totally abol ished. Both increases were inhibited (similar to 50%) by local infusio n of 10 mu M of tetrodotoxin (TTX). Thus, CCK exerts modulatory effect s in the basal ganglia, possibly by interacting with local neostriatal neurones releasing Asp, and with Dyn B-containing neurones projecting to the pars reticulata of the substantia nigra.