Exogenous cholecystokinin (CCK) reduces neonatal rat brain opioid receptor density and CCK levels.

Abstract:

:Newborn rats were given saline or cholecystokinin8 (CCK8) (5 micrograms/kg, twice daily) i.p. for 3 weeks. On day 21, effects on brain development were assessed. CCK-like immunoreactivity was measured in 7 brain regions; a small (12-18%) but significant decrease in endogenous levels of this peptide was detected in cerebral cortex, medulla and pons of the CCK-treated rats. Morphometric measurements revealed a slight reduction in thickness of most cerebral cortical sections within the CCK-treated group. The area of a midsagittal section of the cerebellum was unchanged except for the Purkinje/granule cell layer, which was smaller in CCK-treated animals. Levels of mu-, delta- and kappa-opioid receptors were estimated by homologous displacement binding assays using selective radioligands. The CCK treatment resulted in a significant decrease in levels of mu- (11%) and delta- (13%)-sites in the cerebral cortex. Neither binding affinities nor kappa-receptor densities were altered. Other animals received the same treatment regimens for 21 days and were maintained for an additional 29 days without treatment; these rats had reductions only in cortical mu-sites (15%). Chronic intraventricular administration of CCK (0.1 microgram/h) to adult rats did not elicit a similar down-regulation of cortical mu or delta receptors, suggesting that the effects observed in neonates reflected developmental processes.

journal_name

Brain Res

journal_title

Brain research

authors

Johnson FE,Hudd C,LaRegina MC,Beinfeld MC,Tolbert DL,Spain JW,Szucs M,Coscia CJ

doi

10.1016/0165-3806(87)90147-7

subject

Has Abstract

pub_date

1987-03-01 00:00:00

pages

139-46

issue

1

eissn

0006-8993

issn

1872-6240

journal_volume

429

pub_type

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