In vivo studies on the enhancement of cholecystokinin release in the rat striatum by dopamine depletion

Brain Res. 1989 Dec 25;505(1):119-22. doi: 10.1016/0006-8993(89)90121-2.

Abstract

The release of cholecystokinin-8-like (CCK) immunoreactivity from the rat striatum has been studied in vivo using brain microdialysis. A basal efflux of CCK-like immunoreactivity was not detectable in the majority of experiments. Intrastriatal infusion of veratrine (100 micrograms/ml) increased striatal dialysate levels of CCK-like immunoreactivity above detection limits, representing an overflow into the interstitial fluid. High concentrations of potassium caused similar but less consistent effects. Extracellular dopamine depletion using alpha-methyl-p-tyrosine or reserpine also increased the dialysate content of CCK-like immunoreactivity. In contrast, inhibition of peptidases reported to hydrolyse CCK in vitro did not affect either basal or evoked efflux of CCK-like immunoreactivity. These data demonstrate that CCK-like immunoreactivity may be released from neuronal elements within the striatum by depolarizing stimuli in vivo, and suggest that increased overflow of CCK-like immunoreactivity is associated with dopamine depletion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Corpus Striatum / drug effects
  • Corpus Striatum / metabolism*
  • Dopamine / metabolism
  • Dopamine / physiology*
  • Methyltyrosines / pharmacology
  • Rats
  • Rats, Inbred Strains
  • Reserpine / pharmacology
  • Sincalide / metabolism*
  • Veratridine / pharmacology
  • alpha-Methyltyrosine

Substances

  • Methyltyrosines
  • alpha-Methyltyrosine
  • Veratridine
  • Reserpine
  • Sincalide
  • Dopamine