Involvement of cholecystokinin receptors in the control of striatal dopamine autoreceptors

Naunyn Schmiedebergs Arch Pharmacol. 1990 Sep;342(3):300-4. doi: 10.1007/BF00169441.

Abstract

The interaction of locally perfused cholecystokinin-8 (sulphated) with systemically administered apomorphine was studied on the release of dopamine and its metabolites using microdialysis in the neostriatum of the halothane-anaesthetized male rat. Dialysate levels of dopamine, 3,4-dihydroxyphenylacetic acid and homovanillic acid were assayed by high performance liquid chromatography in combination with electrochemical detection. Perfusion with cholecystokinin-8 (100 microM but not 1 microM or 10 nM) increased the dialysate levels of dopamine without affecting those of DOPAC or HVA. At low concentrations (1 microM and 10 nM but not 1 nM), cholecystokinin-8 counteracted the inhibitory effect of apomorphine (0.05 mg/kg, s.c.) on dopamine release. This counteraction was antagonized by perfusion with the cholecystokinin-8 antagonist proglumide (3 microM). At this concentration, proglumide perfused alone was without effect on basal or apomorphine-reduced levels of dopamine. The results indicate a facilitatory effect of cholecystokinin-8 on dopamine release in rat neostriatum only at high concentrations. At lower concentrations, cholecystokinin-8 appears to modulate dopamine release by an inhibitory effect on dopamine autoreceptors possibly involving an intramembrane interaction between presynaptic cholecystokinin-8 receptors and dopamine autoreceptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3,4-Dihydroxyphenylacetic Acid / metabolism
  • Animals
  • Apomorphine / pharmacology
  • Brain Chemistry / drug effects
  • Corpus Striatum / drug effects
  • Corpus Striatum / metabolism*
  • Dialysis
  • Dopamine / metabolism
  • Homovanillic Acid / metabolism
  • Male
  • Proglumide / pharmacology
  • Rats
  • Rats, Inbred Strains
  • Receptors, Cholecystokinin / physiology*
  • Receptors, Dopamine / metabolism*
  • Sincalide / pharmacology

Substances

  • Receptors, Cholecystokinin
  • Receptors, Dopamine
  • 3,4-Dihydroxyphenylacetic Acid
  • Proglumide
  • Sincalide
  • Apomorphine
  • Dopamine
  • Homovanillic Acid