Antagonism of the anticonflict effects of chlordiazepoxide by beta-carboline carboxylic acid ethyl ester, Ro 15-1788 and ACTH(4--10)

Psychopharmacology (Berl). 1982;78(3):256-60. doi: 10.1007/BF00428161.

Abstract

The antagonism of the anticonflict effect of chlordiazepoxide (CDP) by beta-carboline carboxylic acid ethyl ester (BCCE), Ro 15-1788 and ACTH(4--10) has been evaluated in the Geller-Seifter rat conflict test in which CDP increases punished (conflict), but not unpunished responding. BCCE (0.5--10 micrograms ICV) produced a dose-dependent reduction in the anticonflict activity of CDP. This was also significantly reduced by Ro 15-1788 (25 mg/kg IP) and a high dose of ACTH(4--10) (5 micrograms ICV). None of these test compounds had a marked direct effect on punished or unpunished responding in the dose used. These experiments provide further physiological support for the suggestion from binding studies that BCCE and Ro 15-1788 act on benzodiazepine receptors. However, the ability of ACTH(4--10) to reduce the anticonflict effect of CDP may be by some other, possibly opioid, mechanism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenocorticotropic Hormone / pharmacology*
  • Animals
  • Arousal / drug effects*
  • Benzodiazepinones / pharmacology*
  • Carbolines / pharmacology*
  • Chlordiazepoxide / antagonists & inhibitors*
  • Chlordiazepoxide / pharmacology
  • Conditioning, Operant / drug effects
  • Conflict, Psychological*
  • Fear / drug effects
  • Flumazenil
  • Indoles / pharmacology*
  • Male
  • Muridae
  • Peptide Fragments / pharmacology*
  • Receptors, Cell Surface / drug effects
  • Receptors, GABA-A
  • Reinforcement Schedule

Substances

  • Benzodiazepinones
  • Carbolines
  • Indoles
  • Peptide Fragments
  • Receptors, Cell Surface
  • Receptors, GABA-A
  • Flumazenil
  • Chlordiazepoxide
  • beta-carboline-3-carboxylic acid ethyl ester
  • Adrenocorticotropic Hormone
  • ACTH (4-10)