The effects of cocaine, amphetamine, and the dopamine D1 receptor agonist SKF 38393 on fear extinction as measured with potentiated startle: implications for psychomotor stimulant psychosis

Behav Neurosci. 1998 Aug;112(4):952-65. doi: 10.1037//0735-7044.112.4.952.

Abstract

Using Pavlovian conditioned increases in the amplitude of the acoustic startle reflex as a behavioral indicator of fear motivation, the authors previously showed a resistance to extinction after repeated associations of cocaine with the fear-evoking conditioned stimulus (CS). In Experiment 1, acute administration of cocaine, amphetamine, and the dopamine (DA) D1 receptor agonist SKF 38393 produced a similar fear enhancement. In Experiment 2, a noncontingent injection of cocaine and SKF 38393 provoked a CS potentiation of acoustic startle in fear-extinguished laboratory rats. Potential behavioral, neurochemical, and neuroendocrine explanations for the effects of psychomotor stimulants on conditional fear were discussed. It was suggested that DA agonist drugs increase fear expression possibly by activating mesoamygdaloid associative neurocircuitry involved in excitatory conditioned fear reactions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine / pharmacology
  • Acoustic Stimulation
  • Analysis of Variance
  • Animals
  • Central Nervous System Stimulants / pharmacology*
  • Cocaine / pharmacology
  • Conditioning, Classical / drug effects*
  • Dextroamphetamine / pharmacology
  • Disease Models, Animal
  • Dopamine Agonists / pharmacology*
  • Electroshock
  • Extinction, Psychological / drug effects*
  • Fear / drug effects*
  • Male
  • Motor Activity / drug effects
  • Psychoses, Substance-Induced / physiopathology*
  • Rats
  • Rats, Wistar
  • Reflex, Startle / drug effects

Substances

  • Central Nervous System Stimulants
  • Dopamine Agonists
  • 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine
  • Cocaine
  • Dextroamphetamine