Behavioral effects of psychomotor stimulants in rats with dorsal or ventral subiculum lesions: locomotion, cocaine self-administration, and prepulse inhibition of startle

Behav Neurosci. 2001 Aug;115(4):880-94. doi: 10.1037//0735-7044.115.4.880.

Abstract

Compelling evidence suggests a primary role for the mesoaccumbens dopaminergic pathway in the behavioral effects of amphetamine and cocaine, but the roles of other projections to the accumbens, including those arising in the hippocampal formation, are less clear. The authors evaluated the effects of discrete excitotoxic lesions of either the dorsal or ventral subiculum on the locomotor activating, reinforcing, and sensorimotor gating-disruptive effects of psychomotor stimulant drugs. Whereas dorsal subiculum-lesioned rats were hyperactive in tests of exploratory locomotion and startle reactivity, ventral subiculum-lesioned rats exhibited an attenuated locomotor response to amphetamine, moderately impaired acquisition of cocaine self-administration, and reduced levels of prepulse inhibition of startle. These 2 behavioral profiles overlap considerably with those previously observed in rats with lesions of the rostrodorsal and caudomedial accumbens, respectively, and suggest that projections from dorsal subiculum to accumbens core and ventral subiculum to accumbens shell exert distinct influences on behavioral responses that are amplified by psychomotor stimulant drugs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amphetamine / pharmacology*
  • Animals
  • Apomorphine / pharmacology*
  • Central Nervous System Stimulants / administration & dosage*
  • Cocaine / administration & dosage*
  • Conditioning, Operant / drug effects
  • Dopamine Agonists / pharmacology*
  • Exploratory Behavior / drug effects
  • Locomotion / drug effects
  • Male
  • Nucleus Accumbens / drug effects*
  • Nucleus Accumbens / pathology
  • Nucleus Accumbens / physiology
  • Rats
  • Rats, Inbred Strains
  • Reflex, Startle / drug effects*

Substances

  • Central Nervous System Stimulants
  • Dopamine Agonists
  • Amphetamine
  • Cocaine
  • Apomorphine