Self-administration of intravenous amphetamine is predicted by individual differences in sucrose feeding in rats

Psychopharmacology (Berl). 2000 Jan;148(1):52-8. doi: 10.1007/s002130050024.

Abstract

Rationale: Previous studies have shown that individual differences in oral sucrose consumption are predictive of the psychomotor and dopamine (DA) stimulant properties of amphetamine in rats.

Objectives: The present experiment was designed to examine the relationship between sucrose feeding and the reinforcing properties of amphetamine using the intravenous (i.v.) drug self-administration paradigm.

Methods: Based on a median split of sucrose intake during a final 1-h feeding test session, male Wistar rats were designated as either low (LSF) or high sucrose feeders (HSF). Acquisition of i. v.-amphetamine self-administration across ten daily 30-min sessions was then assessed. Following acquisition, i.v. self-administration of several doses of amphetamine was similarly tested across daily 30-min sessions.

Results: Data from this experiment revealed augmented responding in HSF compared with LSF during acquisition of amphetamine self-administration. Correspondingly, when given access to different doses of amphetamine, responding was greater in HSF than in LSF across several doses (3 microg and 10 microg per infusion).

Conclusions: These data support the notion that individual differences in oral sucrose consumption are predictive of the reinforcing properties of psychostimulant drugs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amphetamine / administration & dosage
  • Amphetamine / pharmacology*
  • Analysis of Variance
  • Animals
  • Dopamine Uptake Inhibitors / administration & dosage
  • Dopamine Uptake Inhibitors / pharmacology*
  • Dose-Response Relationship, Drug
  • Infusions, Intravenous
  • Mice
  • Psychomotor Performance / drug effects
  • Rats
  • Rats, Wistar
  • Reinforcement, Psychology
  • Self Administration*
  • Sucrose / administration & dosage*

Substances

  • Dopamine Uptake Inhibitors
  • Sucrose
  • Amphetamine