Elsevier

Neuropharmacology

Volume 24, Issue 9, September 1985, Pages 823-829
Neuropharmacology

Time course of the development of the enhanced behavioral and biochemical responses to amphetamine after pretreatment with amphetamine

https://doi.org/10.1016/0028-3908(85)90032-2Get rights and content

Abstract

These experiments were designed to examine the time course of development of the enhanced stereotyped behavioral response to amphetamine after withdrawal from chronic pretreatment with amphetamine and to determine whether this time course correlates with that of the enhancement in the amphetamine-induced stimulation of the release of dopamine (DA) from striatal slices. Rats were pretreated with amphetamine (5 mg/kg, i.p.) or saline, twice daily for 5 consecutive days. At 3, 15 and 30 days after withdrawal of the drug the stereotyped behavioral response and the release of endogenous DA from slices of striatum in response to a challenge dose of amphetamine were measured. At all 3 times tested, the stereotyped behavioral response to the challenge dose of amphetamine was enhanced in the rats pretreated with amphetamine, with the greatest degree of enhancement seen at 15 and 30 days after withdrawal of the drug. At these times, the responses were associated with a significant attenuation in the stimulation of locomotor activity produced by the challenge dose of amphetamine, which was probably related to the enhanced stereotyped behavioral response. Amphetamine stimulated the release of endogenous DA from slices of striatum in rats pretreated with saline and amphetamine. However, the release of endogenous DA from slices of rats pretreated with amphetamine was significantly greater than that of saline-pretreated rats at 15 and 30 days after withdrawal of the drug, but not at 3 days after withdrawal. Thus, pretreatment with amphetamine resulted in enhanced behavioral and biochemical responses to amphetamine which increased over time after withdrawal of the drug. These results suggest that the enhanced behavioral response to amphetamine may be due to increased sensitivity of dopaminergic neurons in the striatum to the releasing actions of amphetamine.

References (40)

  • L.R. Steranka et al.

    Long-term effects of continuous exposure to amphetamine on brain dopamine concentration and synaptosomal uptake in mice

    Eur. J. Pharmac.

    (1980)
  • D. Young et al.

    Paranoid psychosis in narcolepsy and the possible danger of benzedrine treatment

    Med. clin. North Am.

    (1938)
  • E.G. Arnold et al.

    The release of endogenous norepinephrine and dopamine from cerebral cortex by amphetamine

    J. Pharmac. exp. Ther.

    (1977)
  • P.H. Connell

    Amphetamine Psychosis

    (1958)
  • P.G. Conway et al.

    Role of striatal dopaminergic receptor in amphetamine-induced behavioral facilitation

    J. Pharmac. exp. Ther.

    (1982)
  • I. Creese et al.

    Amphetamine response after dopamine neuron destruction

    Nature, New Biol.

    (1972)
  • E. Ellinwood et al.

    Stimulant abuse in man, The use of animal models to assess and predict behavioral toxicity

  • A.M. Ernst et al.

    Site of action of dopamine and apomorphine in compulsive gnawing behaviour in rats

    Experientia

    (1966)
  • L.J. Felice et al.

    Determination of catecholamines in rat brain parts by reverse-phase ion-pair liquid chromatography

    J. Neurochem.

    (1978)
  • J.F. Fischer et al.

    Chemical release of dopamine from striatal homogenates. Evidence for an exchange diffusion model

    J. Pharmac. exp. Ther.

    (1979)
  • Cited by (0)

    View full text