It is well established that the repeated administration of stimulant drugs (e.g. amphetamine) results in a progressively enhanced behavioral response to subsequent injections. This phenomenon of 'reverse tolerance', or sensitization, has generated considerable interest because it is thought to provide an animal analogue of amphetamine (AMPH) psychosis in humans. However, a single injection of AMPH may also produce a long-lasting change in brain activity. In preliminary studies using AMPH-induced rotational behavior as an index of mesostriatal dopamine (DA) activity we found that a single injection of a low dose (1.25 mg/kg) of AMPH greatly enhanced the rotational behavior produced by a second injection of AMPH given 3-4 weeks later in intact female, ovariectomized female and castrated male rats. Intact males did not show as robust a change. This behavioral sensitization may be due to changes in DA release, since it is accompanied by a long-lasting enhancement in AMPH-stimulated endogenous DA release from striatal tissue in vitro. The studies proposed here are disigned to: (1) further characterize the phenomenon of long-term changes in rotational behavior produced by a single or repeated injections of AMPH: (2) examine the role of gonadal steroid hormones in modulating this form of neural plasticity; (3) further explore the possibility that long-lasting changes in DA release from terminals in a variety of brain regions are involved in the development of behavioral sensitization; (4) determine whether similar long-lasting changes in brain activity are produced by other stimulant drugs; and (5) determine whether a single injection of AMPH will produce comparable changes in other behaviors thought to be mediated by brain DA systems. We believe the proposed studies integrating both in vivo and in vitro approaches will increase our understanding of the basic neurobiological mechanisms involved in neuroplasticity. The studies are of clinical interest since they may provide some insight as to the neurochemical changes underlying AMPH psychosis. Lastly, the fact that the single administration of psychostimulant drugs may result in long-term physiological alterations should be of obvious practical concern in psychotherapeutics.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Modified Research Career Development Award (K04)
Project #
5K04NS000844-02
Application #
3074711
Study Section
Biopsychology Study Section (BPO)
Project Start
1984-06-01
Project End
1989-05-31
Budget Start
1985-06-01
Budget End
1986-05-31
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
Schools of Arts and Sciences
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Robinson, T E; Yew, J; Paulson, P E et al. (1990) The long-term effects of neurotoxic doses of methamphetamine on the extracellular concentration of dopamine measured with microdialysis in striatum. Neurosci Lett 110:193-8
Robinson, T E; Camp, D M (1990) Does amphetamine preferentially increase the extracellular concentration of dopamine in the mesolimbic system of freely moving rats? Neuropsychopharmacology 3:163-73
Robinson, T E; Whishaw, I Q (1988) Normalization of extracellular dopamine in striatum following recovery from a partial unilateral 6-OHDA lesion of the substantia nigra: a microdialysis study in freely moving rats. Brain Res 450:209-24
Robinson, T E; Jurson, P A; Bennett, J A et al. (1988) Persistent sensitization of dopamine neurotransmission in ventral striatum (nucleus accumbens) produced by prior experience with (+)-amphetamine: a microdialysis study in freely moving rats. Brain Res 462:211-22
Becker, J B; Adams, F; Robinson, T E (1988) Intraventricular microdialysis: a new method for determining monoamine metabolite concentrations in the cerebrospinal fluid of freely moving rats. J Neurosci Methods 24:259-69
Camp, D M; Robinson, T E (1988) Susceptibility to sensitization. II. The influence of gonadal hormones on enduring changes in brain monoamines and behavior produced by the repeated administration of D-amphetamine or restraint stress. Behav Brain Res 30:69-88
Camp, D M; Robinson, T E (1988) Susceptibility to sensitization. I. Sex differences in the enduring effects of chronic D-amphetamine treatment on locomotion, stereotyped behavior and brain monoamines. Behav Brain Res 30:55-68
Castaneda, E; Becker, J B; Robinson, T E (1988) The long-term effects of repeated amphetamine treatment in vivo on amphetamine, KCl and electrical stimulation evoked striatal dopamine release in vitro. Life Sci 42:2447-56
Robinson, T E; Camp, D M (1987) Long-lasting effects of escalating doses of d-amphetamine on brain monoamines, amphetamine-induced stereotyped behavior and spontaneous nocturnal locomotion. Pharmacol Biochem Behav 26:821-7
Robinson, T E; Becker, J B; Young, E A et al. (1987) The effects of footshock stress on regional brain dopamine metabolism and pituitary beta-endorphin release in rats previously sensitized to amphetamine. Neuropharmacology 26:679-91

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