Project Details
Description
DESCRIPTION: (Applicant's Abstract)
The abuse of amphetamine-like psychostimulants is a medical and social
problem throughout the world. The rewarding properties of amphetamine-like
stimulants are linked to the capacity of these drugs to increase
extracellular concentrations of dopamine in the forebrain, notably in the
nucleus accumbens. Despite the advances in our understanding of the
cellular and molecular actions of psychostimulants, effective
pharmacological treatments for amphetamine and cocaine addition remain
elusive. However, several preclinical studies report that calcium channel
antagonists influence psychostimulant self-administration and conditioned
place preference in rodents in a manner similar to dopamine antagonists.
These results suggest that drugs acting on calcium conductances and
associated transduction pathways may be potentially effective therapeutic
agents for treating psychostimulant abuse. Interestingly, repeated
injections of amphetamine-like psychostimulants results in an enhancement in
the ability of these drugs to increase extracellular dopamine in the nucleus
accumbens, and calcium appears to play an important role in this process.
The studies outlined in this proposal will: i)identify the mechanisms that
underlie the influence of calcium and calcium-stimulated kinases on the
enhanced increase in dopamine in the nucleus accumbens of cocaine-pretreated
rats and ii) assess the behavioral relevance of these changes in dopamine
neuronal function. Since the enhanced increase in dopamine in the nucleus
accumbens is observed in both rats that self-administer or receive daily
systemic injections of cocaine, the identification of novel mechanisms
underlying this neurochemical adaptation to repeated cocaine may have direct
clinical significance. Thus, by outlining the role of calcium in the
cellular and molecular effects of psychostimulant drugs, the results of the
experiments outlined in this proposal could guide the development of novel
treatment strategies for amphetamine and cocaine addiction.
Status | Finished |
---|---|
Effective start/end date | 10/2/97 → 10/31/99 |
Funding
- National Institute on Drug Abuse
ASJC
- Psychiatry and Mental health
- Neuroscience(all)
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