Investigations of the neuronal mechanisms of drug actions are necessary for discerning the neurobiological basis of euphoria and drug abuse. Many abused pharmacological agents have several commonalities, including self-administration by non-humans in experimental settings, discriminative stimulus properties that can result in state-dependent learning and the disruption of schedule-controlled behavior. Many studies that have investigated neuronal activity mediating drug reinforcement have used self-administration procedures. Selective dopaminergic or noradrenergic neurotoxin lesions of the nucleus accumbens by receptor antagonists delivered into this area influenced responding maintained by both stimulant and opiate self-administration. However, the changes reported in drug intake and the rate of responding do not necessarily indicate a change in the reinforcing efficacy of a drug. This research project proposes investigations of the involvement of several neurotransmitter systems in the behavioral mechanisms of action of cocaine and d-amphetamine. The behavioral effects of four specific neurotoxin lesions of the nucleus accumbens that destroy either dopaminergic, noradrenergic, serotonergic, or intrinsic and efferent fibers will be studied. Intracranial injections of reversible gamma aminobutyric acid, dopamine, 5-hydroxytryptamine and opiate receptor antagonists delivered directly into the nucleus accumbens will also be used to delineate the neurobiological substrates of the behavioral effects of cocaine and heroin. The behavioral mechanisms that will be investigated include alteration of schedule-controlled behavior, changes in discriminative stimulus properties, and a dose-preference procedure which provides rate-free measure of reinforcing efficacy. These studies will determine the involvement of several neuronal systems located in the nucleus accumbens in modulating the behavioral effects of drugs, thus providing information on the neurobiological basis of these effects.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA003631-02
Application #
3208175
Study Section
Drug Abuse Clinical and Behavioral Research Review Committee (DACB)
Project Start
1985-01-01
Project End
1987-12-31
Budget Start
1986-01-01
Budget End
1986-12-31
Support Year
2
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Louisiana State University Hsc Shreveport
Department
Type
Schools of Medicine
DUNS #
City
Shreveport
State
LA
Country
United States
Zip Code
71103
Dworkin, S I; Smith, J E (1991) Mechanisms of reinforcement and their relation to future developments in pharmacotherapy. Alcohol Alcohol Suppl 1:39-47
Dworkin, S I; Smith, J E (1988) Neurobehavioral pharmacology of cocaine. NIDA Res Monogr 88:185-98
Dworkin, S I; Goeders, N E; Grabowski, J et al. (1987) The effects of 12-hour limited access to cocaine: reduction in drug intake and mortality. NIDA Res Monogr 76:221-5
Goeders, N E; Dworkin, S I (1987) Effects of chlordiazepoxide on intravenous cocaine self-administration in rats. NIDA Res Monogr 76:240-7
Dworkin, S I; Smith, J E (1986) Behavioral contingencies involved in drug-induced neurotransmitter turnover changes. NIDA Res Monogr 74:90-106
Dworkin, S I; Goeders, N E; Smith, J E (1986) The reinforcing and rate effects of intracranial dopamine administration. NIDA Res Monogr 67:242-8