The objectives of the proposed research are to study and identify factors that control drug reinforced behavior. The methodology and principles of operant conditioning will be used. The studies will be limited to drugs that are taken orally and that function as positive reinforcers. Subjects will be rhesus monkeys, rats, and mice. In the upcoming years the principal focus will be on variables that control drug reinforced behavior such as reinforcement schedules, food deprivation, and alternative reinforcers. Genetic factors, specifically strain differences, will be studied. Consequences of drug taking behavior (tolerance and physiological dependence) will also be examined within a context whereby the drug is taken by mouth and functions as a reinforcer. Special emphasis will be given to systematically studying variables over a range of values, and interactions among variables will be parametically explored. For example, the effects of fixed-ratio size will be examined using a broad range of drug concentrations. These studies will build upon an infrahuman model of oral drug dependence that we have developed in this laboratory. The proposed studies will provide an organized group of findings that will complement and extend results obtained by others using the intravenous route. These types of laboratory studies of drug taking behavior will contribute to a systematized body of knowledge that will aid in the analysis of the complicated problem of human drug dependence.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA000944-11
Application #
3206840
Study Section
(SRC)
Project Start
1985-02-01
Project End
1989-01-31
Budget Start
1986-09-01
Budget End
1988-01-31
Support Year
11
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Type
Schools of Medicine
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Meisch, R A; Stewart, R B (1995) Relative reinforcing effects of different doses of orally delivered cocaine. Drug Alcohol Depend 37:141-7
Beardsley, P M; Lemaire, G A; Meisch, R A (1993) Persistence of ethanol self-administration as a function of interreinforcer interval and concentration. Drug Alcohol Depend 34:71-81
Suzuki, T; Koike, Y; Yanaura, S et al. (1992) Sex differences in physical dependence on pentobarbital in four inbred strains of rats. Gen Pharmacol 23:487-92
Meisch, R A; Lemaire, G A; Cutrell, E B (1992) Oral self-administration of pentobarbital by rhesus monkeys: relative reinforcing effects under concurrent signalled differential-reinforcement-of-low-rates schedules. Drug Alcohol Depend 30:215-25
George, F R (1991) Is there a common biological basis for reinforcement from alcohol and other drugs? J Addict Dis 10:127-39
Meisch, R A (1991) Establishment of drug discrimination and drug reinforcement in different animal strains: some methodological issues. J Addict Dis 10:179-87
George, F R; Elmer, G I; Meisch, R A et al. (1991) Orally delivered cocaine functions as a positive reinforcer in C57BL/6J mice. Pharmacol Biochem Behav 38:897-903
Meisch, R A; Lemaire, G A (1991) Effects of feeding condition on orally delivered ethanol as a reinforcer for rhesus monkeys. Alcohol 8:55-63
Meisch, R A; Lemaire, G A (1990) Reinforcing effects of a pentobarbital-ethanol combination relative to each drug alone. Pharmacol Biochem Behav 35:443-50
George, F R; Meisch, R A (1990) Cyclooxygenase inhibitors antagonize the rate-depressant effects of ethanol on fixed-ratio responding. Alcohol 7:355-60

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