Caffeine is the most widely consumed behaviorally active drug in the world. Because it has the principal features usually associated with a drug of abuse, caffeine can be a convenient model drug for studying the behavioral and cellular mechanisms of drug reinforcement and related phenomena, such a tolerance and physical dependence. The broad objectives of this project have been to define and quantify effects of acute and chronic treatment wit caffeine at the behavioral and cellular levels. The following specific aim represent a continuation of established lines of investigation as well as new research approaches suggested by recent findings. 1) To test the hypothesis that some behavioral effects of caffeine are due to enhanced postsynaptic dopaminergic mechanism resulting from blockade of adenosine receptors; continuous blockade of adenosine receptors results in a compensatory desensitization of those dopaminergic mechanism and caffeine tolerance. This hypothesis will be tested in rats using the behavioral measures of locomotor activity and unilateral rotation and by in vitro and in vivo measures of postsynaptic dopamine receptor function. 2) To continu to characterize pharmacologically in rats the qualitative differences between the discriminative effects of low and high doses of caffeine and th ability of caffeine to elevate the reinforcement threshold for intracranial self-stimulation. Experiments will be directed at determining the neurochemical bases of those effects and their relevancy to the positive an negative mood states induced by caffeine in humans. 3) To test the hypothesis that caffeine has potent and previously uncharacterized effects on cyclic AMP metabolism and intracellular Ca2+ stores, that these effects are not mediated by blockade of cell-surface adenosine receptors, and that tolerance develops to these effects. Experiments will be performed on a model cell line of CNS origin, the NG108-15 neuroblastome x glioma hybrid cell line, in order to define more clearly these cellular effects of caffeine. Despite the fact that caffeine usually is consumed on a chronic daily basis, there have been relatively few studies of the behavioral and neurochemical consequences of chronic treatment with caffeine. Basic information obtained on the acute and chronic behavioral and cellular actions of caffeine should have broad applicability to many types of drugs of abuse.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
2R01DA003413-09
Application #
3207898
Study Section
Drug Abuse Clinical and Behavioral Research Review Committee (DACB)
Project Start
1984-07-01
Project End
1997-06-30
Budget Start
1992-07-15
Budget End
1993-06-30
Support Year
9
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Emory University
Department
Type
Schools of Medicine
DUNS #
042250712
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Jain, Raka; Holtzman, Stephen G (2005) Caffeine induces differential cross tolerance to the amphetamine-like discriminative stimulus effects of dopaminergic agonists. Brain Res Bull 65:415-21
Powell, K R; Iuvone, P M; Holtzman, S G (2001) The role of dopamine in the locomotor stimulant effects and tolerance to these effects of caffeine. Pharmacol Biochem Behav 69:59-70
Holtzman, S G (1999) Discriminative effects of CGS 15943, a competitive adenosine receptor antagonist, have a dopamine component in monkeys. Eur J Pharmacol 376:7-15
Powell, K R; Holtzman, S G (1998) Lack of NMDA receptor involvement in caffeine-induced locomotor stimulation and tolerance in rats. Pharmacol Biochem Behav 59:433-8
Easterling, K W; Holtzman, S G (1997) Parametric changes in response equilibrium during an intra-cranial self stimulation (ICSS) task: can reward value be assessed independently of absolute threshold? Neurosci Biobehav Rev 21:55-65
Holtzman, S G (1996) Discriminative effects of CGS 15943, a competitive adenosine receptor antagonist, in monkeys: comparison to methylxanthines. J Pharmacol Exp Ther 277:739-46
Garrett, B E; Holtzman, S G (1996) Comparison of the effects of prototypical behavioral stimulants on locomotor activity and rotational behavior in rats. Pharmacol Biochem Behav 54:469-77
(1996) Caffeine: a model drug of abuse. NIDA Res Monogr 162:73-5
Garrett, B E; Holtzman, S G (1995) Does adenosine receptor blockade mediate caffeine-induced rotational behavior? J Pharmacol Exp Ther 274:207-14
Garrett, B E; Holtzman, S G (1994) Caffeine cross-tolerance to selective dopamine D1 and D2 receptor agonists but not to their synergistic interaction. Eur J Pharmacol 262:65-75

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