This is an application for an ADAMHA Research Scientist Award. A program of research is proposed for characterizing the behavioral effects of two types of drugs of major clinical, social, and theoretical importance: opioids, which have long represented a significant abuse problem, and caffeine, which is the most widely consumed behaviorally-active compound in this country. A theme central to the entire research program is that through systematic and comprehensive behavioral studies it will be possible to characterize the bases of drug actions at the neuronal level. Representative opioid alkaloids--agonists, agonist/antagonists, and antagonists--will be studied in several behavioral procedures, notably, drug discrimination, food-reinforced operant responding (punishment paradigm), and locomotor activity, and in at least two animal species, rat and squirrel monkey for optimal assessment of the generality of experimental findings. Emphasis will be placed on clarifying the role of endogenous opioid peptides in the diverseness of the behavioral effects of opioid alkaloids. Behavioral effects of peptides will be determined after central administration, their effects compared to those of prototypic alkaloids, and interactions studied between peptides administered centrally and alkaloids administered systemically. The effects of chronic caffeine administration will be characterized by an integrated behavioral and neurochemical approach. Most studies will be performed on rats receiving caffeine daily by scheduled access to water bottles containing the drug. Matched controls will receive drug-free tap water. Rate and extent of tolerance development, and time course for loss of tolerance to caffeine-induced stimulation of motor activity will be determined as a function of daily drug dosage. Pharmacologic (i.e., alkylxanthine and nonxanthine drugs) and behavioral (i.e., food-reinforced operant responding) variables in tolerance to caffeine will also be assessed. Changes in various measures of the functional state of brain catecholamine and adenosine systems will be determined in parallel with the behavioral changes as a first step toward identifying the cellular mechanisms that underlie tolerance to caffeine.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Scientist Award (K05)
Project #
5K05DA000008-12
Application #
3075291
Study Section
Drug Abuse Clinical and Behavioral Research Review Committee (DACB)
Project Start
1975-09-01
Project End
1990-08-31
Budget Start
1986-09-01
Budget End
1987-08-31
Support Year
12
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Emory University
Department
Type
Schools of Medicine
DUNS #
042250712
City
Atlanta
State
GA
Country
United States
Zip Code
30322
White, David A; Michaels, Clifford C; Holtzman, Stephen G (2008) Periadolescent male but not female rats have higher motor activity in response to morphine than do adult rats. Pharmacol Biochem Behav 89:188-99
White, David A; Ballard, Michael E; Harmon, Alvin C et al. (2008) Acute delta- and kappa-opioid agonist pretreatment potentiates opioid antagonist-induced suppression of water consumption. Brain Res Bull 76:597-604
Michaels, Clifford C; Holtzman, Stephen G (2007) Enhanced sensitivity to naltrexone-induced drinking suppression of fluid intake and sucrose consumption in maternally separated rats. Pharmacol Biochem Behav 86:784-96
Michaels, Clifford C; Easterling, Keith W; Holtzman, Stephen G (2007) Maternal separation alters ICSS responding in adult male and female rats, but morphine and naltrexone have little affect on that behavior. Brain Res Bull 73:310-8
White, David A; Kalinichev, Mikhail; Holtzman, Stephen G (2007) Locomotor response to novelty as a predictor of reactivity to aversive stimuli in the rat. Brain Res 1149:141-8
Michaels, Clifford C; Holtzman, Stephen G (2006) Neonatal stress and litter composition alter sucrose intake in both rat dam and offspring. Physiol Behav 89:735-41
White, David A; Hwang, M Lisa; Holtzman, Stephen G (2005) Naltrexone-induced conditioned place aversion following a single dose of morphine in the rat. Pharmacol Biochem Behav 81:451-8
White, David A; Holtzman, Stephen G (2005) Periadolescent morphine exposure alters subsequent behavioral sensitivity to morphine in adult rats. Eur J Pharmacol 528:119-23
White, David A; Holtzman, Stephen G (2005) Discriminative stimulus effects of acute morphine followed by naltrexone in the squirrel monkey: a further characterization. J Pharmacol Exp Ther 314:374-82
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

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