Opioids comprise a broad range of compounds, from classical morphine-like agonists to pure antagonists. Between those extremes are drugs with varying spectra of agonist and antagonist properties, probably as a consequence of interactions with multiple subtypes of opiate receptors. Abuse potential also varies considerably among the different types of opioids. Experiments are proposed that will continue an ongoing research program aimed at characterizing systematically and comprehensively the behavioral effects of opioids having different spectra of activities in order to identify and study components of drug action relevant to abuse potential, and to gain insights into the neuronal substrates subserving those components of action. Emphasis will be placed on clarifying the role of endogenous opioid peptides in the diverseness of the behavioral effects of opioid antagonists and agonists. Behavioral effects of opioid peptides will be determined following intracerebroventricular (icv) administration, their effects compared to those of prototypic opioid alkaloids, and interactions studied between opioid peptides administered icv and opioid antagonists and agonists administered systemically. Tests will usually be performed in two animal species (rat and squirrel monkey), and in several behavioral procedures in order to assess the generality of experimental findings. Principal studies will include: a) characterizing the discriminative stimulus effects of opioid peptides and their interactions with various opioid antagonists and agonists in animals trained to discriminate saline from prototypic agonists (e.g., morphine, ethylketocyclazocine, SKF 10,047) of proposed receptor subtypes; b) determining if the discrimination of saline from diprenorphine by monkeys is based on stimuli associated with a blockade of endogenous opioid peptide systems; c) assessing the effects of antagonists, agonists and opioid peptides alone and in combination on schedule-controlled behavior (punishment paradigm) in rats and monkeys, and on motor activity in rats. Experiments will also be continued to elucidate the fole of endogenous opioid peptides in the regulation of appetitive behaviors by testing pure opioid antagonists and peptides administered centrally to rats and monkeys.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA000541-13
Application #
3206784
Study Section
Drug Abuse Clinical and Behavioral Research Review Committee (DACB)
Project Start
1975-06-01
Project End
1988-07-31
Budget Start
1986-08-01
Budget End
1987-07-31
Support Year
13
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; 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
Joyce, Andrew R; Easterling, Keith; Holtzman, Stephen G et al. (2006) Modeling the onset of drug dependence: a consideration of the requirement for protein synthesis. J Theor Biol 240:531-7
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
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
Easterling, Keith W; Holtzman, Stephen G (2004) In rats, acute morphine dependence results in antagonist-induced response suppression of intracranial self-stimulation. Psychopharmacology (Berl) 175:287-95
White, David A; Holtzman, Stephen G (2003) Discriminative stimulus effects of acute morphine followed by naltrexone in the squirrel monkey. Psychopharmacology (Berl) 167:203-10
Holtzman, Stephen G (2003) Discrimination of a single dose of morphine followed by naltrexone: substitution of other agonists for morphine and other antagonists for naltrexone in a rat model of acute dependence. J Pharmacol Exp Ther 304:1033-41
Kalinichev, Mikhail; Holtzman, Stephen G (2003) Changes in urination/defecation, auditory startle response, and startle-induced ultrasonic vocalizations in rats undergoing morphine withdrawal: similarities and differences between acute and chronic dependence. J Pharmacol Exp Ther 304:603-9

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