The roles of specific dopamine (DA) receptors in the behavioral effects of cocaine, including its psychomotor stimulant and subjective interoceptive, and reinforcing effects have been investigated. Using DA receptor knockout mice along with relatively selective DA antagonists we assessed the roles of dopamine receptors in various behavioral effects of cocaine.? The effects on learned operant behavior of agonist actions at dopamine D1-like receptors have not been fully characterized. We compared three D1-like receptor agonists (SKF 38393, SKF 77434 and SKF 82958), both alone and in combination with the D1-like receptor antagonist, SCH 23390. Lever pressing was maintained by food reinforcement under a fixed-ratio 30-response schedule (each thirtieth response produced reinforcement), and the effects of the three agonists were assessed by cumulative dosing. Each drug produced dose-related reductions in response rates, in order of potency: SKF 82958 > SKF 77434 > SKF 38393. Antagonism of these behavioral effects by SCH 23390 was only significant for SKF 82958; surprisingly, SCH 23390 enhanced the effects of SKF 38393. For SKF 82958, the antagonism was receptor subtype-specific, since the D2-like receptor antagonist spiperone was ineffective. The non-selective serotonergic antagonist metergoline produced a significant rightward shift of the SKF 38393 dose-response function, indicating effective antagonism, although the degree of antagonism was not dose-related. These results support the view that the behavioral effects of D1-like receptor agonists differ in their susceptibility to antagonism by D1-like receptor antagonists, and that some effects of SKF 38393 are mediated by serotonergic activity rather than by activity at D1-like receptors.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Intramural Research (Z01)
Project #
1Z01DA000105-17
Application #
7320789
Study Section
(MDRB)
Project Start
Project End
Budget Start
Budget End
Support Year
17
Fiscal Year
2006
Total Cost
Indirect Cost
Name
National Institute on Drug Abuse
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Tanda, Gianluigi; Katz, Jonathan L (2007) Muscarinic preferential M(1) receptor antagonists enhance the discriminative-stimulus effects of cocaine in rats. Pharmacol Biochem Behav 87:400-4
Katz, Jonathan L; Kopajtic, Theresa A; Terry, Philip (2006) Effects of dopamine D1-like receptor agonists on food-maintained operant behavior in rats. Behav Pharmacol 17:303-9
Desai, Rajeev I; Terry, Philip; Katz, Jonathan L (2005) A comparison of the locomotor stimulant effects of D1-like receptor agonists in mice. Pharmacol Biochem Behav 81:843-8
Katz, Jonathan L; Higgins, Stephen T (2003) The validity of the reinstatement model of craving and relapse to drug use. Psychopharmacology (Berl) 168:21-30
McMillan, Donald E; Katz, Jonathan L (2002) Continuing implications of the early evidence against the drive-reduction hypothesis of the behavioral effects of drugs. Psychopharmacology (Berl) 163:251-64
Chausmer, Allison L; Elmer, Gregory I; Rubinstein, Marcelo et al. (2002) Cocaine-induced locomotor activity and cocaine discrimination in dopamine D2 receptor mutant mice. Psychopharmacology (Berl) 163:54-61
Chausmer, Allison L; Katz, Jonathan L (2002) Comparison of interactions of D1-like agonists, SKF 81297, SKF 82958 and A-77636, with cocaine: locomotor activity and drug discrimination studies in rodents. Psychopharmacology (Berl) 159:145-53
Mead, Andy N; Rocha, Beatriz A; Donovan, David M et al. (2002) Intravenous cocaine induced-activity and behavioural sensitization in norepinephrine-, but not dopamine-transporter knockout mice. Eur J Neurosci 16:514-20
Mead, Andy N; Katz, Jonathan L; Rocha, Beatriz A (2002) Intravenous cocaine-induced activity in A/J and C57BL/6J mice: behavioral sensitization and conditioned activity. Neuropharmacology 42:976-86
Bergman, Jack; Katz, Jonathan L; Miczek, Klaus A (2002) The experimental imperative. Psychopharmacology (Berl) 163:249-50

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