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Expression of morphine-conditioned hyperactivity is attenuated by naloxone and pimozide
1Department of Psychology, University of Kentucky, Lexington 40506.
Psychopharmacology
|January 1, 1987
Summary
Morphine-induced hyperactivity in rats can be blocked by naloxone and pimozide. Conditioned hyperactivity responses to morphine were also counteracted by naloxone and attenuated by pimozide.
Area of Science:
- Neuropharmacology
- Behavioral Neuroscience
- Addiction Research
Background:
- Morphine, an opiate agonist, can induce hyperactivity.
- Conditioned responses to drugs are a key aspect of addiction.
- Understanding the neurobiological basis of conditioned drug effects is crucial.
Purpose of the Study:
- To investigate whether naloxone and pimozide can attenuate morphine-conditioned hyperactivity.
- To explore the neuropharmacological substrates underlying morphine-induced unconditioned and conditioned hyperactivity.
Main Methods:
- Rats received repeated pairings of morphine (2 mg/kg) with a distinctive environment.
- Unconditioned hyperactivity was assessed after morphine administration.
- Conditioned hyperactivity was measured upon exposure to the environment without morphine.
- The effects of naloxone and pimozide on both unconditioned and conditioned hyperactivity were evaluated.
Main Results:
- Both naloxone and pimozide blocked morphine-induced unconditioned hyperactivity.
- Rats displayed a hyperactive conditioned response (CR) after drug-environment pairings.
- Naloxone (1 mg/kg) counteracted the CR.
- Pimozide attenuated the CR in a dose-dependent manner (0.25–0.4 mg/kg).
Conclusions:
- The findings suggest that similar neuropharmacological mechanisms underlie morphine's unconditioned and conditioned hyperactive effects.
- Dopaminergic pathways, modulated by pimozide, play a role in conditioned hyperactivity.
- Opiate receptor involvement, indicated by naloxone's effects, is also implicated in conditioned responses.