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Antagonism of eegraphic and behavioural effects of methamphetamine by selective receptor blockers (SCH 23390 and raclopride) in the rabbit
- Source :
- Progress in Neuro-Psychopharmacology and Biological Psychiatry. 15:803-815
- Publication Year :
- 1991
- Publisher :
- Elsevier BV, 1991.
-
Abstract
- 1. The interactions between selective D1 and D2 antagonists (SCH 23390 and raclopride) and methamphetamine on EEG arousal and behaviour was studied in rabbits. Haloperidol, a “classic neuroleptic” was used as reference drug. 2. Both 23390 and raclopride, which were used at low dosage (0.03–0.09 mg/kg iv for the former and 1–3 mg/kg for the latter), were able to block completely the behaviour induced but do not inhibit completely the EEG arousal pattern induced by methamphetamine. 3. The blockade of both behaviour and EEG arousal took only when the two drugs were administered concomitantly at the lower dosage. 4. The antagonistic effects obtained with the concomitantly administration of the two drugs were of higher degree in confront of those obtained with the pretreatment with haloperidol 0.3 mg/kg iv. 5. Our data indicate that both D1 and D2 antagonists are able to block, at the dosage used, motor hyperactivity and stereotyped behaviour typically induced by methamphetamine and that SCH 23390 and raclopride are potentiated also in this experimental model.
- Subjects :
- medicine.medical_specialty
Pharmacology
Methamphetamine
chemistry.chemical_compound
Internal medicine
Salicylamides
medicine
Haloperidol
Animals
Cortical Synchronization
Biological Psychiatry
Raclopride
SCH-23390
Behavior, Animal
Receptors, Dopamine D2
Receptors, Dopamine D1
Motor Cortex
Dopamine antagonist
Electroencephalography
Benzazepines
Blockade
Electrophysiology
Endocrinology
Mechanism of action
chemistry
Dopamine Antagonists
Rabbits
Stereotyped Behavior
medicine.symptom
Arousal
medicine.drug
Subjects
Details
- ISSN :
- 02785846
- Volume :
- 15
- Database :
- OpenAIRE
- Journal :
- Progress in Neuro-Psychopharmacology and Biological Psychiatry
- Accession number :
- edsair.doi.dedup.....53c60338c0cdfd5564a45574bae7b1e3