Blockade of the discriminative stimulus effects of DOI by MDL 100,907 and the ‘atypical’ antipsychotics, clozapine and risperidone
- 1 October 1994
- journal article
- research article
- Published by Elsevier in European Journal of Pharmacology
- Vol. 264 (1) , 99-102
- https://doi.org/10.1016/0014-2999(94)90643-2
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- In vivo properties of SB 200646A, a 5‐HT2C/2B receptor antagonistBritish Journal of Pharmacology, 1994
- Survey on the pharmacodynamics of the new antipsychotic risperidonePsychopharmacology, 1994
- Antagonism of 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane stimulus with a newly identified 5-HT2- versus 5-HT1C-selective antagonistJournal of Medicinal Chemistry, 1993
- A proposed new nomenclature for 5-HT receptorsTrends in Pharmacological Sciences, 1993
- 5-HT2 receptors exert a state-dependent regulation of dopaminergic function: studies with MDL 100,907 and the amphetamine analogue, 3,4-methylenedioxymethamphetamineEuropean Journal of Pharmacology, 1992
- Behavioral pharmacology of antagonists at 5-HT2/5-HT1C receptorsNeuroscience & Biobehavioral Reviews, 1992
- Neurochemical and in vivo pharmacological profile of sertindole, a limbic‐selective neuroleptic compoundDrug Development Research, 1991
- Binding of typical and atypical antipsychotics to 5-HT1C and 5-HT2 sites: clozapine potently interacts with 5-HT1C sitesEuropean Journal of Pharmacology, 1990
- Discriminative stimulus properties of the serotonergic agent 1-(2, 5-dimethoxy-4-iodophenyl)-2-aminopropane (DOI)Life Sciences, 1986