In functional experiments, risperidone is selective, not for the B, but for the A subtype of alpha 1-adrenoceptors.

Article Details

Citation

Eltze M

In functional experiments, risperidone is selective, not for the B, but for the A subtype of alpha 1-adrenoceptors.

Eur J Pharmacol. 1996 Jan 4;295(1):69-73.

PubMed ID
8925876 [ View in PubMed
]
Abstract

The potency of the antipsychotic drug, risperidone, to antagonize alpha 1A-adrenoceptor-mediated contraction in rat vas deferens and vasoconstriction in rat perfused kidney, and alpha 1B-adrenoceptor-mediated contractions in spleen from guinea-pig and mouse was evaluated and compared to that of alpha 1-adrenoceptor subtype-discriminating antagonists. Prazosin was found to be unselective; 2-(2,6-dimethoxyphenoxyethyl)aminomethyl-1,4-benzodioxane (WB 4101), 5-methyl-urapidil, indoramin and (+)-niguldipine were confirmed as selective for the alpha 1A-adrenoceptor, whereas spiperone was weakly alpha 1B-selective. Risperidone was equipotent to prazosin at alpha 1A-adrenoceptors in rat vas deferens and kidney. However, at guinea-pig and mouse splenic alpha 1B-adrenoceptors, the affinity values of risperidone were 10-fold lower than those of prazosin. Thus, in functional experiments the presumed high selectivity of risperidone for the B subtype of alpha 1-adrenoceptors could not be confirmed, the drug instead appears to be moderately selective (10-fold) for the A subtype.

DrugBank Data that Cites this Article

Drug Targets
DrugTargetKindOrganismPharmacological ActionActions
PaliperidoneAlpha-1A adrenergic receptorProteinHumans
Unknown
Antagonist
Details
PaliperidoneAlpha-1B adrenergic receptorProteinHumans
Unknown
Antagonist
Details
PrazosinAlpha-1B adrenergic receptorProteinHumans
Yes
Antagonist
Details