Unbound MEDLINE

Partial agonist actions at dopamine D(2L) receptors are modified by co-transfection of D(3) receptors: Potential role of heterodimer formation. Parkinsonism & related disorders [Parkinsonism Relat Disord] Journal article

 
TitlePartial agonist actions at dopamine D(2L) receptors are modified by co-transfection of D(3) receptors: Potential role of heterodimer formation.
Author(s)Maggio R, Novi F, Rossi M, Corsini GU, Millan MJ 
InstitutionDepartment of Experimental Medicine, University of L'Aquila, Via Vetoi, Coppito 2, 67100 L'Aquila, Italy.
SourceParkinsonism Relat Disord 2008 Jun 25.
AbstractThe effects of aripiprazole, S33592, bifeprunox, N-desmethylclozapine and preclamol acting as partial agonists on recombinant D(2L) and D(3) receptors expressed both separately and concomitantly in COS-7 cells are evaluated here. Aripiprazole, S33592, bifeprunox, N-desmethylclozapine and preclamol behave as partial agonists on D(2L) receptors coupled with adenylyl cyclase, but they behave as antagonists on co-expression of D(3) with D(2L) receptors. These data raise the intriguing hypothesis that antipsychotic actions of "partial agonists" such as aripiprazole may not reflect inefficient stimulation of D(2) and/or D(3) receptors but, by analogy with other antipsychotics, may instead represent a blockade of D(2)/D(3) heterodimers (and/or D(3) receptors) that are "weakly" coupled to transduction mechanisms postsynaptically of the dopaminergic pathway.
LanguageENG
Pub Type(s)JOURNAL ARTICLE
PubMed ID18585083
  
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