Abstract

The role of D 1-like [D 1, D 5] and D 2-like [D 2, D 3, D 4] dopamine receptors and dopamine transduction via DARPP-32 in topographies of orofacial movement was assessed in restrained mice with congenic D 4 vs. D 5 receptor vs. DARPP-32 ‘knockout’. D 4 and DARPP-32 mutants evidenced no material phenotype; also, there were no alterations in topographical responsivity to either the selective D 2-like agonist RU 24213 or the selective D 1-like agonist SK and F 83959. In contrast, D 5 mutants evidenced an increase in spontaneous vertical jaw movements, which habituated more slowly than in wildtypes, and a decrease in horizontal jaw movements; topographical responsivity to SK and F 83959 and RU 24213 was unaltered. D 5 receptors regulate distinct topographies of vertical and horizontal jaw movement in an opposite manner. In assuming that the well-recognised role of the D 1-like family in regulating orofacial movements involves primarily D 1 receptors, a role for their D 5 counterparts may have been overlooked.

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