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- W2328989818 abstract "It has been recently proposed that DARPP-32 participates, as third messenger, in the mediation of effects induced by dopamine at the cellular level. DARPP-32 is indeed localized almost exclusively on dopaminoceptive neurons bearing the D1 receptor subtype and it is phosphorylated by cAMP-dependent protein kinase. In its phospho-form, DARPP-32 acts as an inhibitor of protein phosphatase-1. In vivo pharmacological treatment with selective D1 agonists and antagonists induces changes in the phosphorylation state of DARPP-32 that can be correlated to changes in cAMP, mediated in turn by D1 and D2 receptors. These data demonstrate that the measurement of the phosphorylation state of DARPP-32 with the back-phosphorylation assay can represent a useful biochemical tool to gain further insight into the sequence of events elicited by specific dopaminergic drugs in vivo." @default.
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- W2328989818 date "1992-03-01" @default.
- W2328989818 modified "2023-09-24" @default.
- W2328989818 title "The phosphorylation state of DARPP-32, a third messenger for dopamine, is regulated by in vivo pharmacological treatments" @default.
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- W2328989818 doi "https://doi.org/10.1016/0197-0186(92)90232-g" @default.
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