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- W2324685961 abstract "There has been considerable interest in modulating dopaminergic transmission for drug dependence treatment. However, the fact that dopamine (DA) acts through different receptor subtypes that may have different, perhaps opposing, properties have made the development of viable treatment strategies complex and challenging. It was initially thought that only two receptor subtypes, D1 and D2 receptors, defined on the basis of their distinct transduction mechanisms and pharmacological profiles, mediated the pleiotropic actions of DA. However, soon after D1 (Monsma et al. 1991) and D2 (Bunzow et al. 1988) receptors were cloned, D3 (Sokoloff et al. 1990), D4 (van Tol et al. 1991) and D5 (Sunahara et al. 1991) receptors were also discovered. Those five DA receptor subtypes, termed DRD1–DRD5 are categorized as either D1-like (DRD1 and DRD5) or D2-like (DRD2, DRD3 and DRD4) based on sequence homology and pharmacology (Le Foll et al. 2009). Among those receptors, we and others have proposed that targeting the DRD3 (Heidbreder & Newman, 2010; Le Foll et al. 2005; Newman et al. 2005) and DRD4 (Yan et al. 2012) may be a novel strategy for treatment of drug dependence. However, despite the recent development of promising molecules (particularly DRD3 ligands) by multiple pharmaceutical drug companies, the translational move forward to the clinic has been stalled, in part because of the loss of interest by pharmaceutical companies, of research in the area of neuropsychiatric disorders. In this context, the report recently published by Bergman et al. (2012) suggesting that buspirone binds to DRD3 and DRD4 (among other targets), and may thus aid drug-use cessation, is exciting and timely, especially considering that buspirone is an already-approved medication with a known …" @default.
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- W2324685961 date "2012-10-19" @default.
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- W2324685961 title "Repurposing buspirone for drug addiction treatment" @default.
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- W2324685961 doi "https://doi.org/10.1017/s1461145712000995" @default.
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