Literature DB >> 20888914

A behavioral genetics approach to understanding D1 receptor involvement in phasic dopamine signaling.

Valerie Z Wall1, Jones G Parker, Jonathan P Fadok, Martin Darvas, Larry Zweifel, Richard D Palmiter.   

Abstract

Dopamine-producing neurons fire with both basal level tonic patterns and phasic bursts. Varying affinities of the five dopamine receptors have led to a hypothesis that higher affinity receptors are primarily activated by basal level tonic dopamine, while lower affinity receptors may be tuned to be sensitive to higher levels caused by phasic bursts. Genetically modified mice provide a method to begin to probe this hypothesis. Here we discuss three mouse models. Dopamine-deficient mice were used to determine which behaviors require dopamine. These behaviors were then analyzed in mice lacking D1 receptors and in mice with reduced phasic dopamine release. Comparison of the latter two mouse models revealed a similar failure to learn about and respond normally to cues that indicate either a positive or negative outcome, giving support to the hypothesis that phasic dopamine release and the D1 receptor act in the same pathway. However, the D1 receptor likely has additional roles beyond those of phasic dopamine detection, because D1 receptor knockout mice have deficits in addition to what has been observed in mice with reduced phasic dopamine release. Copyright Â
© 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20888914      PMCID: PMC3035386          DOI: 10.1016/j.mcn.2010.09.011

Source DB:  PubMed          Journal:  Mol Cell Neurosci        ISSN: 1044-7431            Impact factor:   4.314


  102 in total

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Journal:  Neuroscience       Date:  2007-07-17       Impact factor: 3.590

6.  Behavioural assessment of mice lacking D1A dopamine receptors.

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Review 5.  Illicit dopamine transients: reconciling actions of abused drugs.

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9.  Specific contributions of N-methyl-D-aspartate receptors in the dorsal striatum to cognitive flexibility.

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10.  Dopamine D2R is Required for Hippocampal-dependent Memory and Plasticity at the CA3-CA1 Synapse.

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