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Published on: January 27, 2014
Apparent dopamine D1 and D2 receptors in the weaver mutant mouse: receptor binding and coupling to adenylyl cyclase
K M Dewar1, M Paquet, A Sequeira
1Hôpital Louis-H. Lafontaine, Département de Psychiatrie, Université de Montréal, Québec, Canada.
Abstract:
Weaver mutant mice have a selective degeneration of the nigrostriatal dopamine pathway arising between 7-21 days after birth. The goal of this study was to investigate the effects of this mutation on different parameters of the nigrostriatal and mesolimbic dopamine system: apparent D1 and D2 receptor binding sites as well as their signal transduction pathway. Using quantitative autoradiography of ligands for dopamine D1, D2 receptors and the dopamine uptake site, we found a significant loss in apparent D1 receptor binding sites throughout the neostriatum, significant increase of apparent D2 receptor binding in the dorsal aspect of the neostriatum, and almost complete loss of DA uptake sites in these regions of the weaver mouse. In contrast to the neostriatum, the density of dopamine receptors and uptake sites in the nucleus accumbens of the weaver mouse did not differ from controls. Despite alterations in the binding of apparent D1 and D2 receptors, there was no significant difference in either basal, DA stimulated or GTPgammaS stimulated cAMP production. These findings suggest the down-regulation of apparent D1 receptor binding sites reported in this model, probably does not reflect an important physiological mechanism through which these animals compensate for loss of dopamine innervation.
Insights
Weaver mutant mice show dopamine pathway degeneration. Despite altered dopamine D1 and D2 receptor binding, signal transduction pathways remain unaffected, suggesting no compensatory mechanism for dopamine loss.
Area of Science:
- Neuroscience
- Neurodegenerative Diseases
Background:
- Weaver mutant mice exhibit selective degeneration of the nigrostriatal dopamine pathway postnatally.
- This model is crucial for studying dopamine system alterations in neurodegeneration.
Purpose of the Study:
- To investigate the impact of the weaver mutation on dopamine D1 and D2 receptor binding and signal transduction.
- To analyze changes in the nigrostriatal and mesolimbic dopamine systems.
Main Methods:
- Quantitative autoradiography was used to assess dopamine D1, D2 receptors, and dopamine uptake sites.
- Ligand binding assays were performed on brain tissue from weaver mice and controls.
Main Results:
- Significant loss of D1 receptor binding and dopamine uptake sites in the neostriatum of weaver mice.
- Increased D2 receptor binding in the dorsal neostriatum, with no changes in the nucleus accumbens.
- No significant differences in cAMP production (basal, DA-stimulated, or GTPgammaS-stimulated) despite receptor binding alterations.
Conclusions:
- The observed down-regulation of D1 receptor binding in weaver mice may not represent a physiological compensation for dopamine innervation loss.
- The mesolimbic dopamine system appears unaffected by the weaver mutation, unlike the nigrostriatal pathway.
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