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.

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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