Neuronal localization of cannabinoid receptors and second messengers in mutant mouse cerebellum

Brain Res. 1991 Jun 28;552(2):301-10. doi: 10.1016/0006-8993(91)90096-e.


Four lines of mutant mice were used to investigate (1) the neuronal localization of cannabinoid receptors in the cerebellar molecular layer and (2) the anatomical association of these receptors with elements of the two second messenger systems in the brain. Two of the mutant lines--Purkinje cell degeneration and nervous--are selectively deficient in Purkinje cells; the other two--weaver and reeler--are deficient in granule cells. In the heterozygous mice, [3H]CP 55,940 binding to cannabinoid receptors was discretely and densely localized to the molecular layer, as was [3H]forskolin binding to adenylate cyclase and [3H]phorbol 12,13-dibutyrate binding to protein kinase C, a component of the phosphoinositide cycle. [3H]CP 55,940 and [3H]forskolin binding was selectively reduced in weaver and reeler homozygous mice but unchanged in Purkinje cell deficient and nervous homozygotes. No decreases in [3H]phorbol 12,13-dibutyrate binding were found in any of the homozygous mutants relative to the heterozygous littermates. The results suggest that cannabinoid receptors and adenylate cyclase are localized to granule cell axons in the molecular layer, whereas protein kinase C is equally distributed in parallel fibers and Purkinje cell dendrites.

MeSH terms

  • Adenylyl Cyclases / analysis
  • Adenylyl Cyclases / metabolism
  • Animals
  • Autoradiography
  • Cannabinoids / metabolism*
  • Cerebellum / cytology
  • Cerebellum / physiology*
  • Colforsin / metabolism
  • Cyclohexanols / analysis
  • Cyclohexanols / metabolism*
  • Heterozygote
  • Homozygote
  • Mice
  • Mice, Neurologic Mutants
  • Neurons / cytology
  • Neurons / physiology*
  • Phorbol 12,13-Dibutyrate / metabolism
  • Protein Kinase C / analysis
  • Protein Kinase C / metabolism
  • Receptors, Cannabinoid
  • Receptors, Drug / analysis*
  • Receptors, Drug / metabolism
  • Second Messenger Systems*
  • Tritium


  • Cannabinoids
  • Cyclohexanols
  • Receptors, Cannabinoid
  • Receptors, Drug
  • Tritium
  • Colforsin
  • Phorbol 12,13-Dibutyrate
  • 3-(2-hydroxy-4-(1,1-dimethylheptyl)phenyl)-4-(3-hydroxypropyl)cyclohexanol
  • Protein Kinase C
  • Adenylyl Cyclases