Vasopressin immunoreactivity and release in the suprachiasmatic nucleus of wild-type and tau mutant Syrian hamsters

Brain Res. 2002 May 17;936(1-2):38-46. doi: 10.1016/s0006-8993(02)02497-6.

Abstract

Despite the prominent role of the Syrian hamster (Mesocricetus auratus) in studies of circadian rhythms, there are no data available on the temporal dynamics of the neuropeptide vasopressin (AVP), a major output system of the suprachiasmatic nucleus (SCN). We studied the hamster SCN-AVP system in vivo across the light period and in vitro using long-term organotypic SCN cultures. Additionally, we compared wild-type and tau mutant hamsters with an endogenous circadian period of approximately 24 h and approximately 20 h, respectively. The in vivo study revealed no differences in the number of SCN-AVP neurons between the two genotypes of hamsters studied at three time points across the light period of the circadian cycle. A significantly higher level of AVP-immunoreactivity, however, was found in the SCN of wild-type compared to tau mutant hamsters at the beginning and in the middle of the light period, but not at the end of the light period. SCN-AVP cell number and immunostaining decreased significantly across the light period in wild-type hamsters, but not in tau mutants. The in vitro study revealed a significantly higher rate of AVP release per 24 h from the tau mutant SCN compared to the wild-type SCN. Robust circadian oscillations in AVP release were not found in either type of hamster. These results may suggest that the SCN-AVP system of hamsters, irrespective of genotype, is relatively weak compared to other species. Moreover, the tau mutation seems to influence the SCN-AVP system by enhancing the rate of AVP release and by reducing AVP content and its daily fluctuation.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Biological Clocks / genetics*
  • Casein Kinases
  • Cell Count
  • Circadian Rhythm / genetics*
  • Cricetinae
  • Genotype
  • Immunohistochemistry
  • Male
  • Mesocricetus
  • Mutation / physiology*
  • Neurons / cytology
  • Neurons / metabolism*
  • Organ Culture Techniques
  • Photic Stimulation
  • Presynaptic Terminals / metabolism
  • Presynaptic Terminals / ultrastructure
  • Protein Kinases / genetics*
  • Protein Kinases / metabolism
  • Suprachiasmatic Nucleus / cytology
  • Suprachiasmatic Nucleus / metabolism*
  • Vasopressins / metabolism*

Substances

  • Vasopressins
  • Protein Kinases
  • Casein Kinases