An endocannabinoid system is localized to the hypophysial pars tuberalis of Syrian hamsters and responds to photoperiodic changes

Cell Tissue Res. 2010 Apr;340(1):127-36. doi: 10.1007/s00441-010-0930-7. Epub 2010 Feb 18.

Abstract

The hypophysial pars tuberalis (PT), an important interface between neuroendocrine brain centers (hypothalamus, pineal organ) and the pars distalis (PD) of the hypophysis, plays a central role in regulating seasonal reproduction and prolactin release. However, the signaling molecules that transmit photoperiodic information from the PT to the PD and control prolactin release (the so-called "tuberalins") have not yet been identified, despite an intense search for more than three decades. Here, we demonstrate an endocannabinoid system in the PT of the Syrian hamster, a photoperiodic species. By means of in situ hybrization, the PT was found to express N-acylphosphatidylethanolamine-specific phospholipase D (NAPE-PLD), fatty acid amide hydrolase (FAAH), sn-1-selective diacylglycerol lipases (DAGLalpha and DAGLbeta), and monoacylglycerol lipase (MAGL), enzymes involved in endocannabinoid synthesis and degradation. The expression of NAPE-PLD, FAAH, and DAGLalpha was confirmed by immunohistochemistry. Expression and protein levels of DAGLs controlling the synthesis of 2-arachidonoyl glycerol (2-AG), a major endocannabinoid, were upregulated in the PT of Syrian hamsters kept under long-day conditions. Consequently, 2-AG levels were increased in the PT of these hamsters. A primary target of 2-AG, the cannabinoid receptor 1 (CB1), was expressed in the PD. Double-immunolabeling revealed that most of the CB1-immunoreactive cells in the PD were folliculostellate cells that were also immunoreactive for S-100 protein. Thus, the PT comprises an endocannabinoid system, and 2-AG may act as a photoperiodic messenger from the PT to the PD for the regulation of hypophysial hormonal secretion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arachidonic Acids / biosynthesis
  • Arachidonic Acids / genetics
  • Arachidonic Acids / metabolism
  • Biomarkers / analysis
  • Biomarkers / metabolism
  • Cannabinoid Receptor Modulators / genetics*
  • Cannabinoid Receptor Modulators / metabolism*
  • Circadian Rhythm / physiology*
  • Cricetinae
  • Endocannabinoids*
  • Glycerides / biosynthesis
  • Glycerides / genetics
  • Glycerides / metabolism
  • Hydrolases / genetics
  • Hydrolases / metabolism
  • Immunohistochemistry
  • In Situ Hybridization
  • Male
  • Mesocricetus
  • Monoacylglycerol Lipases / genetics
  • Monoacylglycerol Lipases / metabolism
  • Neurosecretory Systems / cytology
  • Neurosecretory Systems / metabolism*
  • Phospholipases / genetics
  • Phospholipases / metabolism
  • Photoperiod*
  • Pituitary Gland / cytology
  • Pituitary Gland / metabolism*
  • RNA, Messenger / analysis
  • RNA, Messenger / metabolism
  • Receptor, Cannabinoid, CB1 / metabolism
  • S100 Proteins / metabolism
  • Second Messenger Systems / genetics
  • Up-Regulation / physiology

Substances

  • Arachidonic Acids
  • Biomarkers
  • Cannabinoid Receptor Modulators
  • Endocannabinoids
  • Glycerides
  • RNA, Messenger
  • Receptor, Cannabinoid, CB1
  • S100 Proteins
  • glyceryl 2-arachidonate
  • Hydrolases
  • Phospholipases
  • Monoacylglycerol Lipases