Effect of photoperiod on the thyroid-stimulating hormone neuroendocrine system in the European hamster (Cricetus cricetus)

J Neuroendocrinol. 2010 Jan;22(1):51-5. doi: 10.1111/j.1365-2826.2009.01937.x. Epub 2009 Nov 14.

Abstract

Recent studies have characterised a retrograde mechanism whereby the pineal hormone melatonin acts in the pars tuberalis (PT) of the pituitary gland to control thyroid hormone action in the hypothalamus, leading to changes in seasonal reproductive function. This involves the release of thyroid-stimulating hormone (TSH) from PT that activates type II deiodinase (DIO2) gene expression in hypothalamic ependymal cells, locally generating biologically active T3, and thus triggering a neuroendocrine cascade. In the present study, we investigated whether a similar regulatory mechanism operates in the European hamster. This species utilises both melatonin signalling and a circannual timer to time the seasonal reproductive cycle. We found that expression of betaTSH RNA in the PT was markedly increased under long compared to short photoperiod, whereas TSH receptor expression was localised in the ependymal cells lining the third ventricle, and in the PT, where its expression varied with time and photoperiod. In the ependymal cells at the base of the third ventricle, DIO2 and type III deiodinase (DIO3) expression was reciprocally regulated, with DIO2 activated under long and repressed under short photoperiod, and the reverse case for DIO3. These data are consistent with recent observations in sheep, and suggest that the PT TSH third ventricle-ependymal cell relay plays a conserved role in initiating the photoperiodic response in both long- and short-day breeding mammals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Body Weight
  • Circadian Rhythm / physiology
  • Cricetinae
  • Ependyma / metabolism
  • Female
  • In Situ Hybridization
  • Iodide Peroxidase / genetics
  • Iodide Peroxidase / metabolism*
  • Iodothyronine Deiodinase Type II
  • Organ Size / physiology
  • Photoperiod*
  • Pineal Gland / metabolism
  • Pituitary Gland, Anterior / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Third Ventricle / metabolism
  • Thyrotropin / genetics
  • Thyrotropin / metabolism*
  • Time Factors
  • Uterus / physiology

Substances

  • RNA, Messenger
  • Thyrotropin
  • Iodide Peroxidase