Thyroxine-induced expression of pyroglutamyl peptidase II and inhibition of TSH release precedes suppression of TRH mRNA and requires type 2 deiodinase

J Endocrinol. 2011 Oct;211(1):73-8. doi: 10.1530/JOE-11-0248. Epub 2011 Jul 25.

Abstract

Suppression of TSH release from the hypothyroid thyrotrophs is one of the most rapid effects of 3,3',5'-triiodothyronine (T(3)) or thyroxine (T(4)). It is initiated within an hour, precedes the decrease in TSHβ mRNA inhibition and is blocked by inhibitors of mRNA or protein synthesis. TSH elevation in primary hypothyroidism requires both the loss of feedback inhibition by thyroid hormone in the thyrotrophs and the positive effects of TRH. Another event in this feedback regulation may be the thyroid hormone-mediated induction of the TRH-inactivating pyroglutamyl peptidase II (PPII) in the hypothalamic tanycytes. This study compared the chronology of the acute effects of T(3) or T(4) on TSH suppression, TRH mRNA in the hypothalamic paraventricular nucleus (PVN), and the induction of tanycyte PPII. In wild-type mice, T(3) or T(4) caused a 50% decrease in serum TSH in hypothyroid mice by 5 h. There was no change in TRH mRNA in PVN over this interval, but there was a significant increase in PPII mRNA in the tanycytes. In mice with genetic inactivation of the type 2 iodothyronine deiodinase, T(3) decreased serum TSH and increased PPII mRNA levels, while T(4)-treatment was ineffective. We conclude that the rapid suppression of TSH in the hypothyroid mouse by T(3) occurs prior to a decrease in TRH mRNA though TRH inactivation may be occurring in the median eminence through the rapid induction of tanycyte PPII. The effect of T(4), but not T(3), requires the type 2 iodothyronine deiodinase.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminopeptidases / metabolism*
  • Animals
  • Antithyroid Agents / adverse effects
  • Disease Models, Animal
  • Hypothyroidism / chemically induced
  • Hypothyroidism / metabolism
  • Injections, Intraperitoneal
  • Iodide Peroxidase / genetics
  • Iodide Peroxidase / metabolism*
  • Iodothyronine Deiodinase Type II
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Paraventricular Hypothalamic Nucleus / metabolism
  • Paraventricular Hypothalamic Nucleus / pathology
  • Pyrrolidonecarboxylic Acid / analogs & derivatives*
  • Pyrrolidonecarboxylic Acid / metabolism
  • RNA, Messenger / antagonists & inhibitors*
  • RNA, Messenger / metabolism
  • Thyrotropin / antagonists & inhibitors*
  • Thyrotropin / metabolism
  • Thyrotropin-Releasing Hormone / antagonists & inhibitors*
  • Thyrotropin-Releasing Hormone / metabolism
  • Thyroxine / administration & dosage
  • Thyroxine / pharmacology*
  • Triiodothyronine / administration & dosage
  • Triiodothyronine / pharmacology

Substances

  • Antithyroid Agents
  • RNA, Messenger
  • Triiodothyronine
  • Thyrotropin-Releasing Hormone
  • Thyrotropin
  • Iodide Peroxidase
  • Aminopeptidases
  • pyroglutamyl-peptidase II
  • Thyroxine
  • Pyrrolidonecarboxylic Acid