Simultaneous changes in central and peripheral components of the hypothalamus-pituitary-thyroid axis in lipopolysaccharide-induced acute illness in mice

J Endocrinol. 2004 Aug;182(2):315-23. doi: 10.1677/joe.0.1820315.

Abstract

During illness, major changes in thyroid hormone metabolism and regulation occur; these are collectively known as non-thyroidal illness and are characterized by decreased serum triiodothyronine (T(3)) and thyroxine (T(4)) without an increase in serum TSH. Whether alterations in the central part of the hypothalamus-pituitary-thyroid (HPT) axis precede changes in peripheral thyroid hormone metabolism instead of vice versa, or occur simultaneously, is presently unknown. We therefore studied the time-course of changes in thyroid hormone metabolism in the HPT axis of mice during acute illness induced by bacterial endotoxin (lipopolysaccharide; LPS).LPS rapidly induced interleukin-1beta mRNA expression in the hypothalamus, pituitary, thyroid and liver. This was followed by almost simultaneous changes in the pituitary (decreased expression of thyroid receptor (TR)-beta2, TSHbeta and 5'-deiodinase (D1) mRNAs), the thyroid (decreased TSH receptor mRNA) and the liver (decreased TRbeta1 and D1 mRNA). In the hypothalamus, type 2 deiodinase mRNA expression was strongly increased whereas preproTRH mRNA expression did not change after LPS. Serum T(3) and T(4) fell only after 24 h. Our results suggested almost simultaneous involvement of the whole HPT axis in the downregulation of thyroid hormone metabolism during acute illness.

MeSH terms

  • Acute Disease
  • Animals
  • Bacterial Infections / metabolism*
  • Female
  • Gene Expression Regulation
  • Hypothalamo-Hypophyseal System / physiology*
  • Interleukin-1 / genetics
  • Iodide Peroxidase / genetics
  • Lipopolysaccharides
  • Liver / metabolism
  • Mice
  • Mice, Inbred BALB C
  • RNA, Messenger / analysis
  • Receptors, Thyrotropin / genetics
  • Thyroid Hormone Receptors beta / metabolism
  • Thyroid Hormones / metabolism*
  • Thyrotropin, beta Subunit / genetics

Substances

  • Interleukin-1
  • Lipopolysaccharides
  • RNA, Messenger
  • Receptors, Thyrotropin
  • Thyroid Hormone Receptors beta
  • Thyroid Hormones
  • Thyrotropin, beta Subunit
  • Iodide Peroxidase