Leptin prevents fasting-induced suppression of prothyrotropin-releasing hormone messenger ribonucleic acid in neurons of the hypothalamic paraventricular nucleus

Gábor Légràdi, Charles H. Emerson, Rexford S Ahima, Jeffrey S. Flier, Ronald M. Lechan

Research output: Contribution to journalArticle

Abstract

Prolonged fasting is associated with a number of changes in the thyroid axis manifested by low serum T3 and T4 levels and, paradoxically, low or normal TSH. This response is, at least partly, caused by suppression of proTRH gone expression in neurons of the hypothalamic paraventricular nucleus (PVN) and reduced hypothalamic TRH release. Because the fall in thyroid hormone levels can be blunted in mice by the systemic administration of leptin, we raised the possibility that leptin may have an important role in the neuroendocrine regulation of the thyroid axis, through effects on hypophysiotropic neurons producing proTRH. Adult male, Sprague-Dawley rats were either fed normally, fasted for 3 days, or fasted and administered leptin at a dose of 0.5μg/gm BW ip every 6 h. Fasted animals showed significant reduction in plasma total and free T4 and T3 levels compared with controls, that were restored toward normal by the administration of leptin. Percent free T4, but not percent free T3 in creased during fasting, further suggesting a reduction in plasma transthyretin levels that did not return to fed levels after leptin administration. By semiquantitative analysis of in situ hybridization autoradiograms, proTRH messenger RNA in medial parvocellular PVN neurons was markedly suppressed in the fasting animals but was restored to normal by leptin administration [fed vs. fast vs. fast/leptin (density units x 108): 8.5 ± 0.4, 3.2 ± 0.2, 8.1 ± 0.8]. In contrast, proTRH messenger RNA in adjacent neurons in the lateral hypothalamus that do not have a hypophysiotropic function remained unchanged by any of the experimental manipulations. These findings indicate that leptin has a selective, central action to modulate the hypothalamic-pituitary- thyroid axis by regulating proTRH gene expression in the PVN but does not have peripheral effects on thyroid-binding proteins. We propose that the fall in circulating leptin levels during fasting resets the set point for feedback inhibition by thyroid hormones on the biosynthesis of hypophysiotropic proTRH, thereby allowing adaptation to starvation.

Original languageEnglish (US)
Pages (from-to)2569-2576
Number of pages8
JournalEndocrinology
Volume138
Issue number6
DOIs
StatePublished - 1997
Externally publishedYes

Fingerprint

Paraventricular Hypothalamic Nucleus
Leptin
Fasting
Hormones
RNA
Neurons
Thyroid Gland
Thyroid Hormones
Lateral Hypothalamic Area
Messenger RNA
Prealbumin
Starvation
In Situ Hybridization
Sprague Dawley Rats
Carrier Proteins
Gene Expression

ASJC Scopus subject areas

  • Endocrinology
  • Endocrinology, Diabetes and Metabolism

Cite this

Leptin prevents fasting-induced suppression of prothyrotropin-releasing hormone messenger ribonucleic acid in neurons of the hypothalamic paraventricular nucleus. / Légràdi, Gábor; Emerson, Charles H.; Ahima, Rexford S; Flier, Jeffrey S.; Lechan, Ronald M.

In: Endocrinology, Vol. 138, No. 6, 1997, p. 2569-2576.

Research output: Contribution to journalArticle

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