Fetal exposure to high maternal thyroid hormone levels causes central resistance to thyroid hormone in adult humans and mice

Panudda Srichomkwun, Joao Anselmo, Xiao Hui Liao, G. Sebastian Hönes, Lars C. Moeller, Manuela Alonso-Sampedro, Roy E. Weiss, Alexandra M. Dumitrescu, Samuel Refetoff

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

Context: Fetuses exposed to the high thyroid hormone (TH) levels of motherswith resistance to thyroid hormone beta (RTH-b), due to mutations in the THRB gene, have low birth weight and suppressed TSH. Objective: Determine if such exposure to high TH levels in embryonic life has a long-term effect into adulthood. Design: Observations in humans with a parallel design on animals to obtain a preliminary information regarding mechanism. Setting: University research centers. Patients or other participants: Humans and mice with no RTH-b exposed during intrauterine life to high TH levels from mothers who were euthyroid due to RTH-b. Controls were humans and mice of the same genotype but born to fathers with RTH-b and mothers without RTH-b and thus, with normal serum TH levels. Interventions: TSH responses to stimulation with thyrotropin-releasing hormone (TRH) during adult life inhumans andmalemice before andafter treatment with triiodothyronine (T3).Wealsomeasured gene expression in anterior pituitaries, hypothalami, and cerebral cortices of mice. Results: Adult humans and mice without RTH-b, exposed to high maternal TH in utero, showed persistent central resistance to TH, as evidenced by reduced responses of serum TSH to TRH when treated with T3. In mice, anterior pituitary TSH-b and deiodinase 3 (D3) mRNAs, but not hypothalamic and cerebral cortex D3, were increased. Conclusions: Adult humans andmice without RTH-b exposed in utero to highmaternal TH levels have persistent central resistance to TH. This is likelymediated by the increased expression ofD3in the anterior pituitary, enhancing local T3 degradation.

Original languageEnglish (US)
Pages (from-to)3234-3240
Number of pages7
JournalJournal of Clinical Endocrinology and Metabolism
Volume102
Issue number9
DOIs
StatePublished - Sep 1 2017

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Biochemistry
  • Endocrinology
  • Clinical Biochemistry
  • Biochemistry, medical

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