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Related Concept Videos

Functions of Thyroid Hormones01:18

Functions of Thyroid Hormones

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The thyroid hormone (TH) plays a pivotal role in the intricate orchestration of physiological processes, exerting profound effects on development, metabolism, and homeostasis throughout different life stages.
TH is indispensable for the normal development and maturation of the skeletal, muscular, and nervous systems during fetal and childhood growth. It facilitates bone mineral turnover and regulates protein synthesis in developing tissues, contributing significantly to overall growth and...
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Synthesis and Regulation of Thyroid Hormones01:20

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Low blood levels of the thyroid hormones — triiodothyronine (T3) and thyroxine (T4) — signal the hypothalamus to release the thyrotropin-releasing hormone (TRH). TRH then reaches the pituitary gland and stimulates the release of thyroid-stimulating hormone(TSH) into the bloodstream.
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Lipid-soluble hormones diffuse across the plasma and nuclear membrane of target cells to bind to their specific intracellular receptors. These receptors act as transcription factors that regulate gene expression and protein synthesis in the target cell
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Hormonal Regulation01:33

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The renin-aldosterone system is an endocrine system which guides the renal absorption of water and electrolytes, thus managing blood pressure and osmoregulation. Activation of the system begins in the kidneys with a small cluster of cells adjacent to the afferent and efferent blood vessels of the renal corpuscle. As the nephrons are filtering blood, juxtaglomerular cells monitor blood pressure. If they detect a decrease in pressure, they release the hormone renin into the bloodstream.
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Hormones regulate a significant portion of digestion through activation of the neuroendocrine system. The neuroendocrine system of digestion contains many different hormones all with multiple functions that are both, directly and indirectly, involved in digestion.
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Hormones can be classified into three main types based on their chemical structures: steroids, peptides, and amines. Their actions are mediated by the specific receptors they bind to on target cells.
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Related Experiment Video

Updated: Jan 29, 2026

Author Spotlight: Accurately Assessing Thyroid Hormone-Driven Motor Alterations in Mouse
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Thyroid hormone receptor function in maturing ovine cardiomyocytes.

Natasha N Chattergoon1,2, Samantha Louey1,2, Thomas Scanlan3

  • 1Center for Developmental Health.

The Journal of Physiology
|February 17, 2019
PubMed
Summary
This summary is machine-generated.

Thyroid hormone receptors (TRs) are essential for regulating fetal sheep heart cell growth and maturation. Blocking TRs impacts tri-iodo-l-thyronine (T3) signaling, with effects varying by fetal age.

Keywords:
Cardiomyocyte proliferationFetalNH3Thyroid hormone

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Area of Science:

  • Cardiovascular Physiology
  • Endocrinology
  • Developmental Biology

Background:

  • Plasma tri-iodo-l-thyronine (T3) increases late in gestation, inhibiting cardiomyocyte proliferation and promoting maturation.
  • Thyroid hormone receptors (TRs) mediate T3's actions in fetal cardiomyocytes, with TRα1 and TRβ1 expression increasing with age.

Purpose of the Study:

  • To investigate whether T3-induced changes in fetal ovine cardiomyocytes are mediated via TRs or non-genomic mechanisms.
  • To assess the role of TRα1/α2 in T3 signaling pathways like ERK and Akt.

Main Methods:

  • Primary fetal ovine cardiomyocytes were isolated at 102 and 135 days of gestational age.
  • Cells were treated with T3, IGF-1, a TR antagonist (NH3), or TRα1/α2 siRNA.
  • Proliferation was measured by BrdU uptake; protein levels (ERK, Akt, TRs, p21) were assessed via Western blot.

Main Results:

  • TRα1 protein levels were consistently higher than TRβ1 in ovine fetal hearts.
  • T3 reduced IGF-1-stimulated proliferation, an effect blocked by NH3 or TRα1/α2 knockdown.
  • TR blockade and knockdown affected ERK and Akt signaling, with age-dependent sensitivity.

Conclusions:

  • TRs are crucial for normal proliferation and T3 signaling in fetal ovine cardiomyocytes.
  • The sensitivity of cardiomyocytes to TR blockade is dependent on gestational age.
  • Genomic actions of TRs, not non-genomic mechanisms, mediate T3's effects on proliferation.