Abstract

The hormone thyroxine that regulates mammalian metabolism is carried and stored in the blood by thyroxine-binding globulin (TBG). We demonstrate here that the release of thyroxine from TBG occurs by a temperature-sensitive mechanism and show how this will provide a homoeostatic adjustment of the concentration of thyroxine to match metabolic needs, as with the hypothermia and torpor of small animals. In humans, a rise in temperature, as in infections, will trigger an accelerated release of thyroxine, resulting in a predictable 23% increase in the concentration of free thyroxine at 39°C. The in vivo relevance of this fever-response is affirmed in an environmental adaptation in aboriginal Australians. We show how two mutations incorporated in their TBG interact in a way that will halve the surge in thyroxine release, and hence the boost in metabolic rate that would otherwise occur as body temperatures exceed 37°C. The overall findings open insights into physiological changes that accompany variations in body temperature, as notably in fevers.

Highlights

  • Thyroxine is the hormone that most directly controls mammalian activity, with its immediate derivatives regulating cellular oxygen consumption and the metabolism of body and brain [1]

  • The steady-state concentration of thyroxine in blood is set centrally by the secretion of thyroid stimulating hormone (TSH) but the maintenance of this concentration throughout the tissues is owing to the equilibrated release of thyroxine from its carrier protein in the blood, thyroxine-binding globulin (TBG) [2,3,4]

  • The steady-state concentration of free thyroxine and the percentage saturation of TBG is determined centrally we demonstrate here, as we have shown with the closely related corticosteroid-binding globulin (CBG) [6,7], how & 2014 The Authors

Read more

Summary

Introduction

Thyroxine is the hormone that most directly controls mammalian activity, with its immediate derivatives regulating cellular oxygen consumption and the metabolism of body and brain [1]. The release of thyroxine from TBG is further adjusted within the circulation by a temperature-sensitive modulation of its binding affinity.

Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.