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Effect of Short-Term Thyroxine Administration on Energy Metabolism and Mitochondrial Efficiency in Humans

The physiologic effects of triiodothyronine (T3) on metabolic rate are well-documented; however, the effects of thyroxine (T4) are less clear despite its wide-spread use to treat thyroid-related disorders and other non-thyroidal conditions. Here, we investigated the effects of acute (3-day) T4 suppl...

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Autores principales: Johannsen, Darcy L., Galgani, Jose E., Johannsen, Neil M., Zhang, Zhengyu, Covington, Jeffrey D., Ravussin, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3406028/
https://www.ncbi.nlm.nih.gov/pubmed/22844412
http://dx.doi.org/10.1371/journal.pone.0040837
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author Johannsen, Darcy L.
Galgani, Jose E.
Johannsen, Neil M.
Zhang, Zhengyu
Covington, Jeffrey D.
Ravussin, Eric
author_facet Johannsen, Darcy L.
Galgani, Jose E.
Johannsen, Neil M.
Zhang, Zhengyu
Covington, Jeffrey D.
Ravussin, Eric
author_sort Johannsen, Darcy L.
collection PubMed
description The physiologic effects of triiodothyronine (T3) on metabolic rate are well-documented; however, the effects of thyroxine (T4) are less clear despite its wide-spread use to treat thyroid-related disorders and other non-thyroidal conditions. Here, we investigated the effects of acute (3-day) T4 supplementation on energy expenditure at rest and during incremental exercise. Furthermore, we used a combination of in situ and in vitro approaches to measure skeletal muscle metabolism before and after T4 treatment. Ten healthy, euthyroid males were given 200 µg T4 (levothyroxine) per day for 3 days. Energy expenditure was measured at rest and during exercise by indirect calorimetry, and skeletal muscle mitochondrial function was assessed by in situ ATP flux ((31)P MRS) and in vitro respiratory control ratio (RCR, state 3/state 4 rate of oxygen uptake using a Clark-type electrode) before and after acute T4 treatment. Thyroxine had a subtle effect on resting metabolic rate, increasing it by 4% (p = 0.059) without a change in resting ATP demand (i.e., ATP flux) of the vastus lateralis. Exercise efficiency did not change with T4 treatment. The maximal capacity to produce ATP (state 3 respiration) and the coupled state of the mitochondria (RCR) were reduced by approximately 30% with T4 (p = 0.057 and p = 0.04, respectively). Together, the results suggest that T4, although less metabolically active than T3, reduces skeletal muscle efficiency and modestly increases resting metabolism even after short-term supplementation. Our findings may be clinically relevant given the expanding application of T4 to treat non-thyroidal conditions such as obesity and weight loss.
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spelling pubmed-34060282012-07-27 Effect of Short-Term Thyroxine Administration on Energy Metabolism and Mitochondrial Efficiency in Humans Johannsen, Darcy L. Galgani, Jose E. Johannsen, Neil M. Zhang, Zhengyu Covington, Jeffrey D. Ravussin, Eric PLoS One Research Article The physiologic effects of triiodothyronine (T3) on metabolic rate are well-documented; however, the effects of thyroxine (T4) are less clear despite its wide-spread use to treat thyroid-related disorders and other non-thyroidal conditions. Here, we investigated the effects of acute (3-day) T4 supplementation on energy expenditure at rest and during incremental exercise. Furthermore, we used a combination of in situ and in vitro approaches to measure skeletal muscle metabolism before and after T4 treatment. Ten healthy, euthyroid males were given 200 µg T4 (levothyroxine) per day for 3 days. Energy expenditure was measured at rest and during exercise by indirect calorimetry, and skeletal muscle mitochondrial function was assessed by in situ ATP flux ((31)P MRS) and in vitro respiratory control ratio (RCR, state 3/state 4 rate of oxygen uptake using a Clark-type electrode) before and after acute T4 treatment. Thyroxine had a subtle effect on resting metabolic rate, increasing it by 4% (p = 0.059) without a change in resting ATP demand (i.e., ATP flux) of the vastus lateralis. Exercise efficiency did not change with T4 treatment. The maximal capacity to produce ATP (state 3 respiration) and the coupled state of the mitochondria (RCR) were reduced by approximately 30% with T4 (p = 0.057 and p = 0.04, respectively). Together, the results suggest that T4, although less metabolically active than T3, reduces skeletal muscle efficiency and modestly increases resting metabolism even after short-term supplementation. Our findings may be clinically relevant given the expanding application of T4 to treat non-thyroidal conditions such as obesity and weight loss. Public Library of Science 2012-07-26 /pmc/articles/PMC3406028/ /pubmed/22844412 http://dx.doi.org/10.1371/journal.pone.0040837 Text en Johannsen et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Johannsen, Darcy L.
Galgani, Jose E.
Johannsen, Neil M.
Zhang, Zhengyu
Covington, Jeffrey D.
Ravussin, Eric
Effect of Short-Term Thyroxine Administration on Energy Metabolism and Mitochondrial Efficiency in Humans
title Effect of Short-Term Thyroxine Administration on Energy Metabolism and Mitochondrial Efficiency in Humans
title_full Effect of Short-Term Thyroxine Administration on Energy Metabolism and Mitochondrial Efficiency in Humans
title_fullStr Effect of Short-Term Thyroxine Administration on Energy Metabolism and Mitochondrial Efficiency in Humans
title_full_unstemmed Effect of Short-Term Thyroxine Administration on Energy Metabolism and Mitochondrial Efficiency in Humans
title_short Effect of Short-Term Thyroxine Administration on Energy Metabolism and Mitochondrial Efficiency in Humans
title_sort effect of short-term thyroxine administration on energy metabolism and mitochondrial efficiency in humans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3406028/
https://www.ncbi.nlm.nih.gov/pubmed/22844412
http://dx.doi.org/10.1371/journal.pone.0040837
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