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Cycling our way to fit fat

Adipose tissue is increasingly being recognized as a key regulator of whole body carbohydrate and lipid metabolism. In conditions of obesity and insulin resistance mitochondrial content in this tissue is reduced, while treatment with insulin sensitizing drugs such as thiazolidinediones (TZDs) increa...

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Detalles Bibliográficos
Autores principales: Townsend, Logan K., Knuth, Carly M., Wright, David C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5392531/
https://www.ncbi.nlm.nih.gov/pubmed/28404813
http://dx.doi.org/10.14814/phy2.13247
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author Townsend, Logan K.
Knuth, Carly M.
Wright, David C.
author_facet Townsend, Logan K.
Knuth, Carly M.
Wright, David C.
author_sort Townsend, Logan K.
collection PubMed
description Adipose tissue is increasingly being recognized as a key regulator of whole body carbohydrate and lipid metabolism. In conditions of obesity and insulin resistance mitochondrial content in this tissue is reduced, while treatment with insulin sensitizing drugs such as thiazolidinediones (TZDs) increase mitochondrial content. It has been known for decades that exercise increases mitochondrial content in skeletal muscle and now several laboratories have shown similar effects in adipose tissue. To date the specific mechanisms mediating this effect have not been fully identified. In this review we highlight recent work suggesting that increases in lipolysis and subsequently fatty acid re‐esterification trigger the activation of 5' AMP‐activated protein kinase (AMP) activated protein kinase and ultimately the induction of mitochondrial biogenesis. It is our current view that this pathway could be a unifying mechanism linking numerous systemic factors (catecholamines, interleukin‐6, meteorin‐like) to induction of mitochondrial biogenesis following exercise.
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spelling pubmed-53925312017-04-17 Cycling our way to fit fat Townsend, Logan K. Knuth, Carly M. Wright, David C. Physiol Rep Review Articles Adipose tissue is increasingly being recognized as a key regulator of whole body carbohydrate and lipid metabolism. In conditions of obesity and insulin resistance mitochondrial content in this tissue is reduced, while treatment with insulin sensitizing drugs such as thiazolidinediones (TZDs) increase mitochondrial content. It has been known for decades that exercise increases mitochondrial content in skeletal muscle and now several laboratories have shown similar effects in adipose tissue. To date the specific mechanisms mediating this effect have not been fully identified. In this review we highlight recent work suggesting that increases in lipolysis and subsequently fatty acid re‐esterification trigger the activation of 5' AMP‐activated protein kinase (AMP) activated protein kinase and ultimately the induction of mitochondrial biogenesis. It is our current view that this pathway could be a unifying mechanism linking numerous systemic factors (catecholamines, interleukin‐6, meteorin‐like) to induction of mitochondrial biogenesis following exercise. John Wiley and Sons Inc. 2017-04-12 /pmc/articles/PMC5392531/ /pubmed/28404813 http://dx.doi.org/10.14814/phy2.13247 Text en © 2017 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Articles
Townsend, Logan K.
Knuth, Carly M.
Wright, David C.
Cycling our way to fit fat
title Cycling our way to fit fat
title_full Cycling our way to fit fat
title_fullStr Cycling our way to fit fat
title_full_unstemmed Cycling our way to fit fat
title_short Cycling our way to fit fat
title_sort cycling our way to fit fat
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5392531/
https://www.ncbi.nlm.nih.gov/pubmed/28404813
http://dx.doi.org/10.14814/phy2.13247
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