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Adiponectin resistance in skeletal muscle: pathophysiological implications in chronic heart failure

Skeletal muscle wasting is a common complication of chronic heart failure (CHF) and linked to poor patient prognosis. In recent years, adiponectin was postulated to be centrally involved in CHF‐associated metabolic failure and muscle wasting. This review discusses current knowledge on the role of ad...

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Autores principales: Sente, Tahnee, Van Berendoncks, An M, Hoymans, Vicky Y, Vrints, Christiaan J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4864225/
https://www.ncbi.nlm.nih.gov/pubmed/27239409
http://dx.doi.org/10.1002/jcsm.12086
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author Sente, Tahnee
Van Berendoncks, An M
Hoymans, Vicky Y
Vrints, Christiaan J
author_facet Sente, Tahnee
Van Berendoncks, An M
Hoymans, Vicky Y
Vrints, Christiaan J
author_sort Sente, Tahnee
collection PubMed
description Skeletal muscle wasting is a common complication of chronic heart failure (CHF) and linked to poor patient prognosis. In recent years, adiponectin was postulated to be centrally involved in CHF‐associated metabolic failure and muscle wasting. This review discusses current knowledge on the role of adiponectin in CHF. Particular emphasis will be given to the complex interaction mechanisms and the intracellular pathways underlying adiponectin resistance in skeletal muscle of CHF patients. In this review, we propose that the resistance process is multifactorial, integrating abnormalities emanating from insulin signalling, mitochondrial biogenesis, and ceramide metabolism.
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spelling pubmed-48642252016-05-27 Adiponectin resistance in skeletal muscle: pathophysiological implications in chronic heart failure Sente, Tahnee Van Berendoncks, An M Hoymans, Vicky Y Vrints, Christiaan J J Cachexia Sarcopenia Muscle Reviews Skeletal muscle wasting is a common complication of chronic heart failure (CHF) and linked to poor patient prognosis. In recent years, adiponectin was postulated to be centrally involved in CHF‐associated metabolic failure and muscle wasting. This review discusses current knowledge on the role of adiponectin in CHF. Particular emphasis will be given to the complex interaction mechanisms and the intracellular pathways underlying adiponectin resistance in skeletal muscle of CHF patients. In this review, we propose that the resistance process is multifactorial, integrating abnormalities emanating from insulin signalling, mitochondrial biogenesis, and ceramide metabolism. John Wiley and Sons Inc. 2015-10-27 2016-06 /pmc/articles/PMC4864225/ /pubmed/27239409 http://dx.doi.org/10.1002/jcsm.12086 Text en © 2015 The Authors Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Reviews
Sente, Tahnee
Van Berendoncks, An M
Hoymans, Vicky Y
Vrints, Christiaan J
Adiponectin resistance in skeletal muscle: pathophysiological implications in chronic heart failure
title Adiponectin resistance in skeletal muscle: pathophysiological implications in chronic heart failure
title_full Adiponectin resistance in skeletal muscle: pathophysiological implications in chronic heart failure
title_fullStr Adiponectin resistance in skeletal muscle: pathophysiological implications in chronic heart failure
title_full_unstemmed Adiponectin resistance in skeletal muscle: pathophysiological implications in chronic heart failure
title_short Adiponectin resistance in skeletal muscle: pathophysiological implications in chronic heart failure
title_sort adiponectin resistance in skeletal muscle: pathophysiological implications in chronic heart failure
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4864225/
https://www.ncbi.nlm.nih.gov/pubmed/27239409
http://dx.doi.org/10.1002/jcsm.12086
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