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Grape seed extract prevents skeletal muscle wasting in interleukin 10 knockout mice

BACKGROUND: Muscle wasting is frequently a result of cancers, AIDS, chronic diseases and aging, which often links to muscle inflammation. Although grape seed extract (GSE) has been widely used as a human dietary supplement for health promotion and disease prevention primarily due to its anti-oxidati...

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Autores principales: Wang, Bo, Yang, Guan, Liang, Xingwei, Zhu, Meijun, Du, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4041050/
https://www.ncbi.nlm.nih.gov/pubmed/24884473
http://dx.doi.org/10.1186/1472-6882-14-162
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author Wang, Bo
Yang, Guan
Liang, Xingwei
Zhu, Meijun
Du, Min
author_facet Wang, Bo
Yang, Guan
Liang, Xingwei
Zhu, Meijun
Du, Min
author_sort Wang, Bo
collection PubMed
description BACKGROUND: Muscle wasting is frequently a result of cancers, AIDS, chronic diseases and aging, which often links to muscle inflammation. Although grape seed extract (GSE) has been widely used as a human dietary supplement for health promotion and disease prevention primarily due to its anti-oxidative and anti-inflammative effects, it is unknown whether GSE affects muscle wasting. The objective is to test the effects of GSE supplementation on inflammation and muscle wasting in interleukin (IL)-10 knockout mice, a recently developed model for human frailty. METHODS: Male IL-10 knockout (IL10KO) C57BL/6 mice at 6 weeks of age were assigned to either 0% or 0.1% GSE (in drinking water) groups (n = 10) for 12 weeks, when skeletal muscle was sampled for analyses. Wild-type C57BL/6 male mice were used as controls. RESULTS: Tibialis anterior muscle weight and fiber size of IL10KO mice were much lower than wild-type mice. IL10KO enhanced nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) signaling and inflammasome formation when compared to wild-type mice. Phosphorylation of anabolic signaling was inhibited, whereas muscle specific ubiquitin ligase, AMP-activated protein kinase (AMPK) and apoptotic signaling were up-regulated in IL10KO mice. GSE supplementation effectively rectified these adverse changes in IL10KO muscle, which provide an explanation for the enhanced muscle mass, reduced protein degradation and apoptosis in GSE supplemented mice compared to IL10KO mice without supplementation. CONCLUSION: GSE supplementation effectively prevents muscle wasting in IL10KO mice, showing that GSE can be used as an auxiliary treatment for muscle loss associated with chronic inflammation and frailty.
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spelling pubmed-40410502014-06-03 Grape seed extract prevents skeletal muscle wasting in interleukin 10 knockout mice Wang, Bo Yang, Guan Liang, Xingwei Zhu, Meijun Du, Min BMC Complement Altern Med Research Article BACKGROUND: Muscle wasting is frequently a result of cancers, AIDS, chronic diseases and aging, which often links to muscle inflammation. Although grape seed extract (GSE) has been widely used as a human dietary supplement for health promotion and disease prevention primarily due to its anti-oxidative and anti-inflammative effects, it is unknown whether GSE affects muscle wasting. The objective is to test the effects of GSE supplementation on inflammation and muscle wasting in interleukin (IL)-10 knockout mice, a recently developed model for human frailty. METHODS: Male IL-10 knockout (IL10KO) C57BL/6 mice at 6 weeks of age were assigned to either 0% or 0.1% GSE (in drinking water) groups (n = 10) for 12 weeks, when skeletal muscle was sampled for analyses. Wild-type C57BL/6 male mice were used as controls. RESULTS: Tibialis anterior muscle weight and fiber size of IL10KO mice were much lower than wild-type mice. IL10KO enhanced nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) signaling and inflammasome formation when compared to wild-type mice. Phosphorylation of anabolic signaling was inhibited, whereas muscle specific ubiquitin ligase, AMP-activated protein kinase (AMPK) and apoptotic signaling were up-regulated in IL10KO mice. GSE supplementation effectively rectified these adverse changes in IL10KO muscle, which provide an explanation for the enhanced muscle mass, reduced protein degradation and apoptosis in GSE supplemented mice compared to IL10KO mice without supplementation. CONCLUSION: GSE supplementation effectively prevents muscle wasting in IL10KO mice, showing that GSE can be used as an auxiliary treatment for muscle loss associated with chronic inflammation and frailty. BioMed Central 2014-05-20 /pmc/articles/PMC4041050/ /pubmed/24884473 http://dx.doi.org/10.1186/1472-6882-14-162 Text en Copyright © 2014 Wang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wang, Bo
Yang, Guan
Liang, Xingwei
Zhu, Meijun
Du, Min
Grape seed extract prevents skeletal muscle wasting in interleukin 10 knockout mice
title Grape seed extract prevents skeletal muscle wasting in interleukin 10 knockout mice
title_full Grape seed extract prevents skeletal muscle wasting in interleukin 10 knockout mice
title_fullStr Grape seed extract prevents skeletal muscle wasting in interleukin 10 knockout mice
title_full_unstemmed Grape seed extract prevents skeletal muscle wasting in interleukin 10 knockout mice
title_short Grape seed extract prevents skeletal muscle wasting in interleukin 10 knockout mice
title_sort grape seed extract prevents skeletal muscle wasting in interleukin 10 knockout mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4041050/
https://www.ncbi.nlm.nih.gov/pubmed/24884473
http://dx.doi.org/10.1186/1472-6882-14-162
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