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Saturated fatty acid palmitate-induced insulin resistance is accompanied with myotube loss and the impaired expression of health benefit myokine genes in C2C12 myotubes

BACKGROUND: Excessive circular fatty acid, particlarly saturated fatty acid, can result in insulin resistance in skeletal muscle, but other adverse effects of fatty acid accumulation in myocytes remain unclear. METHODS: Differentiated C2C12 myotubes were used. The effects of palmitate on cell viabil...

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Autores principales: Yang, Ming, Wei, Dandan, Mo, Chunfen, Zhang, Jie, Wang, Xu, Han, Xiaojuan, Wang, Zhe, Xiao, Hengyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3723881/
https://www.ncbi.nlm.nih.gov/pubmed/23866690
http://dx.doi.org/10.1186/1476-511X-12-104
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author Yang, Ming
Wei, Dandan
Mo, Chunfen
Zhang, Jie
Wang, Xu
Han, Xiaojuan
Wang, Zhe
Xiao, Hengyi
author_facet Yang, Ming
Wei, Dandan
Mo, Chunfen
Zhang, Jie
Wang, Xu
Han, Xiaojuan
Wang, Zhe
Xiao, Hengyi
author_sort Yang, Ming
collection PubMed
description BACKGROUND: Excessive circular fatty acid, particlarly saturated fatty acid, can result in insulin resistance in skeletal muscle, but other adverse effects of fatty acid accumulation in myocytes remain unclear. METHODS: Differentiated C2C12 myotubes were used. The effects of palmitate on cell viability, glucose uptake, gene expression and myotube loss were evaluated by MTT assay, 2NBDG uptake, qRT-PCR, Western Blot and crystal staining-based myotube counting, respectively. In some expreiments, oleate was administrated, or the inhibitors of signaling pathways were applied. RESULTS: Palmitate-induced cellular insulin resistance was clarified by the reduced Akt phosphorylation, glucose uptake and Glut4 expression. Palmitate-caused myotube loss was clearly observed under microscope and proved by myotube counting and expression analysis of myotube marker genes. Moreover, palmitate-induced transcriptional suppression of three health benefit myokine genes (FNDC5, CTRP15 and FGF21) was found, and the different involvement of p38 and PI3K in the transcription of these genes was noticed. CONCLUSIONS: Palmitate-induced insulin resistance accompanys myotube loss and the impaired expression of FNDC5, CTRP15 and FGF21genes in C2C12 myotubes. These results provide novel evidence indicating the negative role of high concentration of palmitate in myotubes.
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spelling pubmed-37238812013-07-27 Saturated fatty acid palmitate-induced insulin resistance is accompanied with myotube loss and the impaired expression of health benefit myokine genes in C2C12 myotubes Yang, Ming Wei, Dandan Mo, Chunfen Zhang, Jie Wang, Xu Han, Xiaojuan Wang, Zhe Xiao, Hengyi Lipids Health Dis Short Report BACKGROUND: Excessive circular fatty acid, particlarly saturated fatty acid, can result in insulin resistance in skeletal muscle, but other adverse effects of fatty acid accumulation in myocytes remain unclear. METHODS: Differentiated C2C12 myotubes were used. The effects of palmitate on cell viability, glucose uptake, gene expression and myotube loss were evaluated by MTT assay, 2NBDG uptake, qRT-PCR, Western Blot and crystal staining-based myotube counting, respectively. In some expreiments, oleate was administrated, or the inhibitors of signaling pathways were applied. RESULTS: Palmitate-induced cellular insulin resistance was clarified by the reduced Akt phosphorylation, glucose uptake and Glut4 expression. Palmitate-caused myotube loss was clearly observed under microscope and proved by myotube counting and expression analysis of myotube marker genes. Moreover, palmitate-induced transcriptional suppression of three health benefit myokine genes (FNDC5, CTRP15 and FGF21) was found, and the different involvement of p38 and PI3K in the transcription of these genes was noticed. CONCLUSIONS: Palmitate-induced insulin resistance accompanys myotube loss and the impaired expression of FNDC5, CTRP15 and FGF21genes in C2C12 myotubes. These results provide novel evidence indicating the negative role of high concentration of palmitate in myotubes. BioMed Central 2013-07-18 /pmc/articles/PMC3723881/ /pubmed/23866690 http://dx.doi.org/10.1186/1476-511X-12-104 Text en Copyright © 2013 Yang 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 cited.
spellingShingle Short Report
Yang, Ming
Wei, Dandan
Mo, Chunfen
Zhang, Jie
Wang, Xu
Han, Xiaojuan
Wang, Zhe
Xiao, Hengyi
Saturated fatty acid palmitate-induced insulin resistance is accompanied with myotube loss and the impaired expression of health benefit myokine genes in C2C12 myotubes
title Saturated fatty acid palmitate-induced insulin resistance is accompanied with myotube loss and the impaired expression of health benefit myokine genes in C2C12 myotubes
title_full Saturated fatty acid palmitate-induced insulin resistance is accompanied with myotube loss and the impaired expression of health benefit myokine genes in C2C12 myotubes
title_fullStr Saturated fatty acid palmitate-induced insulin resistance is accompanied with myotube loss and the impaired expression of health benefit myokine genes in C2C12 myotubes
title_full_unstemmed Saturated fatty acid palmitate-induced insulin resistance is accompanied with myotube loss and the impaired expression of health benefit myokine genes in C2C12 myotubes
title_short Saturated fatty acid palmitate-induced insulin resistance is accompanied with myotube loss and the impaired expression of health benefit myokine genes in C2C12 myotubes
title_sort saturated fatty acid palmitate-induced insulin resistance is accompanied with myotube loss and the impaired expression of health benefit myokine genes in c2c12 myotubes
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3723881/
https://www.ncbi.nlm.nih.gov/pubmed/23866690
http://dx.doi.org/10.1186/1476-511X-12-104
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