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Resveratrol improves palmitic acid‑induced insulin resistance via the DDIT4/mTOR pathway in C2C12 cells

The present study aimed to establish a model of palmitic acid (PA)-induced insulin resistance (IR) in C2C12 cells and to determine the mechanism underlying how resveratrol (RSV) improves IR. C2C12 cells were divided into the control (CON), PA, PA + RSV, PA + RSV + DNA damage-inducible transcript 4 (...

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Autores principales: Pan, Xinyan, Liu, Chunqiao, Wang, Xing, Zhao, Ming, Zhang, Zhimei, Zhang, Xuemei, Wang, Chao, Song, Guangyao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463219/
https://www.ncbi.nlm.nih.gov/pubmed/37594055
http://dx.doi.org/10.3892/mmr.2023.13068
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author Pan, Xinyan
Liu, Chunqiao
Wang, Xing
Zhao, Ming
Zhang, Zhimei
Zhang, Xuemei
Wang, Chao
Song, Guangyao
author_facet Pan, Xinyan
Liu, Chunqiao
Wang, Xing
Zhao, Ming
Zhang, Zhimei
Zhang, Xuemei
Wang, Chao
Song, Guangyao
author_sort Pan, Xinyan
collection PubMed
description The present study aimed to establish a model of palmitic acid (PA)-induced insulin resistance (IR) in C2C12 cells and to determine the mechanism underlying how resveratrol (RSV) improves IR. C2C12 cells were divided into the control (CON), PA, PA + RSV, PA + RSV + DNA damage-inducible transcript 4 (DDIT4)-small interfering (si)RNA and PA + RSV + MHY1485 (mTOR agonist) groups. Glucose contents in culture medium and triglyceride contents in cells were determined. Oil red O staining was performed to observe the pathological changes in the cells. Reverse transcription-quantitative PCR and western blotting were conducted to evaluate the mRNA and protein expression levels, respectively, of DDIT4, mTOR, p70 ribosomal protein S6 kinase (p70S6K), insulin receptor substrate (IRS)-1, PI3K, AKT and glucose transporter 4 (GLUT4). Compared with in the CON group, glucose uptake was decreased, cellular lipid deposition was increased, phosphorylated (p)-IRS-1, p-mTOR and p-p70S6K protein expression levels were increased, and p-PI3K, p-AKT, GLUT4 and DDIT4 protein expression levels were decreased in the PA group. By contrast, compared with in the PA group, culture medium glucose content and cellular lipid deposition were decreased, p-PI3K, p-AKT, GLUT4 and DDIT4 protein expression levels were increased, p-IRS-1 protein expression levels were decreased, and mTOR and p70S6K mRNA and protein expression levels were decreased in the PA + RSV group. Compared with in the PA + RSV group, DDIT4 protein and mRNA expression levels were reduced in the PA + RSV + DDIT4-siRNA group, but showed no change in the PA + RSV + MHY1485 group. Following transfection with DDIT4-siRNA or treatment with MHY1485, the effects of RSV on improving IR and lipid metabolism were weakened, mTOR and p70S6K protein expression levels were upregulated, p-PI3K, p-AKT and GLUT4 protein expression levels were down-regulated, p-IRS-1 protein expression levels were upregulated, and culture medium glucose content and cellular lipid deposition were increased. In conclusion, RSV may improve PA-induced IR in C2C12 cells through the DDIT4/mTOR/IRS-1/PI3K/AKT/GLUT4 signaling pathway, as well as via improvements in glucose and lipid metabolism.
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spelling pubmed-104632192023-08-30 Resveratrol improves palmitic acid‑induced insulin resistance via the DDIT4/mTOR pathway in C2C12 cells Pan, Xinyan Liu, Chunqiao Wang, Xing Zhao, Ming Zhang, Zhimei Zhang, Xuemei Wang, Chao Song, Guangyao Mol Med Rep Articles The present study aimed to establish a model of palmitic acid (PA)-induced insulin resistance (IR) in C2C12 cells and to determine the mechanism underlying how resveratrol (RSV) improves IR. C2C12 cells were divided into the control (CON), PA, PA + RSV, PA + RSV + DNA damage-inducible transcript 4 (DDIT4)-small interfering (si)RNA and PA + RSV + MHY1485 (mTOR agonist) groups. Glucose contents in culture medium and triglyceride contents in cells were determined. Oil red O staining was performed to observe the pathological changes in the cells. Reverse transcription-quantitative PCR and western blotting were conducted to evaluate the mRNA and protein expression levels, respectively, of DDIT4, mTOR, p70 ribosomal protein S6 kinase (p70S6K), insulin receptor substrate (IRS)-1, PI3K, AKT and glucose transporter 4 (GLUT4). Compared with in the CON group, glucose uptake was decreased, cellular lipid deposition was increased, phosphorylated (p)-IRS-1, p-mTOR and p-p70S6K protein expression levels were increased, and p-PI3K, p-AKT, GLUT4 and DDIT4 protein expression levels were decreased in the PA group. By contrast, compared with in the PA group, culture medium glucose content and cellular lipid deposition were decreased, p-PI3K, p-AKT, GLUT4 and DDIT4 protein expression levels were increased, p-IRS-1 protein expression levels were decreased, and mTOR and p70S6K mRNA and protein expression levels were decreased in the PA + RSV group. Compared with in the PA + RSV group, DDIT4 protein and mRNA expression levels were reduced in the PA + RSV + DDIT4-siRNA group, but showed no change in the PA + RSV + MHY1485 group. Following transfection with DDIT4-siRNA or treatment with MHY1485, the effects of RSV on improving IR and lipid metabolism were weakened, mTOR and p70S6K protein expression levels were upregulated, p-PI3K, p-AKT and GLUT4 protein expression levels were down-regulated, p-IRS-1 protein expression levels were upregulated, and culture medium glucose content and cellular lipid deposition were increased. In conclusion, RSV may improve PA-induced IR in C2C12 cells through the DDIT4/mTOR/IRS-1/PI3K/AKT/GLUT4 signaling pathway, as well as via improvements in glucose and lipid metabolism. D.A. Spandidos 2023-08-09 /pmc/articles/PMC10463219/ /pubmed/37594055 http://dx.doi.org/10.3892/mmr.2023.13068 Text en Copyright: © Pan et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , 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 Articles
Pan, Xinyan
Liu, Chunqiao
Wang, Xing
Zhao, Ming
Zhang, Zhimei
Zhang, Xuemei
Wang, Chao
Song, Guangyao
Resveratrol improves palmitic acid‑induced insulin resistance via the DDIT4/mTOR pathway in C2C12 cells
title Resveratrol improves palmitic acid‑induced insulin resistance via the DDIT4/mTOR pathway in C2C12 cells
title_full Resveratrol improves palmitic acid‑induced insulin resistance via the DDIT4/mTOR pathway in C2C12 cells
title_fullStr Resveratrol improves palmitic acid‑induced insulin resistance via the DDIT4/mTOR pathway in C2C12 cells
title_full_unstemmed Resveratrol improves palmitic acid‑induced insulin resistance via the DDIT4/mTOR pathway in C2C12 cells
title_short Resveratrol improves palmitic acid‑induced insulin resistance via the DDIT4/mTOR pathway in C2C12 cells
title_sort resveratrol improves palmitic acid‑induced insulin resistance via the ddit4/mtor pathway in c2c12 cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463219/
https://www.ncbi.nlm.nih.gov/pubmed/37594055
http://dx.doi.org/10.3892/mmr.2023.13068
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