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Effects of omega-7 palmitoleic acids on skeletal muscle differentiation in a hyperglycemic condition
Maternal obesity and diabetes are known to be involved in fetal myogenesis, but the later stages of myogenesis are not well understood. In this study, we investigated the influence of a hyperglycemic environment on L6 skeletal myoblast differentiation and the function of omega-7 palmitoleic acids. E...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Veterinary Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8498828/ https://www.ncbi.nlm.nih.gov/pubmed/34248106 http://dx.doi.org/10.1292/jvms.21-0309 |
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author | TOKUNAGA, Yayoi YOSHIZAKI, Hitomi TORIUMI, Akiyo KAWAHARADA, Ritsuko ISHIDA, Chisato HORI, Masatoshi NAKAMURA, Akio |
author_facet | TOKUNAGA, Yayoi YOSHIZAKI, Hitomi TORIUMI, Akiyo KAWAHARADA, Ritsuko ISHIDA, Chisato HORI, Masatoshi NAKAMURA, Akio |
author_sort | TOKUNAGA, Yayoi |
collection | PubMed |
description | Maternal obesity and diabetes are known to be involved in fetal myogenesis, but the later stages of myogenesis are not well understood. In this study, we investigated the influence of a hyperglycemic environment on L6 skeletal myoblast differentiation and the function of omega-7 palmitoleic acids. Exposure to a high concentration of glucose (25 mM) in high-glucose culture medium (HG) increased the expression of myogenic genes (MyoD, Myogenin, MRF4, Myhc2x, and Myhc2a) and the synthesis of myosin. HG also activated the PI3K/AKT pathway revealed muscle cell differentiation. Furthermore, the levels of reactive oxygen species (ROS) and an inflammatory cytokine (Tnfaip3; tumor necrosis factor alpha-induced protein 3), which are crucial for the growth and differentiation of skeletal muscle, were increased by HG. Palmitoleic acids suppressed the expression levels of myogenic regulatory genes and increased the expression level of a cell proliferation-related gene (Pax3). Trans-palmitoleic acid and eicosapentaenoic acid (TPA and EPA) increased the phosphorylation level of MAPK/ERK1/2 and downregulated ROS generation and Tnfaip3 expression. In contrast, cis-palmitoleic acid inactivated MAPK/ERK1/2, leading to increased ROS generation. In conclusion, a hyperglycemic environment mediated by HG induced excessive muscle differentiation. Palmitoleic acids inhibited myoblast differentiation by downregulating muscle-specific genes. Moreover, trans-palmitoleic acids may have beneficial antioxidant and/or anti-inflammatory effects in cells. |
format | Online Article Text |
id | pubmed-8498828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-84988282021-10-13 Effects of omega-7 palmitoleic acids on skeletal muscle differentiation in a hyperglycemic condition TOKUNAGA, Yayoi YOSHIZAKI, Hitomi TORIUMI, Akiyo KAWAHARADA, Ritsuko ISHIDA, Chisato HORI, Masatoshi NAKAMURA, Akio J Vet Med Sci Pharmacology Maternal obesity and diabetes are known to be involved in fetal myogenesis, but the later stages of myogenesis are not well understood. In this study, we investigated the influence of a hyperglycemic environment on L6 skeletal myoblast differentiation and the function of omega-7 palmitoleic acids. Exposure to a high concentration of glucose (25 mM) in high-glucose culture medium (HG) increased the expression of myogenic genes (MyoD, Myogenin, MRF4, Myhc2x, and Myhc2a) and the synthesis of myosin. HG also activated the PI3K/AKT pathway revealed muscle cell differentiation. Furthermore, the levels of reactive oxygen species (ROS) and an inflammatory cytokine (Tnfaip3; tumor necrosis factor alpha-induced protein 3), which are crucial for the growth and differentiation of skeletal muscle, were increased by HG. Palmitoleic acids suppressed the expression levels of myogenic regulatory genes and increased the expression level of a cell proliferation-related gene (Pax3). Trans-palmitoleic acid and eicosapentaenoic acid (TPA and EPA) increased the phosphorylation level of MAPK/ERK1/2 and downregulated ROS generation and Tnfaip3 expression. In contrast, cis-palmitoleic acid inactivated MAPK/ERK1/2, leading to increased ROS generation. In conclusion, a hyperglycemic environment mediated by HG induced excessive muscle differentiation. Palmitoleic acids inhibited myoblast differentiation by downregulating muscle-specific genes. Moreover, trans-palmitoleic acids may have beneficial antioxidant and/or anti-inflammatory effects in cells. The Japanese Society of Veterinary Science 2021-07-12 2021-09 /pmc/articles/PMC8498828/ /pubmed/34248106 http://dx.doi.org/10.1292/jvms.21-0309 Text en ©2021 The Japanese Society of Veterinary Science https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Pharmacology TOKUNAGA, Yayoi YOSHIZAKI, Hitomi TORIUMI, Akiyo KAWAHARADA, Ritsuko ISHIDA, Chisato HORI, Masatoshi NAKAMURA, Akio Effects of omega-7 palmitoleic acids on skeletal muscle differentiation in a hyperglycemic condition |
title | Effects of omega-7 palmitoleic acids on skeletal muscle differentiation in a hyperglycemic condition |
title_full | Effects of omega-7 palmitoleic acids on skeletal muscle differentiation in a hyperglycemic condition |
title_fullStr | Effects of omega-7 palmitoleic acids on skeletal muscle differentiation in a hyperglycemic condition |
title_full_unstemmed | Effects of omega-7 palmitoleic acids on skeletal muscle differentiation in a hyperglycemic condition |
title_short | Effects of omega-7 palmitoleic acids on skeletal muscle differentiation in a hyperglycemic condition |
title_sort | effects of omega-7 palmitoleic acids on skeletal muscle differentiation in a hyperglycemic condition |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8498828/ https://www.ncbi.nlm.nih.gov/pubmed/34248106 http://dx.doi.org/10.1292/jvms.21-0309 |
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