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Ca(2+)-Dependent Glucose Transport in Skeletal Muscle by Diphlorethohydroxycarmalol, an Alga Phlorotannin: In Vitro and In Vivo Study
Diphlorethohydroxycarmalol (DPHC), a type of phlorotannin isolated from the marine alga Ishige okamurae, reportedly alleviates impaired glucose tolerance. However, the molecular mechanisms of DPHC regulatory activity and by which it exerts potential beneficial effects on glucose transport into skele...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Hindawi
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889350/ https://www.ncbi.nlm.nih.gov/pubmed/33628395 http://dx.doi.org/10.1155/2021/8893679 |
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author | Yang, Hye-Won Jiang, Yun-Fei Lee, Hyo-Geun Jeon, You-Jin Ryu, BoMi |
author_facet | Yang, Hye-Won Jiang, Yun-Fei Lee, Hyo-Geun Jeon, You-Jin Ryu, BoMi |
author_sort | Yang, Hye-Won |
collection | PubMed |
description | Diphlorethohydroxycarmalol (DPHC), a type of phlorotannin isolated from the marine alga Ishige okamurae, reportedly alleviates impaired glucose tolerance. However, the molecular mechanisms of DPHC regulatory activity and by which it exerts potential beneficial effects on glucose transport into skeletal myotubes to control glucose homeostasis remain largely unexplored. The aim of this study was to evaluate the effect of DPHC on cytosolic Ca(2+) levels and its correlation with blood glucose transport in skeletal myotubes in vitro and in vivo. Cytosolic Ca(2+) levels upon DPHC treatment were evaluated in skeletal myotubes and zebrafish larvae by Ca(2+) imaging using Fluo-4. We investigated the effect of DPHC on the blood glucose level and glucose transport pathway in a hyperglycemic zebrafish. DPHC was shown to control blood glucose levels by accelerating glucose transport; this effect was associated with elevated cytosolic Ca(2+) levels in skeletal myotubes. Moreover, the increased cytosolic Ca(2+) level caused by DPHC can facilitate the Glut4/AMPK pathways of the skeletal muscle in activating glucose metabolism, thereby regulating muscle contraction through the regulation of expression of troponin I/C, CaMKII, and ATP. Our findings provide insights into the mechanism of DPHC activity in skeletal myotubes, suggesting that increased cytosolic Ca(2+) levels caused by DPHC can promote glucose transport into skeletal myotubes to modulate blood glucose levels, thus indicating the potential use of DPHC in the prevention of diabetes. |
format | Online Article Text |
id | pubmed-7889350 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-78893502021-02-23 Ca(2+)-Dependent Glucose Transport in Skeletal Muscle by Diphlorethohydroxycarmalol, an Alga Phlorotannin: In Vitro and In Vivo Study Yang, Hye-Won Jiang, Yun-Fei Lee, Hyo-Geun Jeon, You-Jin Ryu, BoMi Oxid Med Cell Longev Research Article Diphlorethohydroxycarmalol (DPHC), a type of phlorotannin isolated from the marine alga Ishige okamurae, reportedly alleviates impaired glucose tolerance. However, the molecular mechanisms of DPHC regulatory activity and by which it exerts potential beneficial effects on glucose transport into skeletal myotubes to control glucose homeostasis remain largely unexplored. The aim of this study was to evaluate the effect of DPHC on cytosolic Ca(2+) levels and its correlation with blood glucose transport in skeletal myotubes in vitro and in vivo. Cytosolic Ca(2+) levels upon DPHC treatment were evaluated in skeletal myotubes and zebrafish larvae by Ca(2+) imaging using Fluo-4. We investigated the effect of DPHC on the blood glucose level and glucose transport pathway in a hyperglycemic zebrafish. DPHC was shown to control blood glucose levels by accelerating glucose transport; this effect was associated with elevated cytosolic Ca(2+) levels in skeletal myotubes. Moreover, the increased cytosolic Ca(2+) level caused by DPHC can facilitate the Glut4/AMPK pathways of the skeletal muscle in activating glucose metabolism, thereby regulating muscle contraction through the regulation of expression of troponin I/C, CaMKII, and ATP. Our findings provide insights into the mechanism of DPHC activity in skeletal myotubes, suggesting that increased cytosolic Ca(2+) levels caused by DPHC can promote glucose transport into skeletal myotubes to modulate blood glucose levels, thus indicating the potential use of DPHC in the prevention of diabetes. Hindawi 2021-02-10 /pmc/articles/PMC7889350/ /pubmed/33628395 http://dx.doi.org/10.1155/2021/8893679 Text en Copyright © 2021 Hye-Won Yang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Yang, Hye-Won Jiang, Yun-Fei Lee, Hyo-Geun Jeon, You-Jin Ryu, BoMi Ca(2+)-Dependent Glucose Transport in Skeletal Muscle by Diphlorethohydroxycarmalol, an Alga Phlorotannin: In Vitro and In Vivo Study |
title | Ca(2+)-Dependent Glucose Transport in Skeletal Muscle by Diphlorethohydroxycarmalol, an Alga Phlorotannin: In Vitro and In Vivo Study |
title_full | Ca(2+)-Dependent Glucose Transport in Skeletal Muscle by Diphlorethohydroxycarmalol, an Alga Phlorotannin: In Vitro and In Vivo Study |
title_fullStr | Ca(2+)-Dependent Glucose Transport in Skeletal Muscle by Diphlorethohydroxycarmalol, an Alga Phlorotannin: In Vitro and In Vivo Study |
title_full_unstemmed | Ca(2+)-Dependent Glucose Transport in Skeletal Muscle by Diphlorethohydroxycarmalol, an Alga Phlorotannin: In Vitro and In Vivo Study |
title_short | Ca(2+)-Dependent Glucose Transport in Skeletal Muscle by Diphlorethohydroxycarmalol, an Alga Phlorotannin: In Vitro and In Vivo Study |
title_sort | ca(2+)-dependent glucose transport in skeletal muscle by diphlorethohydroxycarmalol, an alga phlorotannin: in vitro and in vivo study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889350/ https://www.ncbi.nlm.nih.gov/pubmed/33628395 http://dx.doi.org/10.1155/2021/8893679 |
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