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Mild Electrical Stimulation with Heat Shock Ameliorates Insulin Resistance via Enhanced Insulin Signaling

Low-intensity electrical current (or mild electrical stimulation; MES) influences signal transduction and activates phosphatidylinositol-3 kinase (PI3K)/Akt pathway. Because insulin resistance is characterized by a marked reduction in insulin-stimulated PI3K-mediated activation of Akt, we asked whet...

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Autores principales: Morino, Saori, Kondo, Tatsuya, Sasaki, Kazunari, Adachi, Hironori, Suico, Mary Ann, Sekimoto, Erika, Matsuda, Tomoko, Shuto, Tsuyoshi, Araki, Eiichi, Kai, Hirofumi
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2603588/
https://www.ncbi.nlm.nih.gov/pubmed/19114996
http://dx.doi.org/10.1371/journal.pone.0004068
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author Morino, Saori
Kondo, Tatsuya
Sasaki, Kazunari
Adachi, Hironori
Suico, Mary Ann
Sekimoto, Erika
Matsuda, Tomoko
Shuto, Tsuyoshi
Araki, Eiichi
Kai, Hirofumi
author_facet Morino, Saori
Kondo, Tatsuya
Sasaki, Kazunari
Adachi, Hironori
Suico, Mary Ann
Sekimoto, Erika
Matsuda, Tomoko
Shuto, Tsuyoshi
Araki, Eiichi
Kai, Hirofumi
author_sort Morino, Saori
collection PubMed
description Low-intensity electrical current (or mild electrical stimulation; MES) influences signal transduction and activates phosphatidylinositol-3 kinase (PI3K)/Akt pathway. Because insulin resistance is characterized by a marked reduction in insulin-stimulated PI3K-mediated activation of Akt, we asked whether MES could increase Akt phosphorylation and ameliorate insulin resistance. In addition, it was also previously reported that heat shock protein 72 (Hsp72) alleviates hyperglycemia. Thus, we applied MES in combination with heat shock (HS) to in vitro and in vivo models of insulin resistance. Here we show that 10-min treatment with MES at 5 V (0.1 ms pulse duration) together with HS at 42°C increased the phosphorylation of insulin signaling molecules such as insulin receptor substrate (IRS) and Akt in HepG2 cells maintained in high-glucose medium. MES (12 V)+mild HS treatment of high fat-fed mice also increased the phosphorylation of insulin receptor β subunit (IRβ) and Akt in mice liver. In high fat-fed mice and db/db mice, MES+HS treatment for 10 min applied twice a week for 12–15 weeks significantly decreased fasting blood glucose and insulin levels and improved insulin sensitivity. The treated mice showed significantly lower weight of visceral and subcutaneous fat, a markedly improved fatty liver and decreased size of adipocytes. Our findings indicated that the combination of MES and HS alleviated insulin resistance and improved fat metabolism in diabetes mouse models, in part, by enhancing the insulin signaling pathway.
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spelling pubmed-26035882008-12-30 Mild Electrical Stimulation with Heat Shock Ameliorates Insulin Resistance via Enhanced Insulin Signaling Morino, Saori Kondo, Tatsuya Sasaki, Kazunari Adachi, Hironori Suico, Mary Ann Sekimoto, Erika Matsuda, Tomoko Shuto, Tsuyoshi Araki, Eiichi Kai, Hirofumi PLoS One Research Article Low-intensity electrical current (or mild electrical stimulation; MES) influences signal transduction and activates phosphatidylinositol-3 kinase (PI3K)/Akt pathway. Because insulin resistance is characterized by a marked reduction in insulin-stimulated PI3K-mediated activation of Akt, we asked whether MES could increase Akt phosphorylation and ameliorate insulin resistance. In addition, it was also previously reported that heat shock protein 72 (Hsp72) alleviates hyperglycemia. Thus, we applied MES in combination with heat shock (HS) to in vitro and in vivo models of insulin resistance. Here we show that 10-min treatment with MES at 5 V (0.1 ms pulse duration) together with HS at 42°C increased the phosphorylation of insulin signaling molecules such as insulin receptor substrate (IRS) and Akt in HepG2 cells maintained in high-glucose medium. MES (12 V)+mild HS treatment of high fat-fed mice also increased the phosphorylation of insulin receptor β subunit (IRβ) and Akt in mice liver. In high fat-fed mice and db/db mice, MES+HS treatment for 10 min applied twice a week for 12–15 weeks significantly decreased fasting blood glucose and insulin levels and improved insulin sensitivity. The treated mice showed significantly lower weight of visceral and subcutaneous fat, a markedly improved fatty liver and decreased size of adipocytes. Our findings indicated that the combination of MES and HS alleviated insulin resistance and improved fat metabolism in diabetes mouse models, in part, by enhancing the insulin signaling pathway. Public Library of Science 2008-12-30 /pmc/articles/PMC2603588/ /pubmed/19114996 http://dx.doi.org/10.1371/journal.pone.0004068 Text en Morino et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Morino, Saori
Kondo, Tatsuya
Sasaki, Kazunari
Adachi, Hironori
Suico, Mary Ann
Sekimoto, Erika
Matsuda, Tomoko
Shuto, Tsuyoshi
Araki, Eiichi
Kai, Hirofumi
Mild Electrical Stimulation with Heat Shock Ameliorates Insulin Resistance via Enhanced Insulin Signaling
title Mild Electrical Stimulation with Heat Shock Ameliorates Insulin Resistance via Enhanced Insulin Signaling
title_full Mild Electrical Stimulation with Heat Shock Ameliorates Insulin Resistance via Enhanced Insulin Signaling
title_fullStr Mild Electrical Stimulation with Heat Shock Ameliorates Insulin Resistance via Enhanced Insulin Signaling
title_full_unstemmed Mild Electrical Stimulation with Heat Shock Ameliorates Insulin Resistance via Enhanced Insulin Signaling
title_short Mild Electrical Stimulation with Heat Shock Ameliorates Insulin Resistance via Enhanced Insulin Signaling
title_sort mild electrical stimulation with heat shock ameliorates insulin resistance via enhanced insulin signaling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2603588/
https://www.ncbi.nlm.nih.gov/pubmed/19114996
http://dx.doi.org/10.1371/journal.pone.0004068
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