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Interleukin-6 increases the expression and activity of insulin-degrading enzyme

Impairment of the insulin-degrading enzyme (IDE) is associated with obesity and type 2 diabetes mellitus (T2DM). Here, we used 4-mo-old male C57BL/6 interleukin-6 (IL-6) knockout mice (KO) to investigate the role of this cytokine on IDE expression and activity. IL-6 KO mice displayed lower insulin c...

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Autores principales: Kurauti, Mirian A., Costa-Júnior, José M., Ferreira, Sandra M., Santos, Gustavo J., Sponton, Carlos H. G., Carneiro, Everardo M., Telles, Guilherme D., Chacon-Mikahil, Mara P. T., Cavaglieri, Cláudia R., Rezende, Luiz F., Boschero, Antonio C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399448/
https://www.ncbi.nlm.nih.gov/pubmed/28429777
http://dx.doi.org/10.1038/srep46750
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author Kurauti, Mirian A.
Costa-Júnior, José M.
Ferreira, Sandra M.
Santos, Gustavo J.
Sponton, Carlos H. G.
Carneiro, Everardo M.
Telles, Guilherme D.
Chacon-Mikahil, Mara P. T.
Cavaglieri, Cláudia R.
Rezende, Luiz F.
Boschero, Antonio C.
author_facet Kurauti, Mirian A.
Costa-Júnior, José M.
Ferreira, Sandra M.
Santos, Gustavo J.
Sponton, Carlos H. G.
Carneiro, Everardo M.
Telles, Guilherme D.
Chacon-Mikahil, Mara P. T.
Cavaglieri, Cláudia R.
Rezende, Luiz F.
Boschero, Antonio C.
author_sort Kurauti, Mirian A.
collection PubMed
description Impairment of the insulin-degrading enzyme (IDE) is associated with obesity and type 2 diabetes mellitus (T2DM). Here, we used 4-mo-old male C57BL/6 interleukin-6 (IL-6) knockout mice (KO) to investigate the role of this cytokine on IDE expression and activity. IL-6 KO mice displayed lower insulin clearance in the liver and skeletal muscle, compared with wild type (WT), due to reduced IDE expression and activity. We also observed that after 3-h incubation, IL-6, 50 and 100 ng ml(−1), increased the expression of IDE in HEPG2 and C2C12 cells, respectively. In addition, during acute exercise, the inhibition of IL-6 prevented an increase in insulin clearance and IDE expression and activity, mainly in the skeletal muscle. Finally, IL-6 and IDE concentrations were significantly increased in plasma from humans, after an acute exercise, compared to pre-exercise values. Although the increase in plasma IDE activity was only marginal, a positive correlation between IL-6 and IDE activity, and between IL-6 and IDE protein expression, was observed. Our outcomes indicate a novel function of IL-6 on the insulin metabolism expanding the possibilities for new potential therapeutic strategies, focused on insulin degradation, for the treatment and/or prevention of diseases related to hyperinsulinemia, such as obesity and T2DM.
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spelling pubmed-53994482017-04-21 Interleukin-6 increases the expression and activity of insulin-degrading enzyme Kurauti, Mirian A. Costa-Júnior, José M. Ferreira, Sandra M. Santos, Gustavo J. Sponton, Carlos H. G. Carneiro, Everardo M. Telles, Guilherme D. Chacon-Mikahil, Mara P. T. Cavaglieri, Cláudia R. Rezende, Luiz F. Boschero, Antonio C. Sci Rep Article Impairment of the insulin-degrading enzyme (IDE) is associated with obesity and type 2 diabetes mellitus (T2DM). Here, we used 4-mo-old male C57BL/6 interleukin-6 (IL-6) knockout mice (KO) to investigate the role of this cytokine on IDE expression and activity. IL-6 KO mice displayed lower insulin clearance in the liver and skeletal muscle, compared with wild type (WT), due to reduced IDE expression and activity. We also observed that after 3-h incubation, IL-6, 50 and 100 ng ml(−1), increased the expression of IDE in HEPG2 and C2C12 cells, respectively. In addition, during acute exercise, the inhibition of IL-6 prevented an increase in insulin clearance and IDE expression and activity, mainly in the skeletal muscle. Finally, IL-6 and IDE concentrations were significantly increased in plasma from humans, after an acute exercise, compared to pre-exercise values. Although the increase in plasma IDE activity was only marginal, a positive correlation between IL-6 and IDE activity, and between IL-6 and IDE protein expression, was observed. Our outcomes indicate a novel function of IL-6 on the insulin metabolism expanding the possibilities for new potential therapeutic strategies, focused on insulin degradation, for the treatment and/or prevention of diseases related to hyperinsulinemia, such as obesity and T2DM. Nature Publishing Group 2017-04-21 /pmc/articles/PMC5399448/ /pubmed/28429777 http://dx.doi.org/10.1038/srep46750 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kurauti, Mirian A.
Costa-Júnior, José M.
Ferreira, Sandra M.
Santos, Gustavo J.
Sponton, Carlos H. G.
Carneiro, Everardo M.
Telles, Guilherme D.
Chacon-Mikahil, Mara P. T.
Cavaglieri, Cláudia R.
Rezende, Luiz F.
Boschero, Antonio C.
Interleukin-6 increases the expression and activity of insulin-degrading enzyme
title Interleukin-6 increases the expression and activity of insulin-degrading enzyme
title_full Interleukin-6 increases the expression and activity of insulin-degrading enzyme
title_fullStr Interleukin-6 increases the expression and activity of insulin-degrading enzyme
title_full_unstemmed Interleukin-6 increases the expression and activity of insulin-degrading enzyme
title_short Interleukin-6 increases the expression and activity of insulin-degrading enzyme
title_sort interleukin-6 increases the expression and activity of insulin-degrading enzyme
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399448/
https://www.ncbi.nlm.nih.gov/pubmed/28429777
http://dx.doi.org/10.1038/srep46750
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