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Improving Obesity and Insulin Resistance by Targeting Skeletal Muscle MKP-1

Obesity has reached a global epidemic and it predisposes to the development of insulin resistance, type 2 diabetes and related metabolic diseases. Current interventions against obesity and/or type 2 diabetes such as calorie restriction, exercise, genetic manipulations or established pharmacological...

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Detalles Bibliográficos
Autores principales: Bennett, Anton M., Lawan, Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7654974/
https://www.ncbi.nlm.nih.gov/pubmed/33179019
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author Bennett, Anton M.
Lawan, Ahmed
author_facet Bennett, Anton M.
Lawan, Ahmed
author_sort Bennett, Anton M.
collection PubMed
description Obesity has reached a global epidemic and it predisposes to the development of insulin resistance, type 2 diabetes and related metabolic diseases. Current interventions against obesity and/or type 2 diabetes such as calorie restriction, exercise, genetic manipulations or established pharmacological treatments have not been successful for many patients with obesity and/or type 2 diabetes. There is an urgent need for new strategies to treat insulin resistance, T2D and obesity. Increased activity of stress-responsive pathways has been linked to the pathogenesis of insulin resistance in obesity. In this commentary, we argue that chronic upregulation of MKP-1 in skeletal muscle is part of a stress response that contributes to the development of insulin resistance, T2D and obesity. Therefore, inhibition of MKP-1 in skeletal muscle is a potential strategy for the treatment of T2D and obesity. We highlight therapeutic strategies for potential targeting of MKP-1 in skeletal muscle for the treatment of metabolic diseases as well as other diseases of skeletal muscle.
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spelling pubmed-76549742020-11-10 Improving Obesity and Insulin Resistance by Targeting Skeletal Muscle MKP-1 Bennett, Anton M. Lawan, Ahmed J Cell Signal Article Obesity has reached a global epidemic and it predisposes to the development of insulin resistance, type 2 diabetes and related metabolic diseases. Current interventions against obesity and/or type 2 diabetes such as calorie restriction, exercise, genetic manipulations or established pharmacological treatments have not been successful for many patients with obesity and/or type 2 diabetes. There is an urgent need for new strategies to treat insulin resistance, T2D and obesity. Increased activity of stress-responsive pathways has been linked to the pathogenesis of insulin resistance in obesity. In this commentary, we argue that chronic upregulation of MKP-1 in skeletal muscle is part of a stress response that contributes to the development of insulin resistance, T2D and obesity. Therefore, inhibition of MKP-1 in skeletal muscle is a potential strategy for the treatment of T2D and obesity. We highlight therapeutic strategies for potential targeting of MKP-1 in skeletal muscle for the treatment of metabolic diseases as well as other diseases of skeletal muscle. 2020 /pmc/articles/PMC7654974/ /pubmed/33179019 Text en https://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 credited.
spellingShingle Article
Bennett, Anton M.
Lawan, Ahmed
Improving Obesity and Insulin Resistance by Targeting Skeletal Muscle MKP-1
title Improving Obesity and Insulin Resistance by Targeting Skeletal Muscle MKP-1
title_full Improving Obesity and Insulin Resistance by Targeting Skeletal Muscle MKP-1
title_fullStr Improving Obesity and Insulin Resistance by Targeting Skeletal Muscle MKP-1
title_full_unstemmed Improving Obesity and Insulin Resistance by Targeting Skeletal Muscle MKP-1
title_short Improving Obesity and Insulin Resistance by Targeting Skeletal Muscle MKP-1
title_sort improving obesity and insulin resistance by targeting skeletal muscle mkp-1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7654974/
https://www.ncbi.nlm.nih.gov/pubmed/33179019
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