通过靶向骨骼肌MKP-1改善肥胖和胰岛素抵抗

A. Bennett, A. Lawan
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引用次数: 2

摘要

肥胖已成为全球流行病,它容易导致胰岛素抵抗、2型糖尿病和相关代谢疾病的发展。目前针对肥胖和/或2型糖尿病的干预措施,如热量限制、运动、基因操作或既定的药物治疗,对许多肥胖和/或2型糖尿病患者并不成功。目前迫切需要新的策略来治疗胰岛素抵抗、糖尿病和肥胖症。应激反应通路活性的增加与肥胖患者胰岛素抵抗的发病机制有关。在这篇评论中,我们认为骨骼肌中MKP-1的慢性上调是应激反应的一部分,有助于胰岛素抵抗、T2D和肥胖的发展。因此,抑制骨骼肌中的MKP-1是治疗T2D和肥胖的潜在策略。我们强调了骨骼肌中MKP-1的潜在靶向治疗策略,用于治疗代谢性疾病以及其他骨骼肌疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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 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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