靶向巨噬细胞极化治疗糖尿病-早期改善胰岛素敏感性和胰岛素抵抗的可行性-一项全面的系统综述

K. Kaur, G. Allahbadia, M. Singh
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引用次数: 2

摘要

肥胖的发病率正以巨大的比例增加,以至于相关的2型糖尿病的发病率也显著增加,我们不得不创造一个术语“糖尿病”来同时针对这两者。早些时候,我们试图回顾肥胖和2型糖尿病的发病机制我们发现,无论制定什么药物,通常对一些并发症都不起作用,到目前为止,除了减肥手术,我们没有永久性的长期治疗方法。此外,T2DM可能是一种双重发病机制的疾病,即炎症性和代谢性。尽管代谢性炎症具有全身性,但其共同的起始点是组织常驻巨噬细胞,其对微环境的成功生理或异常病理适应决定了疾病的进程和严重程度。之前我们回顾了巨噬细胞极化在非酒精性脂肪性肝病(NAFLD)中的作用。本文综述了巨噬细胞极化、炎症和非炎症的关键模式,这些模式与胰岛素抵抗(IR)和2型糖尿病(T2DM)的形成有关,并详细讨论了巨噬细胞极化、生物能量学在不同情况下的巨噬细胞适应以及转录因子如干扰素调节因子5(IRF5)、核因子κ B(NFKB)、Toll样受体4 (TLR4)、肝X受体(LXR)、激活蛋白1(AP1)、缺氧诱导因子1(HIF1)、除氧化酶体增殖激活受体(PPAR)外,所有这些信号的信号转导和转录激活因子(STATS)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting macrophage polarization for therapy of diabesity–the feasibility of early improvement of insulin sensitivity and insulin resistance-a comprehensive systematic review
The incidence of obesity is increasing in mammoth proportions so much so that associated comorbidity T2DM incidence is increasing markedly that we had to coin a term Diabesity to target both together. Earlier trying to review etiopathogenesis of both obesity and type 2 DM we found that whatever drugs that are formulated usually do not work with some complications and till now other than bariatric surgery we have no permanent cure for long term maintenance.Further T2DM might be a disease of 2 etiopathogenesis, namely inflammatory, as well as metabolic.Although metabolic inflammation has the properties of being systemic, their common initiating point is tissue resident macrophages, whose successful physiological or abnormal pathological adaptation to its microenvironment dictates disease course as well as severity. Earlierv we reviewed macrophage polarization in case of non alcoholic fatty liver disease (NAFLD) . Here we review it more comprehensively regarding crucial modes, of macrophage polarization, inflammatory, as well as non inflammatory which sees to the formation Of insulin resistance(IR) as well as Type 2 diabetes mellitus(T2DM) .Details of macrophage polarization, bioenergetics macrophage adaptations in different scenario is discussed in detail along with role of transcription factors like Interferon Regulatory Factor 5(IRF5), Nuclear Factor Kappa B(NFKB), Toll Like Receptor 4 (TLR4) Liver X Receptor (LXR), Activator Protein 1(AP1), Hypoxia Inducible Factor 1(HIF1), Signal Transducers and Activators of Transcription (STATS) in all these signaling besides per oxisome Proliferator Activated Receptor (PPAR) .
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