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Molecular Interaction between the Glucocorticoid Receptor and MAPK Signaling Pathway: A novel link in Modulating the Anti-inflammatory Role of Glucocorticoids

机译:糖皮质激素受体和MAPK信号通路之间的分子相互作用:调节糖皮质激素的抗炎作用中的新链接。

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Glucocorticoids (GCs) have a broad spectrum of life-sustaining functions and play an important role in health and diseases. At pharmacologic doses, GCs are potent immunosuppressive and anti-inflammatory agents. Inflammation and its related diseases present a huge ever increasing burden on the health and disease management. A plausible link of inflammation with aging, cardiovascular diseases and cancer makes matter even worst and calls for a better understanding to resolve the mechanisms associated with the cause and cure of inflammation. Understanding the physiological and molecular interlinks is an utmost importance in designing novel therapeutic strategies in combating inflammation. Advancement in research related to the mitogen-activated protein kinase (MAPK) signaling pathway and its regulation on inflammation has open up new and promising avenues in targeting inflammation as well as understanding the anti-inflammatory property of GCs. Molecular interaction between the ligand-activated glucocorticoid receptor (GR) and the MAPK signaling at different junctions inhibit the latter and thus may account for the anti-inflammatory role of GCs. Therapeutic application of GCs in combination with the recently added class of GR modulators having greater transrepresssion over transactivation (dissociative property) might overcome the clinical side effects associated with GCs.
机译:糖皮质激素(GCs)具有广泛的生命维持功能,并在健康和疾病中发挥重要作用。在药理学剂量下,GCs是有效的免疫抑制剂和消炎药。炎症及其相关疾病给健康和疾病管理带来了越来越大的负担。炎症与衰老,心血管疾病和癌症之间的合理联系甚至使事情变得更糟,并要求人们更好地理解以解决与炎症原因和治愈相关的机制。在设计新的治疗炎症的策略时,了解生理和分子的相互联系是至关重要的。与促分裂原活化蛋白激酶(MAPK)信号通路及其对炎症的调控有关的研究进展为靶向炎症以及了解GC的抗炎特性开辟了新的有希望的途径。配体激活的糖皮质激素受体(GR)与MAPK信号在不同的连接点之间的分子相互作用抑制了后者,因此可能解释了GC的抗炎作用。 GC的治疗应用与最近添加的一类具有比反式激活更高的反转录抑制作用(解离性质)的GR调节剂相结合,可能会克服与GC相关的临床副作用。

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