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The emergence of proteinase-activated receptor-2 as a novel target for the treatment of inflammation-related CNS disorders

机译:蛋白酶激活受体2的出现作为治疗炎症相关中枢神经系统疾病的新型靶标

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摘要

The signalling molecules that are involved in inflammatory pathways are now thought to play a part in many disorders of the central nervous system (CNS). In common with peripheral chronic inflammatory diseases such a rheumatoid arthritis and ulcerative colitis, evidence now exists for the involvement of inflammatory cytokines, for example tumour necrosis factor (TNF) and interleukins (IL), in neurological disorders. A common factor observed with the up-regulation of these cytokines in peripheral inflammatory diseases, is the increased expression of the proteinase-activated receptor (PAR) subtype PAR-2. Indeed, recent evidence suggests that targeting PAR-2 helps reduce joint swelling observed in animal models of arthritis. So could targeting this receptor prove to be useful in treating those CNS disorders where inflammatory processes are thought to play an intrinsic role? The aim of this review is to summarize the emerging data regarding the role of PAR-2 in neuroinflammation and ischaemic injury and discuss its potential as an exciting new target for the prevention and/or treatment of CNS disorders.
机译:现在认为涉及炎症途径的信号传导分子在中枢神经系统(CNS)的许多疾病中起作用。与诸如类风湿性关节炎和溃疡性结肠炎的外周慢性炎性疾病一样,现在存在炎性细胞因子例如肿瘤坏死因子(TNF)和白介素(IL)参与神经系统疾病的证据。在外周炎性疾病中这些细胞因子的上调所观察到的共同因素是蛋白酶激活受体(PAR)亚型PAR-2的表达增加。实际上,最近的证据表明,靶向PAR-2有助于减少关节炎动物模型中观察到的关节肿胀。那么靶向这种受体是否可以证明对治疗那些认为炎症过程起内在作用的中枢神经系统疾病有用?这篇综述的目的是总结关于PAR-2在神经炎症和缺血性损伤中作用的新兴数据,并讨论其作为预防和/或治疗CNS疾病的令人兴奋的新靶标的潜力。

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