Dipartimento di Farmacia - Scienze del Farmaco, Universita degli Studi di Bari Aldo Moro, via Orabona, 4, 70125 Bari, Italy.
Mini Rev Med Chem. 2020;20(20):2090-2103. doi: 10.2174/1389557520666200719014433.
Dysregulated inflammation is a central pathological process in diverse disease states, including neurodegenerative disorders. The recent concept of "resolution of inflammation" is offering a conceptual change for the diagnosis and the development of new therapeutic approaches for chronic inflammatory diseases. Resolution of inflammation terminates the inflammatory response promoting the return to tissue homeostasis through the action of several classes of mediators, termed specialized pro-resolving lipid mediators (SPMs), that include lipoxins, resolvins, protectins, and maresins. SPMs provide "stop signals" that reduce the number of immune cells at the site of insult and increase the clearance of apoptotic cells through phagocytosis. SPMs elicit their effects through the interaction with specific G-protein coupled receptors (GPCRs). The elucidation of the pathways downstream of the GPCRs involved in the resolution of chronic inflammation is opening novel opportunities to generate novel anti-inflammatory agents. This review focuses on the SPMs and the receptors through which their effects are mediated. The medicinal chemistry of the modulators of the GPCRs involved in the resolution of inflammation will be illustrated, by highlighting the potential for developing new antiinflammatory drugs.
炎症失调是多种疾病状态(包括神经退行性疾病)的中心病理过程。最近提出的“炎症消退”概念为慢性炎症性疾病的诊断和新治疗方法的开发提供了概念上的改变。炎症消退通过几种称为特异性促炎消退介质(SPM)的介质的作用终止炎症反应,促进组织内稳态的恢复,这些介质包括脂氧素、消退素、保护素和maresin。SPM 提供“停止信号”,减少损伤部位的免疫细胞数量,并通过吞噬作用增加凋亡细胞的清除。SPM 通过与特定的 G 蛋白偶联受体(GPCR)相互作用发挥作用。阐明参与慢性炎症消退的 GPCR 下游途径为生成新型抗炎剂开辟了新的机会。这篇综述重点介绍了介导其作用的 SPM 和受体。通过突出开发新型抗炎药物的潜力,说明了参与炎症消退的 GPCR 调节剂的药物化学。