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新型抗炎—促分解代谢介质及其受体。

Novel anti-inflammatory--pro-resolving mediators and their receptors.

机构信息

Center for Experimental Therapeutics and Reperfusion Injury, Department of Anesthesia, Perioperative and Pain Medicine, Harvard Institute of Medicine, 77 Avenue Louis Pasteur, Boston, MA 02115,USA.

出版信息

Curr Top Med Chem. 2011;11(6):629-47. doi: 10.2174/1568026611109060629.

Abstract

Resolution of inflammation, an actively coordinated program, is essential to maintain host health. It involves effective removal of inflammatory stimuli and the spatio-temporal control of leukocyte trafficking as well as chemical mediator generation. During the active resolution process, new classes of small, local acting endogenous autacoids, namely the lipoxins, D and E series resolvins, (neuro)protectins, and maresins have been identified. These specialized pro-resolving lipid mediators (SPM) prevent excessive inflammation and promote removal of microbes and apoptotic cells, thereby expediting resolution and return to tissue homeostasis. As part of their molecular mechanism, SPM exert their potent actions via activating specific pro-resolving G-protein coupled receptors. Together these SPM and their receptors provide new concepts and opportunities for therapeutics, namely promoting active resolution as opposed to the conventionally used enzyme inhibitors and receptor antagonists. This approach may offer new targets suitable for drug design for treating inflammation related diseases, for the new terrain of resolution pharmacology.

摘要

炎症的消退是一个主动协调的过程,对于维持宿主健康至关重要。它涉及到有效清除炎症刺激物,白细胞迁移的时空控制以及化学介质的产生。在积极的消退过程中,已经鉴定出了新的一类小的、局部作用的内源性自分泌调节剂,即脂氧素、D 和 E 系列的消退素、(神经)保护素和maresins。这些专门的促消退脂质介质 (SPM) 可防止过度炎症,并促进微生物和凋亡细胞的清除,从而加速消退并恢复组织内稳态。作为其分子机制的一部分,SPM 通过激活特定的促消退 G 蛋白偶联受体发挥其强大作用。这些 SPM 及其受体共同为治疗学提供了新的概念和机会,即促进主动消退,而不是传统上使用的酶抑制剂和受体拮抗剂。这种方法可能为治疗炎症相关疾病的药物设计提供新的靶点,开辟了消退药理学的新领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f74b/3094721/9a10a27e4ef4/nihms280746f1.jpg

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