Pro-resolving lipid mediators and therapeutic innovations in resolution of inflammation.

IF 12 1区 医学 Q1 PHARMACOLOGY & PHARMACY
Hong Yong Peh, Jianmin Chen
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引用次数: 0

Abstract

This review summarizes findings presented at the 19th World Congress of Basic & Clinical Pharmacology 2023 (Glasgow, Scotland, July 3rd to 7th, 2023) from 8 speakers in the field of resolution of inflammation, resolution pharmacology and resolution biology. It is now accepted that the acute inflammatory response is protective to defend the host against infection or tissue injury. Acute inflammation is self-limited and programmed to be limited in space and time: this is achieved through endogenous resolution processes that ensure return to homeostasis. Resolution is brought about by agonist mediators that include specialized pro-resolving lipid mediators (SPMs) and pro-resolving proteins and peptides such as annexin A1 and angiotensin-(1-7), all acting to initiate anti-inflammatory and pro-resolving processes. If the inflammatory reaction remains unchecked through dysfunctional resolution mechanism, it can become chronic and contribute to a plethora of human diseases, including respiratory, cardiovascular, metabolic, allergic diseases, and arthritis. Herein, we discuss how non-resolving inflammation plays a role in the pathogenesis of these diseases. In addition to SPMs, we highlight the discovery, biosynthesis, biofunctions, and latest research updates on innovative therapeutics (including annexin-A1 peptide-mimetic RTP-026, small molecule FPR2 agonist BM-986235/LAR-1219, biased agonist for FPR1/FPR2 Cmpd17b, lipoxin mimetics AT-01-KG and AT-02-CT, melanocortin receptor agonist AP1189, gold nanoparticles, angiotensin-(1-7), and CD300a) that can promote resolution of inflammation directly or through modulation of SPMs production. Drug development strategies based on the biology of the resolution of inflammation can offer novel therapeutic means and/or add-on therapies for the treatment of chronic diseases.

有利于消除炎症的脂质介质和创新疗法。
本综述总结了第 19 届世界基础与临床药理学大会(2023 年 7 月 3 日至 7 日,苏格兰格拉斯哥)上 8 位发言者在炎症解析、解析药理学和解析生物学领域的研究成果。目前公认的观点是,急性炎症反应具有保护作用,可保护宿主免受感染或组织损伤。急性炎症反应具有自限性,并在空间和时间上受到限制:这是通过确保恢复平衡的内源性消解过程实现的。炎症的消退是通过激动介质实现的,这些介质包括专门的促进消退的脂质介质(SPMs)和促进消退的蛋白质和肽,如附件素 A1 和血管紧张素-(1-7),所有这些介质都起着启动抗炎和促进消退过程的作用。如果炎症反应通过功能失调的分解机制得不到控制,就会变成慢性炎症反应,并导致大量人类疾病,包括呼吸系统疾病、心血管疾病、代谢性疾病、过敏性疾病和关节炎。在此,我们将讨论非化解性炎症如何在这些疾病的发病机制中发挥作用。除了 SPMs 之外,我们还重点介绍了创新疗法的发现、生物合成、生物功能和最新研究进展(包括附件素-A1 肽模拟物 RTP-026、小分子 FPR2 激动剂 BM-986235/LAR-1219、小分子 FPR2 激动剂 BM-986235/LAR-1219、FPR1/FPR2 偏激动剂 Cmpd17b、脂毒素模拟物 AT-01-KG 和 AT-02-CT、黑色素皮质素受体激动剂 AP1189、金纳米粒子、血管紧张素-(1-7) 和 CD300a),这些药物可直接或通过调节 SPMs 的产生来促进炎症的消退。以消炎生物学为基础的药物开发战略可为治疗慢性疾病提供新的治疗手段和/或附加疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
23.00
自引率
0.70%
发文量
222
审稿时长
90 days
期刊介绍: Pharmacology & Therapeutics, in its 20th year, delivers lucid, critical, and authoritative reviews on current pharmacological topics.Articles, commissioned by the editor, follow specific author instructions.This journal maintains its scientific excellence and ranks among the top 10 most cited journals in pharmacology.
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