Department of Pharmacology, Faculty of Medicine, University of Malaya, Kuala Lumpur 50603, Malaysia.
Trio Medicines Ltd., Hammersmith Medicines Research, London NW10 7EW, UK.
Cells. 2021 Dec 14;10(12):3524. doi: 10.3390/cells10123524.
Our interest in inflammation and its treatment stems from ancient times. Hippocrates used willow bark to treat inflammation, and many centuries later, salicylic acid and its derivative aspirin's ability to inhibit cyclooxygenase enzymes was discovered. Glucocorticoids (GC) ushered in a new era of treatment for both chronic and acute inflammatory disease, but their potentially dangerous side effects led the pharmaceutical industry to seek other, safer, synthetic GC drugs. The discovery of the GC-inducible endogenous anti-inflammatory protein annexin A1 (AnxA1) and other endogenous proresolving mediators has opened a new era of anti-inflammatory therapy. This review aims to recapitulate the last four decades of research on NSAIDs, GCs, and AnxA1 and their anti-inflammatory effects.
我们对炎症及其治疗的兴趣可以追溯到古代。希波克拉底曾使用柳树皮来治疗炎症,几个世纪后,人们发现了水杨酸及其衍生物阿司匹林抑制环氧化酶的能力。糖皮质激素 (GC) 的出现开创了治疗慢性和急性炎症性疾病的新纪元,但它们潜在的危险副作用促使制药行业寻找其他更安全的合成 GC 药物。GC 诱导的内源性抗炎蛋白 annexin A1 (AnxA1) 和其他内源性抗炎介质的发现为抗炎治疗开辟了一个新时代。本文旨在回顾过去四十年关于 NSAIDs、GC 和 AnxA1 及其抗炎作用的研究。