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马急性炎症模型的应用。动物健康研究的汽巴 - 嘉基奖。

Applications of equine models of acute inflammation. The Ciba-Geigy Prize for Research in Animal Health.

作者信息

Lees P, Higgins A J, Sedgwick A D, May S A

机构信息

Royal Veterinary College Field Station, Hatfield, Hertfordshire.

出版信息

Vet Rec. 1987 May 30;120(22):522-9. doi: 10.1136/vr.120.22.522.

Abstract

The development of reproducible models of acute inflammation in which inflammatory heat is easily quantified and from which inflammatory exudate is readily harvested has facilitated studies in the horse of the actions of steroids and non-steroidal anti-inflammatory drugs (NSAIDS). Blockade of the synthesis of eicosanoids and suppression of inflammatory heat by clinical dose rates of NSAIDS suggests a causal link between the two events and provides further evidence for a role of these compounds in acute equine inflammation. The tendency for enolic and carboxylic acids NSAIDS to accumulate in inflammatory exudate may account for the duration of action of these compounds in inhibiting exudate eicosanoid synthesis and the data confirm clinical experiences with these drugs. A novel NSAID which inhibits both cyclo-oxygenase and lipoxygenase pathways of arachidonic acid metabolism, BW540C, and two anti-inflammatory steroids, betamethasone and dexamethasone, have been evaluated in the models of equine inflammation with some interesting and unexpected findings. This paper emphasises the interrelationships between the inflammatory process and the actions and fate of anti-inflammatory drugs.

摘要

可重现的急性炎症模型的建立,使得炎症热易于量化且能轻易获取炎性渗出液,这推动了对马体内类固醇和非甾体抗炎药(NSAIDs)作用的研究。NSAIDs的临床剂量可阻断类花生酸的合成并抑制炎症热,这表明这两个事件之间存在因果关系,并进一步证明了这些化合物在马急性炎症中的作用。烯醇酸和羧酸类NSAIDs倾向于在炎性渗出液中蓄积,这可能解释了这些化合物抑制渗出液类花生酸合成的作用持续时间,并且这些数据证实了使用这些药物的临床经验。一种新型NSAID(BW540C)可抑制花生四烯酸代谢的环氧化酶和脂氧合酶途径,以及两种抗炎类固醇(倍他米松和地塞米松),已在马炎症模型中进行了评估,得出了一些有趣且意想不到的结果。本文强调了炎症过程与抗炎药的作用及转归之间的相互关系。

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