Paul W, Beets J L, Bray M A, Morley J
Agents Actions. 1978 Oct;8(5):509-14. doi: 10.1007/BF02111438.
Five non-steroidal anti-inflammatory drugs (indomethacin, naproxen, meclofenamic acid, feprazone and phenylbutazone: NSAIDs) and three glucocorticosteroids (dexamethasone, hydrocortisone and prednisolone) have been tested as local inhibitors of increased vascular permeability in guinea-pig skin. Lesions were induced by histamine or by antigen to evoke type I (passive cutaneous anaphylaxis), type III (reverse passive Arthus) and type IV (delayed hypersensitivity) allergic reactions. NSAIDs and glucocorticosteroids caused either weak, inconsistent inhibition or slight, high-dose inhibition of the response to histamine. None of the drugs tested showed significant inhibition of the type IV response. The NSAIDs caused dose-related inhibition of both type I and type III responses whereas glucocorticosteroids were ineffective. Maximum inhibition with the NSAIDs was never greater than 50--60% Feprazone, meclofenamic acid and indomethacin were the most potent inhibitors of histamine, PCA and Arthus responses respectively. The possible significance of the effects of these anti-inflammatory agents on vascular permeability is discussed.
五种非甾体抗炎药(吲哚美辛、萘普生、甲氯芬那酸、非普拉宗和保泰松:非甾体抗炎药)和三种糖皮质激素(地塞米松、氢化可的松和泼尼松龙)已作为豚鼠皮肤血管通透性增加的局部抑制剂进行了测试。通过组胺或抗原诱导损伤以引发I型(被动皮肤过敏反应)、III型(反向被动Arthus反应)和IV型(迟发型超敏反应)过敏反应。非甾体抗炎药和糖皮质激素对组胺反应的抑制作用较弱、不一致或在高剂量时有轻微抑制。所测试的药物均未显示出对IV型反应的显著抑制。非甾体抗炎药对I型和III型反应均产生剂量相关的抑制作用,而糖皮质激素则无效。非甾体抗炎药的最大抑制作用从未超过50%-60%。非普拉宗、甲氯芬那酸和吲哚美辛分别是组胺、PCA和Arthus反应的最有效抑制剂。讨论了这些抗炎药对血管通透性影响的可能意义。