Wojnar R J, Hearn T, Starkweather S
J Allergy Clin Immunol. 1980 Jul;66(1):37-45. doi: 10.1016/0091-6749(80)90136-0.
Augmentation of allergic histamine release in vitro with human leukocytes was produced by numerous nonsteroidal anti-inflammatory--analgesic agents, primarily the arylalkanoic and anthranilic acids. Augmentation occurred without release of histamine by the agents in the absence of the allergen (ragweed) and only under conditions of an accompanying release by the allergen. As a consequence of augmentation, less allergen was necessary to produce a given response in the presence of these agents. It is suggested that some of these agents might enhance mediator release in immediate-type hypersensitivity reactions. The same agents reported to exacerbate chronic urticaria, i.e., indomethacin, mefenamic acid, sodium salicylate, aspirin, sodium benzoate, and tartrazine, also augmented allergic histamine release. Pharmacologically mediated augmentation of mediator release from stimulated cells is suggested to be involved in the exacerbation of existing chronic urticaria by the acidic nonsteroidal anti-inflammatory-analgesic agents.
许多非甾体抗炎镇痛药,主要是芳基链烷酸和邻氨基苯甲酸,可在体外增强人白细胞介导的过敏性组胺释放。在没有变应原(豚草)的情况下,这些药物不会释放组胺,只有在变应原伴随释放的条件下才会出现增强作用。由于增强作用,在这些药物存在的情况下,产生给定反应所需的变应原较少。提示其中一些药物可能在速发型超敏反应中增强介质释放。据报道,同样会加重慢性荨麻疹的药物,即吲哚美辛、甲芬那酸、水杨酸钠、阿司匹林、苯甲酸钠和酒石黄,也会增强过敏性组胺释放。酸性非甾体抗炎镇痛药通过药理介导增强受刺激细胞介质释放,提示这与现有慢性荨麻疹的加重有关。