Nagai H, Kelly K, Sehon A H
Int Arch Allergy Appl Immunol. 1978;56(4):307-15. doi: 10.1159/000232036.
Three new antiallergic drugs, Doxantrazole, PRD-92 and N5', as well as disodium cromoglycate, inhibited the IgE-mediated PCA reaction in the rat triggered by the homologous antigen, but did not have an antagonistic effect on histamine itself. Moreover, all the drugs examined caused in vitro inhibition of antigen-mediated histamine release from peritoneal mast cells and chopped lung tissue of sensitized rats producing IgE antibodies. Doxantrazole had a synergistic effect on the inhibition of histamine release by isoproterenol, whereas the other drugs were devoid of this capacity. PRD-92 and N5' inhibited the ionophore A23,187 induced histamine release, but did not have any effect on the D2O-enhanced histamine release which was triggered by antigen.
三种新型抗过敏药物多沙那唑、PRD - 92和N5',以及色甘酸二钠,可抑制大鼠体内由同源抗原引发的IgE介导的被动皮肤过敏反应(PCA反应),但对组胺本身并无拮抗作用。此外,所有检测的药物在体外均能抑制致敏大鼠产生IgE抗体的腹膜肥大细胞和切碎肺组织中抗原介导的组胺释放。多沙那唑对异丙肾上腺素抑制组胺释放具有协同作用,而其他药物则无此能力。PRD - 92和N5'可抑制离子载体A23,187诱导的组胺释放,但对抗原引发的重水增强组胺释放没有任何影响。