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新型苯并吡喃并吡啶衍生物Y-12,141在大鼠体内的抗过敏活性

Anti-allergic activities of a new benzopyranopyridine derivative Y-12,141 in rats.

作者信息

Goto K, Terasawa M, Maruyama Y

出版信息

Int Arch Allergy Appl Immunol. 1979;59(1):13-9. doi: 10.1159/000232234.

Abstract

Passive cutaneous anaphylaxis (PCA) mediated in rats by IgE-like antibodies against egg albumin or the benzylpenicilloyl determinant was inhibited in a dose-dependent manner by intravenous treatment with Y-12,141; the ED50 was 0.09--0.2 mg/kg. The inhibitory effect of Y-12,141 ON PCA was about 5 times as potent as that of disodium cromoglycate (DSCG). Oral treatment with Y-12,141 resulted in the inhibition of PCA, showing an ED50 of 2.5 mg/kg. This action of Y-12,141 on PCA was considered to be due to the inhibition of the release of allergic mediatros from mast cells in a manner similar to DSCG. The results suggest that Y-12,141 may have an anti-allergic activity.

摘要

静脉注射Y-12,141可剂量依赖性地抑制大鼠中由抗卵清蛋白或苄青霉素酰决定簇的IgE样抗体介导的被动皮肤过敏反应(PCA);半数有效剂量(ED50)为0.09--0.2毫克/千克。Y-12,141对PCA的抑制作用约为色甘酸钠二钠(DSCG)的5倍。口服Y-12,141可抑制PCA,半数有效剂量为2.5毫克/千克。Y-12,141对PCA的这种作用被认为是由于其以类似于DSCG的方式抑制肥大细胞释放过敏介质。结果表明Y-12,141可能具有抗过敏活性。

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