Suppr超能文献

[氨来呫诺对白细胞介素-3诱导的人白细胞组胺释放增强作用的抑制作用]

[Inhibitory action amlexanox on interleukin-3-induced enhancement of histamine releasability of human leukocytes].

作者信息

Urisu A, Iimi K, Kondo Y, Horiba F, Masuda S, Tsuruta M, Yazaki T, Torii S

机构信息

Department of Pediatrics, Fujita Health University School of Medicine.

出版信息

Arerugi. 1990 Oct;39(10):1448-54.

PMID:1701989
Abstract

Amlexanox, an anti-allergic drug, showed a concentration-dependent inhibition against hrIL-3-induced enhancement of in vitro histamine release from human leukocytes by anti-IgE. The significant inhibitory action of amlexanox was observed in one out of nine and six out of nine allergic subjects at concentrations of 10(-5) M and 10(-4) M, respectively. This means that the inhibitory effect of amlexanox varied from patient to patient. Post-treatment as well as simultaneous treatment with amlexanox produced an inhibitory action on the enhancing effect of hrIL-3, suggesting that hrIL-3-induced enhancement of releasability is a reversible reaction. AA-861, OKY-046, superoxide dismutase and prostaglandin E2 showed no effects on the hrIL-3-induced enhancement of histamine releasability. The inhibitory action of amlexamox to the hrIL-3-induced enhancement of histamine releasability may be a new anti-allergic mechanism, details of which remains unclear.

摘要

抗组胺药氨来呫诺对人白细胞在抗IgE作用下hrIL-3诱导的体外组胺释放增强具有浓度依赖性抑制作用。在9名过敏受试者中,分别有1名和6名在10(-5)M和10(-4)M浓度下观察到氨来呫诺有显著抑制作用。这意味着氨来呫诺的抑制作用因患者而异。氨来呫诺治疗后以及同时治疗对hrIL-3的增强作用均产生抑制作用,提示hrIL-3诱导的释放能力增强是可逆反应。AA-861、OKY-046、超氧化物歧化酶和前列腺素E2对hrIL-3诱导的组胺释放增强无作用。氨来呫诺对hrIL-3诱导的组胺释放增强的抑制作用可能是一种新的抗过敏机制,其具体细节尚不清楚。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验