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奥沙米特:体外对人肺和白细胞组胺释放的抑制与刺激作用

Oxatomide: inhibition and stimulation of histamine release from human lung and leucocytes in vitro.

作者信息

Church M K, Gradidge C F

出版信息

Agents Actions. 1980 Apr;10(1 Pt 2):4-7. doi: 10.1007/BF02024171.

Abstract

Oxatomide is a very potent inhibitor of histamine release induced by anti-1gE and Timothy pollen extract in passively sensitized human lung fragments and that induced by anti-1gE from human leucocytes. Its spectrum of activity is different from sodium cromoglycate-like drugs. In high concentrations oxatomide, like other antihistamines and related structures, induced histamine release from both lung and leucocytes. However, oxatomide induced histamine release far more effectively from sensitized lung than non-sensitized lung. Inhibition of immunologically induced histamine releast by oxatomide may play a part in its action as an anti-hay fever and, possibly, an anti-asthmatic drug.

摘要

奥沙米特是一种非常有效的组胺释放抑制剂,可抑制被动致敏的人肺组织碎片中由抗IgE和梯牧草花粉提取物诱导的组胺释放,以及人白细胞中由抗IgE诱导的组胺释放。其活性谱与色甘酸钠类药物不同。高浓度时,奥沙米特与其他抗组胺药及相关结构一样,可诱导肺组织和白细胞释放组胺。然而,奥沙米特从致敏肺组织诱导组胺释放的效果远比未致敏肺组织有效得多。奥沙米特对免疫诱导的组胺释放的抑制作用可能在其作为抗花粉热药物以及可能作为抗哮喘药物的作用中发挥作用。

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