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奥沙米特对大鼠腹膜肥大细胞组胺释放的比较作用。

Comparative effects of oxatomide on the release of histamine from rat peritoneal mast cells.

作者信息

De Clerck F, Van Reempts J, Borgers M

出版信息

Agents Actions. 1981 May;11(3):184-92. doi: 10.1007/BF01967612.

Abstract

Oxatomide inhibits the release of histamine from rat peritoneal mast cells in vitro induced by C 48/80, antigen, anti-IgE and ionophore A 23 187, without effect on non-specific release by n-decylamine. Its effect is concentration- and pH-dependent and decreases with increasing extracellular Ca2+-concentrations. Prolonged incubation does not enhance the inhibition, which is lost after one single wash-out. Aminophylline and isoproterenol are not potentiated by oxatomide. The present study points to an effect of oxatomide on a Ca2+-dependent process at the level of cell membrane common to antigen, C 48/80 and ionophore A 23 187.

摘要

奥沙米特可抑制体外培养的大鼠腹腔肥大细胞释放组胺,这些组胺的释放由C 48/80、抗原、抗IgE和离子载体A 23187诱导产生,但对正癸胺引起的非特异性释放没有影响。其作用具有浓度和pH依赖性,且随着细胞外钙离子浓度的增加而减弱。长时间孵育并不会增强这种抑制作用,单次洗脱后抑制作用即消失。氨茶碱和异丙肾上腺素不会因奥沙米特而增强作用。本研究表明,奥沙米特对细胞膜水平上抗原、C 48/80和离子载体A 23187所共有的钙离子依赖性过程有影响。

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