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葡聚糖和离子载体A23187引起的组胺释放差异:抑制剂的作用

Differential histamine release by dextran and the ionophore A23187: the actions of inhibitors.

作者信息

Garland L G, Mongar J L

出版信息

Int Arch Allergy Appl Immunol. 1976;50(1):27-42. doi: 10.1159/000231477.

Abstract

Inhibitors of mast cell membrane activation reduced histamine release from rat mast cells induced by dextran and phosphatidyl serine but not that induced by the calcium ionophore A23187. Such inhibitors included cromoglycate, an orally-active anti-allergic agent 3-(5-tetrazolyl)thioxanthone 10,10-dioxide, dibutyryl cyclic 3':5'-AMP, theophylline and dicumarol. Inhibitors of mast cell metabolism reduced both types of release and these included oligomycin, papevevime, and the two uncouplers of oxidative phosphorylation-alpha2,4-dinitrophenol and CCCP. Inhibition of histamine release from rat isolated peritoneal mast cells by either a mixture of dextran and phosphatidyl serine or the ionophore A23187 thus allows inhibitors of mast cell membrane activation to be distinguished from those affecting cell metabolism or the later stages of the secretory process.

摘要

肥大细胞膜激活抑制剂可减少由右旋糖酐和磷脂酰丝氨酸诱导的大鼠肥大细胞组胺释放,但不能减少由钙离子载体A23187诱导的组胺释放。这类抑制剂包括色甘酸、口服活性抗过敏剂3-(5-四唑基)噻吨酮10,10-二氧化物、二丁酰环3':5'-AMP、茶碱和双香豆素。肥大细胞代谢抑制剂可减少两种类型的释放,这些抑制剂包括寡霉素、帕佩韦韦姆以及氧化磷酸化的两种解偶联剂——α2,4-二硝基苯酚和CCCP。因此,通过右旋糖酐和磷脂酰丝氨酸混合物或离子载体A23187抑制大鼠分离腹膜肥大细胞的组胺释放,可区分肥大细胞膜激活抑制剂与影响细胞代谢或分泌过程后期阶段的抑制剂。

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