方军, 郑钦岳. 商陆皂甙甲抑制大鼠腹腔巨噬细胞释放血小板活化因子J. 药学学报, 1991, 26(10): 721-724.
引用本文: 方军, 郑钦岳. 商陆皂甙甲抑制大鼠腹腔巨噬细胞释放血小板活化因子J. 药学学报, 1991, 26(10): 721-724.
J Fang, QY Zheng. INHIBITORY EFFECT OF ESCULENTOSIDE A ON PLATELET ACTIVATING FACTOR RELEASED FROM CALCIMYCIN INDUCED RAT PERITONEAL MACROPHAGES.J. Acta Pharmaceutica Sinica, 1991, 26(10): 721-724.
Citation: J Fang, QY Zheng. INHIBITORY EFFECT OF ESCULENTOSIDE A ON PLATELET ACTIVATING FACTOR RELEASED FROM CALCIMYCIN INDUCED RAT PERITONEAL MACROPHAGES.J. Acta Pharmaceutica Sinica, 1991, 26(10): 721-724.

商陆皂甙甲抑制大鼠腹腔巨噬细胞释放血小板活化因子

INHIBITORY EFFECT OF ESCULENTOSIDE A ON PLATELET ACTIVATING FACTOR RELEASED FROM CALCIMYCIN INDUCED RAT PERITONEAL MACROPHAGES.

  • 摘要: 卡西霉素(A23187)刺激大鼠腹腔巨噬细胞释放血小板活化因子(PAF),用洗涤血小板聚集的方法测定,证明商陆皂甙甲在0.1~100μmol/L浓度范围内及所试的时间范围内,呈剂量及时间依赖性抑制大鼠腹腔巨噬细胞释放PAF:商陆皂甙甲可能就是通过抑制体内PAF生成而起抗炎作用的。

     

    Abstract: Platelet activating factor (PAF)is a kind of inflammatory mediator. We used the method of aggregation of washed rabbit platelet to study the effect of esculentoside A (EsA) on the release of PAF from calcimycin (A23187) stimulated rat peritoneal macrophages and found that the release of PAF was inhibited by EsA in a time and dose dependent manner. The IC50 of EsA for the inhibition of PAF release was 1.5μmol/L.Under the same condition, the release of PAF was also inhibited by mepacrine at 100 μmol/L. The results indicate that EsA is a potent inhibitor of PAF synthsis in rat peritoneal macrophages.

     

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