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C5ades Arg过敏毒素刺激豚鼠肺释放白三烯。

Release of leukotrienes from guinea pig lung stimulated by C5ades Arg anaphylatoxin.

作者信息

Stimler N P, Bach M K, Bloor C M, Hugli T E

出版信息

J Immunol. 1982 May;128(5):2247-52.

PMID:6174625
Abstract

The complement anaphylatoxins C5a and C5Ades Arg contract guinea pig peripheral airway preparations and trachea by a mechanism largely independent of histamine release. In trachea the contractions are inhibited by FPL 55712, a relatively specific inhibitor of slow-reacting substance of anaphylaxis (SRS-A). SRS-A is now known to be a mixture of leukotrienes C4, D4, and E4 (LTC4, LTD4, LTE4). These data suggest that C5-derived anaphylatoxins stimulate production and release of leukotrienes in pulmonary tissues. To define these observations more precisely, fragments of guinea pig lung were incubated with porcine C5ades Arg, and the supernatant fluids were analyzed for leukotrienes by using both pharmacologic and chemical methods. In addition to histamine, a smooth muscle contracting activity characteristic of SRS-A was released from C5a-treated lung preparations. The contractile substance was identified as a leukotriene based on: 1) the characteristic contraction of guinea pig ileum, 2) inhibition of the contractile activity by FPL 55712, 3) enhanced release of activity in the presence of indomethacin or L-cysteine, 4) chromatographic behavior of ethanol-extracted active material on Amberlite XAD-7 resin, and 5) cochromatography of the active material on reverse-phase, high performance liquid chromatography with standard LTD4. We therefore concluded the humoral factor C5ades Arg induces a leukotriene release reaction in guinea pig lung tissue. This particular response of pulmonary tissue to anaphylatoxin has not been appreciated previously as an immediate effect of complement activation on the pathophysiology of the lung.

摘要

补体过敏毒素C5a和C5ades Arg通过一种很大程度上独立于组胺释放的机制使豚鼠外周气道制剂和气管收缩。在气管中,收缩受到FPL 55712的抑制,FPL 55712是过敏反应慢反应物质(SRS-A)的一种相对特异性抑制剂。现在已知SRS-A是白三烯C4、D4和E4(LTC4、LTD4、LTE4)的混合物。这些数据表明,C5衍生的过敏毒素刺激肺组织中白三烯的产生和释放。为了更精确地界定这些观察结果,将豚鼠肺组织碎片与猪C5ades Arg一起孵育,并用药理学和化学方法分析上清液中的白三烯。除了组胺外,经C5a处理的肺组织制剂还释放出具有SRS-A特征的平滑肌收缩活性。基于以下几点,收缩物质被鉴定为白三烯:1)豚鼠回肠的特征性收缩;2)FPL 55712对收缩活性的抑制;3)在吲哚美辛或L-半胱氨酸存在下活性增强释放;4)乙醇提取的活性物质在Amberlite XAD-7树脂上的色谱行为;5)活性物质与标准LTD4在反相高效液相色谱上的共色谱分析。因此,我们得出结论,体液因子C5ades Arg在豚鼠肺组织中诱导白三烯释放反应。肺组织对过敏毒素的这种特殊反应以前未被视为补体激活对肺病理生理学的直接影响。

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