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C5adesArg过敏毒素对豚鼠肺实质条的致痉挛活性:白三烯介导成分对环氧化酶抑制剂的敏感性

Spasmogenic activity of C5adesArg anaphylatoxin on guinea pig lung parenchymal strips: sensitivity of the leukotriene-mediated component to cyclooxygenase inhibitors.

作者信息

Stimler N P

出版信息

Biochem Biophys Res Commun. 1984 Dec 28;125(3):852-8. doi: 10.1016/0006-291x(84)91361-5.

Abstract

The leukotriene-dependent component of C5adesArg-induced contractile activity on guinea pig lung parenchymal strips is inhibited by cyclooxygenase inhibitors. Indomethacin simultaneously increased leukotriene release while inhibiting both cyclooxygenase-dependent mediator release and the contractile force generated. Tissue responses to LTC4 and LTD4 are also inhibited by cyclooxygenase blockade, while contractions induced by the thromboxane A2 analog, U-46619, histamine or acetylcholine are not affected. These data indicate a functional role for cyclooxygenase metabolites in leukotriene-induced contractile responses in lung.

摘要

环氧化酶抑制剂可抑制C5adesArg诱导豚鼠肺实质条收缩活性中白三烯依赖性成分。吲哚美辛在抑制环氧化酶依赖性介质释放和所产生的收缩力的同时,还能增加白三烯的释放。环氧化酶阻断也会抑制组织对LTC4和LTD4的反应,而血栓素A2类似物U-46619、组胺或乙酰胆碱诱导的收缩则不受影响。这些数据表明环氧化酶代谢产物在肺中白三烯诱导的收缩反应中发挥功能性作用。

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