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血小板与肺的体内相互作用:一种多用途模型的人为现象?

Platelet-lung in vivo interactions: an artifact of a multi-purpose model?

作者信息

Vargaftig B B, Lefort J, Prancan A V, Chignard M, Benveniste J

出版信息

Haemostasis. 1979;8(3-5):171-82. doi: 10.1159/000214309.

Abstract

The simultaneous evaluation of platelet behaviour in vivo and of the accompanying bronchoconstriction in the guinea pig is described. Arachidonic acid induces bronchoconstriction, accompanied by, but independent from, thrombocytopenia, whereas collagen induces bronchoconstriction also accompanied by, but dependent from, thrombocytopenia. In both cases bronchoconstriction is due to cyclo-oxygenase metabolites of arachidonic acid. Use of potential inhibitors of thromboxane synthetase failed to reveal which of prostaglandin endoperoxides or thromboxane A2 is responsible for aspirin-inhibitive bronchoconstriction and thrombocytopenia. In contrast to PGE1 prostacyclin failed to interfere with bronchoconstriction by serotonin or by arachidonic acid, even though thrombocytopenia by the latter was suppressed. Bronchoconstriction by collagen, in contrast, was inhibited by nanogram doses of prostacyclin, confirming platelet-dependency. The combined bronchoconstriction/thrombocytopenia test in guinea pigs can discriminate sites of action of anti-inflammatory drugs, of agents which block specific platelet and/or bronchial receptors, which stimulate the cyclic AMP system, or generically which interfere with the mechanisms of bronchoconstriction and of thrombocytopenia.

摘要

本文描述了对豚鼠体内血小板行为及伴随的支气管收缩进行同步评估的情况。花生四烯酸可诱导支气管收缩,同时伴有血小板减少,但二者相互独立;而胶原蛋白诱导支气管收缩时也伴有血小板减少,且二者相互依赖。在这两种情况下,支气管收缩均归因于花生四烯酸的环氧化酶代谢产物。使用血栓素合成酶的潜在抑制剂未能揭示前列腺素内过氧化物或血栓素A2中哪一种是阿司匹林抑制性支气管收缩和血小板减少的原因。与前列腺素E1不同,前列环素未能干扰5-羟色胺或花生四烯酸引起的支气管收缩,尽管后者引起的血小板减少得到了抑制。相比之下,纳克剂量的前列环素可抑制胶原蛋白引起的支气管收缩,证实了其对血小板的依赖性。豚鼠的支气管收缩/血小板减少联合试验可区分抗炎药物、阻断特定血小板和/或支气管受体的药物、刺激环磷酸腺苷系统的药物或一般干扰支气管收缩和血小板减少机制的药物的作用部位。

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