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巴西日圆线虫致敏大鼠中的血小板活化因子与全身性过敏反应:血小板活化因子拮抗剂的不同作用

Platelet activating factor and systemic anaphylaxis in Nippostrongylus brasiliensis-sensitized rats: differential effects of PAF antagonists.

作者信息

Mathison R, Davison J S, Befus A D

机构信息

Department of Medical Physiology, Faculty of Medicine, University of Calgary, Alberta, Canada.

出版信息

Br J Pharmacol. 1992 Jun;106(2):263-6. doi: 10.1111/j.1476-5381.1992.tb14326.x.

Abstract
  1. The effects of two platelet-activating factor (PAF) antagonists, WEB 2086 and BN 52021, in reducing the changes in extravasation (Evans blue technique) and blood flow (radiolabelled microsphere method) to various organs and tissues following anaphylactic shock in the Nippostrongylus brasiliensis-sensitized rat were investigated. 2. Both antagonists attenuated anaphylaxis-induced increases in plasma protein leak in the trachea, stomach and small intestine, although they did not block extravasation in the colon and kidneys. 3. Anaphylaxis-induced decreases in blood flow to the adrenals were effectively antagonized by WEB 2086, although this antagonist did not reverse blood flow decreases to any other tissues. BN 52021, on the other hand, did not alter anaphylaxis-induced decreases in blood flow to the adrenals, but effectively prevented dramatic decreases in blood flow to the large and small bowel and spleen. 4. Anaphylactic shock produced marked reduction in blood pressure that was partly reversed by WEB 2086, whereas BN 52021 effectively blocked the decreases in cardiac output. 5. Thus, PAF is responsible for some of the haemodynamic and extravasation of protein changes associated with systemic anaphylaxis in the rat, although the differential inhibition observed with the two antagonists suggests that PAF alters vascular responsiveness through different mechanisms in selected tissues.
摘要
  1. 研究了两种血小板活化因子(PAF)拮抗剂WEB 2086和BN 52021对巴西日圆线虫致敏大鼠过敏性休克后各器官和组织渗出(伊文思蓝技术)和血流(放射性标记微球法)变化的影响。2. 两种拮抗剂均减轻了过敏性反应诱导的气管、胃和小肠血浆蛋白渗漏增加,尽管它们并未阻止结肠和肾脏的渗出。3. WEB 2086有效拮抗了过敏性反应诱导的肾上腺血流减少,尽管该拮抗剂并未逆转其他任何组织的血流减少。另一方面,BN 52021并未改变过敏性反应诱导的肾上腺血流减少,但有效防止了大肠、小肠和脾脏血流的显著减少。4. 过敏性休克导致血压显著降低,WEB 2086可部分逆转,而BN 52021有效阻断心输出量的减少。5. 因此,PAF与大鼠全身性过敏反应相关的一些血液动力学和蛋白渗出变化有关,尽管两种拮抗剂观察到的差异抑制表明PAF通过不同机制改变了特定组织中的血管反应性。

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