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组胺和白三烯非依赖性豚鼠过敏性休克不能用血小板活化因子来解释。

Histamine and leukotriene-independent guinea-pig anaphylactic shock unaccounted for by Paf-acether.

作者信息

Detsouli A, Lefort J, Vargaftig B B

出版信息

Br J Pharmacol. 1985 Apr;84(4):801-10. doi: 10.1111/j.1476-5381.1985.tb17374.x.

Abstract

Ovalbumin induced dose-dependent contractions of lung parenchyma strips from sensitized guinea-pigs, whereas Paf-acether (1-alkyl-2-acetyl-sn-glycero-3-phosphoryl choline), a potential mediator of immediate hypersensitivity, induced a single contraction, followed by specific desensitization to a second exposure. Lung strips desensitized to Paf-acether contracted to ovalbumin as did non-desensitized controls, even in the presence of inhibitors of other mediators of anaphylaxis. Contractions by Paf-acether and by ovalbumin were reduced by nordihydroguaiaretic acid (NDGA) and by the phospholipase A2 inhibitor p-bromophenacyl bromide (0.1-0.3 mM). Three other anti-lipoxygenase agents (diethylcarbamazine, 5 mM; eicosatetraynoic acid and BW755c, 0.1 mM), reduced the contractions by ovalbumin but also those due to acetylcholine, indicating non-specific effects. Neither the anti-allergic compound sodium cromoglycate (3 mM) nor the anti-leukotriene agent, FPL 55712 (0.01 mM), inhibited the contractions by ovalbumin or by Paf-acether. A sensitized strip stimulated with ovalbumin released substances which contracted a non-sensitized strip mounted in the same organ bath. The contractions of the non-sensitized strip were abolished by FPL 55712 (0.01 mM), by NDGA and BW755c, (0.1 mM), whereas those of the sensitized one were unaffected. Leukotrienes are formed by the lung strips during shock but alone, they do not explain the contractile activity. The intravenous administration of ovalbumin (1 mg kg-1) led to bronchoconstriction and thrombocytopenia, which were not modified by the anti-leukotriene substance FPL 55712 nor by aspirin. Bronchoconstriction was suppressed if FPL 55712 was used in combination with aspirin (20 mg kg-1), mepyramine and methysergide (200 micrograms kg-1 of either). Pretreatment of the guinea-pigs with propranolol reduced this inhibition to approximately 60%. In no instance was thrombocytopenia prevented. In vitro contractions of the actively sensitized lung strip are not fully accounted for by histamine, FPL 55712-inhibitable leukotrienes or Paf-acether, whereas in systemic anaphylaxis histamine and leukotrienes (inhibited respectively by mepyramine and by FPL 55712) have a significant role.

摘要

卵清蛋白可引起致敏豚鼠肺实质条带剂量依赖性收缩,而血小板活化因子(1-烷基-2-乙酰基-sn-甘油-3-磷酸胆碱)作为速发型超敏反应的潜在介质,可引起单次收缩,随后对第二次暴露产生特异性脱敏。对血小板活化因子脱敏的肺条带对卵清蛋白的收缩反应与未脱敏的对照条带相同,即使存在其他过敏介质抑制剂时也是如此。去甲二氢愈创木酸(NDGA)和磷脂酶A2抑制剂对溴苯甲酰溴(0.1 - 0.3 mM)可降低血小板活化因子和卵清蛋白引起的收缩。另外三种抗脂氧合酶药物(二乙氨基甲嗪,5 mM;二十碳四炔酸和BW755c,0.1 mM)可降低卵清蛋白引起的收缩,但也会降低乙酰胆碱引起的收缩,表明存在非特异性作用。抗过敏化合物色甘酸钠(3 mM)和抗白三烯药物FPL 55712(0.01 mM)均不能抑制卵清蛋白或血小板活化因子引起的收缩。用卵清蛋白刺激致敏条带会释放出能使安装在同一器官浴槽中的未致敏条带收缩的物质。FPL 55712(0.01 mM)、NDGA和BW755c(0.1 mM)可消除未致敏条带的收缩,而致敏条带的收缩不受影响。白三烯在休克期间由肺条带形成,但单独存在时,它们并不能解释收缩活性。静脉注射卵清蛋白(1 mg/kg)会导致支气管收缩和血小板减少,抗白三烯物质FPL 55712和阿司匹林对此均无影响。如果将FPL 55712与阿司匹林(20 mg/kg)、美吡拉敏和甲基麦角新碱(200 μg/kg其中任何一种)联合使用,支气管收缩会受到抑制。用普萘洛尔预处理豚鼠可使这种抑制作用降低至约60%。在任何情况下,血小板减少均未得到预防。主动致敏肺条带的体外收缩不能完全由组胺、FPL 55712可抑制的白三烯或血小板活化因子来解释,而在全身性过敏反应中,组胺和白三烯(分别被美吡拉敏和FPL 55712抑制)起重要作用。

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