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首页> 外文期刊>Prostaglandins, Leukotrienes, and Essential Fatty Acids >Studies on the mechanism of PAF-induced vasopermeability in rat lungs.
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Studies on the mechanism of PAF-induced vasopermeability in rat lungs.

机译:PAF诱导的大鼠肺血管通透性机制的研究。

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摘要

The present study evaluated the effect of platelet activating factor (PAF) instilled into rat airways on vascular permeability assessed in isolated lung tissues by Evans blue (EB)-labelled plasma protein extravasation. It was found that intratracheal instillation of PAF induces a dose-dependent increase of EB extravasation in the bronchi (upper and inner) but not in the lung parenchyma. The contribution of eicosanoids to PAF-induced increase of vascular permeability was investigated by treating the animals with selected inhibitors prior to PAF administration. Mepacrine (5 mg/kg), L-663,536 (10 mg/kg), indomethacin (4 mg/kg) and dazoxiben (10 mg/kg) significantly reduced EB extravasation in the bronchi. The PAF antagonists BN-52021 (5 mg/kg), WEB-2086 (1 mg/kg), WEB-2170 (5 mg/kg) and PCA-4248 (3 mg/kg) were all effective in reducing the extravasation. These results suggest that PAF-induced increase of vascular permeability in rat bronchi is mediated by cyclooxygenase and lipoxygenase products of arachidonic acid metabolism.
机译:本研究评估了通过伊文思蓝(EB)标记的血浆蛋白外渗评估了注入大鼠气道的血小板活化因子(PAF)对分离的肺组织中血管通透性的影响。发现气管内滴注PAF会引起支气管(上部和内部)的EB外渗剂量依赖性增加,但不会导致肺实质内的EB外渗。类花生酸对PAF诱导的血管通透性增加的贡献是通过在施用PAF之前用选定的抑制剂处理动物来研究的。 Mepacrine(5 mg / kg),L-663,536(10 mg / kg),消炎痛(4 mg / kg)和dazoxiben(10 mg / kg)显着降低了支气管EB的外渗。 PAF拮抗剂BN-52021(5 mg / kg),WEB-2086(1 mg / kg),WEB-2170(5 mg / kg)和PCA-4248(3 mg / kg)在减少外渗方面均有效。这些结果表明,PAF诱导的大鼠支气管血管通透性增加是由花生四烯酸代谢的环氧合酶和脂氧合酶产物介导的。

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