Platelet-activating factor mediates the ozone-induced increase in airway microvascular leakage in guinea pigs

Takeshi Kaneko, Hirotada Ikeda, Li Fu, Harumi Nishiyama, Takao Okubo
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引用次数: 13

Abstract

In the present study, we asked whether platelet-activating factor (PAF) mediates the ozone-induced increase in airway microvascular leakage. To answer this question, we examined the effect of a PAF receptor antagonist on the ozone-induced increase in airway microvascular leakage quantified by the extravasation of Evans blue dye in the guinea pig trachea and main bronchi. Guinea pigs were pretreated with the PAF receptor antagonist, E6123 ((S)-(+)-6-(2-chlorophenyl)-3-cyclopropane-carbonyl-8,11- dimethyl-2,3,4,5-tetrahydro-8H-pyrido[4′,3′:4,5]thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine) (0.01, 0.1 and 1.0 mg/kg i.v.) and then exposed to 3 ppm ozone for 30 min. The PAF receptor antagonist significantly reduced the ozone-induced increase in microvascular leakage in a dose-dependent manner in both the trachea and main bronchi. Our results indicate that PAF mediates the ozone-induced increase in airway microvascular leakage. We therefore suggest that PAF may be involved in ozone-induced airway inflammation.

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血小板活化因子介导臭氧诱导豚鼠气道微血管渗漏增加
在本研究中,我们询问血小板活化因子(PAF)是否介导臭氧诱导的气道微血管渗漏增加。为了回答这个问题,我们研究了PAF受体拮抗剂对臭氧诱导的气道微血管渗漏增加的影响,通过Evans蓝染料在豚鼠气管和主支气管的外渗来量化。用PAF受体拮抗剂E6123 ((S)-(+)-6-(2-氯苯基)-3-环丙烷-羰基-8,11-二甲基-2,3,4,5-四氢- 8h -吡啶[4 ',3 ':4,5]噻唑[3,2-f][1,2,4]三唑[4,3-a][1,4]二氮平)(0.01,0.1和1.0 mg/kg i.v)预处理豚鼠,然后暴露于3ppm臭氧中30分钟。PAF受体拮抗剂显著降低臭氧诱导的气管和主支气管微血管渗漏增加,并呈剂量依赖性。我们的研究结果表明,PAF介导臭氧诱导的气道微血管渗漏增加。因此,我们认为PAF可能参与了臭氧诱导的气道炎症。
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