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首页> 外文期刊>Japanese Journal of Pharmacology >Effects of a Specific Cysteinyl Leukotriene Antagonist, Pranlukast, on Antigen-Induced Cysteinyl Leukotriene-Mediated Rhinitis in Guinea Pigs
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Effects of a Specific Cysteinyl Leukotriene Antagonist, Pranlukast, on Antigen-Induced Cysteinyl Leukotriene-Mediated Rhinitis in Guinea Pigs

机译:特定的半胱氨酰白三烯拮抗剂Pranlukast对豚鼠抗原诱导的半胱氨酸白三烯介导的鼻炎的影响

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References(23) Cited-By(11) To examine the effects of a specific cysteinyl leukotriene (cysLT) antagonist, pranlukast, on allergic rhinitis, antigen-induced rhinitis in guinea pigs was modified by pretreatment with an cyclooxygenase inhibitor (indomethacin) followed by an H1-blocker (pyrilamine). Intranasal ovalbumin (OVA) administration in actively sensitized guinea pigs resulted in concentration-dependent increases in nasal permeability and nasal airway resistance (NAR). Although pyrilamine (1 mg/kg, i.v.) abolished these antigen-induced changes, pretreatment with indomethacin (5 mg/kg, i.v.) followed by pyrilamine enhanced these responses to a degree similar to that observed with OVA challenge alone. Analyses of nasal perfusate in indomethacin/pyrilamine-pretreated animals showed that cysLTs increased by 270.8%, whereas thromboxane B2 decreased by 88.3% as compared with those on challenged with OVA alone. Oral administration of pranlukast (1-10 mg/kg) dose-dependently prevented increases in nasal permeability and NAR of indomethacin/pyrilamine-pretreated animals. However, an anti-allergic agent, azelastine, did not affect these responses. These results indicate that pranlukast suppresses antigen-induced cysLT-mediated responses of allergic rhinitis in actively sensitized guinea pigs. A cysLT antagonist, pranlukast, may thus prevent cysLT-mediated symptoms of allergic rhinitis.
机译:参考文献(23)(11)为了检查特定的半胱氨酰白三烯(cysLT)拮抗剂普仑司特对变应性鼻炎的影响,对抗原诱导的豚鼠鼻炎进行了改良,方法是先用环氧合酶抑制剂(吲哚美辛)预处理H1受体阻滞剂(吡咯胺)。积极致敏的豚鼠鼻内卵清蛋白(OVA)给药导致鼻通透性和鼻气道阻力(NAR)浓度依赖性增加。尽管吡拉明(1 mg / kg,静脉内)消除了这些抗原诱导的变化,但是用吲哚美辛(5 mg / kg,静脉内)预处理然后吡咯胺增强了这些反应,其程度与单独使用OVA激发所观察到的相似。与吲哚美辛/吡咯胺预处理的动物相比,经鼻灌洗液分析发现,与仅用OVA刺激的人相比,cysLTs增加了270.8%,而血栓烷B2减少了88.3%。口服普仑司特(1-10 mg / kg)剂量依赖性地防止了消炎痛/吡咯胺预处理的动物鼻通透性和NAR的增加。但是,抗过敏药氮卓斯汀不影响这些反应。这些结果表明,在主动致敏的豚鼠中,普仑司特抑制抗原诱导的cysLT介导的变应性鼻炎反应。 cysLT拮抗剂普鲁司特可以预防cysLT介导的过敏性鼻炎症状。

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