Suppr超能文献

血小板活化因子受体拮抗剂SDZ 64 - 412对豚鼠变应原激发后非特异性气道高反应性的预防作用

Prevention of non-specific airway hyperreactivity after allergen challenge in guinea-pigs by the PAF receptor antagonist SDZ 64-412.

作者信息

Havill A M, Van Valen R G, Handley D A

机构信息

Sandoz Research Institute, East Hanover, NJ 07936.

出版信息

Br J Pharmacol. 1990 Feb;99(2):396-400. doi: 10.1111/j.1476-5381.1990.tb14715.x.

Abstract
  1. Allergen challenge by aerosol in sensitized guinea-pigs elicited non-specific airway hyperreactivity assessed by reactivity to i.v. histamine or acetylcholine. Airway hyperreactivity to histamine persisted for at least 48 h and was accompanied by pulmonary eosinophilia as determined by bronchoalveolar lavage cell analysis. 2. Airway hyperreactivity was independent of vagal reflex mechanisms since it was not abrogated by bilateral vagotomy. 3. The novel platelet-activating factor (PAF) receptor antagonist SDZ 64-412 inhibited the development of airway hyperreactivity, as measured 24 h after aerosol allergen challenge, when given as a single treatment orally 2 h before allergen challenge. The PAF receptor antagonist WEB 2086 as well as methylprednisolone and ketotifen also showed efficacy in preventing development of airway hyperreactivity. 4. Neither the two PAF antagonists nor ketotifen had any effect on bronchoalveolar lavage (BAL) eosinophil numbers. Methylprednisolone was the only substance which readily prevented eosinophil recruitment in addition to airway hyperreactivity. 5. We conclude that allergen-induced airway hyperreactivity in guinea-pigs is inhibited by prophylactic anti-asthma drugs and specific PAF receptor antagonists, thus demonstrating a pivotal role of PAF in this response. There was a lack of correlation between airway hyperreactivity and the presence of BAL eosinophils.
摘要
  1. 对致敏豚鼠进行气溶胶变应原激发试验,通过静脉注射组胺或乙酰胆碱的反应性来评估非特异性气道高反应性。对组胺的气道高反应性持续至少48小时,并伴有支气管肺泡灌洗细胞分析所确定的肺嗜酸性粒细胞增多。2. 气道高反应性与迷走神经反射机制无关,因为双侧迷走神经切断术并未消除该反应。3. 新型血小板活化因子(PAF)受体拮抗剂SDZ 64 - 412在变应原激发试验前2小时口服单次给药时,抑制了气溶胶变应原激发24小时后所测量的气道高反应性的发展。PAF受体拮抗剂WEB 2086以及甲基强的松龙和酮替芬在预防气道高反应性发展方面也显示出疗效。4. 两种PAF拮抗剂和酮替芬对支气管肺泡灌洗(BAL)嗜酸性粒细胞数量均无影响。甲基强的松龙是唯一除了能预防气道高反应性外还能轻易阻止嗜酸性粒细胞募集的物质。5. 我们得出结论,预防性抗哮喘药物和特异性PAF受体拮抗剂可抑制豚鼠变应原诱导的气道高反应性,从而证明PAF在该反应中起关键作用。气道高反应性与BAL嗜酸性粒细胞的存在之间缺乏相关性。

相似文献

引用本文的文献

本文引用的文献

10
Evidence favouring PAF rather than leukotrienes in the pathogenesis of asthma.
Pharmacol Res Commun. 1986 Aug;18 Suppl:217-37. doi: 10.1016/0031-6989(86)90055-x.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验