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Br J Pharmacol. 1990 Feb;99(2):396-400. doi: 10.1111/j.1476-5381.1990.tb14715.x.
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The effect of the selective PAF antagonist WEB 2170 on PAF and antigen induced airway hyperresponsiveness and eosinophil infiltration.选择性血小板活化因子拮抗剂WEB 2170对血小板活化因子及抗原诱导的气道高反应性和嗜酸性粒细胞浸润的影响。
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Activity of a novel thienodiazepine derivative as a platelet-activating factor antagonist in guinea pig lungs. Effects on platelet-activating factor and allergen induced eosinophil accumulation.一种新型噻吩二氮卓衍生物在豚鼠肺中作为血小板活化因子拮抗剂的活性。对血小板活化因子和变应原诱导的嗜酸性粒细胞积聚的影响。
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Limited interference of specific Paf antagonists with hyper-responsiveness to Paf itself of lungs from actively sensitized guinea-pigs.特定血小板活化因子拮抗剂对主动致敏豚鼠肺脏对血小板活化因子自身高反应性的有限干扰。
Br J Pharmacol. 1989 Jun;97(2):433-42. doi: 10.1111/j.1476-5381.1989.tb11970.x.

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Platelet-activating factor (PAF) plays an important role in the immediate asthmatic response in guinea-pig by augmenting the response to histamine.血小板活化因子(PAF)通过增强对组胺的反应,在豚鼠的速发型哮喘反应中起重要作用。
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Effects of bradykinin receptor antagonists on antigen-induced respiratory distress, airway hyperresponsiveness and eosinophilia in guinea-pigs.缓激肽受体拮抗剂对豚鼠抗原诱导的呼吸窘迫、气道高反应性和嗜酸性粒细胞增多的影响。
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Agents Actions. 1992 Nov;37(3-4):195-7. doi: 10.1007/BF02028107.

本文引用的文献

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Glucocorticoid protection against PAF-acether toxicity in mice.糖皮质激素对小鼠血小板活化因子-乙醚毒性的保护作用。
Br J Pharmacol. 1983 Jun;79(2):595-8. doi: 10.1111/j.1476-5381.1983.tb11034.x.
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Increased biosynthesis of platelet-activating factor in activated human eosinophils.活化的人嗜酸性粒细胞中血小板活化因子的生物合成增加。
J Biol Chem. 1984 May 10;259(9):5526-30.
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A comparison of the in vivo effects of ketotifen, clemastine, chlorpheniramine and sodium cromoglycate on histamine and allergen induced weals in human skin.酮替芬、氯马斯汀、氯苯那敏和色甘酸钠对组胺和变应原诱导的人体皮肤风团的体内作用比较。
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Antigen-induced bronchial anaphylaxis in actively sensitized guinea-pigs: effect of long-term treatment with sodium cromoglycate and aminophylline.抗原诱导的主动致敏豚鼠支气管过敏反应:色甘酸钠和氨茶碱长期治疗的效果
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Role of the vagus nerves in anaphylaxis and histamine-induced bronchoconstrictions in guinea-pigs.迷走神经在豚鼠过敏反应和组胺诱导的支气管收缩中的作用。
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Evidence for a direct effect on vascular permeability of platelet-activating factor induced hemoconcentration in the guinea pig.血小板激活因子诱导豚鼠血液浓缩对血管通透性产生直接影响的证据。
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Eosinophils, bronchial hyperreactivity and late-phase asthmatic reactions.嗜酸性粒细胞、支气管高反应性与迟发性哮喘反应。
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Damage of the airway epithelium and bronchial reactivity in patients with asthma.哮喘患者气道上皮损伤与支气管反应性
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Bronchoalveolar eosinophilia during allergen-induced late asthmatic reactions.变应原诱导的迟发型哮喘反应期间的支气管肺泡嗜酸性粒细胞增多
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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.

DOI:10.1111/j.1476-5381.1990.tb14715.x
PMID:2328403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1917390/
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。