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5-脂氧合酶抑制剂和白三烯拮抗剂(PF 5901)对新生期免疫家兔抗原诱导的气道反应的影响。

Effect of a 5-lipoxygenase inhibitor and leukotriene antagonist (PF 5901) on antigen-induced airway responses in neonatally immunized rabbits.

作者信息

Herd C M, Donigi-Gale D, Shoupe T S, Burroughs D A, Yeadon M, Page C P

机构信息

Department of Pharmacology, Kings College London.

出版信息

Br J Pharmacol. 1994 May;112(1):292-8. doi: 10.1111/j.1476-5381.1994.tb13067.x.

Abstract
  1. The effect of a single intratracheal dose (10 mg) of PF 5901 (2-[3(1-hydroxyhexyl) phenoxymethyl] quinoline hydrochloride, a specific inhibitor of the 5-lipoxygenase pathway of arachidonic acid metabolism and a leukotriene D4 antagonist) on airway changes induced in response to Alternaria tenuis aerosol challenge was assessed in adult rabbits neonatally immunized. Leukotriene generation was determined in vivo by measuring leukotriene B4 (LTB4) levels in bronchoalveolar lavage (BAL) fluid and ex vivo by measuring calcium ionophore-stimulated production of LTB4 in whole blood. 2. While PF 5901 (10 mg) had no significant effect on the acute bronchoconstriction induced by antigen, this dose was sufficient to inhibit significantly the increase in airway responsiveness to inhaled histamine 24 h following antigen challenge (P < 0.05). 3. Total leucocyte infiltration into the airways induced by antigen, as assessed by bronchoalveolar lavage, was significantly inhibited by pretreatment with PF 5901 (10 mg). However, the pulmonary infiltration of neutrophils and eosinophils induced by antigen was unaltered by prior treatment with PF 5901 (10 mg). 4. PF 5901 (10 mg) had no effect on ex vivo LTB4 synthesis in whole blood. However, the antigen-induced increase in LTB4 levels in BAL 24 h following challenge was significantly inhibited (P < 0.05). 5. We suggest from the results of the present study that the antigen-induced airway hyperresponsiveness to inhaled histamine in immunized rabbits is mediated, at least in part, by products of the 5-lipoxygenase metabolic pathway, and is not dependent on the extent of eosinophil or neutrophil influx into the airway lumen.
摘要
  1. 评估了单次气管内给予剂量为10毫克的PF 5901(2-[3-(1-羟基己基)苯氧基甲基]喹啉盐酸盐,一种花生四烯酸代谢5-脂氧合酶途径的特异性抑制剂及白三烯D4拮抗剂)对新生期免疫的成年兔因链格孢菌气溶胶激发而引起的气道变化的影响。通过测量支气管肺泡灌洗(BAL)液中的白三烯B4(LTB4)水平在体内测定白三烯生成,并通过测量全血中钙离子载体刺激产生的LTB4在体外测定白三烯生成。2. 虽然PF 5901(10毫克)对抗原诱导的急性支气管收缩无显著影响,但该剂量足以在抗原激发后24小时显著抑制气道对吸入组胺反应性的增加(P<0.05)。3. 通过支气管肺泡灌洗评估,PF 5901(10毫克)预处理可显著抑制抗原诱导的气道总白细胞浸润。然而,PF 5901(10毫克)预先处理并未改变抗原诱导的中性粒细胞和嗜酸性粒细胞的肺浸润。4. PF 5901(10毫克)对全血中体外LTB4合成无影响。然而,激发后24小时BAL中抗原诱导的LTB4水平增加被显著抑制(P<0.05)。5. 从本研究结果我们推测,免疫兔中抗原诱导的气道对吸入组胺的高反应性至少部分由5-脂氧合酶代谢途径的产物介导,且不依赖于嗜酸性粒细胞或中性粒细胞流入气道腔的程度。

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