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半胱氨酰白三烯拮抗剂(ONO-1078)对变应性绵羊抗原诱导反应的影响

The effects of a cysteinyl leukotriene antagonist (ONO-1078) on antigen-induced responses in allergic sheep.

作者信息

Abraham W M, Ahmed A, Cortes A, Sielczak M, Hallmon J

机构信息

Department of Research, Mount Sinai Medical Center, Miami Beach, Florida 33140.

出版信息

Prostaglandins Leukot Essent Fatty Acids. 1993 Mar;48(3):233-9. doi: 10.1016/0952-3278(93)90091-a.

DOI:10.1016/0952-3278(93)90091-a
PMID:8469683
Abstract

The cysteinyl leukotrienes (LTC4/D4/E4) are putative mediators of asthma. In this study we used sheep allergic to Ascaris suum antigen to examine the effects of a novel orally active cysteinyl LT antagonist, ONO-1078, on antigen-induced early and late responses, airway inflammation, post challenge (24 h) airway hyperresponsiveness (AHR) and mucociliary clearance. Airway responses to antigen were determined by measuring specific lung resistance (SRL) before and for 8 h after challenge, bronchoalveolar lavage (BAL) was used to estimate airway inflammation, and airway responsiveness was measured by determining the carbachol dose that increased SRL by 400% (PC400). We also used a radiographic technique to measure the antigen-induced change in tracheal mucus velocity (TMV), a marker of mucociliary clearance. In two trials separated by at least 21 days, sheep were treated once with ONO-1078 (30 mg/kg, p.o.) and once with placebo (0.5% methylcellulose), 2 h before and 4 h after antigen challenge. Treatment with ONO-1078 (n = 7) provided 40% protection (p < 0.10) against the peak early increase in SRL, resulted in a more rapid reversal of the early response, and provided 96% protection against the peak late (6-8 h) increase in SRL. ONO-1078 also inhibited the AHR 24 h after challenge. In the drug trial, PC400 was unchanged as compared to pre-challenge, whereas in the placebo trial, PC400 was decreased 1.4-fold (p < 0.05). Treatment however, did not affect BAL cell numbers or differential.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

半胱氨酰白三烯(LTC4/D4/E4)被认为是哮喘的介质。在本研究中,我们使用对猪蛔虫抗原过敏的绵羊来检测一种新型口服活性半胱氨酰白三烯拮抗剂ONO-1078对抗原诱导的早期和晚期反应、气道炎症、激发后(24小时)气道高反应性(AHR)以及黏液纤毛清除功能的影响。通过测量激发前及激发后8小时的特异性肺阻力(SRL)来确定气道对抗原的反应,采用支气管肺泡灌洗(BAL)来评估气道炎症,并通过测定使SRL增加400%的卡巴胆碱剂量(PC400)来测量气道反应性。我们还使用一种放射学技术来测量抗原诱导的气管黏液速度(TMV)变化,TMV是黏液纤毛清除功能的一个指标。在至少间隔21天的两项试验中,绵羊在抗原激发前2小时和激发后4小时分别接受一次ONO-1078(30毫克/千克,口服)治疗和一次安慰剂(0.5%甲基纤维素)治疗。用ONO-1078治疗(n = 7)可对SRL早期峰值增加提供40%的保护作用(p < 0.10),使早期反应逆转更快,并对SRL晚期(6 - 8小时)峰值增加提供96%的保护作用。ONO-1078还可抑制激发后24小时的AHR。在药物试验中,与激发前相比,PC400无变化,而在安慰剂试验中,PC400降低了1.4倍(p < 0.05)。然而,治疗并未影响BAL细胞数量或分类。(摘要截断于250字)

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