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以高反应性大鼠变应原诱导的支气管收缩抑制作为测试5-脂氧合酶抑制剂和白三烯D4受体拮抗剂的模型。

Inhibition of allergen-induced bronchoconstriction in hyperreactive rats as a model for testing 5-lipoxygenase inhibitors and leukotriene D4 receptor antagonists.

作者信息

Piechuta H, Ford-Hutchinson A W, Letts L G

机构信息

Department of Pharmacology, Merck Frosst Canada Inc., Pointe Claire-Dorval, Québec, Canada.

出版信息

Agents Actions. 1987 Oct;22(1-2):69-74. doi: 10.1007/BF01968819.

Abstract

Sensitized inbred hyperreactive rats showed reproducible episodes of dyspnea when exposed to aerosols of antigen. Following inhibition of the serotonin component of the response by pretreatment with methysergide, the model was shown to be useful for studying the oral activity of compounds that affect the production or action of leukotrienes. This was shown through inhibition of the duration of dyspnea by two selective 5-lipoxygenase inhibitors, L-651,392 and L-615,919, and two selective leukotriene D4 receptor antagonists, L-647,438 and L-649,923. Selectivity of the compounds could be demonstrated by reducing inhibition of the antigen response in the absence of methysergide and failure to inhibit serotonin-induced dyspnea. It is concluded that the model provides a reproducible method for screening large numbers of leukotriene inhibitors and antagonists and gives a measurement of their duration of biological activity.

摘要

致敏的近交高反应性大鼠在接触抗原气雾剂时会出现可重复的呼吸困难发作。在用麦角新碱预处理抑制反应中的血清素成分后,该模型被证明可用于研究影响白三烯产生或作用的化合物的口服活性。两种选择性5-脂氧合酶抑制剂L-651,392和L-615,919以及两种选择性白三烯D4受体拮抗剂L-647,438和L-649,923对白喉持续时间的抑制作用证明了这一点。在没有麦角新碱的情况下减少对抗原反应的抑制以及未能抑制血清素诱导的呼吸困难,可以证明化合物的选择性。得出的结论是,该模型为筛选大量白三烯抑制剂和拮抗剂提供了一种可重复的方法,并能测量它们的生物活性持续时间。

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