首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Prevention by the tachykinin NK2 receptor antagonist SR 48968 of antigen-induced airway hyperresponsiveness in sensitized guinea-pigs.
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Prevention by the tachykinin NK2 receptor antagonist SR 48968 of antigen-induced airway hyperresponsiveness in sensitized guinea-pigs.

机译:通过速激肽NK2受体拮抗剂SR 48968预防致敏豚鼠中抗原诱导的气道高反应性。

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摘要

The involvement of tachykinins in antigen-induced airway hyperresponsiveness (AHR) was characterized pharmacologically in guinea-pigs sensitized to ovalbumin with antagonists of tachykinin NK1 and NK2 receptors, namely SR 140333 and SR 48968, respectively. AHR was illustrated by increased sensitivity to bronchoconstriction provoked by aerosolized acetylcholine in anaesthetized, ventilated animals, administrated 48 h after ovalbumin aerosol challenge. SR 48968 (1 mg kg-1, i.p.), when given once 30 min before the antigen challenge, prevented AHR, whereas SR 140333 did not. These findings suggest that the tachykinin NK2 receptor antagonist, SR 48968, may be useful for investigating mechanisms of tachykinins in the development of airway hyperresponsiveness.
机译:速激肽参与抗原诱导的气道高反应性(AHR)的药理学特征是,对速激肽NK1和NK2受体拮抗剂SR 140333和SR 48968分别对卵清蛋白致敏的豚鼠。卵清蛋白气雾剂攻击后48小时给予麻醉,通风的动物,气雾化的乙酰胆碱对支气管收缩的敏感性增加,说明了AHR。 SR 48968(1 mg kg-1,i.p.)在抗原攻击前30分钟给药一次,可预防AHR,而SR 140333则不能。这些发现表明,速激肽NK2受体拮抗剂SR 48968可用于研究速激肽在气道高反应性发展中的机制。

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