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色甘酸酯及新型抗过敏药物U - 42,585E对过敏反应的抑制作用。II. 在灵长类动物中对雾化猪蛔虫抗原的活性。

Inhibition of allergic reactions by cromoglycate and by a new antiallergy drug U-42,585E. II. Activity in primates against aerosolized Ascaris suum antigen.

作者信息

Johnson H G, VanHout C A, Wright J B

出版信息

Int Arch Allergy Appl Immunol. 1978;56(6):481-7. doi: 10.1159/000232062.

Abstract

Immediate type hypersensitivity to Ascaris antigen in Rhesus reactor monkeys was used to assess the pharmacologic profile of cromolyn Na (DSCG) and a new inhibitor of IgE-mediated lung function changes (U-42,585E). Two parameters used to measure lung function, respiratory rate increase and tidal volume decrease, were significantly altered in a dose-related fashion by U-42,585E when the latter was administered either by the intravenous, intrabronchial, or the oral route. Oral activity of U-42,585E was demonstrated with doses as low as 5 mg/kg in Ascaris reactor primates.

摘要

利用恒河猴对蛔虫抗原的速发型超敏反应,来评估色甘酸钠(DSCG)和一种新型IgE介导的肺功能变化抑制剂(U-42,585E)的药理学特征。当通过静脉内、支气管内或口服途径给予U-42,585E时,用于测量肺功能的两个参数,即呼吸频率增加和潮气量减少,会以剂量相关的方式发生显著改变。在蛔虫反应性灵长类动物中,低至5mg/kg的剂量就证明了U-42,585E的口服活性。

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