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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.

DOI:10.1159/000232062
PMID:415987
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。

相似文献

1
Inhibition of allergic reactions by cromoglycate and by a new antiallergy drug U-42,585E. II. Activity in primates against aerosolized Ascaris suum antigen.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。
Int Arch Allergy Appl Immunol. 1978;56(6):481-7. doi: 10.1159/000232062.
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引用本文的文献

1
Ascaris-induced bronchoconstriction in primates experimentally infected with Ascaris suum ova.猪蛔虫卵实验感染灵长类动物中蛔虫引起的支气管收缩。
Clin Exp Immunol. 1983 Nov;54(2):461-8.
2
Inhalation challenge with specific grass pollen antigens in asthmatics and the effect of lodoxamide tromethamine.哮喘患者吸入特定草花粉抗原的激发试验及三甲噻米哒洛草酰胺的作用
Thorax. 1983 Jun;38(6):458-62. doi: 10.1136/thx.38.6.458.
3
Inhibition of oxidative enzymes by anti-allergy drugs.
Agents Actions. 1981 Nov;11(5):503-9. doi: 10.1007/BF02004713.
4
Alternative modes of action of sodium cromoglycate.色甘酸钠的其他作用方式。
Agents Actions. 1986 Jun;18(3-4):294-300. doi: 10.1007/BF01964987.
5
The characterization of lodoxamide, a very active inhibitor of mediator release, in animal and human models of asthma.洛度沙胺(一种非常有效的介质释放抑制剂)在哮喘动物和人体模型中的特性研究。
Agents Actions. 1986 Jun;18(3-4):301-5. doi: 10.1007/BF01964988.
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The effect of lodoxamide ethyl [diethyl N,N'-(2-chloro-5-cyano-m-phenylene)dioxamate] on in vivo anaphylactic reactions.
Agents Actions. 1979 Aug;9(3):235-8. doi: 10.1007/BF01966693.