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血清 IL-4 和 IgE 对绿原酸诱导的过敏反应的早期预测的贡献。

Contribution of serum IL-4 and IgE to the early prediction of allergic reactions induced by chlorogenic acid.

机构信息

Department of Pharmacology and Toxicology, Guangdong Institute for Food and Drug Control, 2 Jin Bu Li, Hui Fu Xi Road, Guangzhou 510180, People's Republic of China.

出版信息

Eur J Pharmacol. 2013 Jan 15;699(1-3):1-5. doi: 10.1016/j.ejphar.2012.11.047. Epub 2012 Dec 5.

Abstract

Chlorogenic acid (CA) is one of the active ingredients in some Chinese herbal injections, which may cause allergic reactions in clinic therapy. However, the criterion of test for allergen had not been employed in current Pharmacopeia of United States, European Pharmacopeia, Japanese Pharmacopeia and British Pharmacopeia. In order to find a new way to predict allergic reactions induced by CA earlier, the guinea pigs were sensitized successively by injecting CA intravenously once a day for three times, the results were compared that of Chinese Pharmacopeia by injecting CA intraperitoneally once every other day for three times, serum IL-4 and total IgE were detected by method of enzyme linked immunosorbent assay (ELISA) before guinea pigs were challenged once by injecting the same drug intravenously. The time-effectiveness and dose-effect of allergic reactions induced by CA were also studied. We found that contents of serum IL-4 and total IgE increased significantly before guinea pigs were challenged, either in D8 after intravenous sensitization (1.5 g/l CA, 0.5 ml) or in D14 and D21 after intraperitoneal sensitization (1.5 g/l CA, 0.5 ml), and allergic reactions occurred in all guinea pigs after challenged once by injecting CA (1.5 g/l, 1.0 ml) intravenously. It provides a new way to predict whether CA (or Chinese herbal injections contained CA) can provoke allergic reactions by detecting serum IL-4 and total IgE earlier; the examination period is reduced by 1-2 weeks. It has a good prospect of application in drug emergency test.

摘要

绿原酸(CA)是一些中药注射液的有效成分之一,在临床治疗中可能引起过敏反应。然而,目前的《美国药典》、《欧洲药典》、《日本药典》和《英国药典》都没有采用过敏原检测标准。为了寻找更早预测 CA 引起的过敏反应的新方法,我们通过连续 3 天每天静脉注射 CA 对豚鼠进行致敏,将结果与通过每 2 天腹腔注射 CA 进行致敏 3 次的《中国药典》进行比较,在豚鼠静脉注射相同药物进行单次激发前,通过酶联免疫吸附试验(ELISA)检测血清白细胞介素 4(IL-4)和总 IgE。还研究了 CA 引起的过敏反应的时效和量效关系。我们发现,在豚鼠接受激发前,无论是静脉致敏后第 8 天(1.5g/L CA,0.5ml)还是腹腔致敏后第 14 天和第 21 天(1.5g/L CA,0.5ml),血清 IL-4 和总 IgE 的含量均显著增加,且所有豚鼠在静脉注射 CA(1.5g/L,1.0ml)激发后均发生过敏反应。通过更早地检测血清 IL-4 和总 IgE,为预测 CA(或含有 CA 的中药注射液)是否能引起过敏反应提供了新的方法;检查期缩短了 1-2 周。它在药物应急测试中有很好的应用前景。

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