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TYB-2285对主动致敏的棕色挪威大鼠抗原暴露诱导的气道嗜酸性粒细胞积聚的影响。

Effects of TYB-2285 on the accumulation of eosinophils in the airway induced by antigen exposure in actively sensitized brown Norway rats.

作者信息

Tominaga T, Watanabe A, Tsuji J, Koda A, Nagai H, Kumazawa Y, Shimada H

机构信息

Department of Pharmacology, Toyobo Co. Ltd., Shiga, Japan.

出版信息

Gen Pharmacol. 1997 Feb;28(2):301-3. doi: 10.1016/s0306-3623(96)00227-3.

DOI:10.1016/s0306-3623(96)00227-3
PMID:9013208
Abstract
  1. The effect of TYB-2285 on the antigen-induced accumulation of eosinophils into the airway was investigated in two models (inhalant sensitization and noninhalant sensitization) using Brown Norway (BN) rats. 2. In the method of inhalant sensitization, BN rats were sensitized by weekly exposure to ovalbumin (OA). The accumulation of eosinophils was inhibited by the oral administration of TYB-2285 for the first 2 days of each sensitization in a dose-dependent manner. 3. With noninhalant sensitization, BN rats were sensitized by i.m. injection of OA and i.p. injection of killed Bordetella pertussis. The accumulation of eosinophils was inhibited by TYB-2285 in a dose-dependent manner, when TYB-2285 is given p.o. 5 mm before and 5 hr after the antigen exposure. Moreover, this accumulation of eosinophils was inhibited by a single administration of TYB-2285 5 hr after the antigen exposure, presumably when the mast cell degranulation was already finished. 4. In the method with noninhalant sensitization, the accumulation of eosinophils was not inhibited by mast cell stabilizers such as ketotifen, tranilast, or DSCG. 5. The present study demonstrates that TYB-2285, unlike other mast cell stabilizers, inhibits the antigen-induced accumulation of eosinophils into the airway. It also suggests that this drug might be effective in asthmatic patients.
摘要
  1. 使用褐家鼠(BN大鼠)在两种模型(吸入致敏和非吸入致敏)中研究了TYB - 2285对抗原诱导的嗜酸性粒细胞在气道内积聚的影响。2. 在吸入致敏方法中,BN大鼠通过每周暴露于卵清蛋白(OA)进行致敏。在每次致敏的前2天口服TYB - 2285可剂量依赖性地抑制嗜酸性粒细胞的积聚。3. 对于非吸入致敏,BN大鼠通过肌肉注射OA和腹腔注射灭活的百日咳博德特氏菌进行致敏。当在抗原暴露前5小时和暴露后5小时口服给予TYB - 2285时,嗜酸性粒细胞的积聚被TYB - 2285剂量依赖性地抑制。此外,在抗原暴露后5小时单次给予TYB - 2285也可抑制嗜酸性粒细胞的这种积聚,推测此时肥大细胞脱颗粒已经完成。4. 在非吸入致敏方法中,肥大细胞稳定剂如酮替芬、曲尼司特或色甘酸钠不能抑制嗜酸性粒细胞的积聚。5. 本研究表明,与其他肥大细胞稳定剂不同,TYB - 2285可抑制抗原诱导的嗜酸性粒细胞在气道内的积聚。这也表明该药物可能对哮喘患者有效。

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1
Effects of TYB-2285 on the accumulation of eosinophils in the airway induced by antigen exposure in actively sensitized brown Norway rats.TYB-2285对主动致敏的棕色挪威大鼠抗原暴露诱导的气道嗜酸性粒细胞积聚的影响。
Gen Pharmacol. 1997 Feb;28(2):301-3. doi: 10.1016/s0306-3623(96)00227-3.
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A similarity and a difference between two models of late eosinophil accumulation into the airway induced by antigen exposure in actively sensitized brown Norway (BN) rats.在主动致敏的棕色挪威(BN)大鼠中,抗原暴露诱导嗜酸性粒细胞晚期积聚至气道的两种模型之间的一个相似点和一个不同点。
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Effect of TYB-2285 on peritoneal anaphylaxis in passively sensitized rats.TYB-2285对被动致敏大鼠腹膜过敏反应的影响。
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Role of very late activation antigen-4 in the antigen-induced accumulation of eosinophils and lymphocytes in the lungs and airway lumen of sensitized brown Norway rats.极晚期活化抗原-4在致敏棕色挪威大鼠肺部和气道腔内抗原诱导的嗜酸性粒细胞和淋巴细胞聚集中的作用。
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