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两性抗组胺药HSR-609对棕色挪威大鼠抗原诱导的晚期鼻嗜酸性粒细胞增多的影响。

Effects of an amphoteric antiallergic agent, HSR-609, on antigen-induced late phase nasal eosinophilia in brown Norway rats.

作者信息

Musoh K, Nakamura N, Nagai H

机构信息

Department of Pharmacology, Gifu Pharmaceutical University, Gifu, Japan.

出版信息

Pharmacology. 2000 Nov;61(4):230-7. doi: 10.1159/000028406.

Abstract

The effect of a newly synthesized compound, HSR-609, on rat experimental rhinitis was investigated. In the first part of the study, a new experimental nasal allergic late phase eosinophilia model in Brown Norway (BN) rats was investigated. The increase in the number of antigen inhalations resulted in the proportional increase in the number of inflammatory cells such as macrophages, eosinophils and neutrophils in the nasal cavity lavage fluid (NCLF) at 5 h after each inhalation. The number of inflammatory cells reached a maximum 8 h after the antigen perfusion. Submaximum response was observed at 5 h after the antigen provocation. In this system, the serum IgG and IgE antibody titers measured by homologous passive cutaneous anaphylaxis were 160 and 640, respectively. In the second part of the study, the effects of prednisolone, cetirizine and a newly synthesized amphoteric antiallergic agent, HSR-609, on this allergic late nasal eosinophilia and neutrophilia in BN rats were investigated. Prednisolone and HSR-609 significantly inhibited the increase in the number of eosinophils in the NCLF but not cetirizine. Furthermore, prednisolone showed the inhibition of the increase in the number of macrophages and neutrophils in NCLF. These results suggest that this late phase eosinophilia model in the nose of BN rats may be useful for investigating the therapeutic drugs for nasal allergy and a newly synthesized amphoteric antiallergic agent, HSR-609, may be useful for the treatment of allergic rhinitis with eosinophilia.

摘要

研究了一种新合成的化合物HSR - 609对大鼠实验性鼻炎的影响。在研究的第一部分,对一种新的棕色挪威(BN)大鼠实验性鼻过敏迟发性嗜酸性粒细胞增多模型进行了研究。抗原吸入次数的增加导致每次吸入后5小时鼻腔灌洗液(NCLF)中巨噬细胞、嗜酸性粒细胞和中性粒细胞等炎症细胞数量成比例增加。抗原灌注后8小时炎症细胞数量达到最大值。抗原激发后5小时观察到次最大反应。在该系统中,通过同源被动皮肤过敏反应测得的血清IgG和IgE抗体滴度分别为160和640。在研究的第二部分,研究了泼尼松龙、西替利嗪和一种新合成的两性抗过敏剂HSR - 609对BN大鼠这种过敏性鼻迟发性嗜酸性粒细胞增多和嗜中性粒细胞增多的影响。泼尼松龙和HSR - 609显著抑制了NCLF中嗜酸性粒细胞数量的增加,但西替利嗪没有。此外,泼尼松龙还抑制了NCLF中巨噬细胞和中性粒细胞数量的增加。这些结果表明,BN大鼠鼻部的这种迟发性嗜酸性粒细胞增多模型可能有助于研究鼻过敏的治疗药物,并且一种新合成的两性抗过敏剂HSR - 609可能对治疗伴有嗜酸性粒细胞增多的过敏性鼻炎有用。

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