Suppr超能文献

基于蛋白质组学的“小青龙汤”对哮喘气道炎症的抗炎作用机制研究

Proteomic Analysis of Anti-inflammatory Effects of a Kampo (Japanese Herbal) Medicine "Shoseiryuto (Xiao-Qing-Long-Tang)" on Airway Inflammation in a Mouse Model.

机构信息

Kitasato Institute for Life Sciences and Graduate School of Infection Control Sciences, Japan.

出版信息

Evid Based Complement Alternat Med. 2011;2011:604196. doi: 10.1093/ecam/nep151. Epub 2011 Mar 10.

Abstract

Effects of a Kampo (Japanese herbal) medicine "shoseiryuto (SST, xiao-qing-long-tang in Chinese)", which has been used for the treatment of allergic bronchial asthma clinically, were examined on ovalbumin (OVA)-sensitized allergic airway inflammation model (i.e., bronchial asthma) in a mouse. When SST was orally administered at 0.5 g kg(-1) day(-1) from day 1 to 6 after OVA inhalation, SST reduced the inflammation in lung tissue, the number of eosinophils and the OVA-specific immunoglobulin E (IgE) antibody titer in bronchoalveolar lavage (BAL) fluids at 7 days after the OVA inhalation. SST also reduced the airway hyperreactivity at 6 days after the OVA inhalation. Proteomic analysis with the agarose two-dimensional electrophoresis showed that the expression of spectrin α2 was reduced in the lung tissue of OVA-sensitized mice and SST recovered the expression. Western blot and immunohistochemical analyses of lung tissue also confirmed this result. When prednisolone was orally administered at 3 mg kg(-1) day(-1) from day 1 to 6 after OVA inhalation, the inflammation in lung tissue, the number of eosinophils in BAL fluids and airway hyperreactivity were reduced in the OVA-sensitized mice. However, prednisolone did not reduce the OVA-specific IgE antibody titer in BAL fluids and did not recover the expression of spectrin α2 in lung tissue. These results suggest that at least a part of action mechanism of SST against OVA-sensitized allergic airway inflammation in a mouse model is different from that of prednisolone.

摘要

一种名为“消风散(SST,小青龙汤)”的汉方药已被用于治疗过敏性支气管哮喘,本研究考察了其对卵清蛋白(OVA)致敏的过敏性气道炎症模型(即支气管哮喘)的作用。当 SST 在 OVA 吸入后第 1 天至第 6 天每天口服 0.5g/kg 时,SST 可减少肺组织炎症、肺泡灌洗液(BAL)中嗜酸性粒细胞数量和 OVA 特异性免疫球蛋白 E(IgE)抗体滴度,在 OVA 吸入后第 7 天。SST 还可降低 OVA 吸入后第 6 天的气道高反应性。琼脂糖二维电泳的蛋白质组学分析显示,OVA 致敏小鼠肺组织中 spectrin α2 的表达减少,而 SST 可恢复其表达。肺组织的 Western blot 和免疫组织化学分析也证实了这一结果。当泼尼松龙在 OVA 吸入后第 1 天至第 6 天每天口服 3mg/kg 时,OVA 致敏小鼠的肺组织炎症、BAL 液中的嗜酸性粒细胞数量和气道高反应性均降低。然而,泼尼松龙并未降低 BAL 液中的 OVA 特异性 IgE 抗体滴度,也未恢复肺组织中 spectrin α2 的表达。这些结果表明,SST 对 OVA 致敏的过敏性气道炎症的作用机制至少有一部分与泼尼松龙不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/917f/3136714/49f07068df61/ECAM2011-604196.001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验