期刊文献+

温补肾阳汤早期干预对哮喘小鼠EOS祖细胞分化的影响 被引量:2

Effect on EOS Differentiation of Progenitor Cell in Asthmatic Mice by the Intervention of Wenbu Shenyang Tang
下载PDF
导出
摘要 目的:观察温补肾阳汤早期干预对哮喘小鼠EOS祖细胞分化的影响,并探讨其作用机制。方法:将30只BALB/c小鼠按随机数字表单盲法分为空白对照组、模型组、温补肾阳汤组,每组各10只。造模开始即给药,每天1次,共29 d。观察哮喘小鼠外周血IgE、IL-5、Eotaxin表达,肺组织病理学改变,骨髓悬液EOS、CD34+、CD34+/CCR3+细胞的表达。结果:与模型组相比,温补肾阳汤组小鼠外周血IgE、IL-5、Eotaxin表达明显降低(P<0.01),骨髓悬液EOS计数、CD34+细胞数及CD34+/CCR3+细胞数明显减少(P<0.01)。结论:温补肾阳汤早期干预治疗可以抑制哮喘小鼠过敏反应,抑制外周血和气道炎症反应;预防服用温补肾阳汤可能通过抑制哮喘小鼠过敏反应,改变小鼠骨髓腔内环境,抑制CD34+祖细胞向EOS分化,减少炎症因子向外周组织的释放和聚集,控制哮喘发作。 Objective:To observe the influence of wenbu shenyang tang (WBSYT)on the EOS differentiation of progenitor cells in asth- matic mice, and explore its possible mechanism. Methods:All 30 BALB / e mice were randomly equally divided into three groups:blank control group, model group and WBSYT group. All groups were treated at the beginning of modeling, once daily for 29 days. Peripheral blood IgE,IL-5,Eotaxin,pathological changes of lung tissue,and the express of the EOS, CD34 +cell, CD34 +/CCR3+ cells in the bone marrow suspension were observed. Results:Compared with model group, the mice peripheral blood IgE, IL-5 and Eotaxin expression, the bone marrow suspension EOS count, CD34+ cell count and CD34 +/CCR3 + cell count in WBSYT group were decreased significantly ( P 〈0. 01 ). Conclusions :Early intervention treatment can restrain anaphylaxis ,inflammatory response of peripheral blood and airway in asthmatic mice by wenbu shenyang tang. Prevention taking wenbu shenyang tang may restrain anaphylaxis, differentiation CD34 + pro- genitor cells into EOS cells, change internal environment of marrow cavity in mice, and reduce release and gather of inflammatory factor.
出处 《中医学报》 CAS 2013年第5期681-682,I0001,共3页 Acta Chinese Medicine
基金 浙江省中医药科技计划项目(编号:2008YA006)
关键词 哮喘 温补肾阳汤 EOS 祖细胞分化 小鼠 asthma wenbu shenyang tang EOS differentiation of progenitor cell mice
  • 相关文献

参考文献4

  • 1陆再英,钟南山.内科学[M].北京:人民卫生出版社,2008:121.
  • 2沈璐,赖克方,姜华,洪燕华,钟南山.不同激发方式对小鼠过敏性支气管哮喘模型的影响[J].中华哮喘杂志(电子版),2009,3(6):5-8. 被引量:17
  • 3Shen, H. H. , Ochkur, S. I. , McGarry, M. P. , et al. A causative rela- tionship exists between eosinophils and the development of allergy pulmonary pathologies in the mouse [ J ]. J Immunol, 2003,170 ( 6 ) : 3296 - 3305.
  • 4Sabine, H. , Carole, O.. Present status on the genetic studies of asthma [J].C urr 0pin Immuno1,2002,14 (6) :709.

二级参考文献3

共引文献1703

同被引文献33

  • 1徐立,时乐,冯里,俞晶华,范欣生.偏苯三酸酐诱导职业性哮喘大鼠模型的研究[J].中华哮喘杂志(电子版),2012,6(6):410-414. 被引量:3
  • 2黄霞,刘杰,刘惠霞.熟地黄多糖对血虚模型小鼠的影响[J].中国中药杂志,2004,29(12):1168-1170. 被引量:49
  • 3杨欣,张永华,丁彩飞,颜志中,杜静.巴戟天水提物对人精子膜功能氧化损伤的保护作用[J].中国中药杂志,2006,31(19):1614-1617. 被引量:11
  • 4Lemifere C, Malo JL, Gautrin D, et al. Nonsensi-tizing causes of occupational asthma [J]. MedClin North Am, 1996,80(4) : 749 -774.
  • 5林佩琴原著,李德新编校.类证治裁[M].北京:人民卫生出版社,2005:108.
  • 6Kitayama J, Mackay CR, Ponath PD, et al. TheC-C chemokine receptor CCR3 participates instimulation of eosinophil arrest on inflammatoryendothelium in shear flow [ J ]. J Clin Invest,1998,101 (9) : 2017 -2024.
  • 7Inman MD, Ellis R, Wattie J, et al. Allergen-in-duced increase in airway responsiveness, airwayeosinophilia,and bone-marrow eosinophil progen-itors in mice [ J ]. Am J Respir Cell Mol Biol,1999’ 21 (4) : 473 -479.
  • 8Dorman SC, Babirad I, Post J, et al. Progenitoregress from the bone marrow after allergen chal-lenge: role of stromal cell-derived factor 1 alphaand eotaxin [ J ]. J Allergy Clin Immunol, 2005,115 (3) : 501 -507.
  • 9Collins PD, Marleau S, Griffiths-Johndson DA, et al.Cooperation between interleukin-5 and the chemo-kine eotaxin to induce eosinophil accumulation invitro [J], J Exp Med, 1995,182(4): 1167-1174.
  • 10王晓敏,王建红,邹志坚,刘海云.菟丝子黄酮对去势雌性大鼠血脂和血管雌激素受体的影响[J].中成药,2008,30(2):255-256. 被引量:26

引证文献2

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部