山东大学耳鼻喉眼学报 ›› 2016, Vol. 30 ›› Issue (4): 30-33.doi: 10.6040/j.issn.1673-3770.0.2016.162

• 变应性鼻炎 • 上一篇    下一篇

γ干扰素对变应性鼻炎大鼠鼻腔灌洗液中嗜酸粒细胞凋亡及Eotaxin水平的影响

李钦1,陈彦林1,马焱燚1,张永东2   

  1. 1. 临沂市人民医院耳鼻咽喉科, 山东 临沂 276003;
    2. 山东医学高等专科学校药理学教研室, 山东 临沂 276002
  • 收稿日期:2016-04-11 出版日期:2016-08-16 发布日期:2016-08-16
  • 通讯作者: 陈彦林. E-mail:ylch8618@163.com E-mail:liqin8226@163.co
  • 作者简介:李钦. E-mail: liqin8226@163.co
  • 基金资助:
    山东省自然科学基金资助项目(ZR2013HL020)

Effects of interferon gamma on Eosinophil apoptosis and Eotaxin levels in nasal lavage fluid of allergic rhinitis rats.

LI Qin1, CHEN Yanlin1, MA Yanyi1, ZHANG Yongdong   

  1. 1. Department of Otorhinolaryngology, Linyi Peoples Hospital, Linyi 276003, Shandong, China;2. Department of Phamacology, Shandong Medical College, Linyi 276002, Shandong, China
  • Received:2016-04-11 Online:2016-08-16 Published:2016-08-16

摘要: 目的 建立大鼠变应性鼻炎( allergic rhinitis, AR)模型,探讨鼻腔滴入γ干扰素(interferon gamma, IFN-γ)对AR大鼠鼻腔灌洗液中嗜酸粒细胞(eosinophil, EOS)凋亡及嗜酸粒细胞趋化因子(Eotaxin)水平的影响。 方法 将40只Wistar 大鼠按随机数字表法分为对照组(A组)、AR组(B组)、布地奈德组(C组)和IFN-γ组(D组),每组10只。B、C和D组大鼠采用卵清蛋白(OVA)、氢氧化铝建立AR大鼠模型,分别于模型建立后第31~38天,每只每日每侧鼻腔滴入磷酸盐缓冲液50 μL、布地奈德50 μL(1.28 μg/μL),IFN-γ 50 μL(0.02 μg/μL)。A组以生理盐水代替OVA。各组大鼠于第39天取鼻腔灌洗液,检测其EOS百分比,流式细胞术检测EOS凋亡率,酶联免疫吸附试验(ELISA)检测Eotaxin水平。 结果 C、D组大鼠鼻腔灌洗液中EOS百分比明显低于B组(P均<0.01);C、D组鼻腔灌洗液中EOS凋亡率明显高于B组(P均<0.01);C、D组鼻腔灌洗液中Eotaxins明显低于B组。D组大鼠鼻腔灌洗液中EOS 百分比与其凋亡率呈显著负相关(r=-0.769,P<0.05); D组大鼠鼻腔灌洗液中EOS 百分比与Eotaxin水平呈显著正相关(r=0.750,P<0.05)。 结论 IFN-γ可显著增加AR大鼠鼻腔灌洗液中EOS的凋亡,降低Eotaxins水平,明显减少了鼻腔内EOS的浸润,从而减轻了AR的炎症反应,对AR有一定的治疗作用。

关键词: 模型, 嗜酸粒细胞趋化因子, 凋亡, γ干扰素, 鼻腔灌洗液, 嗜酸粒细胞, 变应性鼻炎

Abstract: Objective To explore the effect of interferon gamma(IFN-γ)on the apoptosis of Eosinophils and Eotaxin levels from nasal lavage fluid in allergic rhinitis(AR)rats. Methods AR model was established by the sensitizer of ovalbumin and aluminum hydroxide. The 40 rats were randomly divided into the control group(group A, n=10), the allergic rhinitis group(group B, n=10), the budesonide group(group C, n=10)and the IFN-γ group(group D, n=10). In days 31 to 38 after the establishment of AR rats, each rat of the group D was administrated by instillation of 1 μg(1 μg/50 μL)IFN-γ into each of the nasal cavities one time a day, while each rat of the group B was administrated by instillation of 50 μL phosphate buffer in the same way, and each rat of the group C was administrated by instillation of 50 μL(1.28 μg/μL)budesonide in the same way. In days 39, the nasal lavage fluid was obtained to measure the apoptotic percentage of eosinophils and the apoptotic ratios were analyzed by flow cytometry. The levels of Eotaxin were detected by enzyme-linked immunosorbent assay(ELISA). Results The percentage of EOS in nasal lavage fluid of group C and group D was evidently lower than that of group B(all P<0.01). The eosinophil apoptotic ratio in group C and group D was evidently higher than that in group B(all P<0.01). The levels of Eotaxin in nasal lavage fluid of group C and group D were evidently lower than those in group B(all P<0.01);Furthermore significantly negative correlation was observed between the percentage of EOS and apoptotic ratio in the nasal lavage fluid of group D (r=-0.769,P<0.05). While significantly positive correlation was observed between the percentage of EOS and Eotaxin in the nasal lavage fluid of group D (r=0.750,P<0.05). Conclusion IFN-γcan significantly reduce the eosinophil infiltration and increase eosinophil apoptosis. It can reduce the levels of Eotaxin so as to achieve the purpose of treating allergic rhinitis.

Key words: Apoptosis, Nasal lavage fluid, Models, Allergic rhinitis, Eotaxin, Eosinophil, IFN-γ

中图分类号: 

  • R765.21
[1] 李钦, 张永东, 孙崇伟, 等. 鼻腔吸入γ干扰素对大鼠变应性鼻炎的治疗作用[J]. 中华耳鼻咽喉头颈外科杂志, 2008, 43(2):134-138. LI Qin, ZHANG Yongdong, SUN Chongwei, et al. Treatment of allergic rhinitis rats by intranasal interferon gamma[J]. Chin J Otorhinolaryngol Head Neck Surgery, 2008, 43(2):134-138.
[2] 李钦,李玉芬,陈彦林,等.白细胞介素5和13受体对变应性鼻炎大鼠血管细胞黏附分子1及γ干扰素的影响[J].中华耳鼻咽喉头颈外科杂志,2012,47(8):638-641. LI Qin, LI Yufen, CHEN Yanlin, et al. Effect of combined use of sIL-5Rα and sIL-13Rα2 on VCAM-1 and IFN-γ in allergic rhinitis rats[J]. Chin J Otorhinolaryngol Head Neck Surgery, 2012, 47(8):638-641.
[3] 庄晓艳,李钦,陈彦林,等. 布地奈德对变应性鼻炎大鼠鼻腔灌洗液中嗜酸性粒细胞凋亡的影响[J]. 山东大学耳鼻喉眼学报,2014,28(2):68-71. ZHUANG Xiaoyan, LI Qin, CHEN Yanlin, et al. Effects of budesonide on eosinophil apoptosis in nasal lavage fluid of allergic rhinitis rats[J]. J Otolaryngol Ophthalmol Shandong Univ, 2014, 28(2):68-71.
[4] Peric A, Vojvodic D, Vukomanovic- D-ur(-overd)evic B, et al. Eosinophilic inflammation in allergic rhinitis and nasal polyposis[J]. Arh Hig Rada Toksiko, 2011, 62(4):341-348.
[5] Cheng K J, Xu Y Y, Liu H Y, et al. Serum eosinophil cationic protein level in Chinese subjects with nonallergic and local allergic rhinitis and its relation to the severity of disease[J].Am J Rhinol Allergy, 2013, 27(1):8-12.
[6] Foresi A, Teodoro C, Leone C, et al. Eosinophil apoptosis in induced sputum from patients with seasonal allergic rhinitis and with asymptomatic and symptomatic asthma[J]. Ann Allergy Asthma Immunol, 2000, 84(4):411-416.
[7] Maskrey B H, Megson I L, Whitfield P D, et al. Mechanisms of resolution of inflammation: a focus on cardiovascular disease[J]. Arterioscler Thromb Vasc Biol, 2011, 31(5):1001-1006.
[8] Fujisawa T, Kato Y, Nagase H, et al. Chemokines induce eosinophil degranulation through CCR-3 [J]. J Allergy Clin Immunol, 2000, 106(3):507-513.
[9] Menzies-Gow A, Robinson D S. Eosinophil chemokines and chemokine receptors: their role in eosinophil accumulation and activation in asthma and potential as therapeutic targets[J]. J Asthma, 2001, 38(8):605-613.
[10] 燕志强, 章如新, 余少卿, 等. 嗜酸细胞活化趋化因子在变应性鼻炎中的作用[J]. 中国耳鼻咽喉头颈外科杂志, 2008, 15(5):262-266. YAN Zhiqiang, ZHANG Ruxin, YU Shaoqin, et al. Role of eotaxin in allergic rhinitis[J]. Chin Arch Otolaryngol Head Neck Surgery, 2008, 15(5):262-266.
[11] Bousquet J, Khaltaev N, Cruz A A, et al. Allergic rhinitis and its impact on asthma(ARIA)2008 update(in collaboration with the World Health Organization,GA2LEN and AllerGen)[J]. Allergy, 2008, 63(1):8-160.
[12] Brozek J L, Bousquet J, Baena-Cagnani C E, et al. Allergic rhinitis and its impact on asthma(ARIA)guidelines:2010 revision[J]. J Allergy Clin Immunol,2010,126(3):466-476.
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