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[吸收的INF-γ抑制JNK磷酸化对变应性鼻炎大鼠鼻黏膜重塑的影响]

[Effects of inhibiting the phosphorylation of JNK by absorbed INF-γon the remodeling of nasal mucosa in allergic rhinitis rats].

作者信息

Li Q, Chen Y L, Ma Y Y, Zhang Y D, Sun C W, You C P

机构信息

Department of Otorhinolaryngology,Linyi People's Hospital,Linyi,276003,China.

Department of Pharmacology,Shandong Medical College.

出版信息

Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2016 Jul 5;30(13):1034-1037. doi: 10.13201/j.issn.1001-1781.2016.13.007.

Abstract

To study the role of phosphorylated JNK(c-Jun N-terminal kinase) on nasal mucosa remodeling in allergic rhinitis(AR) rats and the influence of IFN-γon IL-1β,JNK and nasal mucosa remodeling.According to random number table,48 Wistar rats were divided into control group(A group),AR group(B group),IFN-γgroup(C group) and triamcinolone acetonide group(D group).The rats in group B,C and D were sensitized and provocated for inducing AR by intraperitoneal injection of ovalbumin(OVA) and Al(OH)₃.Thirty minutes before intranasally challenged,rats in three groups were administrated by instillation of PBS,IFN-γand triamcinolone acetonide into nasal cavities,while the group A rats were administrated by saline solution.Ten rats in each group were selected to enter the final experiment.The density of IL-1βin serum and nasal lavage fluid were tested by ELISA.The mean absorbance (m) of phosphorylated JNK and c-Jun were tested by immunohistochemistry.Western Blot detected the P-JNK level in nasal tissue homogenate.The density of IL-1βin serum and nasal lavage fluid in group C and group D were significantly lower than that of group B (<0.01).Immunohistochemistry study showed that the protein expression level of phosphorylated JNK and c-Jun of nasal mucosa were significantly increased in group B,but significantly reduced in group C and group D .The mA of phosphorylated JNK and c-Jun in group B were significantly higher than those in the group C and group D(<0.01).The Western blot showed that the P-JNK of nasal tissue homogenate in group B was higher than that of group C and group D (<0.01). The phosphorylation of JNK played an important role in nasal mucosa remodeling.IFN-γcould inhibit the phosphorylation of JNK and reduce the nasal mucosa remodeling.The mechanisms may be achieved through down-regulation of IL-1β.

摘要

研究磷酸化JNK(c-Jun氨基末端激酶)在变应性鼻炎(AR)大鼠鼻黏膜重塑中的作用以及干扰素-γ(IFN-γ)对白细胞介素-1β(IL-1β)、JNK和鼻黏膜重塑的影响。将48只Wistar大鼠按随机数字表法分为对照组(A组)、AR组(B组)、IFN-γ组(C组)和曲安奈德组(D组)。B、C、D组大鼠通过腹腔注射卵清蛋白(OVA)和氢氧化铝(Al(OH)₃)致敏并激发以诱导AR。在鼻内激发前30分钟,对三组大鼠鼻腔分别滴注磷酸盐缓冲液(PBS)、IFN-γ和曲安奈德,而A组大鼠滴注生理盐水。每组选取10只大鼠进入最终实验。采用酶联免疫吸附测定(ELISA)检测血清和鼻灌洗液中IL-1β的浓度。采用免疫组织化学法检测磷酸化JNK和c-Jun的平均吸光度(m)。蛋白质免疫印迹法(Western Blot)检测鼻组织匀浆中磷酸化JNK(P-JNK)水平。C组和D组血清及鼻灌洗液中IL-1β浓度均显著低于B组(<0.01)。免疫组织化学研究显示,B组鼻黏膜磷酸化JNK和c-Jun蛋白表达水平显著升高,而C组和D组显著降低。B组磷酸化JNK和c-Jun的平均吸光度显著高于C组和D组(<0.01)。蛋白质免疫印迹法显示,B组鼻组织匀浆中P-JNK高于C组和D组(<0.01)。JNK的磷酸化在鼻黏膜重塑中起重要作用。IFN-γ可抑制JNK的磷酸化并减轻鼻黏膜重塑。其机制可能是通过下调IL-1β实现的。

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