虫草活力素对大鼠慢性支气管哮喘模型气道重塑作用初探  被引量:2

Role of cordycepin on transforming growth factor-β_1 in a rat model of chronic bronchial asthma

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作  者:张旻[1] 周新[1] 唐亮 余伯成 李群[1] 张杏怡[1] 张国清[1] 

机构地区:[1]上海交通大学附属第一人民医院呼吸科,200080 [2]上海国宝企业发展中心,200001

出  处:《中华哮喘杂志(电子版)》2011年第2期1-5,共5页Chinese Journal of Asthma(Electronic Version)

基  金:国家"十一五"863计划课题资助项目

摘  要:目的对虫草活力素(简称虫草)在大鼠支气管哮喘(简称哮喘)模型气道重塑中的作用及相关机制进行初步探讨。方法 50只Wister大鼠[6~8周龄,(200±20)g],随机数字表法分为阴性对照组(A)、慢性哮喘单纯模型组(B)(卵清白蛋白系统致敏和反复激发)、慢性哮喘+虫草50mg/kg治疗8周组(C)、慢性哮喘+布地奈德(BUD)8周治疗组(D)及慢性哮喘+BUD联合虫草8周治疗组(E)。肺组织切片HE染色观察病理变化并检测气道管壁厚度,采用免疫组织化学法检测气道转化生长因子β1(TGF-β1)表达水平,应用逆转录PCR法检测肺组织A2a腺苷受体(A2aAR)mRNA表达。数据统计采用ANOVA检验进行组间分析,Mann-Whitney检验进行组内两两比较,Spearman等级相关分析。结果①HE染色显示所有药物干预组较单纯模型组炎症细胞浸润、平滑肌肥厚及黏膜肺组织水肿等炎症表现明显减轻,以D和E组最为明显;②5组气道管壁厚度依次分别为(9.89±2.09)、(21.72±3.16)、(14.94±1.96)、(12.29±2.75)和(12.25±2.32)μm2/μm,F=31.37,P<0.0001,所有药物干预组气道壁厚度均高于对照组(C组、D组和E组与A组比较后的P值分别为0.0001、0.0524、0.0524),且低于单纯模型组(C组、D组和E组与B组比较后的P值均<0.0001),差异有统计学意义,C组气道壁较D组和E组增厚,差异有统计学意义(P值分别为0.0232和0.0147);③5组TGF-β1表达强阳性率分别为(2.08±1.63)%、(29.37±5.08)%、(12.30±3.26)%、(10.78±3.35)%及(7.43±2.84)%,F=86.45,P<0.0001,所有药物干预组TGF-β1蛋白表达均高于对照组(C组、D组和E组与A组比较后的P值均<0.0001),且低于单纯模型组(C组、D组和E组与B组比较后的P值均<0.0001),差异有统计学意义;E组较C组的蛋白表达有统计学意义下降(P=0.0052);④5组肺组织A2aARmRNA表达相对强度依次为(0.35±0.06)、(0.27±0.10)、(0.52±0.07)、(0.24±0.05)及(0.47±0.08),F=26.46,P<0.0001,C组和E组A2aARmRNA表达高于A组(P值分别为0.0001Objective To investigate the potential suppression role of cordycepin in airway remodeling by observing the expression of transforming growth factor-β1(TGF-β1)and A2a adenosine receptor(A2aAR)on a rat model of chronic bronchial asthma(asthma).Methods 50 rats were randomized into control group(A),asthma group(B),50 mg/kg cordycepin treatment group(C),budesonide(BUD)treatment group(D)and combination treatment group(BUD + cordycepin 50 mg/kg)(E).After 8 weeks therapy on ovalbumin challenged asthma model,histologic examination were performed to observe the general pathologic alteration and analyze the thickness of airway wall.The protein expressions of TGF-β1 were calculated by immunohistochemistry,and the transcriptions of A2aAR mRNA in the lung tissues were measured by reverse transcriptase-polymerase chain reaction(RT-PCR).Data were evaluated using One-way ANOVA followed by Turkey's test and Mann-Whitney test.Results ① HE staining showed that compared with the treatment groups,there were a large number of inflammatory cells infiltration,heavier smooth muscle hypertrophy and mucous membrane hyperemia in the asthma group.② The thickness of airway in each group was(9.89±2.09),(21.72±3.16),(14.94±1.96),(12.29±2.75)and(12.25±2.32)μm2/μm respectively,F=31.37,P0.000 1,airway thickness in group C,D and E were all significantly higher than group A(P=0.000 1,0.052 4 and 0.052 4 respectively),and lower than group B(P0.000 1).Airway in group C also showed remarkably thicker than group D and E(P=0.023 and 0.015 respectively).③ The expressions of TGF-β1 in each group was(2.08±1.63)%,(29.37±5.08)%,(12.30±3.26)%,(10.78±3.35)% and(7.43±2.84)% respectively,F=86.45,P0.000 1,protein expressions in group C,D and E were all higher than group A(P0.000 1,0.000 1 and =0.000 1 respectively),and lower than group B significantly(P0.000 1),expression in group E also decreased remarkably than group C(P=0.005 2).

关 键 词:哮喘 虫草 气道重塑 转化生长因子Β1 腺苷A2A受体 

分 类 号:R562.25[医药卫生—呼吸系统]

 

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