首页|基于TLR4/MyD88/NF-κB与p38 MAPK信号通路研究麻杏石甘汤减轻咳嗽变异性哮喘大鼠炎症反应的作用及机制

基于TLR4/MyD88/NF-κB与p38 MAPK信号通路研究麻杏石甘汤减轻咳嗽变异性哮喘大鼠炎症反应的作用及机制

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探讨麻杏石甘汤对咳嗽变异性哮喘(CVA)大鼠炎症反应的作用及机制。6~8周龄SPF级SD大鼠随机分为正常组、模型组、孟鲁司特钠组以及麻杏石甘汤低、中、高剂量组,每组8只;采用卵蛋白(OVA)和氢氧化铝[Al(OH)3]致敏并用OVA激发的方法复制大鼠CVA模型,正常组、模型组给予等体积生理盐水灌胃,各受试药组给予相应药物灌胃。实验结束后,检测各组大鼠血液白细胞计数,血清白细胞介素-6(IL-6)、白细胞介素-10(IL-10)、肿瘤坏死因子-α(TNF-α)含量;苏木素-伊红(HE)染色观察肺组织病理变化;蛋白免疫印迹法检测肺组织中Toll样受体4(TLR4)、髓样分化因子88(MyD88)、核转录因子-κB p65(NF-κB p65)和磷酸化核转录因子-κB p65(p-p65)、p38丝裂原活化蛋白激酶(p38 MAPK)和磷酸化p38丝裂原活化蛋白激酶(p-p38 MAPK)水平,实时荧光定量分析法检测肺组织中TLR4、MyD88 mRNA表达水平。结果显示,与正常组比较,模型组大鼠具有明显哮喘表型,血液白细胞计数和IL-6、TNF-α水平显著升高(P<0。01),IL-10水平显著降低(P<0。01),气道周围炎症细胞浸润明显,细胞排列紊乱,肺组织中TLR4、MyD88、p-p65/NF-κB p65、p-p38 MAPK/p38 MAPK水平以及TLR4、MyD88 mRNA水平显著升高(P<0。01)。与模型组比较,孟鲁司特钠组、麻杏石甘汤高剂量组白细胞计数和IL-6、TNF-α水平显著降低(P<0。01),IL-10水平显著升高(P<0。01),气道炎症细胞浸润、细胞排列紊乱程度明显减轻,肺组织中TLR4、MyD88、p-p65/NF-κB p65、p-p38 MAPK/p38 MAPK水平以及TLR4、MyD88 mRNA水平显著降低(P<0。01)。与孟鲁司特钠组比较,麻杏石甘汤高剂量组大鼠血液白细胞数,血清中IL-10和TNF-α含量,肺组织中TLR4、MyD88、p-p65/NF-κB p65、p-p38 MAPK/p38 MAPK水平及TLR4、MyD88 mRNA水平,均无显著差异。麻杏石甘汤具有抑制CVA大鼠气道炎症反应的作用,其作用机制可能与抑制TLR4/MyD88/NF-κB以及p38 MAPK信号通路的激活相关。
Effect and mechanism of Maxing Shigan Decoction on reducing inflammatory response in rats with cough variant asthma via TLR4/MyD88/NF-κB and p38 MAPK signaling pathways
This study aims to investigate the effect and mechanism of Maxingshigan Decoction on inflammation in the rat model of cough variant asthma(CVA).The SPF-grade SD rats of 6-8 weeks were randomized into normal,model,Montelukast sodium,and low-,medium-,and high-dose Maxing Shigan Decoction groups,with 8 rats in each group.The CVA rat model was induced by ovalbu-min(OVA)and aluminum hydroxide sensitization and ovalbumin stimulation.The normal group and model group were administrated with equal volume of normal saline by gavage,and other groups with corresponding drugs by gavage.After the experiment,the number of white blood cells in blood and the levels of interleukin-6(IL-6),interleukin-10(IL-10),and tumor necrosis factor-α(TNF-α)in the serum were measured.The lung tissue was stained with hematoxylin-eosin(HE).Western blot was employed to determine the pro-tein levels of nuclear factor-κB(NF-κB),Toll-like receptor 4(TLR4),myeloid differentiation protein(MyD88),and mitogen-acti-vated protein kinase(MAPK)in the lung tissue.Real-time PCR was carried out to measure the mRNA levels of TLR4 and MyD88 in the lung tissue.Compared with the normal group,the model group showed increased white blood cells,elevated IL-6 and TNF-α levels(P<0.01),lowered IL-10 level(P<0.01),up-regulated protein levels of TLR4,MyD88,p-p65/NF-κB p65,and p-p38 MAPK/p38 MAPK(P<0.01)and mRNA levels of TLR4 and MyD88(P<0.01)in the lung tissue.HE staining showed obvious infiltration of in-flammatory cells around the airway and cell disarrangement in the model group.Compared with the model group,Montelukast sodium and high-dose Maxing Shigan Decoction reduced the white blood cells,lowered the IL-6 and TNF-α levels(P<0.01),and elevated the IL-10 level(P<0.01).Moreover,they down-regulated the protein levels of TLR4,MyD88,p-p65/NF-κB p65,p-p38 MAPK/p38 MAPK in the lung tissue(P<0.01)and the mRNA levels of TLR4 and MyD88 in the lung tissue(P<0.01).HE staining showed that Montelukast sodium and high-dose Maxing Shigan Decoction reduced inflammatory cell infiltration and cell disarrangement.The number of white blood cells,the levels of IL-10 and TNF-α in the serum,the protein levels of TLR4,MyD88,p-p65/NF-κB p65,and p-p38 MAPK/p38 MAPK,and the mRNA levels of TLR4 and MyD88 in the lung tissue showed no significant differences between the Monte-lukast sodium group and high-dose Maxing Shigan Decoction group.Maxing Shigan Decoction can inhibit airway inflammation in CVA rats by inhibiting the activation of TLR4/MyD88/NF-κB and p38 MAPK signaling pathways.

Maxing Shigan Decoctioncough variant asthmainflammatory responseTLR4/MyD88/NF-κB signaling pathwayp38 MAPK signaling pathway

付智慧、周霖、聂安政

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郑州大学第一附属医院中医药学部,河南郑州 450052

郑州大学第一附属医院药学部,河南 郑州 450052

河南省精准医学临床质谱工程研究中心,河南郑州 450052

麻杏石甘汤 咳嗽变异性哮喘 炎症反应 TLR4/MyD88/NF-κB信号通路 p38 MAPK信号通路

河南省科技发展计划河南省高等学校重点科研项目郑州大学第一附属医院院内青年基金

21210231034621A360026YNQN2017198

2024

中国中药杂志
中国药学会

中国中药杂志

CSTPCD北大核心
影响因子:1.718
ISSN:1001-5302
年,卷(期):2024.49(4)
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