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平喘方通过调节核苷酸结合寡聚化结构域样受体蛋白3/白细胞介素-1β和c-Jun氨基末端激酶通路改善气道重塑。

Pingchuan formula improve airway remodeling via regulation of the nucleotide-binding domain, leucine-rich-containing family, pyrin domain-containing-3/interleukin-1β and C-Jun N-terminal kinase pathways.

作者信息

Xu W-C, Lu Z-Y, Liu X-M, Wu R-F, Cao L, Chen L-N, Chen S-Y, Yu J-E, Zhuang C

机构信息

Department of Paediatrics, Seventh People's Hospital of Shanghai University of Traditional Chinese Medicine, Shanghai Province, China.

出版信息

J Physiol Pharmacol. 2024 Oct;75(5). doi: 10.26402/jpp.2024.5.04. Epub 2024 Dec 4.

DOI:10.26402/jpp.2024.5.04
PMID:39652899
Abstract

Asthma is a prevalent chronic inflammatory airway disease that affects both adults and children. Inflammation-induced airway remodeling can lead to irreversible damage to the airways. Traditional Chinese medicine (TCM) plays a significant role in healthcare, offering potential improvements for chronic airway inflammation associated with asthma. The objective of this study is to investigate the efficacy of Pingchuan formula (PCF) in treating asthma and explore its underlying mechanisms. The asthmatic model mice were sensitized on days 1 and 7, followed by aerosolized OVA challenge for a total of 21 times starting from day 14, spanning weeks 3 to 9. PCF was administered daily after the first challenge. The mice were orally dosed daily based on their individual body weights for a continuous period of 47 days. The examined items encompassed proteomic analysis of the target proteins impacted by PCF. The levels of interleukins IL-1β, IL-18, and transforming growth factor-β (TGF-β) in bronchoalveolar lavage fluid (BALF) were measured using ELISA. Immunohistochemistry was employed to assess the expression levels of nucleotide-binding domain, leucine-rich-containing family, pyrin domain-containing-3 (NLRP3), caspase-1, and TGF-β in the airways. Western blotting and real-time quantitative PCR analysis were conducted to determine NLRP3 and caspase-1 expression levels. Additionally, Western blotting was performed to evaluate C-Jun N-terminal kinase (JNK), phosphorylated JNK (p-JNK), matrix metalloproteinase-9 (MMP-9), N-cadherin, E-cadherin, and tenascin C (T-NC) expression. Compared to the asthma model group, histological analysis using hematoxylin and eosin (HE) staining and Masson staining revealed that PCF exhibited a significant reduction in airway inflammation exudation and collagen fiber production in asthmatic mice. The proteomics analysis revealed that there were 174 proteins exhibiting differential expression in the PCF group compared to the asthma model group, indicating a strong association with negative regulation of the cell cycle and inflammation in the airways of asthmatic individuals. The PCF also exhibited a significant reduction in the protein and mRNA expressions of NLRP3 and caspase-1 in lung tissue (P<0.05). Additionally, it decreased the protein expressions of ASC, p-JNK, MMP-9, E-cadherin, and T-NC while increasing N-cadherin levels (P<0.05). The inflammatory factors IL-1β, IL-18 and TGF-β were reduced (P<0.05). This study revealed that Pingchuan Decoction can inhibit airway remodeling by inhibiting NLRP/IL-1β and JNK pathway activation, and effectively improve airway histological inflammation and remodeling in mice.

摘要

哮喘是一种常见的慢性炎症性气道疾病,影响成人和儿童。炎症诱导的气道重塑可导致气道不可逆转的损伤。中医在医疗保健中发挥着重要作用,为与哮喘相关的慢性气道炎症提供了潜在的改善方法。本研究的目的是探讨平喘方(PCF)治疗哮喘的疗效并探索其潜在机制。哮喘模型小鼠在第1天和第7天致敏,从第14天开始进行总共21次雾化卵清蛋白激发,持续3至9周。首次激发后每天给予PCF。根据小鼠个体体重每日口服给药,持续47天。检测项目包括对受PCF影响的靶蛋白进行蛋白质组学分析。使用酶联免疫吸附测定法(ELISA)测量支气管肺泡灌洗液(BALF)中白细胞介素IL-1β、IL-18和转化生长因子-β(TGF-β)的水平。采用免疫组织化学法评估气道中核苷酸结合寡聚化结构域样受体蛋白3(NLRP3)、半胱天冬酶-1(caspase-1)和TGF-β的表达水平。进行蛋白质免疫印迹法(Western blotting)和实时定量聚合酶链反应(PCR)分析以确定NLRP3和caspase-1的表达水平。此外,进行蛋白质免疫印迹法以评估c-Jun氨基末端激酶(JNK)、磷酸化JNK(p-JNK)、基质金属蛋白酶-9(MMP-9)、N-钙黏蛋白、E-钙黏蛋白和肌腱蛋白C(T-NC)的表达。与哮喘模型组相比,苏木精-伊红(HE)染色和Masson染色的组织学分析显示,PCF可显著减少哮喘小鼠气道炎症渗出和胶原纤维生成。蛋白质组学分析显示,与哮喘模型组相比,PCF组有174种蛋白质表达存在差异,表明与哮喘个体气道中细胞周期的负调控和炎症密切相关。PCF还显著降低了肺组织中NLRP3和caspase-1的蛋白质和mRNA表达(P<0.05)。此外,它降低了凋亡相关斑点样蛋白(ASC)、p-JNK、MMP-9、E-钙黏蛋白和T-NC的蛋白质表达,同时增加了N-钙黏蛋白水平(P<0.05)。炎症因子IL-1β、IL-18和TGF-β减少(P<0.05)。本研究表明,平喘方可以通过抑制NLRP/IL-1β和JNK通路激活来抑制气道重塑,并有效改善小鼠气道组织学炎症和重塑。

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