KM Convergence Research Division, Korea Institute of Oriental Medicine, Yuseong-daero 1672, Yuseong-gu, Daejeon 34054, Republic of Korea.
KM Convergence Research Division, Korea Institute of Oriental Medicine, Yuseong-daero 1672, Yuseong-gu, Daejeon 34054, Republic of Korea; Korean Convergence Medicine Major KIOM, University of Science & Technology (UST), Daejeon 34054, Republic of Korea.
Biomed Pharmacother. 2022 Aug;152:113264. doi: 10.1016/j.biopha.2022.113264. Epub 2022 Jun 10.
Veronica persica is a flowering plant belonging to the family Scrophulariaceae. Here, we aimed to evaluate the pharmacological activity of the ethanol extract of Veronica persica (EEVP) in an airway inflammation model. We examined airway responsiveness to aerosolized methacholine, serum immunoglobulin (Ig)E levels, and total cell numbers in the lung and bronchoalveolar lavage fluid (BALF). Histological analysis of the lung tissue was performed using hematoxylin-eosin, Masson trichrome, or periodic acid-Schiff staining. Fluorescence-activated cell sorting analysis in the lung and BALF was applied to clarify the changes in immune cell types. Enzyme-linked immunosorbent assay and quantitative real-time polymerase chain reaction were applied to investigate cytokine levels and gene expression related to airway inflammation. STAT-3/6 phosphorylation was examined in primary bronchial/tracheal epithelial cells using western blot analysis. EEVP significantly suppressed total IgE levels and methacholine-induced increase of Penh value in the HDM-challenged mouse model. EEVP also attenuated the severity of airway remodeling in lung tissues and decreased eosinophil and neutrophil infiltration in the lungs and BALF. EEVP significantly reduced the production of cytokines in BAL and splenocyte culture medium, and the expression of mRNAs related to airway inflammation in the lung tissue. EEVP suppressed IL-4/13-induced STAT-3/6 phosphorylation in the epithelial cells. We showed for the first time that EEVP effectively inhibits eosinophilic airway inflammation by suppressing the expression of inflammatory factors for T cell activation and polarization, and inhibits MCP-1 production of bronchial/tracheal epithelial cells by suppressing STAT-3/6 activation. EEVP may be a potential pharmacological agent to prevent inflammatory airway diseases.
贯叶连翘是玄参科的一种开花植物。在这里,我们旨在评估贯叶连翘乙醇提取物(EEVP)在气道炎症模型中的药理活性。我们检查了气道对雾化乙酰甲胆碱的反应性、血清免疫球蛋白(Ig)E 水平以及肺和支气管肺泡灌洗液(BALF)中的总细胞数。使用苏木精-伊红、马松三色或过碘酸-希夫染色对肺组织进行组织学分析。对肺和 BALF 中的荧光激活细胞分选分析用于阐明免疫细胞类型的变化。酶联免疫吸附试验和实时定量聚合酶链反应用于研究与气道炎症相关的细胞因子水平和基因表达。使用 Western blot 分析检查原代支气管/气管上皮细胞中的 STAT-3/6 磷酸化。EEVP 显著抑制了 HDM 挑战小鼠模型中的总 IgE 水平和乙酰甲胆碱诱导的 Penh 值升高。EEVP 还减轻了肺组织中气道重塑的严重程度,并减少了肺部和 BALF 中的嗜酸性粒细胞和中性粒细胞浸润。EEVP 显著减少了 BAL 和脾细胞培养物中细胞因子的产生,以及肺组织中与气道炎症相关的 mRNA 的表达。EEVP 抑制了上皮细胞中 IL-4/13 诱导的 STAT-3/6 磷酸化。我们首次表明,EEVP 通过抑制 T 细胞激活和极化的炎症因子表达,以及通过抑制 STAT-3/6 激活来抑制 MCP-1 产生的支气管/气管上皮细胞,有效抑制嗜酸性气道炎症。EEVP 可能是预防炎症性气道疾病的潜在药物。