Details

Autor(en) / Beteiligte

• Shim, Ki-Shuk
• Song, Hyun-Kyung
• Hwang, Youn-Hwan
• Chae, Sungwook
• Kim, Ho Kyoung
• Jang, Seol
• Kim, Yun Hee
• Choo, Byung-Kil
• Yang, Won-Kyung
• Kim, Seung-Hyung
• Kim, Taesoo
• Kim, Ki Mo

Titel

Ethanol extract of Veronica persica ameliorates house dust mite-induced asthmatic inflammation by inhibiting STAT-3 and STAT-6 activation

Ist Teil von

• Biomedicine & pharmacotherapy, 2022-08, Vol.152, p.113264-113264, Article 113264

Ort / Verlag

France: Elsevier Masson SAS

Erscheinungsjahr

2022

Quelle

Elsevier ScienceDirect Journals

Beschreibungen/Notizen

• 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. [Display omitted] •EEVP can reduce HDM-sensitized asthmatic inflammation.•EEVP can inhibit eosinophilic infiltration and the expression of T cell activation factors.•EEVP can inhibit MCP-1 production and STAT-3/6 activation in bronchial/tracheal epithelial cells.