Effects of total alkaloids from (L.) R. Br. on ovalbumin-induced asthma mice

卵清蛋白 嗜酸性粒细胞趋化因子 支气管肺泡灌洗 免疫学 医学 哮喘 免疫球蛋白E 嗜酸性粒细胞 胸腺基质淋巴细胞生成素 白三烯 白细胞介素 白三烯C4 药理学 免疫系统 内科学 细胞因子 抗体
作者
Xiaoyun Tong,Yun‐Li Zhao,Rongbing Fu,Min Hu,Qiushi Zhang,Xiangnong Wu,Lu Qu,Bao-Jing Li,Jian Nie,Chunyan Hu,Xiaoling Yu,Yuhuan Xie,Xiao‐Dong Luo,Feng Huang
出处
期刊:Journal of Ethnopharmacology [Elsevier BV]
卷期号:318: 116887-116887 被引量:5
标识
DOI:10.1016/j.jep.2023.116887
摘要

More than 300 million people worldwide suffer from asthma, a chronic respiratory inflammatory disease. Total alkaloids (TA) were extracted from the ethnic medicinal plant Alstonia solaris (L.) R.Br., which is used to treat respiratory diseases. They may be effective drugs for treating asthma, but research is still needed to determine their effectiveness and mechanism in treating asthma. To further understand TA's role in the treatment of asthma and to support the phase II trial of the drug. In this study, we investigated the effects of TA in a mouse asthma model produced by Ovalbumin (OVA). H&E and PAS staining were used to observe the histopathological features of lung. airway hyperresponsiveness (AHR) was detected by ventilator; The expression of interleukin (IL)-33, suppression of tumorigenicity 2 (ST2) and E-cadherin in the lungs was evaluated by IHC. The concentrations of Mucin5AC (MUC5AC), eotaxin, IL-4, IL-5, IL-9, IL-13, interferon (IFN)-γ, IL-6, IL-8, IL-17A, IL-33, IL-25, thymic stromal lymphopoietin (TSLP), monocyte chemoattractant protein 1 (MCP-1), leukotriene (LT) B4, LTC4, LTD4, LTE4 in bronchoalveolar lavage fluid (BALF) and total IgE (tIgE), OVA-Specific IgE (OVA-IgE) in serum were measured by ELISA. ILC2s and eosinophils were detected in lung tissue by flow cytometry. The gene expression levels of IL-33 and ST2 were detected by RT-qPCR. Administration of TA reduced pulmonary inflammatory symptoms, MUC5AC production in the BALF, and AHR. At the same time, TA inhibited eotaxin production and eosinophil recruitment. Moreover, TA significantly decreased Th2 and Th17 cytokines and increased Th1 cytokines, contributing to restore the balance between Th1 and Th2 and Th17 cytokines. TA may reduce ILC2s numbers by inhibiting IL-33, IL-25, and TSLP levels in BALF and IL-33/ST2 signaling in lung tissue. Finally, TA decreased tIgE, OVA-IgE, and MCP-1 levels and subsequently inhibited mast cell activation and leukotriene release. These findings imply that TA may be an effective immunoregulatory medication for the management and prevention of asthma.
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