鱼腥草素钠对中性粒细胞哮喘小鼠炎性细胞因子和黏蛋白表达的影响
黄晨凤, 李淼中国医科大学附属盛京医院小儿呼吸内科, 沈阳 110004
收稿日期:
2021-12-08发布日期:
2022-11-09通讯作者:
李淼E-mail:Lmpediatrician@126.com作者简介:
黄晨凤(1996-),女,硕士研究生.基金资助:
国家自然科学基金青年基金(81400016)关键词: 鱼腥草素钠, 中性粒细胞哮喘, 肿瘤坏死因子-α, 白细胞介素-1β, 黏蛋白5AC, 丝氨酸/苏氨酸蛋白激酶磷酸化
Abstract: Objective To investigate the effect of sodium houttuyfonate(SH)on the levels of inflammatory factors,such as tumor necrosis factor(TNF)-α,interleukin(IL)-1β ,and mucin 5 subtype AC(MUC5AC)in mice with neutrophilic asthma(NA).Methods Forty BALB/c mice were randomly divided into NC,NA,SH,dexamethasone(DXM),and SH+DXM groups. Airway resistance was determined for mice in each group and the total number of leukocytes in the bronchoalveolar lavage fluid(BALF)was determined. Wright-Giemsa staining was performed to classify and count leukocytes and hematoxylin and eosin,periodic acid-Schiff,and Masson’s trichrome staining were performed to observe the distribution of inflammatory cells,mucus secretion in lung tissue and around the airways,and the degree of fibrosis,respectively. Immunohistochemistry was performed to detect differences in the expression levels of MUC5AC in lung tissue and real-time polymerase chain reaction was used to determine MUC5AC mRNA levels in lung tissue. Western blotting was used to detect differences in TNF-α,IL-1β ,and phosphorylated(p)-AKT/AKT protein levels in lung tissue.Results Compared with the NA group,airway resistance,and the total number of leukocytes and neutrophils in BALF were lower in the SH,DXM,and SH+DXM groups(P < 0.05). Inflammation,mucus secretion,and fibrosis in the lung tissue and around the airways were reduced and MUC5AC protein expression levels in lung tissue and airway epithelial cells decreased(P < 0.05). MUC5AC mRNA levels and TNF-α,IL-1β ,and p-AKT/AKT protein levels in lung tissue decreased(P < 0.05).Conclusion SH may reduce the expression levels of inflammatory factors and mucin by inhibiting the phosphorylation of AKT,thus alleviating the symptoms of NA.
Key words: sodium houttuyfonate, neutrophilic asthma, tumor necrosis factor-α, interleukin-1β, mucin 5 subtype AC, serine/threonine protein kinase phosphorylation
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