Regulation of Th1/Th2 balance through OX40/OX40L signalling by glycyrrhizic acid in a murine model of asthma

被引:87
|
作者
Wu, Qiaozhen [1 ,2 ]
Tang, Ying [2 ]
Hu, Xiaoyun [2 ]
Wang, Qin [3 ]
Lei, Wei [1 ]
Zhou, Linfu [4 ]
Huang, Jianan [1 ]
机构
[1] Soochow Univ, Affiliated Hosp 1, Dept Resp & Crit Med, Suzhou 215006, Peoples R China
[2] Soochow Univ, Peoples Hosp Wujiang 1, Dept Resp Med, Suzhou 215006, Peoples R China
[3] Soochow Univ, Inst Med Biotechnol, Suzhou 215006, Peoples R China
[4] Nanjing Med Univ, Affiliated Hosp 1, Dept Resp Med, Nanjing, Peoples R China
关键词
asthma; cytokine; glycyrrhizic acid; OX40; ligand; NF-KAPPA-B; OX40; LIGAND; CELL REGULATION; IN-VIVO; INFLAMMATION; ACTIVATION; EXPRESSION; BLOCKADE; DISEASE; MICE;
D O I
10.1111/resp.12655
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background and objectiveGlycyrrhizic acid (GA) has been reported to have attenuating airway inflammation effects in asthma mouse model. However, the potential molecular mechanisms by which GA exerts anti-inflammatory effects on ovalbumin (OVA)-induced allergic asthma have not been well elaborated. MethodsThe effect of GA on OVA-sensitized and challenged mice was investigated. The effect of GA on anti-OX40 mAb stimulated splenocytes from asthma mice model was also examined. ResultsIn OVA-induced asthmatic mice, GA treatment prevented the decrease of T helper1 cytokine (interferon (IFN)-) and the increase of T helper2 cytokines (interleukin (IL)-4, IL-5, IL-13) in bronchoalveolar lavage fluid (BALF), reduced serum immunoglobulin (Ig)E and OVA-specific IgE levels, prohibited the protein and mRNA expression of OX40 and OX40 Ligand (OX40L) in lung tissues, and the expression of OX40 in CD4(+) T cells and OX40L in CD11b(+) monocytes and CD19(+) B cells in spleens in a dose-dependent manner compared with the vehicle treatment (all P<0.05). Moreover, OVA significantly increased the activation of p38 mitogen-activated protein kinase (MAPK) in lung tissues, whereas GA and anti-OX40L mAb markedly reduced phosphorylation of p38 MAPK. In addition, GA could inhibit the T cell proliferation and modulate the balance of Th1/Th2 in anti-OX40 mAb stimulated CD4(+) T cells from asthmatic spleens (all P<0.05). ConclusionsGA may exert a therapeutic effect on OVA-induced experimental asthma partly by regulating the Th1/Th2 balance through suppressing OX40-OX40L signalling and p38 MAPK activity. GA may be a promising treatment for asthma. We investigated the effect of glycyrrhizic acid (GA) on an OVA-challenged model of asthma. GA-modulated Th2 and Th1 reduced OX40, OX40L and p-p38 MAPK in OVA-challenged asthma mice model. GA also suppressed OVA-induced and anti-OX40 mAb stimulated splenocyte proliferation and Th2 production. GA has potential as a treatment for asthma.
引用
收藏
页码:102 / 111
页数:10
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