益气温阳方调控SIRT1抑制变应性鼻炎小鼠线粒体过度分裂及炎症反应的研究

Yiqi Wenyang Recipe ameliorates Excessive Mitochondrial Fission and Inflammatory Response in a Murine Model of Allergic Rhinitis through Regulating SITR1

  • 摘要:
    目的 探讨益气温阳方干预变应性鼻炎(AR)小鼠的潜在效应机制。
    方法 C57/BL6小鼠随机分为空白、模型、益气温阳方及益气温阳方+EX-527(SIRT1)抑制剂组,以卵白蛋白基础联合攻击致敏的方法建立小鼠AR模型,各组予对应措施干预后,评估小鼠行为学变化;以HE及甲苯胺蓝染色观察鼻黏膜病变;ELISA法测定血清白介素-4(IL-4)、小鼠干扰素γ(IFN-γ)、免疫球蛋白E(IgE)水平;Western blot联合免疫荧光法测定鼻黏膜组织中磷酸化Janus激酶2(p-JAK2)、磷酸化信号转导与转录因子6(p-STAT6)、磷酸化动力样蛋白1(p-Drp1)、SIRT1、过氧化物酶体增殖物激活受体γ共激活因子1α(PGC-1α)表达水平;荧光探针法检测活性氧(ROS)水平;透射电镜观察鼻黏膜微观结构中线粒体形态改变。
    结果 与空白组比较,模型组小鼠搔鼻与喷嚏频次升高,鼻黏膜见大量嗜酸性粒细胞及肥大细胞浸润(P < 0.05);与模型组比较,益气温阳方组小鼠鼻过敏症状及鼻黏膜炎症反应水平显著改善(P < 0.05);与益气温阳方组比较,益气温阳方+EX-527组小鼠搔鼻与喷嚏升高,鼻黏膜见嗜酸性粒细胞及肥大细胞计数显著增加(P < 0.05)。与模型组比较,益气温阳方组小鼠血清IL-4、IgE水平降低,血清IFN-γ水平回升(P < 0.05);而益气温阳方+EX-527组小鼠血清IL-4、IgE较益气温阳方组小鼠升高(P < 0.05)。Western blot与免疫荧光均表明,益气温阳方可有效抑制卵白蛋白致敏诱导的p-JAK2、p-STAT6、p-Drp1(Ser616)水平的升高,以及SIRT1、PGC-1α表达降低(P < 0.01);但EX-527的介入钝化了益气温阳方对上述信号分子的调节作用(P < 0.05,P < 0.01)。透射电镜及荧光探针结果表明,模型组鼻黏膜线粒体见大量圆球状线粒体分布,ROS水平显著升高(P < 0.01);益气温阳方干预恢复了线粒体长管状形态并降低ROS水平(P < 0.01),而EX-527的介入削弱了上述改善效应(P < 0.01)。
    结论 益气温阳方可通过调控SIRT1以激活PGC-1α,进而抑制Drp1介导的线粒体过度分裂,起到干预AR的效应。SIRT1可能为益气温阳方干预AR的重要靶点之一。

     

    Abstract:
    OBJECTIVE To explore the potential mechanism of Yiqi Wenyang Recipe in the intervention of allergic rhinitis (AR) mice.
    METHODS C57/BL6 mice were randomly divided into blank, model, Yiqi Wenyang Recipe and Yiqi Wenyang Recipe+EX-527 Sirtuin 1 (SIRT1) inhibitor groups. The AR model of mice was established by ovalbumin based challenge sensitization method, each group received corresponding intervention measures. Assessment of behavioral changes in mice; nasal mucosal lesions were observed by HE and toluidine blue staining; the serum levels of interleukin-4 (IL-4), interferon-γ (IFN-γ), and immunoglobulin E (IgE) were measured by ELISA; the expression levels of phospho-Janus kinase 2 (p-JAK2), phospho-signal transducer and activator of transcription 6 (p-STAT6), phospho-dynamin-related protein 1 (p-Drp1), SIRT1, peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) in nasal mucosa were determined by Western blot combined with immunofluorescence; reactive oxygen species (ROS) levels were detected by fluorescent probe method; the morphological changes of mitochondria in the microstructure of nasal mucosa were observed by transmission electron microscopy.
    RESULTS Compared with the blank group, the frequency of scratching and sneezing in the model group was significantly increased, and a large number of eosinophils and mast cells were found in the nasal mucosa (P < 0.05); compared with the model group, the nasal allergic symptoms and the level of nasal mucosal inflammatory reaction in the Yiqi Wenyang Recipe group were significantly improved (P < 0.05); compared with the Yiqi Wenyang Recipe group, the scratching and sneezing of mice in the Yiqi Wenyang Recipe+EX-527 group increased again, and the counts of eosinophils and mast cells in nasal mucosa increased significantly (P < 0.05). Compared with the model group, the levels of serum IL-4 and IgE in the Yiqi Wenyang Recipe group decreased, while the level of serum IFN-γ increased (P < 0.05); the serum IL-4 and IgE of mice in the Yiqi Wenyang Recipe+ex-527 group were significantly higher than those in the Yiqi Wenyang Recipe group (P < 0.05). Western blot and immunofluorescence showed that Yiqi Wenyang Recipe could effectively inhibit the increase of p-JAK2, p-STAT6, p-Drp1(ser616) levels induced by ovalbumin sensitization, as well as the decrease of SIRT1 and PGC-1 α expression(P < 0.01); however, the intervention of EX-527 significantly blunted the regulatory effect of Yiqi Wenyang Recipe on the above signaling molecules(P < 0.05, P < 0.01). The results of transmission electron microscopy and fluorescent probe showed that in the model group, a large number of spherical mitochondria were found in the mitochondria of nasal mucosa, and the level of ROS was significantly increased(P < 0.01);; the intervention of Yiqi Wenyang recipe effectively restored the long tubular morphology of mitochondria and reduced ROS level(P < 0.01);, while the intervention of EX-527 weakened the above improvement effect(P < 0.01).
    CONCLUSION Yiqi Wenyang Recipe can regulate SIRT1 to activate PGC-1α, and then inhibit Drp1 mediated excessive mitochondrial fission to intervene AR; SIRT1 may be one of the important targets of Yiqi Wenyang Recipe in the intervention of AR.

     

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