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Dexamethasone reduces serum level of IL-17 in Bleomycin-A5-induced rats model of pulmonary fibrosis

机译:地塞米松降低博来霉素-A5诱导的大鼠肺纤维化模型的血清IL-17水平

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Abstract Background: Pulmonary fibrosis is a chronic progressive disease with limited therapeutic options and inflammatory cytokines play important roles in the pathogenesis of pulmonary fibrosis. Material and method: Here, we investigated the changes of TGF-β1, IL-8, and IL-17 in the serum of bleomycin-A5-induced rats model of pulmonary fibrosis. 120 healthy male Wistar rats were randomly divided into three groups, the control group (n?=?30), the model group (n?=?45) and the dexamethasone (DEX) group (n?=?45). The rats of both model group and DEX group were injected with Bleomycin-A5 (5?mg/kg) through tracheofistulization to induce pulmonary fibrosis, while the rats of the control group were injected with equivalent physiological saline. After operation, DEX (4?mg/kg) was given to the DEX group rats intraperitoneally once a day. Equivalent saline was administered to rats of both the control group and the model group. Results: On the 1st, 14th, and 28th day after operation, pathological changes of the lung tissues, and the levels of serum IL-8, TGF-β1, and IL-17 were measured. The concentrations of serum TGF-β1, IL-8, and IL-17 were significantly increased after bleomycin-A5 treatment, especially on the 14th day (p?p??.01). Conclusions: DEX protect bleomycin-A5-induced pulmonary fibrosis in rats through reduced the level of IL-17 in serum.
机译:摘要背景:肺纤维化是一种慢性进行性疾病,治疗选择有限,炎性细胞因子在肺纤维化的发病机制中起着重要作用。材料和方法:在这里,我们研究了博来霉素A5诱导的大鼠肺纤维化模型血清中TGF-β1,IL-8和IL-17的变化。将120只健康的雄性Wistar大鼠随机分为三组,对照组(n≥30),模型组(n≥45)和地塞米松(DEX)组(n≥45)。模型组和DEX组大鼠均通过气管切开术注射博来霉素A5(5?mg / kg)诱发肺纤维化,而对照组大鼠则注射等量生理盐水。手术后,每天一次腹膜内给予DEX组大鼠DEX(4?mg / kg)。对照组和模型组大鼠均给予等量生理盐水。结果:在术后第1、14和28天,测量肺组织的病理变化,并检测血清IL-8,TGF-β1和IL-17的水平。博来霉素-A5处理后,血清TGF-β1,IL-8和IL-17的浓度显着升高,尤其是在第14天(p?p?

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