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首页> 外文期刊>Naunyn-Schmiedeberg's Archives of Pharmacology >Sitagliptin exerts anti-inflammatory and anti-allergic effects in ovalbumin-induced murine model of allergic airway disease
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Sitagliptin exerts anti-inflammatory and anti-allergic effects in ovalbumin-induced murine model of allergic airway disease

机译:西他列汀在卵白蛋白诱导的小鼠过敏性气道疾病模型中发挥抗炎和抗过敏作用

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摘要

Sitagliptin, a new oral glucose lowering medication, is used for treatment of type 2 diabetes mellitus. The anti-inflammatory property of sitagliptin is reported, yet no studies have been done on asthma. In the present study, the effect of sitagliptin on allergic asthma was investigated using ovalbumin (OVA)-induced asthma model in mice. Swiss male albino mice sensitized and challenged to ovalbumin were treated with sitagliptin (8 mg/kg administered orally twice a day). Drug treatment was done on each day from days 16 to 23, 1 h before the challenge on the days of challenge. Sitagliptin treatment markedly decreased inflammatory cell accumulation in bronchoalveolar lavage (BAL) fluid and in the lungs, as revealed by histopathological examination. Furthermore, the levels of interleukin (IL)-13 in BAL fluid, total and OVA specific immunoglobulins (Ig)-E in serum, were significantly reduced as compared to the OVA group. In addition, sitagliptin significantly increased superoxidase dismutase (SOD) and reduced glutathione (GSH) activities with significant decrease in malondialdehyde (MDA) content in the lung. Importantly, sitagliptin decreased mRNA expression of the inflammatory cytokines tumor necrosis factor-α (TNF-α) and transforming growth factor-β1 (TGF-β1) in lung tissues as compared to the OVA group. Moreover, nitric oxide content as well as the mRNA expression of inducible nitric oxide synthase (iNOS) was remarkably decreased by sitagliptin treatment. Sitagliptin attenuates the allergic airway inflammation suggesting that sitagliptin may have applications in the treatment of bronchial asthma.
机译:西他列汀是一种新型的口服降糖药物,用于治疗2型糖尿病。据报道西他列汀具有抗炎特性,但尚未进行哮喘研究。在本研究中,使用卵清蛋白(OVA)诱导的小鼠哮喘模型研究了西他列汀对过敏性哮喘的作用。用西他列汀(每天两次口服8 mg / kg)治疗对卵白蛋白致敏和攻击的瑞士雄性白化病小鼠。在攻击日的第16天至第23天,即攻击前1小时,每天进行药物治疗。组织病理学检查显示,西他列汀治疗显着降低了支气管肺泡灌洗液(BAL)和肺中炎性细胞的蓄积。此外,与OVA组相比,BAL液中白介素(IL)-13的水平,血清中总和OVA特异性免疫球蛋白(Ig)-E的水平明显降低。此外,西他列汀显着增加了过氧化物酶歧化酶(SOD)并降低了谷胱甘肽(GSH)活性,同时肺中丙二醛(MDA)含量显着降低。重要的是,与OVA组相比,西他列汀可降低肺组织中炎性细胞因子肿瘤坏死因子-α(TNF-α)和转化生长因子-β1(TGF-β1)的mRNA表达。此外,西他列汀处理显着降低了一氧化氮含量以及诱导型一氧化氮合酶(iNOS)的mRNA表达。西他列汀减轻了过敏性气道炎症,提示西他列汀可能在支气管哮喘的治疗中有应用。

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