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白杨素可减轻慢性哮喘小鼠模型中的过敏性炎症和气道重塑。

Chrysin alleviates allergic inflammation and airway remodeling in a murine model of chronic asthma.

作者信息

Yao Jing, Jiang Mingzi, Zhang Yunshi, Liu Xing, Du Qiang, Feng Ganzhu

机构信息

Department of Respiratory Medicine, the Second Affiliated Hospital of Nanjing Medical University, 121 Jiangjiayuan Road, Nanjing, Jiangsu 210000, PR China.

Department of Respiratory Medicine, The First People's Hospital of Kunshan, Qianjinxi Road No. 91, Kunshan, Jiangsu 215300, PR China.

出版信息

Int Immunopharmacol. 2016 Mar;32:24-31. doi: 10.1016/j.intimp.2016.01.005. Epub 2016 Jan 15.

Abstract

Asthma is a chronic airway inflammatory disorder and progresses mainly due to airway remodeling. Chrysin, a natural flavonoid, has been reported to possess multiple biologic activities, including anti-inflammation, anti-oxidation and anti-proliferation. The present study aimed to investigate whether chrysin could relieve allergic airway inflammation and remodeling in a murine model of chronic asthma and the mechanism involved. The female BALB/c mice sensitized and challenged with ovalbumin (OVA) successfully developed airway hyperresponsiveness (AHR), inflammation and remodeling. The experimental data showed that chrysin could alleviate OVA-induced AHR. Chrysin could also reduce OVA-induced increases in the number of inflammatory cells, especially eosinophils, interleukin (IL) -4, and IL-13 in bronchoalveolar lavage fluid (BALF) and total IgE in serum. The decreased interferon-γ (IFN-γ) level in BALF was also upregulated by chrysin. In addition, inflammatory cell infiltration, goblet cell hyperplasia and the expression of α-smooth muscle actin (α-SMA) around bronchioles were suppressed by chrysin. Furthermore, the phosphorylation levels of Akt and extracellular signal-regulated kinase (ERK) could be decreased by chrysin, which are associated with airway smooth muscle cell (ASMC) proliferation. These results indicate the promising therapeutic effect of chrysin on chronic asthma, especially the progression of airway remodeling.

摘要

哮喘是一种慢性气道炎症性疾病,主要因气道重塑而进展。白杨素是一种天然黄酮类化合物,据报道具有多种生物学活性,包括抗炎、抗氧化和抗增殖作用。本研究旨在探讨白杨素是否能缓解慢性哮喘小鼠模型中的过敏性气道炎症和重塑及其相关机制。用卵清蛋白(OVA)致敏和激发的雌性BALB/c小鼠成功出现气道高反应性(AHR)、炎症和重塑。实验数据表明,白杨素可减轻OVA诱导的AHR。白杨素还可减少OVA诱导的支气管肺泡灌洗液(BALF)中炎症细胞数量的增加,尤其是嗜酸性粒细胞、白细胞介素(IL)-4和IL-13,以及血清中总IgE的增加。白杨素还上调了BALF中降低的干扰素-γ(IFN-γ)水平。此外,白杨素抑制了炎症细胞浸润、杯状细胞增生以及细支气管周围α平滑肌肌动蛋白(α-SMA)的表达。此外,白杨素可降低与气道平滑肌细胞(ASMC)增殖相关的Akt和细胞外信号调节激酶(ERK)的磷酸化水平。这些结果表明白杨素对慢性哮喘,尤其是气道重塑的进展具有良好的治疗效果。

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