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川芎嗪减轻卵清蛋白诱导的小鼠哮喘模型中的炎症及相关趋化因子和受体。

Ligustrazine attenuates inflammation and the associated chemokines and receptors in ovalbumine-induced mouse asthma model.

机构信息

Department of Integrative Medicine, Huashan Hospital, Fudan University, China; The Academy of Integrative Medicine, Fudan University, China.

Department of Integrative Medicine, Huashan Hospital, Fudan University, China; The Academy of Integrative Medicine, Fudan University, China.

出版信息

Environ Toxicol Pharmacol. 2016 Sep;46:55-61. doi: 10.1016/j.etap.2016.07.005. Epub 2016 Jul 12.

Abstract

Ligustrazine which is isolated from Chinese herb ligusticum chuanxiong hort, has been widely used in traditional Chinese medicine (TCM) for asthma treatment. In this study, we aim to observe the effect of ligustrazine on inflammation and the associated chemokines and receptors in ovalbumin (OVA)-induced mouse asthma model. Our data demonstrates that ligustrazine suppresses airway hyperresponsiveness to methacholine and lung inflammation in OVA-induced mouse asthma model. Ligustrazine also induces inhibition of inflammatory cells including neutrophils, lymphocytes and eosinophils. In addition, ligustrazine significantly reduces IL-4, IL-5, IL-17A, CCL3, CCL19 and CCL21 level in BALF of asthma mice. Furthermore, ligustrazine induces down-regulation of CCL19 receptor CCR7, STAT3 and p38 MAPK protein expression. Collectively, these results suggest that ligustrazine is effective in attenuation of allergic airway inflammatory changes and related chemokines and receptors in OVA-induced asthma model, and this action might be associated with inhibition of STAT3 and p38 MAPK pathway, which indicates that ligustrazine may be used as a potential therapeutic method to treat asthma.

摘要

川芎嗪是从中药川芎中分离出来的,已广泛用于哮喘的治疗。在这项研究中,我们旨在观察川芎嗪对卵清蛋白(OVA)诱导的小鼠哮喘模型中炎症及相关趋化因子和受体的影响。我们的数据表明,川芎嗪抑制了 OVA 诱导的小鼠哮喘模型中气道对乙酰甲胆碱的高反应性和肺炎症。川芎嗪还诱导抑制炎症细胞,包括中性粒细胞、淋巴细胞和嗜酸性粒细胞。此外,川芎嗪显著降低哮喘小鼠 BALF 中 IL-4、IL-5、IL-17A、CCL3、CCL19 和 CCL21 的水平。此外,川芎嗪诱导 CCL19 受体 CCR7、STAT3 和 p38 MAPK 蛋白表达下调。总之,这些结果表明,川芎嗪可有效减轻 OVA 诱导的哮喘模型中过敏性气道炎症变化及相关趋化因子和受体,其作用可能与抑制 STAT3 和 p38 MAPK 通路有关,提示川芎嗪可能作为一种潜在的治疗哮喘的方法。

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