Quanzhen Yiqi decoction attenuates inflammation in mice with smoking-induced COPD by activating the Nrf2/HO-1 pathway and inhibiting the NLRP3 inflammasome.

Jiamin Zeng, Zhenqiu Li, Wanyan Li, Zhu Liang, Yuewen Luo, Caiping Li, Sida Liao, Kexin Wang, Yuanlong Hu, Yuanyuan Li, Qiuling Liang, Wenju Lu, Lu Li, Zhijuan Wu, Da-Peng Zhang, Zhiming Zhang
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Abstract

OBJECTIVE Quanzhen Yiqi decoction (QZYQ) is a traditional Chinese medicine for treating chronic obstructive pulmonary disease. METHODS Mice were exposed to cigarette smoke (CS) 6 days/week (40 cigarettes/day) for 24 weeks and then intragastrically administered QZYQ (4.72, 9.45, or 18.89 g/kg) or dexamethasone (DEX, 0.6 mg/kg) for 6 weeks. We examined the lung function and collected bronchoalveolar lavage fluid for inflammatory cell and cytokine quantification. The pathological lung changes, ROS and oxidative biomarkers were measured. We used immunohistochemistry and western blotting to evaluate the levels of Nrf2/HO-1, NLRP3/ASC/Caspase1/IL-1β/IL-18. RESULTS The CS group showed significant increases in the forced vital capacity, lung resistance, and chord compliance and a lower FEV50/FVC compared with the control, and QZYQ improved these changes. In addition, QZYQ effectively reduced emphysema, immune cell infiltration, and airway remodeling. QZYQ stimulated HO-1 expression and reduced oxidative stress through the Nrf2 pathway. QZYQ inhibited the production of NLRP3/ASC/Caspase-1 to inhibit IL-1β and IL-18. CONCLUSION Our study suggested that QZYQ can improve the function and histology of the lungs and reduce inflammatory cell recruitment. QZYQ inhibits ROS production and NLRP3 inflammasome activation by upregulating Nrf2 to reduce lung injury. The anti-inflammatory effects of QZYQ are similar to those of DEX.
全真益气煎剂通过激活Nrf2/HO-1通路和抑制NLRP3炎性体,减轻吸烟诱导的慢性阻塞性肺病小鼠的炎症反应。
方法将小鼠暴露于香烟烟雾(CS)中,每周 6 天(每天 40 支香烟),持续 24 周,然后胃内注射 QZYQ(4.72、9.45 或 18.89 克/千克)或地塞米松(DEX,0.6 毫克/千克),持续 6 周。我们检查了患者的肺功能,并收集了支气管肺泡灌洗液,用于炎症细胞和细胞因子的定量分析。我们还测量了肺部病理变化、ROS 和氧化生物标志物。结果与对照组相比,CS 组的用力肺活量、肺阻力和弦顺应性显著增加,FEV50/FVC 降低,而 QZYQ 则改善了这些变化。此外,QZYQ 还能有效减少肺气肿、免疫细胞浸润和气道重塑。QZYQ 通过 Nrf2 途径刺激了 HO-1 的表达并降低了氧化应激。结论我们的研究表明,QZYQ 可以改善肺功能和组织学,减少炎症细胞的招募。QZYQ通过上调Nrf2抑制ROS的产生和NLRP3炎性体的激活,从而减轻肺损伤。QZYQ 的抗炎作用与 DEX 相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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