Xu Yifan, Li Jing, Lin Zhiwei, Liang Weiquan, Qin Lijie, Ding Jiabin, Chen Shuqi, Zhou Luqian
State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Institute of Combination Chinese and Western Medicine, Guangzhou Medical University, Guangzhou, China.
Front Pharmacol. 2022 Mar 24;13:860362. doi: 10.3389/fphar.2022.860362. eCollection 2022.
Chronic obstructive pulmonary disease (COPD) is a severely disabling chronic lung disease characterized by persistent airway inflammation, which leads to limited expiratory airflow that deteriorates over time. Isorhamnetin (Iso) is one of the most important active components in the fruit of and leaves of , which is widely used in many pulmonary disease studies because of its anti-inflammatory effects. Here, we investigated the pharmacological action of Iso in CS-induced airway inflammation and dissected the anti-inflammation mechanisms of Iso in COPD mice. A mouse model of COPD was established by exposure to cigarette smoke (CS) and intratracheal inhalation of lipopolysaccharide (LPS). Our results illustrated that Iso treatment significantly reduced leukocyte recruitment and excessive secretion of interleukin-6 (IL-6), monocyte chemoattractant protein-1 (MCP-1), and regulated upon activation, normal T-cell expressed and secreted (RANTES) in BALF of CS-induced COPD mice in a dose-dependent manner. This improved airway collagen deposition and emphysema, and further alleviated the decline in lung functions and systemic symptoms of hypoxia and weight loss. Additionally, Iso treatment obviously improves the T lymphocyte dysregualtion in peripheral blood of COPD mice. Mechanistically, Iso may degrade Keap1 through ubiquitination of p62, thereby activating the nuclear factor erythroid 2-related factor (Nrf2) pathway to increase the expression of protective factors, such as heme oxygenase-1 (HO-1), superoxide dismutase (SOD) 1, and SOD2, in lungs of CS-exposed mice, which plays an anti-inflammatory role in COPD. In conclusion, our study indicates that Iso significantly alleviates the inflammatory response in CS-induced COPD mice mainly by affecting the Nrf2/Keap1 pathway. More importantly, Iso exhibited anti-inflammatory effects comparable with Dex in COPD and we did not observe discernible side effects of Iso. The high safety profile of Iso may make it a potential drug candidate for COPD.
慢性阻塞性肺疾病(COPD)是一种严重致残的慢性肺部疾病,其特征为持续性气道炎症,可导致呼气气流受限,并随时间推移而恶化。异鼠李素(Iso)是[植物名称1]果实和[植物名称2]叶子中最重要的活性成分之一,因其抗炎作用而广泛应用于许多肺部疾病研究。在此,我们研究了异鼠李素在香烟烟雾(CS)诱导的气道炎症中的药理作用,并剖析了异鼠李素在COPD小鼠中的抗炎机制。通过暴露于香烟烟雾(CS)并气管内吸入脂多糖(LPS)建立COPD小鼠模型。我们的结果表明,异鼠李素治疗以剂量依赖性方式显著减少了CS诱导的COPD小鼠支气管肺泡灌洗液(BALF)中的白细胞募集以及白细胞介素-6(IL-6)、单核细胞趋化蛋白-1(MCP-1)和活化正常T细胞表达和分泌因子(RANTES)的过度分泌。这改善了气道胶原沉积和肺气肿,并进一步缓解了肺功能下降以及缺氧和体重减轻等全身症状。此外,异鼠李素治疗明显改善了COPD小鼠外周血中的T淋巴细胞失调。机制上,异鼠李素可能通过p62的泛素化降解Keap1,从而激活核因子红细胞2相关因子(Nrf2)途径,增加CS暴露小鼠肺中血红素加氧酶-1(HO-1)、超氧化物歧化酶(SOD)1和SOD2等保护因子的表达,这些因子在COPD中发挥抗炎作用。总之,我们的研究表明,异鼠李素主要通过影响Nrf2/Keap1途径显著减轻CS诱导的COPD小鼠的炎症反应。更重要的是,异鼠李素在COPD中表现出与地塞米松相当的抗炎作用,并且我们未观察到异鼠李素明显的副作用。异鼠李素的高安全性可能使其成为COPD的潜在候选药物。