Zhang Li, Tong Xiang, Huang Jizhen, Wu Man, Zhang Shijie, Wang Dongguang, Liu SiTong, Fan Hong
Department of Respiratory and Critical Care Medicine, West China Hospital/West China School of Medicine, Chengdu, China.
Front Pharmacol. 2020 Dec 14;11:553690. doi: 10.3389/fphar.2020.553690. eCollection 2020.
Idiopathic pulmonary fibrosis is an aging-associated disease, satisfactory therapies are not yet available. Accelerated senescence of alveolar epithelial cells plays an important part in Idiopathic pulmonary fibrosis pathogenesis. Fisetin (FIS) is a natural non-toxic flavonoid, which has many pharmacological functions. However, the role of FIS in pulmonary fibrosis has not been established. In this study, we found that FIS treatment apparently alleviated BLM-induced weight loss, inflammatory cells infiltration, inflammatory factors expression, collagen deposition and alveolar epithelial cell senescence, along with AMPK activation and the down regulation of NF-κB and TGF-β/Smad3 . , FIS administration significantly inhibited the senescence of alveolar epithelial cells and senescence-associated secretory phenotype, followed by reduced transdifferentiation of fibroblasts to myofibroblasts as well as collagen deposition in fibroblasts, which was blocked by an AMPK inhibitor, Compound C. Together, these results suggest that FIS can alleviate the development of BLM-induced pulmonary fibrosis, which is related to the inhibition of TGF-β/Smad3 signaling and the reduction of alveolar epithelium cell senescence by regulating AMPK/NF-κB signaling pathway. FIS may be a promising candidate for patients with pulmonary fibrosis.
特发性肺纤维化是一种与衰老相关的疾病,目前尚无令人满意的治疗方法。肺泡上皮细胞的加速衰老在特发性肺纤维化发病机制中起重要作用。漆黄素(FIS)是一种天然无毒的类黄酮,具有多种药理功能。然而,FIS在肺纤维化中的作用尚未明确。在本研究中,我们发现FIS治疗明显减轻了博来霉素诱导的体重减轻、炎性细胞浸润、炎性因子表达、胶原沉积和肺泡上皮细胞衰老,同时激活了AMPK并下调了NF-κB和TGF-β/Smad3。此外,FIS给药显著抑制了肺泡上皮细胞的衰老和衰老相关分泌表型,随后减少了成纤维细胞向肌成纤维细胞的转分化以及成纤维细胞中的胶原沉积,而这被AMPK抑制剂Compound C所阻断。总之,这些结果表明FIS可以减轻博来霉素诱导的肺纤维化的发展,这与通过调节AMPK/NF-κB信号通路抑制TGF-β/Smad3信号传导和减少肺泡上皮细胞衰老有关。FIS可能是肺纤维化患者的一个有前途的候选药物。