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一种中药配方通过上调Nrf2抑制氧化应激来改善肺纤维化。

A Chinese Herbal Formula Ameliorates Pulmonary Fibrosis by Inhibiting Oxidative Stress via Upregulating Nrf2.

作者信息

Bai Yunping, Li Jiansheng, Zhao Peng, Li Ya, Li Meng, Feng Suxiang, Qin Yanqin, Tian Yange, Zhou Tiqiang

机构信息

Henan Key Laboratory of Chinese Medicine for Respiratory Disease, Henan University of Chinese Medicine, Zhengzhou, China.

Collaborative Innovation Center for Respiratory Disease Diagnosis and Treatment - Chinese Medicine Development of Henan Province, Zhengzhou, China.

出版信息

Front Pharmacol. 2018 Jun 12;9:628. doi: 10.3389/fphar.2018.00628. eCollection 2018.

Abstract

This study aimed to explore the protective effects of a Chinese herbal formula, Jinshui Huanxian formula (JHF), on experimental pulmonary fibrosis and its underlying mechanisms. After being treated with single dose of bleomycin (5 mg/kg) intratracheally, rats were orally administered with JHF and pirfenidone from day 1 to 42, then sacrificed at 7, 14, 28, or 42 days post-bleomycin instillation. JHF ameliorated bleomycin-induced pathological changes, collagen deposition in the rat lung and recovered pulmonary function at different days post-bleomycin instillation. In lungs of JHF-treated rats, the levels of total superoxide dismutase, catalase and glutathione were higher, and myeloperoxidase and methane dicarboxylic aldehyde were lower than those in vehicle-treated rats, respectively. Additionally, JHF inhibited the expression of NADPH oxidase 4 (NOX4) and increased the Nuclear Factor Erythroid 2-Related Factor 2 (Nrf2) in lung tissues. , JHF and ruscogenin, a compound of Ophiopogonis Radix contained in JHF, significantly inhibited transforming growth factor β1 (TGF-β1)-induced differentiation of fibroblasts. Furthermore, JHF markedly decreased the level of reactive oxygen species in TGF-β1-induced fibroblast. In line with this, upregulation of NAD(P)H: quinone oxidoreductase 1 and heme oxygenase 1, and downregulation of NOX4 were found in JHF-treated fibroblast induced by TGF-β1. While on the other hand, Nrf2 siRNA could suppress the JHF-mediated inhibition effect on alpha-smooth muscle actin (α-SMA), and FN1 expression induced by TGF-β in fibroblasts. These results indicated that JHF performed remarkably therapeutic and long-term effects on pulmonary fibrosis in rat and suppressed the differentiation of fibroblast into myofibroblast through reducing the oxidative response by upregulating Nrf2 signaling. It might provide a new potential natural drug for the treatment of pulmonary fibrosis.

摘要

本研究旨在探讨中药金水还仙方(JHF)对实验性肺纤维化的保护作用及其潜在机制。大鼠经气管内单次注射博莱霉素(5 mg/kg)后,从第1天至第42天口服给予JHF和吡非尼酮,然后在博莱霉素滴注后7、14、28或42天处死。JHF改善了博莱霉素诱导的大鼠肺病理变化、胶原沉积,并在博莱霉素滴注后的不同时间恢复了肺功能。在JHF治疗的大鼠肺中,总超氧化物歧化酶、过氧化氢酶和谷胱甘肽水平较高,而髓过氧化物酶和丙二醛水平分别低于载体治疗的大鼠。此外,JHF抑制肺组织中NADPH氧化酶4(NOX4)的表达并增加核因子红细胞2相关因子2(Nrf2)。JHF及其所含的麦冬皂苷元,能显著抑制转化生长因子β1(TGF-β1)诱导的成纤维细胞分化。此外,JHF显著降低了TGF-β1诱导的成纤维细胞中的活性氧水平。与此一致,在TGF-β1诱导的JHF处理的成纤维细胞中发现NAD(P)H:醌氧化还原酶1和血红素加氧酶1上调,NOX4下调。另一方面,Nrf2 siRNA可抑制JHF介导的对TGF-β诱导的成纤维细胞中α-平滑肌肌动蛋白(α-SMA)和FN1表达的抑制作用。这些结果表明,JHF对大鼠肺纤维化具有显著的治疗和长期作用,并通过上调Nrf2信号通路减少氧化反应,抑制成纤维细胞向肌成纤维细胞的分化。它可能为治疗肺纤维化提供一种新的潜在天然药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2e3/6005894/e717e8f590bc/fphar-09-00628-g001.jpg

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