Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, 210029, PR China; The First Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, 210023, PR China.
Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, 210029, PR China; Department of Respiratory and Critical Care Medicine, Jiangsu Province Hospital of Chinese Medicine, Nanjing, 210029, PR China.
J Ethnopharmacol. 2021 Apr 6;269:113761. doi: 10.1016/j.jep.2020.113761. Epub 2020 Dec 29.
Peel of Citrus reticulata, a Chinese herbal drug with functions of regulating Qi and expelling phlegm, has been used for the treatment of lung related diseases in Chinese medicine for a long time. Its detailed effects on collagen in anti-idiopathic pulmonary fibrosis (IPF) is still unclear.
To explore the effects of citrus alkaline extract (CAE) on collagen synthesis, crosslinking and deposition in pulmonary fibrosis and understand the possible signal pathways involved in the activity.
CAE was prepared from C. reticulata. Bleomycin-induced pulmonary fibrosis mouse model was applied. Pulmonary fibrosis of lung was estimated with histopathology analysis, and collagen deposition was evaluated with immunohistochemistry. Collagen crosslinking related biomarkers and enzymes were analyzed with chemical methods, immunohistochemical and western blot analyses.
CAE oral administration lowered hydroxyproline content, inhibited the collagen deposition including expressions of collagen I and III, and relieved bleomycin-induced pulmonary fibrosis in mice model. The productions of a collagen crosslink pyridinoline and crosslinking related enzymes including lysyl oxidase (LOX), lysyl oxidase-like protein 1 (LOXL1) in lung were suppressed by CAE treatment. Furthermore, the protein expressions of TGF-β1 and Smad3 levels in lungs were also downregulated by CAE.
This study demonstrated that CAE inhibited collagen synthesis, crosslinking and deposition, and ameliorated bleomycin-induced pulmonary fibrosis. Preliminary mechanism study revealed that CAE exerted its bioactivity at least via downregulation of TGF-β1/Smad3 pathway. Our findings provided a great potential in fighting IPF based on CAE.
陈皮是一种中草药,具有理气化痰的功效,长期以来一直用于中医治疗肺部相关疾病。其对特发性肺纤维化(IPF)胶原的详细作用尚不清楚。
探讨陈皮碱性提取物(CAE)对肺纤维化胶原合成、交联和沉积的影响,并了解其活性可能涉及的信号通路。
从柑橘属制备 CAE。应用博来霉素诱导的肺纤维化小鼠模型。通过组织病理学分析评估肺纤维化,通过免疫组化评估胶原蛋白沉积。采用化学方法、免疫组化和 Western blot 分析分析胶原蛋白交联相关生物标志物和酶。
CAE 口服给药降低羟脯氨酸含量,抑制包括胶原 I 和 III 表达在内的胶原蛋白沉积,并缓解博来霉素诱导的小鼠肺纤维化模型。CAE 处理抑制了肺中胶原蛋白交联吡咯啉和交联相关酶(包括赖氨酰氧化酶(LOX)、赖氨酰氧化酶样蛋白 1(LOXL1))的产生。此外,CAE 还下调了肺中 TGF-β1 和 Smad3 水平的蛋白表达。
本研究表明 CAE 抑制胶原合成、交联和沉积,并改善博来霉素诱导的肺纤维化。初步的机制研究表明,CAE 通过下调 TGF-β1/Smad3 通路发挥其生物活性。我们的研究结果为基于 CAE 治疗 IPF 提供了巨大的潜力。