Qilongtian Ameliorate Bleomycin-induced Pulmonary Fibrosis in Mice via Inhibiting IL-17 signal pathway

Author:

Zhang Qiang1,Luo Ting2,Yuan Dezheng2,Liu Jing2,Fu Yi3,Yuan Jiali1

Affiliation:

1. Shanghai University of traditional Chinese medicine

2. Yunnan University of Chinese medicine

3. Third Affiliated Hospital of Yunnan University of Traditional Chinese Medicine, Kunming Municipal Hospital of Traditional Chinese Medicine

Abstract

Abstract Pulmonary fibrosis (PF) is a special type of pulmonary parenchymal disease, with chronic, progressive, fibrosis, high mortality. There is a lack of safe, effective, and affordable treatment methods. Qilongtian (QLT) is a traditional Chinese prescription that is composed of Panax notoginseng, Earthworm, and Rhodiola, and shows the remarkable clinical curative effect of PF. However, the mechanism of QLT remains to be clarified. Therefore, we studied the effectivity of QLT in treating Bleomycin (BLM) induced PF mice. Our studies have shown that QLT significantly reduced the inflammatory injury, hydroxyproline content and collagen deposition of lung tissue in BLM induced PF mice and downregulated the cytokine related to inflammation and fibrosis and PF expression on the mRNA and protein level in PF mice. To identify the mechanism of QLT, the Transcriptome was measured, and the IL-17 signal pathway was screened out for further research. Further studies indicated that QLT reduced the mRNA level of CCL12, CXCL5, FOSL1, MMP9, and AREG, which are inflammation and fibrosis-related genes in the IL-17 signal pathway. In summary, the results indicated that the potential mechanism of QLT in preventing PF progress was by inhibiting the inflammation resulting in IL-17 signal pathway. Our study provides the novel scientific basis of QLT and represents new therapeutics for PF in clinical.

Publisher

Research Square Platform LLC

Reference45 articles.

1. 1. Zhan, X.; Liu, B.; Tong, Z.. Current situation and thinking of pulmonary fibrosis after New Coronavirus pneumonia inflammation. Chinese Journal of Tuberculosis and Respiration 2020, 43, 728–732. doi: 10.3760/cma.j.cn112147-20200317-00359

2. 2. Guzy, R.D.; LI, L.; Smith, C.; et al. Pulmonary fibrosis requires cellautonomous mesenchymal fibroblast growth factor (FGF) signaling. J Biol Chem 2017, 292: 10364–10378. doi: 10.1074/jbc.M117.791764

3. 3. Yang, C.M.; Zhang H.C.; Liu D. Systematic evaluation of Supplementing Qi, nourishing yin and dredging collaterals in the treatment of idiopathic pulmonary fibrosis. Journal of China Japan Friendship Hospital, 2021, 35, 172–174. doi: 10.13463/j.cnki.cczyy. 2018.01.027

4. 4. Rahmati, S.; Li, Q.; Rahman, P.; et al. Insights into the pathogenesis of psoriatic arthritis from genetic studies. Semin Immunopathol 2021, 43, 21–234. doi: 10.1007/s00281-021-00843-2

5. 5. Meyer, K.C.. Pulmonary fibrosis, part I: epidemiology, pathogenesis, and diagnosis. Expert Rev Respir Med 2017, 11, 343–359. doi: 10.1080/17476348.2017.1312346

全球学者库

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"全球学者库"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前全球学者库共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2023 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3