Literature DB >> 35576111

Efficacy of Qingfei oral liquid for idiopathic pulmonary fibrosis in rats and related network pharmacology study.

Yiwen Zhang, Kongsheng Sheng, Feifeng Song, Zongfu Pan, Xiaozhou Zou, Yujia Liu, Ping Huang.   

Abstract

To investigate the therapeutic effect and mechanism of Qingfei oral liquid in idiopathic pulmonary fibrosis. Seventy-two male SD rats were divided into control group, model group, pirofenidone group and Qingfei group with 18 animals in each group. The idiopathic pulmonary fibrosis was induced in last three groups by intratracheal injection of bleomycin; pirofenidone group was given oral administration of pirofenidone b.i.d for 21 d, and Qingfei group was given Qingfei oral liquid 3.6 mL/kg q.d for Lung tissues were obtained for HE staining, Masson staining and transforming growth factor (TGF)-β immunohistochemical staining. Superoxide dismutase (SOD), malondialdehyde (MDA) and glutathione (GSH) were detected in tissue homogenates. The BATMAN-TCM database was used to retrieve the chemical components and their corresponding targets of Qingfei oral solution by network pharmacology method, and then the component-target-disease network diagram was constructed. Finally, the pathway enrichment analysis was carried out to explore the molecular mechanism of Qingfei oral liquid against idiopathic fibrosis. Histopathology results showed that Qingfei oral liquid had a similar relieving effect on pulmonary fibrosis as the positive drug pirfenidone; TGF-β secretion had a significant reduction in lung tissues of Qingfei group; and Qingfei oral liquid had better regulatory effect on SOD, MDA and GSH than pirfenidone. The results of component-target-disease network and pathway enrichment analysis showed that the related molecular pathways were concentrated in inflammation, extracellular matrix and cytokines. Qingfei oral liquid has a good therapeutic effect on idiopathic pulmonary fibrosis in rats via regulation of inflammation, extracellular matrix and cytokines.

Entities:  

Keywords:  Idiopathic pulmonary fibrosis; Network pharmacology; Oxidation-reduction; Qingfei oral liquid; Rats; Transforming growth factor-β

Mesh:

Substances:

Year:  2022        PMID: 35576111      PMCID: PMC9109760          DOI: 10.3724/zdxbyxb-2021-0203

Source DB:  PubMed          Journal:  Zhejiang Da Xue Xue Bao Yi Xue Ban        ISSN: 1008-9292


  24 in total

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Journal:  JCI Insight       Date:  2018-08-23

Review 5.  Pirfenidone safety and adverse event management in idiopathic pulmonary fibrosis.

Authors:  Lisa H Lancaster; Joao A de Andrade; Joseph D Zibrak; Maria L Padilla; Carlo Albera; Steven D Nathan; Marlies S Wijsenbeek; John L Stauffer; Klaus-Uwe Kirchgaessler; Ulrich Costabel
Journal:  Eur Respir Rev       Date:  2017-12-06

6.  N-acetylcysteine downregulation of lysyl oxidase activity alleviating bleomycin-induced pulmonary fibrosis in rats.

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Journal:  Eur J Pharm Biopharm       Date:  2021-04-18       Impact factor: 5.589

Review 8.  Efficacy and Safety of Nintedanib for the Treatment of Idiopathic Pulmonary Fibrosis: An Update.

Authors:  José Antonio Rodríguez-Portal
Journal:  Drugs R D       Date:  2018-03

9.  Telomere length and risk of idiopathic pulmonary fibrosis and chronic obstructive pulmonary disease: a mendelian randomisation study.

Authors:  Anna Duckworth; Michael A Gibbons; Richard J Allen; Howard Almond; Robin N Beaumont; Andrew R Wood; Katie Lunnon; Mark A Lindsay; Louise V Wain; Jess Tyrrell; Chris J Scotton
Journal:  Lancet Respir Med       Date:  2020-11-13       Impact factor: 30.700

10.  Bronchoalveolar lavage (BAL) cells in idiopathic pulmonary fibrosis express a complex pro-inflammatory, pro-repair, angiogenic activation pattern, likely associated with macrophage iron accumulation.

Authors:  Jungnam Lee; Ivan Arisi; Ermanno Puxeddu; Lazarus K Mramba; Massimo Amicosante; Carmen M Swaisgood; Marco Pallante; Mark L Brantly; C Magnus Sköld; Cesare Saltini
Journal:  PLoS One       Date:  2018-04-12       Impact factor: 3.240

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