Pharmacodynamic and pharmacokinetic assessment of pulmonary rehabilitation mixture for the treatment of pulmonary fibrosis

Abstract Pulmonary rehabilitation mixture (PRM), a Chinese herbal medicine formula, has been used to treat pulmonary fibrosis for decades. In this study, we systematically evaluated the pharmacodynamic and pharmacokinetic performance of PRM. The pharmacodynamic results showed that PRM could improve...

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Autores principales: Juanjuan Zhao, Yan Ren, Yubei Qu, Wanglin Jiang, Changjun Lv
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Lenguaje:EN
Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/121ab20e0e60459e8a32835b7b03323a
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spelling oai:doaj.org-article:121ab20e0e60459e8a32835b7b03323a2021-12-02T11:52:22ZPharmacodynamic and pharmacokinetic assessment of pulmonary rehabilitation mixture for the treatment of pulmonary fibrosis10.1038/s41598-017-02774-12045-2322https://doaj.org/article/121ab20e0e60459e8a32835b7b03323a2017-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-02774-1https://doaj.org/toc/2045-2322Abstract Pulmonary rehabilitation mixture (PRM), a Chinese herbal medicine formula, has been used to treat pulmonary fibrosis for decades. In this study, we systematically evaluated the pharmacodynamic and pharmacokinetic performance of PRM. The pharmacodynamic results showed that PRM could improve the condition of CoCl2-stimulated human type II alveolar epithelial cells, human pulmonary microvascular endothelial cells, human lung fibroblasts and pulmonary fibrosis rats induced by bleomycin, PRM treatment reduced the expression of platelet-derived growth factor, fibroblast growth factor, toll-like receptor 4, high-mobility group box protein 1 and hypoxia-inducible factor 1α. In the pharmacokinetic study, an accurate and sensitive ultra-high performance liquid chromatography tandem mass spectrometry method was developed and validated for the simultaneous determination of calycosin, calycosin-7-O-glucoside, formononetin, ononin and mangiferin of PRM in the rat plasma for the first time. The method was then successfully applied to the comparative pharmacokinetic study of PRM in normal and pulmonary fibrosis rats. The five constituents could be absorbed in the blood after the oral administration of PRM and exhibited different pharmacokinetic behaviors in normal and pulmonary fibrosis rats. In summary, PRM exhibited a satisfactory pharmacodynamic and pharmacokinetic performance, which highlights PRM as a potential multi-target oral drug for the treatment of pulmonary fibrosis.Juanjuan ZhaoYan RenYubei QuWanglin JiangChangjun LvNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Juanjuan Zhao
Yan Ren
Yubei Qu
Wanglin Jiang
Changjun Lv
Pharmacodynamic and pharmacokinetic assessment of pulmonary rehabilitation mixture for the treatment of pulmonary fibrosis
description Abstract Pulmonary rehabilitation mixture (PRM), a Chinese herbal medicine formula, has been used to treat pulmonary fibrosis for decades. In this study, we systematically evaluated the pharmacodynamic and pharmacokinetic performance of PRM. The pharmacodynamic results showed that PRM could improve the condition of CoCl2-stimulated human type II alveolar epithelial cells, human pulmonary microvascular endothelial cells, human lung fibroblasts and pulmonary fibrosis rats induced by bleomycin, PRM treatment reduced the expression of platelet-derived growth factor, fibroblast growth factor, toll-like receptor 4, high-mobility group box protein 1 and hypoxia-inducible factor 1α. In the pharmacokinetic study, an accurate and sensitive ultra-high performance liquid chromatography tandem mass spectrometry method was developed and validated for the simultaneous determination of calycosin, calycosin-7-O-glucoside, formononetin, ononin and mangiferin of PRM in the rat plasma for the first time. The method was then successfully applied to the comparative pharmacokinetic study of PRM in normal and pulmonary fibrosis rats. The five constituents could be absorbed in the blood after the oral administration of PRM and exhibited different pharmacokinetic behaviors in normal and pulmonary fibrosis rats. In summary, PRM exhibited a satisfactory pharmacodynamic and pharmacokinetic performance, which highlights PRM as a potential multi-target oral drug for the treatment of pulmonary fibrosis.
format article
author Juanjuan Zhao
Yan Ren
Yubei Qu
Wanglin Jiang
Changjun Lv
author_facet Juanjuan Zhao
Yan Ren
Yubei Qu
Wanglin Jiang
Changjun Lv
author_sort Juanjuan Zhao
title Pharmacodynamic and pharmacokinetic assessment of pulmonary rehabilitation mixture for the treatment of pulmonary fibrosis
title_short Pharmacodynamic and pharmacokinetic assessment of pulmonary rehabilitation mixture for the treatment of pulmonary fibrosis
title_full Pharmacodynamic and pharmacokinetic assessment of pulmonary rehabilitation mixture for the treatment of pulmonary fibrosis
title_fullStr Pharmacodynamic and pharmacokinetic assessment of pulmonary rehabilitation mixture for the treatment of pulmonary fibrosis
title_full_unstemmed Pharmacodynamic and pharmacokinetic assessment of pulmonary rehabilitation mixture for the treatment of pulmonary fibrosis
title_sort pharmacodynamic and pharmacokinetic assessment of pulmonary rehabilitation mixture for the treatment of pulmonary fibrosis
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/121ab20e0e60459e8a32835b7b03323a
work_keys_str_mv AT juanjuanzhao pharmacodynamicandpharmacokineticassessmentofpulmonaryrehabilitationmixtureforthetreatmentofpulmonaryfibrosis
AT yanren pharmacodynamicandpharmacokineticassessmentofpulmonaryrehabilitationmixtureforthetreatmentofpulmonaryfibrosis
AT yubeiqu pharmacodynamicandpharmacokineticassessmentofpulmonaryrehabilitationmixtureforthetreatmentofpulmonaryfibrosis
AT wanglinjiang pharmacodynamicandpharmacokineticassessmentofpulmonaryrehabilitationmixtureforthetreatmentofpulmonaryfibrosis
AT changjunlv pharmacodynamicandpharmacokineticassessmentofpulmonaryrehabilitationmixtureforthetreatmentofpulmonaryfibrosis
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