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Bioactive Components from Qingwen Baidu Decoction against LPS-Induced Acute Lung Injury in Rats

Qingwen Baidu Decoction (QBD) is an extraordinarily “cold” formula. It was traditionally used to cure epidemic hemorrhagic fever, intestinal typhoid fever, influenza, sepsis and so on. The purpose of this study was to discover relationships between the change of the constituents in different extract...

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Autores principales: Zhang, Qi, Lei, Hai-Min, Wang, Peng-Long, Ma, Zhi-Qiang, Zhang, Yan, Wu, Jing-Jing, Nie, Jing, Chen, Su-Juan, Han, Wen-Jie, Wang, Qing, Chen, Dan-Yang, Cai, Cheng-Ke, Li, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154387/
https://www.ncbi.nlm.nih.gov/pubmed/28445422
http://dx.doi.org/10.3390/molecules22050692
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author Zhang, Qi
Lei, Hai-Min
Wang, Peng-Long
Ma, Zhi-Qiang
Zhang, Yan
Wu, Jing-Jing
Nie, Jing
Chen, Su-Juan
Han, Wen-Jie
Wang, Qing
Chen, Dan-Yang
Cai, Cheng-Ke
Li, Qiang
author_facet Zhang, Qi
Lei, Hai-Min
Wang, Peng-Long
Ma, Zhi-Qiang
Zhang, Yan
Wu, Jing-Jing
Nie, Jing
Chen, Su-Juan
Han, Wen-Jie
Wang, Qing
Chen, Dan-Yang
Cai, Cheng-Ke
Li, Qiang
author_sort Zhang, Qi
collection PubMed
description Qingwen Baidu Decoction (QBD) is an extraordinarily “cold” formula. It was traditionally used to cure epidemic hemorrhagic fever, intestinal typhoid fever, influenza, sepsis and so on. The purpose of this study was to discover relationships between the change of the constituents in different extracts of QBD and the pharmacological effect in a rat model of acute lung injury (ALI) induced by lipopolysaccharide (LPS). The study aimed to discover the changes in constituents of different QBD extracts and the pharmacological effects on acute lung injury (ALI) induced by LPS. The results demonstrated that high dose and middle dose of QBD had significantly potent anti-inflammatory effects and reduced pulmonary edema caused by ALI in rats (p < 0.05). To explore the underlying constituents of QBD, we assessed its influence of six different QBD extracts on ALI and analyzed the different constituents in the corresponding HPLC chromatograms by a Principal Component Analysis (PCA) method. The results showed that the pharmacological effect of QBD was related to the polarity of its extracts, and the medium polarity extracts E2 and E5 in particular displayed much better protective effects against ALI than other groups. Moreover, HPLC-DAD-ESI-MS(n) and PCA analysis showed that verbascoside and angoroside C played a key role in reducing pulmonary edema. In addition, the current study revealed that ethyl gallate, pentagalloylglucose, galloyl paeoniflorin, mudanpioside C and harpagoside can treat ALI mainly by reducing the total cells and infiltration of activated polymorphonuclear leukocytes (PMNs).
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spelling pubmed-61543872018-11-13 Bioactive Components from Qingwen Baidu Decoction against LPS-Induced Acute Lung Injury in Rats Zhang, Qi Lei, Hai-Min Wang, Peng-Long Ma, Zhi-Qiang Zhang, Yan Wu, Jing-Jing Nie, Jing Chen, Su-Juan Han, Wen-Jie Wang, Qing Chen, Dan-Yang Cai, Cheng-Ke Li, Qiang Molecules Article Qingwen Baidu Decoction (QBD) is an extraordinarily “cold” formula. It was traditionally used to cure epidemic hemorrhagic fever, intestinal typhoid fever, influenza, sepsis and so on. The purpose of this study was to discover relationships between the change of the constituents in different extracts of QBD and the pharmacological effect in a rat model of acute lung injury (ALI) induced by lipopolysaccharide (LPS). The study aimed to discover the changes in constituents of different QBD extracts and the pharmacological effects on acute lung injury (ALI) induced by LPS. The results demonstrated that high dose and middle dose of QBD had significantly potent anti-inflammatory effects and reduced pulmonary edema caused by ALI in rats (p < 0.05). To explore the underlying constituents of QBD, we assessed its influence of six different QBD extracts on ALI and analyzed the different constituents in the corresponding HPLC chromatograms by a Principal Component Analysis (PCA) method. The results showed that the pharmacological effect of QBD was related to the polarity of its extracts, and the medium polarity extracts E2 and E5 in particular displayed much better protective effects against ALI than other groups. Moreover, HPLC-DAD-ESI-MS(n) and PCA analysis showed that verbascoside and angoroside C played a key role in reducing pulmonary edema. In addition, the current study revealed that ethyl gallate, pentagalloylglucose, galloyl paeoniflorin, mudanpioside C and harpagoside can treat ALI mainly by reducing the total cells and infiltration of activated polymorphonuclear leukocytes (PMNs). MDPI 2017-04-26 /pmc/articles/PMC6154387/ /pubmed/28445422 http://dx.doi.org/10.3390/molecules22050692 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhang, Qi
Lei, Hai-Min
Wang, Peng-Long
Ma, Zhi-Qiang
Zhang, Yan
Wu, Jing-Jing
Nie, Jing
Chen, Su-Juan
Han, Wen-Jie
Wang, Qing
Chen, Dan-Yang
Cai, Cheng-Ke
Li, Qiang
Bioactive Components from Qingwen Baidu Decoction against LPS-Induced Acute Lung Injury in Rats
title Bioactive Components from Qingwen Baidu Decoction against LPS-Induced Acute Lung Injury in Rats
title_full Bioactive Components from Qingwen Baidu Decoction against LPS-Induced Acute Lung Injury in Rats
title_fullStr Bioactive Components from Qingwen Baidu Decoction against LPS-Induced Acute Lung Injury in Rats
title_full_unstemmed Bioactive Components from Qingwen Baidu Decoction against LPS-Induced Acute Lung Injury in Rats
title_short Bioactive Components from Qingwen Baidu Decoction against LPS-Induced Acute Lung Injury in Rats
title_sort bioactive components from qingwen baidu decoction against lps-induced acute lung injury in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154387/
https://www.ncbi.nlm.nih.gov/pubmed/28445422
http://dx.doi.org/10.3390/molecules22050692
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