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The underlying mechanisms of Jie-Du-Hua-Yu granule for protecting rat liver failure

OBJECTIVES: Jie-Du-Hua-Yu (JDHY) granule is a combination of six traditional Chinese medicines with known therapeutic effect in treating acute liver failure (ALF). The aim of this study was to investigate the amelioration efficacy of JDHY in lipopolysaccharide/D-galactosamine (LPS/D-GalN)-induced AL...

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Autores principales: Qiu, Hua, Mao, Dewen, Tang, Nong, Long, Fuli, Zhang, Rongzhen, Wang, Minggang, Shi, Qinglan, Li, Jiahuan, Jiang, Qin, Chen, Yueqiao, Wang, Xiufeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376884/
https://www.ncbi.nlm.nih.gov/pubmed/30809090
http://dx.doi.org/10.2147/DDDT.S180969
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author Qiu, Hua
Mao, Dewen
Tang, Nong
Long, Fuli
Zhang, Rongzhen
Wang, Minggang
Shi, Qinglan
Li, Jiahuan
Jiang, Qin
Chen, Yueqiao
Wang, Xiufeng
author_facet Qiu, Hua
Mao, Dewen
Tang, Nong
Long, Fuli
Zhang, Rongzhen
Wang, Minggang
Shi, Qinglan
Li, Jiahuan
Jiang, Qin
Chen, Yueqiao
Wang, Xiufeng
author_sort Qiu, Hua
collection PubMed
description OBJECTIVES: Jie-Du-Hua-Yu (JDHY) granule is a combination of six traditional Chinese medicines with known therapeutic effect in treating acute liver failure (ALF). The aim of this study was to investigate the amelioration efficacy of JDHY in lipopolysaccharide/D-galactosamine (LPS/D-GalN)-induced ALF in rat and explore the possible molecular mechanism underlying the therapeutic efficacy. MATERIALS AND METHODS: The efficacy of JDHY was determined by assessing hepatic pathology and function in LPS and D-GalN challenged Wistar rat. We also evaluated the effect of JDHY on LPS-induced Kupffer cells by measuring inflammatory cytokines and determining the phenotypic function. By means of bioinformatics analysis of liver tissue and validation in Kupffer cells, we identified possible pathways involved in the pharmacologic action of mechanism of JDHY. RESULTS: JDHY could attenuate LPS-induced liver injury in rat by inhibiting apoptosis and increasing hepatic activity. In vitro study showed that JDHY could decrease the production of proinflammatory cytokines (tumor necrosis factor-α, IL6, and interferon-γ), increase anti-inflammatory cytokines (IL10, IL13), and promote cell survival and proliferation, possibly due to inhibition of IκB/nuclear factor-κB (NF-κB) signaling pathway and expression of CD14 and CXCL2, which was consistent with the findings from bioinformatics analysis. CONCLUSION: Our results revealed that JDHY protected against LPS-induced liver damage both in vitro and in vivo, by inhibiting the NF-κB-mediated inflammatory pathway, indicating its potential function to treat liver diseases.
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spelling pubmed-63768842019-02-26 The underlying mechanisms of Jie-Du-Hua-Yu granule for protecting rat liver failure Qiu, Hua Mao, Dewen Tang, Nong Long, Fuli Zhang, Rongzhen Wang, Minggang Shi, Qinglan Li, Jiahuan Jiang, Qin Chen, Yueqiao Wang, Xiufeng Drug Des Devel Ther Original Research OBJECTIVES: Jie-Du-Hua-Yu (JDHY) granule is a combination of six traditional Chinese medicines with known therapeutic effect in treating acute liver failure (ALF). The aim of this study was to investigate the amelioration efficacy of JDHY in lipopolysaccharide/D-galactosamine (LPS/D-GalN)-induced ALF in rat and explore the possible molecular mechanism underlying the therapeutic efficacy. MATERIALS AND METHODS: The efficacy of JDHY was determined by assessing hepatic pathology and function in LPS and D-GalN challenged Wistar rat. We also evaluated the effect of JDHY on LPS-induced Kupffer cells by measuring inflammatory cytokines and determining the phenotypic function. By means of bioinformatics analysis of liver tissue and validation in Kupffer cells, we identified possible pathways involved in the pharmacologic action of mechanism of JDHY. RESULTS: JDHY could attenuate LPS-induced liver injury in rat by inhibiting apoptosis and increasing hepatic activity. In vitro study showed that JDHY could decrease the production of proinflammatory cytokines (tumor necrosis factor-α, IL6, and interferon-γ), increase anti-inflammatory cytokines (IL10, IL13), and promote cell survival and proliferation, possibly due to inhibition of IκB/nuclear factor-κB (NF-κB) signaling pathway and expression of CD14 and CXCL2, which was consistent with the findings from bioinformatics analysis. CONCLUSION: Our results revealed that JDHY protected against LPS-induced liver damage both in vitro and in vivo, by inhibiting the NF-κB-mediated inflammatory pathway, indicating its potential function to treat liver diseases. Dove Medical Press 2019-02-11 /pmc/articles/PMC6376884/ /pubmed/30809090 http://dx.doi.org/10.2147/DDDT.S180969 Text en © 2019 Qiu et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Qiu, Hua
Mao, Dewen
Tang, Nong
Long, Fuli
Zhang, Rongzhen
Wang, Minggang
Shi, Qinglan
Li, Jiahuan
Jiang, Qin
Chen, Yueqiao
Wang, Xiufeng
The underlying mechanisms of Jie-Du-Hua-Yu granule for protecting rat liver failure
title The underlying mechanisms of Jie-Du-Hua-Yu granule for protecting rat liver failure
title_full The underlying mechanisms of Jie-Du-Hua-Yu granule for protecting rat liver failure
title_fullStr The underlying mechanisms of Jie-Du-Hua-Yu granule for protecting rat liver failure
title_full_unstemmed The underlying mechanisms of Jie-Du-Hua-Yu granule for protecting rat liver failure
title_short The underlying mechanisms of Jie-Du-Hua-Yu granule for protecting rat liver failure
title_sort underlying mechanisms of jie-du-hua-yu granule for protecting rat liver failure
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376884/
https://www.ncbi.nlm.nih.gov/pubmed/30809090
http://dx.doi.org/10.2147/DDDT.S180969
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