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Dendrobium officinale Flower Extraction Mitigates Alcohol-Induced Liver Injury in Mice: Role of Antisteatosis, Antioxidative, and Anti-Inflammatory

The study aimed to evaluate the protective effect of Dendrobium officinale flower extraction (DOFE) on alcohol-induced liver injury and its probable mechanisms in mice. The chemical composition of DOFE was performed via UPLC/MS. Male Kunming mice were used to establish alcohol-induced liver injury m...

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Autores principales: Wu, Yu-Lin, Huang, Si-Han, He, Chun-Mei, Qiu, Bo, Liu, Jing-Jing, Li, Jia, Lin, Ying, Yu, Sheng-Lu, Wang, Hong-Feng, Zhang, Gui-Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603571/
https://www.ncbi.nlm.nih.gov/pubmed/33149748
http://dx.doi.org/10.1155/2020/1421853
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author Wu, Yu-Lin
Huang, Si-Han
He, Chun-Mei
Qiu, Bo
Liu, Jing-Jing
Li, Jia
Lin, Ying
Yu, Sheng-Lu
Wang, Hong-Feng
Zhang, Gui-Fang
author_facet Wu, Yu-Lin
Huang, Si-Han
He, Chun-Mei
Qiu, Bo
Liu, Jing-Jing
Li, Jia
Lin, Ying
Yu, Sheng-Lu
Wang, Hong-Feng
Zhang, Gui-Fang
author_sort Wu, Yu-Lin
collection PubMed
description The study aimed to evaluate the protective effect of Dendrobium officinale flower extraction (DOFE) on alcohol-induced liver injury and its probable mechanisms in mice. The chemical composition of DOFE was performed via UPLC/MS. Male Kunming mice were used to establish alcohol-induced liver injury models by oral gavage of 56% alcohol. Results showed that DOFE dramatically attenuated the increased serum levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), total cholesterol (TC), and triacylglycerol (TG). Meanwhile, hematoxylin and eosin and Oil Red O staining showed that DOFE attenuated degeneration, inflammatory infiltration, and lipid droplet accumulation. DOFE was also found to suppress the activity of malonaldehyde (MDA) and enhanced the level of glutathione (GSH) and the activities of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), and catalase (CAT) in the liver. The protection of DOFE against oxidative stress was associated with the downregulation of hepatic cytochrome P450 2E1 (CYP2E1) and upregulation of nuclear factor erythroid 2-related factor 2 (Nrf2), heme oxygenase-1 (HO-1), and NAD(P)H quinone oxidoreductase l (NQO1). Additionally, DOFE suppressed inflammation via downregulating Toll-like receptor-4 (TLR-4) and nuclear factor kappa-B P65 (NF-κB P65). Thus, DOFE exhibited a significant protective effect against alcohol-induced liver injury through its antisteatosis, antioxidative, and anti-inflammatory effect.
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spelling pubmed-76035712020-11-03 Dendrobium officinale Flower Extraction Mitigates Alcohol-Induced Liver Injury in Mice: Role of Antisteatosis, Antioxidative, and Anti-Inflammatory Wu, Yu-Lin Huang, Si-Han He, Chun-Mei Qiu, Bo Liu, Jing-Jing Li, Jia Lin, Ying Yu, Sheng-Lu Wang, Hong-Feng Zhang, Gui-Fang Evid Based Complement Alternat Med Research Article The study aimed to evaluate the protective effect of Dendrobium officinale flower extraction (DOFE) on alcohol-induced liver injury and its probable mechanisms in mice. The chemical composition of DOFE was performed via UPLC/MS. Male Kunming mice were used to establish alcohol-induced liver injury models by oral gavage of 56% alcohol. Results showed that DOFE dramatically attenuated the increased serum levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), total cholesterol (TC), and triacylglycerol (TG). Meanwhile, hematoxylin and eosin and Oil Red O staining showed that DOFE attenuated degeneration, inflammatory infiltration, and lipid droplet accumulation. DOFE was also found to suppress the activity of malonaldehyde (MDA) and enhanced the level of glutathione (GSH) and the activities of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), and catalase (CAT) in the liver. The protection of DOFE against oxidative stress was associated with the downregulation of hepatic cytochrome P450 2E1 (CYP2E1) and upregulation of nuclear factor erythroid 2-related factor 2 (Nrf2), heme oxygenase-1 (HO-1), and NAD(P)H quinone oxidoreductase l (NQO1). Additionally, DOFE suppressed inflammation via downregulating Toll-like receptor-4 (TLR-4) and nuclear factor kappa-B P65 (NF-κB P65). Thus, DOFE exhibited a significant protective effect against alcohol-induced liver injury through its antisteatosis, antioxidative, and anti-inflammatory effect. Hindawi 2020-10-14 /pmc/articles/PMC7603571/ /pubmed/33149748 http://dx.doi.org/10.1155/2020/1421853 Text en Copyright © 2020 Yu-Lin Wu et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wu, Yu-Lin
Huang, Si-Han
He, Chun-Mei
Qiu, Bo
Liu, Jing-Jing
Li, Jia
Lin, Ying
Yu, Sheng-Lu
Wang, Hong-Feng
Zhang, Gui-Fang
Dendrobium officinale Flower Extraction Mitigates Alcohol-Induced Liver Injury in Mice: Role of Antisteatosis, Antioxidative, and Anti-Inflammatory
title Dendrobium officinale Flower Extraction Mitigates Alcohol-Induced Liver Injury in Mice: Role of Antisteatosis, Antioxidative, and Anti-Inflammatory
title_full Dendrobium officinale Flower Extraction Mitigates Alcohol-Induced Liver Injury in Mice: Role of Antisteatosis, Antioxidative, and Anti-Inflammatory
title_fullStr Dendrobium officinale Flower Extraction Mitigates Alcohol-Induced Liver Injury in Mice: Role of Antisteatosis, Antioxidative, and Anti-Inflammatory
title_full_unstemmed Dendrobium officinale Flower Extraction Mitigates Alcohol-Induced Liver Injury in Mice: Role of Antisteatosis, Antioxidative, and Anti-Inflammatory
title_short Dendrobium officinale Flower Extraction Mitigates Alcohol-Induced Liver Injury in Mice: Role of Antisteatosis, Antioxidative, and Anti-Inflammatory
title_sort dendrobium officinale flower extraction mitigates alcohol-induced liver injury in mice: role of antisteatosis, antioxidative, and anti-inflammatory
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603571/
https://www.ncbi.nlm.nih.gov/pubmed/33149748
http://dx.doi.org/10.1155/2020/1421853
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