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Lycium barbarum polysaccharides protect rat liver from non-alcoholic steatohepatitis-induced injury
BACKGROUND: Lycium barbarum polysaccharides (LBPs) are antioxidant and neuroprotective derivative from Wolfberry. However, whether LBP has a protective effect in non-alcoholic steatohepatitis (NASH)-induced hepatic injury is still unknown. OBJECTIVE: We aimed to study the possible hepatoprotective e...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3730220/ https://www.ncbi.nlm.nih.gov/pubmed/23877747 http://dx.doi.org/10.1038/nutd.2013.22 |
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author | Xiao, J Liong, E C Ching, Y P Chang, R C C Fung, M L Xu, A M So, K F Tipoe, G L |
author_facet | Xiao, J Liong, E C Ching, Y P Chang, R C C Fung, M L Xu, A M So, K F Tipoe, G L |
author_sort | Xiao, J |
collection | PubMed |
description | BACKGROUND: Lycium barbarum polysaccharides (LBPs) are antioxidant and neuroprotective derivative from Wolfberry. However, whether LBP has a protective effect in non-alcoholic steatohepatitis (NASH)-induced hepatic injury is still unknown. OBJECTIVE: We aimed to study the possible hepatoprotective effects and mechanisms of LBP on a diet-induced NASH rat model. METHODS AND DESIGN: In this study, female rats were fed a high-fat diet to induce NASH with or without an oral 1 mg kg(−1) LBP feeding daily for 8 weeks. After 8 weeks, blood serum and liver samples from each rat were subjected to histological analysis, biochemical and molecular measurements. RESULTS: Compared with control rats, NASH rats showed typical NASH features including an increase in liver injury, lipid content, fibrosis, oxidative stress, inflammation and apoptosis. In contrast, NASH+LBP-co-treated rats showed (1) improved histology and free fatty acid levels; (2) re-balance of lipid metabolism; (3) reduction in profibrogenic factors through the TGF-β/SMAD pathway; (4) improved oxidative stress through cytochrome P450 2E1-dependent pathway; (5) reduction in hepatic pro-inflammatory mediators and chemokines production; and (6) amelioration of hepatic apoptosis through the p53-dependent intrinsic and extrinsic pathways. The preventive effects of LBP were partly modulated through the PI3K/Akt/FoxO1, LKB1/AMPK, JNK/c-Jun and MEK/ERK pathways and the downregulation of transcription factors in the liver, such as nuclear factor-κB and activator protein-1. CONCLUSION: LBP is a novel hepatoprotective agent against NASH caused by abnormal liver metabolic functions. |
format | Online Article Text |
id | pubmed-3730220 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-37302202013-08-01 Lycium barbarum polysaccharides protect rat liver from non-alcoholic steatohepatitis-induced injury Xiao, J Liong, E C Ching, Y P Chang, R C C Fung, M L Xu, A M So, K F Tipoe, G L Nutr Diabetes Original Article BACKGROUND: Lycium barbarum polysaccharides (LBPs) are antioxidant and neuroprotective derivative from Wolfberry. However, whether LBP has a protective effect in non-alcoholic steatohepatitis (NASH)-induced hepatic injury is still unknown. OBJECTIVE: We aimed to study the possible hepatoprotective effects and mechanisms of LBP on a diet-induced NASH rat model. METHODS AND DESIGN: In this study, female rats were fed a high-fat diet to induce NASH with or without an oral 1 mg kg(−1) LBP feeding daily for 8 weeks. After 8 weeks, blood serum and liver samples from each rat were subjected to histological analysis, biochemical and molecular measurements. RESULTS: Compared with control rats, NASH rats showed typical NASH features including an increase in liver injury, lipid content, fibrosis, oxidative stress, inflammation and apoptosis. In contrast, NASH+LBP-co-treated rats showed (1) improved histology and free fatty acid levels; (2) re-balance of lipid metabolism; (3) reduction in profibrogenic factors through the TGF-β/SMAD pathway; (4) improved oxidative stress through cytochrome P450 2E1-dependent pathway; (5) reduction in hepatic pro-inflammatory mediators and chemokines production; and (6) amelioration of hepatic apoptosis through the p53-dependent intrinsic and extrinsic pathways. The preventive effects of LBP were partly modulated through the PI3K/Akt/FoxO1, LKB1/AMPK, JNK/c-Jun and MEK/ERK pathways and the downregulation of transcription factors in the liver, such as nuclear factor-κB and activator protein-1. CONCLUSION: LBP is a novel hepatoprotective agent against NASH caused by abnormal liver metabolic functions. Nature Publishing Group 2013-07 2013-07-22 /pmc/articles/PMC3730220/ /pubmed/23877747 http://dx.doi.org/10.1038/nutd.2013.22 Text en Copyright © 2013 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Original Article Xiao, J Liong, E C Ching, Y P Chang, R C C Fung, M L Xu, A M So, K F Tipoe, G L Lycium barbarum polysaccharides protect rat liver from non-alcoholic steatohepatitis-induced injury |
title | Lycium barbarum polysaccharides protect rat liver from non-alcoholic steatohepatitis-induced injury |
title_full | Lycium barbarum polysaccharides protect rat liver from non-alcoholic steatohepatitis-induced injury |
title_fullStr | Lycium barbarum polysaccharides protect rat liver from non-alcoholic steatohepatitis-induced injury |
title_full_unstemmed | Lycium barbarum polysaccharides protect rat liver from non-alcoholic steatohepatitis-induced injury |
title_short | Lycium barbarum polysaccharides protect rat liver from non-alcoholic steatohepatitis-induced injury |
title_sort | lycium barbarum polysaccharides protect rat liver from non-alcoholic steatohepatitis-induced injury |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3730220/ https://www.ncbi.nlm.nih.gov/pubmed/23877747 http://dx.doi.org/10.1038/nutd.2013.22 |
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