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Soyasaponin Bb Protects Rat Hepatocytes from Alcohol-Induced Oxidative Stress by Inducing Heme Oxygenase-1

BACKGROUND: It has been known that oxidative stress induced by alcohol played a crucial role in the formation of alcoholic liver disease. Although the formation mechanisms underlying liver injury induced by alcohol still remained largely unknown, it has been considered that oxidative stress played a...

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Detalles Bibliográficos
Autores principales: Lijie, Zhu, Ranran, Fu, Xiuying, Liu, Yutang, He, Bo, Wang, Tao, Ma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096277/
https://www.ncbi.nlm.nih.gov/pubmed/27867273
http://dx.doi.org/10.4103/0973-1296.192203
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author Lijie, Zhu
Ranran, Fu
Xiuying, Liu
Yutang, He
Bo, Wang
Tao, Ma
author_facet Lijie, Zhu
Ranran, Fu
Xiuying, Liu
Yutang, He
Bo, Wang
Tao, Ma
author_sort Lijie, Zhu
collection PubMed
description BACKGROUND: It has been known that oxidative stress induced by alcohol played a crucial role in the formation of alcoholic liver disease. Although the formation mechanisms underlying liver injury induced by alcohol still remained largely unknown, it has been considered that oxidative stress played a core role in the pathogenesis of hepatocyte damage. OBJECTIVE: The aim of this study was to investigate the effects of soyasaponin Bb (Ss-Bb) on oxidative stress in alcohol-induced rat hepatocyte injury. RESULTS: It has been shown that the administration of Ss-Bb could significantly restore antioxidant activity in BRL 3A cells. Moreover, the impaired liver function and morphology changes resulting from ethanol exposure were improved by Ss-Bb treatment. Treatment with a pharmacological inhibitor of haem oxygenase-1 (HO-1) indicated a critical role of HO-1 in mediating the protective role. Finally, we found that pretreatment with Ss-Bb to ethanol exposure cells increased the expression level of HO-1. CONCLUSION: It was suggested that Ss-Bb may protect against alcohol-induced hepatocyte injury through ameliorating oxidative stress, and the induction of HO-1 was an important protective mechanism. SUMMARY: Effects of soyasaponin Bb was investigated on oxidative stress in rat hepatocytes. Cell viability and antioxidant capacities were evaluated to determine the effects. The expression level of HO-1 was measured to reveal the proptective mechanisms.
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spelling pubmed-50962772016-11-18 Soyasaponin Bb Protects Rat Hepatocytes from Alcohol-Induced Oxidative Stress by Inducing Heme Oxygenase-1 Lijie, Zhu Ranran, Fu Xiuying, Liu Yutang, He Bo, Wang Tao, Ma Pharmacogn Mag Original Article BACKGROUND: It has been known that oxidative stress induced by alcohol played a crucial role in the formation of alcoholic liver disease. Although the formation mechanisms underlying liver injury induced by alcohol still remained largely unknown, it has been considered that oxidative stress played a core role in the pathogenesis of hepatocyte damage. OBJECTIVE: The aim of this study was to investigate the effects of soyasaponin Bb (Ss-Bb) on oxidative stress in alcohol-induced rat hepatocyte injury. RESULTS: It has been shown that the administration of Ss-Bb could significantly restore antioxidant activity in BRL 3A cells. Moreover, the impaired liver function and morphology changes resulting from ethanol exposure were improved by Ss-Bb treatment. Treatment with a pharmacological inhibitor of haem oxygenase-1 (HO-1) indicated a critical role of HO-1 in mediating the protective role. Finally, we found that pretreatment with Ss-Bb to ethanol exposure cells increased the expression level of HO-1. CONCLUSION: It was suggested that Ss-Bb may protect against alcohol-induced hepatocyte injury through ameliorating oxidative stress, and the induction of HO-1 was an important protective mechanism. SUMMARY: Effects of soyasaponin Bb was investigated on oxidative stress in rat hepatocytes. Cell viability and antioxidant capacities were evaluated to determine the effects. The expression level of HO-1 was measured to reveal the proptective mechanisms. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC5096277/ /pubmed/27867273 http://dx.doi.org/10.4103/0973-1296.192203 Text en Copyright: © Pharmacognosy Magazine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Lijie, Zhu
Ranran, Fu
Xiuying, Liu
Yutang, He
Bo, Wang
Tao, Ma
Soyasaponin Bb Protects Rat Hepatocytes from Alcohol-Induced Oxidative Stress by Inducing Heme Oxygenase-1
title Soyasaponin Bb Protects Rat Hepatocytes from Alcohol-Induced Oxidative Stress by Inducing Heme Oxygenase-1
title_full Soyasaponin Bb Protects Rat Hepatocytes from Alcohol-Induced Oxidative Stress by Inducing Heme Oxygenase-1
title_fullStr Soyasaponin Bb Protects Rat Hepatocytes from Alcohol-Induced Oxidative Stress by Inducing Heme Oxygenase-1
title_full_unstemmed Soyasaponin Bb Protects Rat Hepatocytes from Alcohol-Induced Oxidative Stress by Inducing Heme Oxygenase-1
title_short Soyasaponin Bb Protects Rat Hepatocytes from Alcohol-Induced Oxidative Stress by Inducing Heme Oxygenase-1
title_sort soyasaponin bb protects rat hepatocytes from alcohol-induced oxidative stress by inducing heme oxygenase-1
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096277/
https://www.ncbi.nlm.nih.gov/pubmed/27867273
http://dx.doi.org/10.4103/0973-1296.192203
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