Hepatoprotective effect of Alhagi sparsifolia against Alcoholic Liver injury in mice

Detalhes bibliográficos
Autor(a) principal: Maimaitimin, Kuerbanjiang
Data de Publicação: 2018
Outros Autores: Jiang, Zhihui, Aierken, Aili, Shayibuzhati, Mikeremu, Zhang, Xiaoying
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Pharmaceutical Sciences
Texto Completo: https://www.revistas.usp.br/bjps/article/view/153872
Resumo: Overconsumption of alcohol leads to alcoholic liver disease (ALD). Natural compounds have been investigated previously for their hepatoprotective activities against liver injury. This study investigated the protective effect of Alhagi sparsifolia on ALD. Alcohol was administered to mice for three consecutive days; either alone or in combination with Alhagi sparsifolia extract (150, 300, 600 mg/kg). Serum aspartate aminotransferase and alanine transaminase as biomarkers of liver injury, the content of malonaldehyde, hydrogen peroxide (H2O2) and glutathione which indicated the redox status of liver and the antioxidant enzyme activity of super oxide dismutase were detected, respectively. Moreover, the expression of protein cytochrome P450 2E1 (CYP2E1) the key enzyme of alcohol metabolism, and also tested by western blot experiment. Subsequently, the mRNA levels of inflammatory factors including TNF- α and TLR4 was determined real-time PCR. Results showed that Alhagi sparsifolia significantly alleviated alcohol-induced liver injury by reducing serum ALT and AST, inhibiting MDA and H2O2 content, increasing SOD, and GSH level in the liver (P< 0.05). In addition, the Alhagi sparsifolia treatment inhibited the expression of CYP2E1 (P< 0.05). The results suggest that Alhagi sparsifolia could be a promising natural substance for ameliorating acute alcohol-induced oxidative stress and hepatic injury.
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spelling Hepatoprotective effect of Alhagi sparsifolia against Alcoholic Liver injury in miceAlcoholic liver diseaseAlhagi sparsifoliaHepatoprotective effectAntioxidantionCYP2E1Overconsumption of alcohol leads to alcoholic liver disease (ALD). Natural compounds have been investigated previously for their hepatoprotective activities against liver injury. This study investigated the protective effect of Alhagi sparsifolia on ALD. Alcohol was administered to mice for three consecutive days; either alone or in combination with Alhagi sparsifolia extract (150, 300, 600 mg/kg). Serum aspartate aminotransferase and alanine transaminase as biomarkers of liver injury, the content of malonaldehyde, hydrogen peroxide (H2O2) and glutathione which indicated the redox status of liver and the antioxidant enzyme activity of super oxide dismutase were detected, respectively. Moreover, the expression of protein cytochrome P450 2E1 (CYP2E1) the key enzyme of alcohol metabolism, and also tested by western blot experiment. Subsequently, the mRNA levels of inflammatory factors including TNF- α and TLR4 was determined real-time PCR. Results showed that Alhagi sparsifolia significantly alleviated alcohol-induced liver injury by reducing serum ALT and AST, inhibiting MDA and H2O2 content, increasing SOD, and GSH level in the liver (P< 0.05). In addition, the Alhagi sparsifolia treatment inhibited the expression of CYP2E1 (P< 0.05). The results suggest that Alhagi sparsifolia could be a promising natural substance for ameliorating acute alcohol-induced oxidative stress and hepatic injury.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2018-11-29info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/15387210.1590/s2175-97902018000317732Brazilian Journal of Pharmaceutical Sciences; Vol. 54 Núm. 3 (2018); e17732Brazilian Journal of Pharmaceutical Sciences; v. 54 n. 3 (2018); e17732Brazilian Journal of Pharmaceutical Sciences; Vol. 54 No. 3 (2018); e177322175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/153872/150222Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso)info:eu-repo/semantics/openAccessMaimaitimin, KuerbanjiangJiang, ZhihuiAierken, AiliShayibuzhati, MikeremuZhang, Xiaoying2019-03-17T13:19:35Zoai:revistas.usp.br:article/153872Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2019-03-17T13:19:35Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Hepatoprotective effect of Alhagi sparsifolia against Alcoholic Liver injury in mice
title Hepatoprotective effect of Alhagi sparsifolia against Alcoholic Liver injury in mice
spellingShingle Hepatoprotective effect of Alhagi sparsifolia against Alcoholic Liver injury in mice
Maimaitimin, Kuerbanjiang
Alcoholic liver disease
Alhagi sparsifolia
Hepatoprotective effect
Antioxidantion
CYP2E1
title_short Hepatoprotective effect of Alhagi sparsifolia against Alcoholic Liver injury in mice
title_full Hepatoprotective effect of Alhagi sparsifolia against Alcoholic Liver injury in mice
title_fullStr Hepatoprotective effect of Alhagi sparsifolia against Alcoholic Liver injury in mice
title_full_unstemmed Hepatoprotective effect of Alhagi sparsifolia against Alcoholic Liver injury in mice
title_sort Hepatoprotective effect of Alhagi sparsifolia against Alcoholic Liver injury in mice
author Maimaitimin, Kuerbanjiang
author_facet Maimaitimin, Kuerbanjiang
Jiang, Zhihui
Aierken, Aili
Shayibuzhati, Mikeremu
Zhang, Xiaoying
author_role author
author2 Jiang, Zhihui
Aierken, Aili
Shayibuzhati, Mikeremu
Zhang, Xiaoying
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Maimaitimin, Kuerbanjiang
Jiang, Zhihui
Aierken, Aili
Shayibuzhati, Mikeremu
Zhang, Xiaoying
dc.subject.por.fl_str_mv Alcoholic liver disease
Alhagi sparsifolia
Hepatoprotective effect
Antioxidantion
CYP2E1
topic Alcoholic liver disease
Alhagi sparsifolia
Hepatoprotective effect
Antioxidantion
CYP2E1
description Overconsumption of alcohol leads to alcoholic liver disease (ALD). Natural compounds have been investigated previously for their hepatoprotective activities against liver injury. This study investigated the protective effect of Alhagi sparsifolia on ALD. Alcohol was administered to mice for three consecutive days; either alone or in combination with Alhagi sparsifolia extract (150, 300, 600 mg/kg). Serum aspartate aminotransferase and alanine transaminase as biomarkers of liver injury, the content of malonaldehyde, hydrogen peroxide (H2O2) and glutathione which indicated the redox status of liver and the antioxidant enzyme activity of super oxide dismutase were detected, respectively. Moreover, the expression of protein cytochrome P450 2E1 (CYP2E1) the key enzyme of alcohol metabolism, and also tested by western blot experiment. Subsequently, the mRNA levels of inflammatory factors including TNF- α and TLR4 was determined real-time PCR. Results showed that Alhagi sparsifolia significantly alleviated alcohol-induced liver injury by reducing serum ALT and AST, inhibiting MDA and H2O2 content, increasing SOD, and GSH level in the liver (P< 0.05). In addition, the Alhagi sparsifolia treatment inhibited the expression of CYP2E1 (P< 0.05). The results suggest that Alhagi sparsifolia could be a promising natural substance for ameliorating acute alcohol-induced oxidative stress and hepatic injury.
publishDate 2018
dc.date.none.fl_str_mv 2018-11-29
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/bjps/article/view/153872
10.1590/s2175-97902018000317732
url https://www.revistas.usp.br/bjps/article/view/153872
identifier_str_mv 10.1590/s2175-97902018000317732
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/bjps/article/view/153872/150222
dc.rights.driver.fl_str_mv Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso)
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso)
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
dc.source.none.fl_str_mv Brazilian Journal of Pharmaceutical Sciences; Vol. 54 Núm. 3 (2018); e17732
Brazilian Journal of Pharmaceutical Sciences; v. 54 n. 3 (2018); e17732
Brazilian Journal of Pharmaceutical Sciences; Vol. 54 No. 3 (2018); e17732
2175-9790
1984-8250
reponame:Brazilian Journal of Pharmaceutical Sciences
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Brazilian Journal of Pharmaceutical Sciences
collection Brazilian Journal of Pharmaceutical Sciences
repository.name.fl_str_mv Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)
repository.mail.fl_str_mv bjps@usp.br||elizabeth.igne@gmail.com
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