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Protective effect of Atriplex suberecta extract against oxidative and apoptotic hepatotoxicity

Atriplex suberecta I. Verd is a known phytomedicinal species of Atriplex; however, studies into its bioactivity remain inconclusive. The in vitro and in vivo antioxidative and hepatoprotective potential of A. suberecta ethanol-extract (ASEE) was assessed in the present study. 1,1-diphenyl-2-picrylhy...

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Autores principales: Parvez, Mohammad K., Arbab, Ahmad H., Al-Dosari, Mohammed S., Al-Rehaily, Adnan J., Alam, Perwez, Ibrahim, Khalid E., Alsaid, Mansour S., Rafatullah, Syed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5863606/
https://www.ncbi.nlm.nih.gov/pubmed/29581744
http://dx.doi.org/10.3892/etm.2018.5919
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author Parvez, Mohammad K.
Arbab, Ahmad H.
Al-Dosari, Mohammed S.
Al-Rehaily, Adnan J.
Alam, Perwez
Ibrahim, Khalid E.
Alsaid, Mansour S.
Rafatullah, Syed
author_facet Parvez, Mohammad K.
Arbab, Ahmad H.
Al-Dosari, Mohammed S.
Al-Rehaily, Adnan J.
Alam, Perwez
Ibrahim, Khalid E.
Alsaid, Mansour S.
Rafatullah, Syed
author_sort Parvez, Mohammad K.
collection PubMed
description Atriplex suberecta I. Verd is a known phytomedicinal species of Atriplex; however, studies into its bioactivity remain inconclusive. The in vitro and in vivo antioxidative and hepatoprotective potential of A. suberecta ethanol-extract (ASEE) was assessed in the present study. 1,1-diphenyl-2-picrylhydrazyl radical scavenging and β-carotene bleaching assays revealed that ASEE possesses free radical scavenging and anti-lipid peroxidative activities. These results were supported by the in vitro protection of HepG2 hepatoblastoma cells via abating 2,7-dichlorofluorescein-activated oxidative and apoptotic molecules (caspase-3/-7). In carbon tetrachloride-treated rats, the oral administration of ASEE significantly normalized serum biomarkers of liver function (serum glutamate oxaloacetate, serum pyruvate transaminase, alkaline phosphatase, γ-glutamyl transferase and bilirubin) and the lipid profile (total cholesterol, high-density lipoprotein, low-density lipoprotein, triglycerides and malondialdehyde), including tissue non-protein sulfhydryl and total protein levels. These results were also supported by liver histopathology, which demonstrated that the therapeutic effect of ASEE was comparable to silymarin. Furthermore, phytochemical analysis of ASEE revealed the presence of flavonoids, alkaloids, tannins and saponins. Rutin, an antioxidant flavonoid, was identified using the validated high-performance thin-layer chromatography method. In conclusion, this is the first report on the therapeutic potential of A. suberecta against chemical-induced oxidative stress and liver damage.
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spelling pubmed-58636062018-03-26 Protective effect of Atriplex suberecta extract against oxidative and apoptotic hepatotoxicity Parvez, Mohammad K. Arbab, Ahmad H. Al-Dosari, Mohammed S. Al-Rehaily, Adnan J. Alam, Perwez Ibrahim, Khalid E. Alsaid, Mansour S. Rafatullah, Syed Exp Ther Med Articles Atriplex suberecta I. Verd is a known phytomedicinal species of Atriplex; however, studies into its bioactivity remain inconclusive. The in vitro and in vivo antioxidative and hepatoprotective potential of A. suberecta ethanol-extract (ASEE) was assessed in the present study. 1,1-diphenyl-2-picrylhydrazyl radical scavenging and β-carotene bleaching assays revealed that ASEE possesses free radical scavenging and anti-lipid peroxidative activities. These results were supported by the in vitro protection of HepG2 hepatoblastoma cells via abating 2,7-dichlorofluorescein-activated oxidative and apoptotic molecules (caspase-3/-7). In carbon tetrachloride-treated rats, the oral administration of ASEE significantly normalized serum biomarkers of liver function (serum glutamate oxaloacetate, serum pyruvate transaminase, alkaline phosphatase, γ-glutamyl transferase and bilirubin) and the lipid profile (total cholesterol, high-density lipoprotein, low-density lipoprotein, triglycerides and malondialdehyde), including tissue non-protein sulfhydryl and total protein levels. These results were also supported by liver histopathology, which demonstrated that the therapeutic effect of ASEE was comparable to silymarin. Furthermore, phytochemical analysis of ASEE revealed the presence of flavonoids, alkaloids, tannins and saponins. Rutin, an antioxidant flavonoid, was identified using the validated high-performance thin-layer chromatography method. In conclusion, this is the first report on the therapeutic potential of A. suberecta against chemical-induced oxidative stress and liver damage. D.A. Spandidos 2018-04 2018-03-02 /pmc/articles/PMC5863606/ /pubmed/29581744 http://dx.doi.org/10.3892/etm.2018.5919 Text en Copyright: © Parvez et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Parvez, Mohammad K.
Arbab, Ahmad H.
Al-Dosari, Mohammed S.
Al-Rehaily, Adnan J.
Alam, Perwez
Ibrahim, Khalid E.
Alsaid, Mansour S.
Rafatullah, Syed
Protective effect of Atriplex suberecta extract against oxidative and apoptotic hepatotoxicity
title Protective effect of Atriplex suberecta extract against oxidative and apoptotic hepatotoxicity
title_full Protective effect of Atriplex suberecta extract against oxidative and apoptotic hepatotoxicity
title_fullStr Protective effect of Atriplex suberecta extract against oxidative and apoptotic hepatotoxicity
title_full_unstemmed Protective effect of Atriplex suberecta extract against oxidative and apoptotic hepatotoxicity
title_short Protective effect of Atriplex suberecta extract against oxidative and apoptotic hepatotoxicity
title_sort protective effect of atriplex suberecta extract against oxidative and apoptotic hepatotoxicity
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5863606/
https://www.ncbi.nlm.nih.gov/pubmed/29581744
http://dx.doi.org/10.3892/etm.2018.5919
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