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Zingiber officinale (Roscoe) mitigates CCl(4)-induced liver histopathology and biochemical derangements through antioxidant, membrane-stabilizing and tissue-regenerating potentials
The world-wide increasing incidence of liver injury has attracted scientific interest in the exploration of better treatment or adjuvant treatment therapies. This study investigated the effects of methanol extract of Zingiber officinale (Roscoe) rhizome (MEZOR) in a Wistar rat model of carbon tetrac...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514439/ https://www.ncbi.nlm.nih.gov/pubmed/31193041 http://dx.doi.org/10.1016/j.toxrep.2019.05.001 |
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author | Oke, Gracious Oluwamayowa Abiodun, Adegboyega Adeleke Imafidon, Christian Eseigbe Monsi, Barinem Fortune |
author_facet | Oke, Gracious Oluwamayowa Abiodun, Adegboyega Adeleke Imafidon, Christian Eseigbe Monsi, Barinem Fortune |
author_sort | Oke, Gracious Oluwamayowa |
collection | PubMed |
description | The world-wide increasing incidence of liver injury has attracted scientific interest in the exploration of better treatment or adjuvant treatment therapies. This study investigated the effects of methanol extract of Zingiber officinale (Roscoe) rhizome (MEZOR) in a Wistar rat model of carbon tetrachloride (CCl(4))-induced liver injury. The study recruited thirty female Wistar rats that received graded doses of MEZOR (determined by its LD(50)) by oral gavage through an oral canula, for 4 consecutive weeks following 1 week oral administration of CCl(4) (0.7 ml/kg in olive oil; 1:1, v/v) while livolin forte® (5.2 mg/kg p.o.) was used as a standard. CCl(4) induced deleterious hepatic effects as revealed by the liver function biomarkers (AST, ALT, ALP and total protein), antioxidant indicators (GSH and CAT) and histopathological effects, demonstrated by H & E, Gordon and Sweet, Masson’s trichrome, PAS staining techniques as well as by quantificational analyses of the liver micrographs, using image–J. MEZOR treatment was associated with a dose-dependent and significant mitigation of the aforementioned parameters (p < 0.05). This study concluded that MEZOR is a potential therapeutic choice in the adjuvant treatment of subjects with chemically-induced liver injury. |
format | Online Article Text |
id | pubmed-6514439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-65144392019-05-20 Zingiber officinale (Roscoe) mitigates CCl(4)-induced liver histopathology and biochemical derangements through antioxidant, membrane-stabilizing and tissue-regenerating potentials Oke, Gracious Oluwamayowa Abiodun, Adegboyega Adeleke Imafidon, Christian Eseigbe Monsi, Barinem Fortune Toxicol Rep Article The world-wide increasing incidence of liver injury has attracted scientific interest in the exploration of better treatment or adjuvant treatment therapies. This study investigated the effects of methanol extract of Zingiber officinale (Roscoe) rhizome (MEZOR) in a Wistar rat model of carbon tetrachloride (CCl(4))-induced liver injury. The study recruited thirty female Wistar rats that received graded doses of MEZOR (determined by its LD(50)) by oral gavage through an oral canula, for 4 consecutive weeks following 1 week oral administration of CCl(4) (0.7 ml/kg in olive oil; 1:1, v/v) while livolin forte® (5.2 mg/kg p.o.) was used as a standard. CCl(4) induced deleterious hepatic effects as revealed by the liver function biomarkers (AST, ALT, ALP and total protein), antioxidant indicators (GSH and CAT) and histopathological effects, demonstrated by H & E, Gordon and Sweet, Masson’s trichrome, PAS staining techniques as well as by quantificational analyses of the liver micrographs, using image–J. MEZOR treatment was associated with a dose-dependent and significant mitigation of the aforementioned parameters (p < 0.05). This study concluded that MEZOR is a potential therapeutic choice in the adjuvant treatment of subjects with chemically-induced liver injury. Elsevier 2019-05-06 /pmc/articles/PMC6514439/ /pubmed/31193041 http://dx.doi.org/10.1016/j.toxrep.2019.05.001 Text en © 2019 The Authors. Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Oke, Gracious Oluwamayowa Abiodun, Adegboyega Adeleke Imafidon, Christian Eseigbe Monsi, Barinem Fortune Zingiber officinale (Roscoe) mitigates CCl(4)-induced liver histopathology and biochemical derangements through antioxidant, membrane-stabilizing and tissue-regenerating potentials |
title | Zingiber officinale (Roscoe) mitigates CCl(4)-induced liver histopathology and biochemical derangements through antioxidant, membrane-stabilizing and tissue-regenerating potentials |
title_full | Zingiber officinale (Roscoe) mitigates CCl(4)-induced liver histopathology and biochemical derangements through antioxidant, membrane-stabilizing and tissue-regenerating potentials |
title_fullStr | Zingiber officinale (Roscoe) mitigates CCl(4)-induced liver histopathology and biochemical derangements through antioxidant, membrane-stabilizing and tissue-regenerating potentials |
title_full_unstemmed | Zingiber officinale (Roscoe) mitigates CCl(4)-induced liver histopathology and biochemical derangements through antioxidant, membrane-stabilizing and tissue-regenerating potentials |
title_short | Zingiber officinale (Roscoe) mitigates CCl(4)-induced liver histopathology and biochemical derangements through antioxidant, membrane-stabilizing and tissue-regenerating potentials |
title_sort | zingiber officinale (roscoe) mitigates ccl(4)-induced liver histopathology and biochemical derangements through antioxidant, membrane-stabilizing and tissue-regenerating potentials |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514439/ https://www.ncbi.nlm.nih.gov/pubmed/31193041 http://dx.doi.org/10.1016/j.toxrep.2019.05.001 |
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