Evaluation the role of Ferula gummosa essential oil against the hepatoxicity induced by acetaminophen in animal model

Background: Acetaminophen as a common antipyretic drug, in overdoses, is poisonous for the liver. Objective: The current study aimed to assess the protective effects of Ferula (F.) gummosa essential oils against the liver toxicity of acetaminophen in rats. Methods: 80 male Wistar rats were randoml...

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Main Authors: AF Dadkhah, Gh Khalaj, F Fatemi, S Dini, S Hesaraki, S Naij, M Babaei, HR Attaran
Format: Article
Language:English
Published: Institue of Medicinal Plants, ACECR 2016-10-01
Series:Journal of Medicinal Plants
Subjects:
Online Access:http://jmp.ir/article-1-1103-en.html
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author AF Dadkhah
Gh Khalaj
F Fatemi
S Dini
S Hesaraki
S Naij
M Babaei
HR Attaran
author_facet AF Dadkhah
Gh Khalaj
F Fatemi
S Dini
S Hesaraki
S Naij
M Babaei
HR Attaran
author_sort AF Dadkhah
collection DOAJ
description Background: Acetaminophen as a common antipyretic drug, in overdoses, is poisonous for the liver. Objective: The current study aimed to assess the protective effects of Ferula (F.) gummosa essential oils against the liver toxicity of acetaminophen in rats. Methods: 80 male Wistar rats were randomly divided into 16 groups (n=5). Negative control group received only DMSO and the positive control group received acetaminophen 500 mg/kg b.w i.p. The treatment groups received F. gummosa essential oils (100 and 200 mg/kg b.w) i.p immediately after acetaminophen administration. The blood were collected for estimating the values of total antioxidant of plasma (FRAP) and liver enzymes; alanin teransferase (ALT), aspartate teransferase (AST), and alkaline phosphatase (ALP). Also, a piece of liver was used for determining of glutathione (GSH), lipid peroxidation (LP) concentrations, the activity of glutathione s-transferase (GST) and histopathological studies.  Results: The data showed that F. gummosa essential oil modulate significantly the changes in the levels of GSH, GST and FRAP as well as the liver enzymes and lipid peroxidation compared to negative control group. Furthermore, the histopathological findings of the liver tissue was confirmed the biochemical results. Conclusion: The essential oil extracted from F. gummosa possessed antioxidant activity which protects the liver against the toxic effects of acetaminophen.
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spelling doaj.art-003eb370f075445b8fb3885509f1a4982022-12-21T18:35:09ZengInstitue of Medicinal Plants, ACECRJournal of Medicinal Plants2717-204X2717-20582016-10-0115601423Evaluation the role of Ferula gummosa essential oil against the hepatoxicity induced by acetaminophen in animal modelAF Dadkhah0Gh Khalaj1F Fatemi2S Dini3S Hesaraki4S Naij5M Babaei6HR Attaran7 Faculty of Medicine, Qom Branch, Islamic Azad University, Qom, I.R. Iran. Faculty of science, Qom Branch, Islamic Azad University, Qom, I.R. Iran. Nuclear Fuel Cycle Research School, Nuclear Science and Technology Research Institute, Tehran, I.R. Iran Young Researchers and Elite Club, Karaj Branch, Islamic Azad University, Karaj, Iran. Department of Pathobiology, College of Veterinary medicine, Tehran Science and Research branch, Islamic Azad University, Tehran, Iran Faculty of Botany, Payam Noor University, Tehran, Iran. Department of chemistry, Qom Branch, Islamic Azad University, Qom, I.R. Iran. Department of Medicine, Faculty of Medicine, Qom Branch, Islamic Azad University, Qom, I.R. Iran Background: Acetaminophen as a common antipyretic drug, in overdoses, is poisonous for the liver. Objective: The current study aimed to assess the protective effects of Ferula (F.) gummosa essential oils against the liver toxicity of acetaminophen in rats. Methods: 80 male Wistar rats were randomly divided into 16 groups (n=5). Negative control group received only DMSO and the positive control group received acetaminophen 500 mg/kg b.w i.p. The treatment groups received F. gummosa essential oils (100 and 200 mg/kg b.w) i.p immediately after acetaminophen administration. The blood were collected for estimating the values of total antioxidant of plasma (FRAP) and liver enzymes; alanin teransferase (ALT), aspartate teransferase (AST), and alkaline phosphatase (ALP). Also, a piece of liver was used for determining of glutathione (GSH), lipid peroxidation (LP) concentrations, the activity of glutathione s-transferase (GST) and histopathological studies.  Results: The data showed that F. gummosa essential oil modulate significantly the changes in the levels of GSH, GST and FRAP as well as the liver enzymes and lipid peroxidation compared to negative control group. Furthermore, the histopathological findings of the liver tissue was confirmed the biochemical results. Conclusion: The essential oil extracted from F. gummosa possessed antioxidant activity which protects the liver against the toxic effects of acetaminophen.http://jmp.ir/article-1-1103-en.html<i>ferula gummosa</i>acetaminophenhepatotoxicityoxidative stresses
spellingShingle AF Dadkhah
Gh Khalaj
F Fatemi
S Dini
S Hesaraki
S Naij
M Babaei
HR Attaran
Evaluation the role of Ferula gummosa essential oil against the hepatoxicity induced by acetaminophen in animal model
Journal of Medicinal Plants
<i>ferula gummosa</i>
acetaminophen
hepatotoxicity
oxidative stresses
title Evaluation the role of Ferula gummosa essential oil against the hepatoxicity induced by acetaminophen in animal model
title_full Evaluation the role of Ferula gummosa essential oil against the hepatoxicity induced by acetaminophen in animal model
title_fullStr Evaluation the role of Ferula gummosa essential oil against the hepatoxicity induced by acetaminophen in animal model
title_full_unstemmed Evaluation the role of Ferula gummosa essential oil against the hepatoxicity induced by acetaminophen in animal model
title_short Evaluation the role of Ferula gummosa essential oil against the hepatoxicity induced by acetaminophen in animal model
title_sort evaluation the role of ferula gummosa essential oil against the hepatoxicity induced by acetaminophen in animal model
topic <i>ferula gummosa</i>
acetaminophen
hepatotoxicity
oxidative stresses
url http://jmp.ir/article-1-1103-en.html
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