Hepatoprotective Effect of Metadoxine on Acetaminophen-induced Liver Toxicity in Mice

Background: Metadoxine (pyridoxine pyrrolidone carboxylate) is considered to be a beneficial agent for the treatment of experimental hepatotoxicity due to alcohol, CCl4, and bile duct ligation. Hence, the therapeutic effect of metadoxine and N-acetylcysteine (NAC) as reference drug was investigated...

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Main Authors: Parvin Mazraati, Mohsen Minaiyan
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2018-01-01
Series:Advanced Biomedical Research
Subjects:
Online Access:http://www.advbiores.net/article.asp?issn=2277-9175;year=2018;volume=7;issue=1;spage=67;epage=67;aulast=Mazraati
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spelling doaj-ff093a4bc3594928b1a7aa41789208ac2020-11-24T22:03:14ZengWolters Kluwer Medknow PublicationsAdvanced Biomedical Research2277-91752018-01-0171676710.4103/abr.abr_142_17Hepatoprotective Effect of Metadoxine on Acetaminophen-induced Liver Toxicity in MiceParvin MazraatiMohsen MinaiyanBackground: Metadoxine (pyridoxine pyrrolidone carboxylate) is considered to be a beneficial agent for the treatment of experimental hepatotoxicity due to alcohol, CCl4, and bile duct ligation. Hence, the therapeutic effect of metadoxine and N-acetylcysteine (NAC) as reference drug was investigated in mice exposed to acute hepatotoxicity induced by a single oral toxic dose of acetaminophen (650 mg/kg). Materials and Methods: Metadoxine (200 and 400 mg/kg) and NAC (300 mg/kg) were given orally (p. o.), 2 h after acetaminophen administration. Serum aminotransferases, aspartate transaminase (AST), alanine transaminase (ALT), alkaline phosphatase (ALP), total bilirubin, hepatic glutathione (GSH), and malondialdehyde (MDA) levels were determined for evaluating the extent of hepatotoxicity due to acetaminophen and its protection by metadoxine. Results: Findings indicated that metadoxine significantly reduced the level of serum ALT, AST, and ALP but not total bilirubin which increased by acetaminophen intoxication. Administration of metadoxine also attenuated oxidative stress by suppressing lipid peroxidation (MDA) and prevented the depletion of reduced GSH level which caused by acetaminophen toxicity. Besides, metadoxine ameliorated histopathological hepatic tissue injury induced by acetaminophen. Conclusion: In most parameters examined, the effect of metadoxine was comparable to NAC. Hence, metadoxine could be considered as a beneficial therapeutic candidate to protect against acute acetaminophen hepatotoxicity.http://www.advbiores.net/article.asp?issn=2277-9175;year=2018;volume=7;issue=1;spage=67;epage=67;aulast=MazraatiAcetaminophenhepatoprotectionliver injurymetadoxinemice
collection DOAJ
language English
format Article
sources DOAJ
author Parvin Mazraati
Mohsen Minaiyan
spellingShingle Parvin Mazraati
Mohsen Minaiyan
Hepatoprotective Effect of Metadoxine on Acetaminophen-induced Liver Toxicity in Mice
Advanced Biomedical Research
Acetaminophen
hepatoprotection
liver injury
metadoxine
mice
author_facet Parvin Mazraati
Mohsen Minaiyan
author_sort Parvin Mazraati
title Hepatoprotective Effect of Metadoxine on Acetaminophen-induced Liver Toxicity in Mice
title_short Hepatoprotective Effect of Metadoxine on Acetaminophen-induced Liver Toxicity in Mice
title_full Hepatoprotective Effect of Metadoxine on Acetaminophen-induced Liver Toxicity in Mice
title_fullStr Hepatoprotective Effect of Metadoxine on Acetaminophen-induced Liver Toxicity in Mice
title_full_unstemmed Hepatoprotective Effect of Metadoxine on Acetaminophen-induced Liver Toxicity in Mice
title_sort hepatoprotective effect of metadoxine on acetaminophen-induced liver toxicity in mice
publisher Wolters Kluwer Medknow Publications
series Advanced Biomedical Research
issn 2277-9175
publishDate 2018-01-01
description Background: Metadoxine (pyridoxine pyrrolidone carboxylate) is considered to be a beneficial agent for the treatment of experimental hepatotoxicity due to alcohol, CCl4, and bile duct ligation. Hence, the therapeutic effect of metadoxine and N-acetylcysteine (NAC) as reference drug was investigated in mice exposed to acute hepatotoxicity induced by a single oral toxic dose of acetaminophen (650 mg/kg). Materials and Methods: Metadoxine (200 and 400 mg/kg) and NAC (300 mg/kg) were given orally (p. o.), 2 h after acetaminophen administration. Serum aminotransferases, aspartate transaminase (AST), alanine transaminase (ALT), alkaline phosphatase (ALP), total bilirubin, hepatic glutathione (GSH), and malondialdehyde (MDA) levels were determined for evaluating the extent of hepatotoxicity due to acetaminophen and its protection by metadoxine. Results: Findings indicated that metadoxine significantly reduced the level of serum ALT, AST, and ALP but not total bilirubin which increased by acetaminophen intoxication. Administration of metadoxine also attenuated oxidative stress by suppressing lipid peroxidation (MDA) and prevented the depletion of reduced GSH level which caused by acetaminophen toxicity. Besides, metadoxine ameliorated histopathological hepatic tissue injury induced by acetaminophen. Conclusion: In most parameters examined, the effect of metadoxine was comparable to NAC. Hence, metadoxine could be considered as a beneficial therapeutic candidate to protect against acute acetaminophen hepatotoxicity.
topic Acetaminophen
hepatoprotection
liver injury
metadoxine
mice
url http://www.advbiores.net/article.asp?issn=2277-9175;year=2018;volume=7;issue=1;spage=67;epage=67;aulast=Mazraati
work_keys_str_mv AT parvinmazraati hepatoprotectiveeffectofmetadoxineonacetaminopheninducedlivertoxicityinmice
AT mohsenminaiyan hepatoprotectiveeffectofmetadoxineonacetaminopheninducedlivertoxicityinmice
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