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Hepatoprotective and antioxidant activity of N-acetyl cysteine in carbamazepine-administered rats
OBJECTIVES: The present study evaluates the hepatoprotective activity of N-acetyl cysteine (NAC) against carbamazepine (CBZ)-induced hepatotoxicity. MATERIALS AND METHODS: Rats were treated with CBZ (50 mg/kg p.o.) and CBZ supplemented with NAC 50, 100 and 200 mg/kg for 45 days, after which blood sa...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987193/ https://www.ncbi.nlm.nih.gov/pubmed/24741196 http://dx.doi.org/10.4103/0253-7613.129321 |
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author | Maheswari, Eswaran Saraswathy, Ganesan Raja Lekshmi Santhranii, Thakur |
author_facet | Maheswari, Eswaran Saraswathy, Ganesan Raja Lekshmi Santhranii, Thakur |
author_sort | Maheswari, Eswaran |
collection | PubMed |
description | OBJECTIVES: The present study evaluates the hepatoprotective activity of N-acetyl cysteine (NAC) against carbamazepine (CBZ)-induced hepatotoxicity. MATERIALS AND METHODS: Rats were treated with CBZ (50 mg/kg p.o.) and CBZ supplemented with NAC 50, 100 and 200 mg/kg for 45 days, after which blood samples were collected and subjected to liver function tests. Animals were killed, liver was separated, weighed and the levels of antioxidants and liver enzymes were estimated. In addition, histopathological investigation was also performed. RESULTS: Serum glutamate pyruvate transaminase (SGPT), serum glutamate oxaloacetate (SGOT) transaminase, alkaline phosphatase (ALP), bilirubin, lipid peroxidation, absolute and relative liver weights were significantly (P < 0.05) elevated, whereas serum levels of albumin, total protein and body weight were decreased in the CBZ-treated animals. CBZ also produced vacuolar degeneration, centrilobular congestion and hepatic necrosis as evidenced from histopathological report. NAC significantly reduced the levels of serum transaminase, ALP, bilirubin and liver weight and increased the levels of total protein, albumin and body weight. CONCLUSION: It was observed that NAC increased the glutathione (GSH) content, reduced lipid peroxidation and reversed the CBZ-induced histopathological abnormalities. CBZ-induced hepatotoxicity may be due its toxic epoxide metabolite-induced oxidative stress. |
format | Online Article Text |
id | pubmed-3987193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-39871932014-04-16 Hepatoprotective and antioxidant activity of N-acetyl cysteine in carbamazepine-administered rats Maheswari, Eswaran Saraswathy, Ganesan Raja Lekshmi Santhranii, Thakur Indian J Pharmacol Research Article OBJECTIVES: The present study evaluates the hepatoprotective activity of N-acetyl cysteine (NAC) against carbamazepine (CBZ)-induced hepatotoxicity. MATERIALS AND METHODS: Rats were treated with CBZ (50 mg/kg p.o.) and CBZ supplemented with NAC 50, 100 and 200 mg/kg for 45 days, after which blood samples were collected and subjected to liver function tests. Animals were killed, liver was separated, weighed and the levels of antioxidants and liver enzymes were estimated. In addition, histopathological investigation was also performed. RESULTS: Serum glutamate pyruvate transaminase (SGPT), serum glutamate oxaloacetate (SGOT) transaminase, alkaline phosphatase (ALP), bilirubin, lipid peroxidation, absolute and relative liver weights were significantly (P < 0.05) elevated, whereas serum levels of albumin, total protein and body weight were decreased in the CBZ-treated animals. CBZ also produced vacuolar degeneration, centrilobular congestion and hepatic necrosis as evidenced from histopathological report. NAC significantly reduced the levels of serum transaminase, ALP, bilirubin and liver weight and increased the levels of total protein, albumin and body weight. CONCLUSION: It was observed that NAC increased the glutathione (GSH) content, reduced lipid peroxidation and reversed the CBZ-induced histopathological abnormalities. CBZ-induced hepatotoxicity may be due its toxic epoxide metabolite-induced oxidative stress. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC3987193/ /pubmed/24741196 http://dx.doi.org/10.4103/0253-7613.129321 Text en Copyright: © Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Maheswari, Eswaran Saraswathy, Ganesan Raja Lekshmi Santhranii, Thakur Hepatoprotective and antioxidant activity of N-acetyl cysteine in carbamazepine-administered rats |
title | Hepatoprotective and antioxidant activity of N-acetyl cysteine in carbamazepine-administered rats |
title_full | Hepatoprotective and antioxidant activity of N-acetyl cysteine in carbamazepine-administered rats |
title_fullStr | Hepatoprotective and antioxidant activity of N-acetyl cysteine in carbamazepine-administered rats |
title_full_unstemmed | Hepatoprotective and antioxidant activity of N-acetyl cysteine in carbamazepine-administered rats |
title_short | Hepatoprotective and antioxidant activity of N-acetyl cysteine in carbamazepine-administered rats |
title_sort | hepatoprotective and antioxidant activity of n-acetyl cysteine in carbamazepine-administered rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987193/ https://www.ncbi.nlm.nih.gov/pubmed/24741196 http://dx.doi.org/10.4103/0253-7613.129321 |
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