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Assessment of the biomarkers of hepatotoxicity following carbamazepine, levetiracetam, and carbamazepine-levetiracetam adjunctive treatment in male Wistar rats

OBJECTIVE: This study examined some of the biomarkers of hepatotoxicity following chronic treatment with carbamazepine (CBZ), levetiracetam (LEV), and CBZ + LEV adjunctive treatment in male rats. METHOD: Twenty-four male Wistar rats (140−150 g) were randomized into four groups (n = 6) to receive ora...

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Autores principales: Osuntokun, Opeyemi Samson, Babatunde, Ademola Adeniyi, Olayiwola, Gbola, Atere, Tope Gafar, Oladokun, Olayemi Olutobi, Adedokun, Kabiru Isola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7994541/
https://www.ncbi.nlm.nih.gov/pubmed/33786324
http://dx.doi.org/10.1016/j.toxrep.2021.03.008
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author Osuntokun, Opeyemi Samson
Babatunde, Ademola Adeniyi
Olayiwola, Gbola
Atere, Tope Gafar
Oladokun, Olayemi Olutobi
Adedokun, Kabiru Isola
author_facet Osuntokun, Opeyemi Samson
Babatunde, Ademola Adeniyi
Olayiwola, Gbola
Atere, Tope Gafar
Oladokun, Olayemi Olutobi
Adedokun, Kabiru Isola
author_sort Osuntokun, Opeyemi Samson
collection PubMed
description OBJECTIVE: This study examined some of the biomarkers of hepatotoxicity following chronic treatment with carbamazepine (CBZ), levetiracetam (LEV), and CBZ + LEV adjunctive treatment in male rats. METHOD: Twenty-four male Wistar rats (140−150 g) were randomized into four groups (n = 6) to receive oral dose of normal saline (0.1 mL), CBZ (25 mg/kg), LEV (50 mg/kg) or sub-therapeutic dose of CBZ (12.5 mg/kg) together with LEV (25 mg/kg) for 28 days. Activities of the liver enzymes and oxidative stress markers were determined while liver histomorphology was also carried out. Data were analyzed using descriptive and inferential statistics. The results were presented as mean ± SEM in graphs or tables, while the level of significance was taken at p < 0.05. RESULTS: The activities of alkaline-phosphatase and malondialdehyde concentrations increased significantly in all the drug treatment groups, while the activities of superoxide dismutase decreased significantly following CBZ, and CBZ + LEV treatment. Alanine-aminotransferase activities increased significantly in the CBZ and CBZ + LEV treated rats compared with control. The liver section of CBZ treated rats showed mild vascular congestion. CONCLUSION: None of these AEDs treatment is devoid of hepatotoxicity. However, the adverse effects in CBZ were greater than LEV, or CBZ + LEV adjunctive treatment.
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spelling pubmed-79945412021-03-29 Assessment of the biomarkers of hepatotoxicity following carbamazepine, levetiracetam, and carbamazepine-levetiracetam adjunctive treatment in male Wistar rats Osuntokun, Opeyemi Samson Babatunde, Ademola Adeniyi Olayiwola, Gbola Atere, Tope Gafar Oladokun, Olayemi Olutobi Adedokun, Kabiru Isola Toxicol Rep Regular Article OBJECTIVE: This study examined some of the biomarkers of hepatotoxicity following chronic treatment with carbamazepine (CBZ), levetiracetam (LEV), and CBZ + LEV adjunctive treatment in male rats. METHOD: Twenty-four male Wistar rats (140−150 g) were randomized into four groups (n = 6) to receive oral dose of normal saline (0.1 mL), CBZ (25 mg/kg), LEV (50 mg/kg) or sub-therapeutic dose of CBZ (12.5 mg/kg) together with LEV (25 mg/kg) for 28 days. Activities of the liver enzymes and oxidative stress markers were determined while liver histomorphology was also carried out. Data were analyzed using descriptive and inferential statistics. The results were presented as mean ± SEM in graphs or tables, while the level of significance was taken at p < 0.05. RESULTS: The activities of alkaline-phosphatase and malondialdehyde concentrations increased significantly in all the drug treatment groups, while the activities of superoxide dismutase decreased significantly following CBZ, and CBZ + LEV treatment. Alanine-aminotransferase activities increased significantly in the CBZ and CBZ + LEV treated rats compared with control. The liver section of CBZ treated rats showed mild vascular congestion. CONCLUSION: None of these AEDs treatment is devoid of hepatotoxicity. However, the adverse effects in CBZ were greater than LEV, or CBZ + LEV adjunctive treatment. Elsevier 2021-03-10 /pmc/articles/PMC7994541/ /pubmed/33786324 http://dx.doi.org/10.1016/j.toxrep.2021.03.008 Text en © 2021 The Authors 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 Regular Article
Osuntokun, Opeyemi Samson
Babatunde, Ademola Adeniyi
Olayiwola, Gbola
Atere, Tope Gafar
Oladokun, Olayemi Olutobi
Adedokun, Kabiru Isola
Assessment of the biomarkers of hepatotoxicity following carbamazepine, levetiracetam, and carbamazepine-levetiracetam adjunctive treatment in male Wistar rats
title Assessment of the biomarkers of hepatotoxicity following carbamazepine, levetiracetam, and carbamazepine-levetiracetam adjunctive treatment in male Wistar rats
title_full Assessment of the biomarkers of hepatotoxicity following carbamazepine, levetiracetam, and carbamazepine-levetiracetam adjunctive treatment in male Wistar rats
title_fullStr Assessment of the biomarkers of hepatotoxicity following carbamazepine, levetiracetam, and carbamazepine-levetiracetam adjunctive treatment in male Wistar rats
title_full_unstemmed Assessment of the biomarkers of hepatotoxicity following carbamazepine, levetiracetam, and carbamazepine-levetiracetam adjunctive treatment in male Wistar rats
title_short Assessment of the biomarkers of hepatotoxicity following carbamazepine, levetiracetam, and carbamazepine-levetiracetam adjunctive treatment in male Wistar rats
title_sort assessment of the biomarkers of hepatotoxicity following carbamazepine, levetiracetam, and carbamazepine-levetiracetam adjunctive treatment in male wistar rats
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7994541/
https://www.ncbi.nlm.nih.gov/pubmed/33786324
http://dx.doi.org/10.1016/j.toxrep.2021.03.008
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