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

•Common etiology for carbamazepine (CBZ) toxicity is coadministration of other medications such as levetiracetam (LEV).•Adjuvant use of antiepileptic drugs with varying mechanisms of action is the mainstay in refractory epilepsy management.•This study showed that neither CBZ, nor LEV treatment is de...

Full description

Saved in:
Bibliographic Details
Published inToxicology reports Vol. 8; pp. 592 - 598
Main Authors Osuntokun, Opeyemi Samson, Babatunde, Ademola Adeniyi, Olayiwola, Gbola, Atere, Tope Gafar, Oladokun, Olayemi Olutobi, Adedokun, Kabiru Isola
Format Journal Article
LanguageEnglish
Published Ireland Elsevier B.V 01.01.2021
Elsevier
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:•Common etiology for carbamazepine (CBZ) toxicity is coadministration of other medications such as levetiracetam (LEV).•Adjuvant use of antiepileptic drugs with varying mechanisms of action is the mainstay in refractory epilepsy management.•This study showed that neither CBZ, nor LEV treatment is devoid of hepatotoxicity.•The adverse effects in CBZ were greater than LEV, or CBZ + LEV adjunctive treatment. 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. 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. 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. None of these AEDs treatment is devoid of hepatotoxicity. However, the adverse effects in CBZ were greater than LEV, or CBZ + LEV adjunctive treatment.
ISSN:2214-7500
2214-7500
DOI:10.1016/j.toxrep.2021.03.008