Protective Effect of β-Carotene on Methotrexate–Induced Oxidative Liver Damage

Author:

Vardi Nigar1,Parlakpinar Hakan2,Cetin Asli1,Erdogan Ali3,Cetin Ozturk I.4

Affiliation:

1. Department of Embryology and Histology, Inonu University, Malatya, Turkey

2. Department of Pharmacology, Inonu University, Malatya, Turkey

3. Department of Chemistry, Inonu University, Malatya, Turkey

4. Department of Biochemistry, Inonu University, Malatya, Turkey

Abstract

In this study, the authors aimed to investigate the role of oxidative stress on the hepatic damage caused by methotrexate (MTX) and the possible protective effects of β-carotene against this damage. The rats were divided into four groups as control, MTX (20 mg/kg ip), β-carotene (10 mg/kg/day ip) + MTX, and β-carotene. Histopathologic alterations were evaluated for defining the liver damage. The tissue, malondialdehyde (MDA), superoxide dismutase (SOD), and glutathione peroxidase (GP-x) contents and serum aspartate aminotransferase (AST) and alanine aminotranferase (ALT) activities were also examined. Histopathologic damage for each group score findings have been determined as control: 0.66 ± 0.33; MTX: 7.0 ± 0.68; β-carotene + MTX: 3.3 ± 0.42; and β-carotene: 0.5 ± 0.3. In the MTX-treated group, MDA, AST, and ALT values were increased, while SOD and GP-x values were decreased compared with the control group. In the β-carotene + MTX-treated group, AST and ALT values significantly decreased, while all other parameters were similar to the control group. This study shows that β-carotene has a protective effect on MTX-induced oxidative hepatic damage. Consequently, it seems that an antioxidant agents like β-carotene may be useful in decreasing the side effects of chemotherapy.

Publisher

SAGE Publications

Subject

Cell Biology,Toxicology,Molecular Biology,Pathology and Forensic Medicine

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