Effects of Urtica dioica L. seed on lipid peroxidation,antioxidants and liver pathology in aflatoxin-induced tissue injury in rats |
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Authors: | Zabit Yener Ismail Celik Fatma Ilhan Ramazan Bal |
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Affiliation: | 1. Department of Pathology, Yuzuncu Yil University, Faculty of Veterinary Medicine, 65080 Van, Turkey;2. Department of Biology, Faculty of Arts and sciences, Yuzuncu Yil University, 65080 Van, Turkey;3. Department of Biophysics, Faculty of Medicine, Firat University, Elazig, Turkey |
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Abstract: | This study was carried out to investigate the hepatoprotective and antioxidant properties of Urtica dioica L. seeds (UDS) extract against aflatoxin (AF)-exposure in rats. The preventive potential and antioxidant capacity of the plant’s extract was evaluated by liver histopathological changes, measuring serum marker enzymes, antioxidant defense systems and lipid peroxidation (Malondialdehyde, MDA) content in some tissues of rats. Eighteen rats were randomly divided into one of three experimental groups: control, AF-treated group and AF+UDS-treated group. Rats in control group were fed with a diet without AF. Rats in AF-treated group and AF+UDS-treated group received approximately 25 μgr of AF/rat/day. AF+UDS groups also received 2 mL of UDS oils/rat/day by gavage for 90 days. Administration of UDS extract restored the AF-induced imbalance between MDA and antioxidant system towards near normal particularly in liver. Hepatoprotection by UDS is further substantiated by the almost normal histologic findings in AF+UDS-treated group as against degenerative changes in the AF-treated rats. It is concluded that UDS has a hepatoprotective effect in rats with aflatoxicosis, probably acting by promoting the antioxidative defense systems. |
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Keywords: | AF, aflatoxin AFB1, aflatoxin B1 UD, Urtica dioica L. UDS, Urtica dioica L. seed TLC, thin layer chromatography MDA, malondialdehyde AST, aspartate aminotransferase ALT, alanin aminotransferase GGT, gamma glutamil transpeptidase GSH, reduced glutathione GR, glutathione reductase SOD, superoxide dismutase GST, glutathione-S-transferase CAT, catalase ROS, reactive oxygen species |
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