Affiliation:
1. Department of Biology, Faculty of Arts and Science, Bozok University, Yozgat, Turkey
2. Department of Science Education, Gazi Education Faculty, Gazi University, Ankara, Turkey
Abstract
Abstract
Furan forms as a result of thermal treatment of food and induces harmful effects on organisms. In our work, lycopene, furan, and a combination of the two were given to diabetic male rats for 28 days. Hematological changes, total protein and cholesterol, triglyceride, and albumin levels, alanine aminotransferase, aspartate aminotransferase, lactate dehydrogenase, and alkaline phosphatase activities of the serum, malondialdehyde levels, glutathione peroxidase, catalase, glutathione-S-transferase, superoxide dismutase activities, DNA damage in liver tissues and hepatic histopathological alterations were compared to a control group. There were significant changes in the liver function tests, DNA damage, activities of antioxidant enzymes, and malondialdehyde levels between diabetic control and non-diabetic control groups, between diabetic control and diabetic lycopene groups, and also between diabetic furan and diabetic control groups. In diabetic lycopene and diabetic furan + lycopene treated groups we designated the preventive effects of lycopene against diabetes and furan, however, on the analysed parameters only. In spite of some pathological alterations designated in diabetic furan treated group’s liver, fewer pathological alterations were observed in furan+lycopene treated groups at the end of week 4. Consequently, lycopene significantly reduced furan- and diabetes-induced toxicity in rat liver.
Subject
Public Health, Environmental and Occupational Health,Toxicology
Reference48 articles.
1. 1. Moro S, Chipman JK, Antczak P, Turan N, Dekant W, Falciani F, Mally A. Identification and pathway mapping of furan target proteins reveal mitochondrial energy production and redox regulation as critical targets of furan toxicity. Toxicol Sci 2012;126:336-52. doi: 10.1093/toxsci/kfs005
2. 2. Terrell AN, Huynh M, Grill AE, Kovi RC, O’Sullivan MG, Guttenplan JB, Ho YY, Peterson LA. Mutagenicity of furan in female Big Blue B6C3F1 mice. Mutat Res Genet Toxicol Environ Mutagen 2014;770:46-54. doi: 10.1016/j. mrgentox.2014.04.024
3. 3. Amin AH, El-Missiry MA, Othman AI. Melatonin ameliorates metabolic risk factors, modulates apoptotic proteins, and protects the rat heart against diabetes-induced apoptosis. Eur J Pharmacol 2015;747:166-73. doi: 10.1016/j. ejphar.2014.12.002
4. 4. Apaydin FG, Kalender S, Bas H, Demir F, Kalender Y. Lead nitrate induced testicular toxicity in diabetic and non-diabetic rats: protective role of sodium selenite. Braz Arch Biol Technol 2015;58:68-74. doi: 10.1590/S1516-8913201400025
5. 5. Tanaka T, Shnimizu M, Moriwaki H. Cancer chemoprevention by carotenoids. Molecules 2012;17:3202-42. doi: 10.3390/ molecules17033202
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