The protective role of oleuropein against diethylnitrosamine and phenobarbital induced damage in rats

Author:

Özeren Nurefşan1,Kisacam Mehmet Ali2ORCID,Ozan Kocamuftuoglu Gonca3ORCID,Kaya Nalan4ORCID,Ozan Sema Temizer5ORCID

Affiliation:

1. Firat University , Faculty of Veterinary Medicine, Department of Biochemistry , Elazig , Turkey

2. Mustafa Kemal University, Faculty of Veterinary Medicine , Department of Biochemistry , Hatay , Turkey

3. Mehmet Akif Ersoy University , Faculty of Veterinary Medicine, Department of Biochemistry , Burdur , Turkey

4. Firat University , Faculty of Medicine, Department of Histology and Embryology , Elazig , Turkey

5. Firat University , Faculty of Veterinary Medicine, Department of Biochemistry , Elazig 23119 , Turkey

Abstract

Abstract Objective Liver cancer is amongst the most lethal cancers worldwide. Diethylnitrosamine (DEN) and phenobarbital (PB) are common agents that form reactive oxygen species (ROS). Oleuropein (OLE) has efficient biological properties and used as a therapeutic agent. In this study, we aimed at investigating OLE against DEN + PB induced liver damage. Methods Adult Sprague-Dawley rats were divided into 5 groups (n = 10): Control, DEN, DEN + PB, DEN + PB + OLE and OLE. DEN, DEN + PB, DEN + PB + OLE groups were administered a single dose of 150 mg/kg DEN. After two weeks, DEN + PB and DEN + PB + OLE groups received 500 ppm of PB. 10 mg/kg/day of OLE was orally administered to DEN + PB + OLE and OLE groups. Biochemical and histopathological changes evaluated after the 8 weeks study. Results DEN and PB application with OLE treatment resulted significant differences, alone or combined. Although there was a significant difference among the groups in terms of liver GSH and MDA levels and CAT activities, there was no significant difference among the groups in SOD activity. In the liver sections of the DEN, DEN + PB and OLE groups, increase in some histopathological findings and TUNEL positive cells were increased compared to the control group. Conclusion OLE can be used as a protector against the effects of carcinogens causing liver damage.

Funder

Firat University Research Fund

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry, medical,Clinical Biochemistry,Molecular Biology,Biochemistry

Reference40 articles.

1. Hanahan D, Weinberg RA. The hallmarks of cancer: the next Generation. Cell 2011;144:646–74.

2. McGlynn KA, London WT. The global epidemiology of hepatocellular carcinoma: present and future. Clin Liver Dis 2011;15:223–43.

3. Munoz N, Bosch X. Epidemiology of hepatocellular carcinoma. In: Okuda K, Ishak KG, editors. Neoplasms of the liver. Tokyo: Springer, 1989:3–19.

4. Okuda K. Epidemiology of primary liver cancer. In: Tobe T, editor.Primary liver cancer in Japan. Tokyo: Springer-Verlag, 1992:353–64.

5. Aydinlik H, Nguyen TD, Moennikes O, Buchmann A, Schwarz M. Selective pressure during tumor promotion by phenobarbital leads to clonal outgrowth of beta-catenin-mutated mouse liver tumors. Oncogene 2001;20:7812–6.

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