Investigation of protective effect of resveratrol and coenzyme Q10 against cyclophosphamide-induced lipid peroxidation, oxidative stress and DNA damage in rats

Author:

Akbel Erten1,Kucukkurt Ismail23ORCID,Ince Sinan43,Demirel Hasan Huseyin5,Acaroz Damla Arslan23,Zemheri-Navruz Fahriye67,Kan Fahriye23

Affiliation:

1. Usak Health Training School, Usak University , 64200, Uşak , Turkey

2. Department of Biochemistry , Faculty of Veterinary Medicine, , 03200, Afyonkarahisar , Turkey

3. Afyon Kocatepe University , Faculty of Veterinary Medicine, , 03200, Afyonkarahisar , Turkey

4. Department of Pharmacology and Toxicology , Faculty of Veterinary Medicine, , 03200, Afyonkarahisar , Turkey

5. Bayat Vocational School, Afyon Kocatepe University , 03780, Afyonkarahisar , Turkey

6. Faculty of Science , Department of Molecular Biology and Genetics, , 74110, Bartın , Turkey

7. Bartın University , Department of Molecular Biology and Genetics, , 74110, Bartın , Turkey

Abstract

Abstract It is seen that cyclophosphamide, which is used in treating many diseases, especially cancer, causes toxicity in studies, and its metabolites induce oxidative stress. This study aimed to investigate the protective effects of resveratrol and Coenzyme Q10, known for their antioxidant properties, separately and together, against oxidative stress induced by cyclophosphamide. In this study, 35 Wistar albino male rats were divided into five groups. Groups; Control group, cyclophosphamide (CP) group (CP as 75 mg kg i.p. on day 14), coenzyme Q10 (CoQ10) + CP group (20 mg/kg i.p. CoQ10 + 75 mg kg i.p. CP), resveratrol (Res) + CP group (20 mg/kg i.p. Res + 75 mg/kg i.p. CP), CoQ10 + Res + CP group (20 mg/kg i.p Res + 20 mg/kg i.p CoQ10 and 75 mg/kg i.p.CP). At the end of the experiment, the cholesterol, creatinine and urea levels of the group given CP increased, while a decrease was observed in the groups given Res and CoQ10. Malondialdehyde level was high, glutathione level, superoxide dismutase and catalase activities were decreased in the blood and all tissues (liver, kidney, brain, heart and testis) of the CP given group. DNA damage and histopathological changes were also observed. In contrast, Res and CoQ10, both separately and together, reversed the CP-induced altered level and enzyme activities and ameliorated DNA damage and histopathological changes. In this study, the effects of Res and CoQ10 against CP toxicity were examined both separately and together.

Funder

Scientific Research Projects Coordination Unit of Usak University

Publisher

Oxford University Press (OUP)

Subject

Health, Toxicology and Mutagenesis,Toxicology

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