Volume 3, Issue 2 (2017)
Pharm Biomed Res 2017, 3(2): 8-18 |
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Chaabane M, Elwej A, Ghorbel I, Boudawara T, Zeghal N, Soudani N. Citrus aurantium L. peel extract mitigates hexavalent chromium-induced oxidative stress and cardiotoxicity in adult rats. Pharm Biomed Res 2017; 3 (2) :8-18
URL: http://pbr.mazums.ac.ir/article-1-164-en.html
URL: http://pbr.mazums.ac.ir/article-1-164-en.html
Mariem Chaabane * 
1, Awatef Elwej1 , Imen Ghorbel1 , Tahia Boudawara2 , Najiba Zeghal1 , Nejla Soudani3
1, Awatef Elwej1 , Imen Ghorbel1 , Tahia Boudawara2 , Najiba Zeghal1 , Nejla Soudani3
1- Animal Physiology Laboratory, Department of Life Sciences, Sciences Faculty of Sfax, University of Sfax, BP 1171, 3000 Sfax, T unisia
2- Hist opathology Laboratory, University of Sfax, CHU Habib Bourguiba, 3029 Sfax, Tunisia
3- Unit of P hysiology and Aquat ic Environment, T unis Facult y of Science, University of T unis El Manar, 2092, T unis, Tunisia
2- Hist opathology Laboratory, University of Sfax, CHU Habib Bourguiba, 3029 Sfax, Tunisia
3- Unit of P hysiology and Aquat ic Environment, T unis Facult y of Science, University of T unis El Manar, 2092, T unis, Tunisia
Abstract: (5000 Views)
In the present study, we aimed to examine the potential protective effect of C. aurantinum L. peel extract against oxidative damage induced by hexavalent chromium in the heart of adult rats. Rats were divided into six groups. Group I served as controls and received standard diet. Group II received via drinking water potassium dichromate (K2Cr2O7) alone (700 ppm) during 3 weeks. Groups III and IV were pre-treated for 10 days by gavage with the ethanolic extract of C. aurantium peels at doses of 100 and 300 mg/kg body weight/day, respectively, and then K2Cr2O7 was administrated during 3 weeks. Groups V and VI received by gavage only C. aurantium peel ethanolic extract at doses of 100 and 300 mg/kg body weight/day, respectively, during 10 days. K2Cr2O7 treatment increased the cardiac levels of malondialdehyde (MDA), protein carbonyls (PCO), advanced oxidation protein products (AOPP), non-protein thiols, glutathione and vitamin C, as well as the activities of catalase, superoxide dismutase and glutathione peroxidase. Cardiac histological alterations, manifested by hemorrhage and cytoplasmic vacuolization, were also observed. Pre-treatment with C. aurantium peel extract (300 mg/kg) attenuated significantly the biochemical and histopathological changes observed following K2Cr2O7 exposure in rat’s heart. Our findings indicated that C. aurantium peel extract was able to hamper K2Cr2O7-induced myocardial injury, which could be attributed to its antioxidant activity.
Type of Study: Original Research |
Subject:
Toxicology
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