In Vivo Prevention of Bladder Urotoxicity

Author:

Rouissi Kamel1,Hamrita Bechr1,Kouidi Soumaya1,Messai Yosra1,Jaouadi Bassem2,Hamden Khaled3,Medimegh Imen1,Ouerhani Slah4,Cherif Mohamed5,Elgaaied Amel Benammar1

Affiliation:

1. Laboratory of Genetics, Immunology and Human Pathology, Faculty of Sciences of Tunis, University of El-Manar I, Tunis, Tunisia

2. Laboratory of Microorganisms and Biomolecules, Centre of Biotechnology of Sfax, University of Sfax, Tunisia

3. Laboratory of Animal Ecophysiology, Faculty of Science of Sfax, Sfax, Tunisia

4. Laboratory of Molecular and Cellular Hematology, Pasteur Institute of Tunis, Tunis, Tunisia

5. Department of Urology, Charles Nicole Hospital, Tunis, Tunisia

Abstract

Urotoxicity is a troublesome complication associated with cyclophosphamide (CP) and L-buthionine-SR-sulfoximine (BSO) treatment in chemotherapy. With this concern in mind, the present study investigated the potential effects of a hydroxytyrosol extract from olive mill waste (OMW) on urotoxicity induced by acute CP and BSO doses using a Swiss albino mouse model. Toxicity modulation was evaluated by measuring lipid peroxidation (LPO) and antioxidants in urinary bladder. The findings revealed that the hydroxytyrosol extract exerted a protective effect not only on LPO but also on enzymatic antioxidants. When compared to the controls, the CP-treated animals underwent significant decreases in the glutathione S-transferase (GST), glutathione reductase (GR), glutathione peroxidase (GP), and catalase (CAT) activities. The level of glutathione (GSH) was also reduced with increased doses of LPO in the CP-treated animals. L-Buthionine-SR-sulfoximine treatment exerted an additive toxic effect on the CP-treated animals. Interestingly, pretreatment with the hydroxytyrosol extract restored the activities of all enzymes back to normal levels and exhibited an overall protective effect on the CP- and BSO-induced toxicities in urinary bladder. The restoration of GSH through the treatment with the hydroxytyrosol extract can play an important role in reversing CP-induced apoptosis and free radical-mediated LPO. 

Publisher

SAGE Publications

Subject

Toxicology

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