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Lucrative antioxidant effect of metformin against cyclophosphamide induced nephrotoxicity.
Tohamy, Adel F; Hussein, Shaymaa; Moussa, Ihab M; Rizk, Hamdy; Daghash, Samer; Alsubki, Roua A; Mubarak, Ayman S; Alshammari, Hanan O; Al-Maary, Khalid S; Hemeg, Hassan A.
Affiliation
  • Tohamy AF; Department of Toxicology and Forensic Medicine, Faculty of Veterinary Medicine, Cairo University, Egypt.
  • Hussein S; Department of Cytology and Histology, Faculty of Veterinary Medicine, Cairo University, Egypt.
  • Moussa IM; Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
  • Rizk H; Department of Microbiology, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.
  • Daghash S; Department of Anatomy and Embryology, Faculty of Veterinary Medicine, Cairo University, Egypt.
  • Alsubki RA; Department of Anatomy and Embryology, Faculty of Veterinary Medicine, Cairo University, Egypt.
  • Mubarak AS; Department of Clinical Laboratory Science, Chair of Medical and Molecular Genetics Research, College of Applied Medical Science, King Saud University, Saudi Arabia.
  • Alshammari HO; Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
  • Al-Maary KS; Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
  • Hemeg HA; Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
Saudi J Biol Sci ; 28(5): 2755-2761, 2021 May.
Article in En | MEDLINE | ID: mdl-34025161
Cyclophosphamide is anticancer drug with a well-Known nephrotoxicity. This work was applied to study the lucrative antioxidant influence of metformin as co-therapy on the nephrotoxicity induced by cyclophosphamide in the treatment of different cancer diseases. Four groups of male Sprague Dawley rats were used; Control group (C) received single I.P. injection of 0.2 ml saline, Metformin (MET) group received daily gavage of 200 mg/kg metformin for two weeks, Cyclophosphamide (CP) group received single I.P. injection of 200 mg/kg CP, Protector group (CP.MET) received daily gavage of 200 mg/kg metformin for two weeks and single I.P. injection of 200 mg/kg CP at day 7. By day 14 rats were euthanized. Samples were collected from kidney tissues and blood for kidney function evaluation, histopathological and assessment of oxidative stress markers. The results disclosed that CP yields many functional and structural damage to the kidney, worsened oxidative stress markers and kidney function indicators. The protector group displayed better kidney tissue morphology, acceptable kidney function indicators as well as satisfactory oxidative stress markers. In assumption, metformin could be combined with CP owing to its lucrative effect counter to CP persuaded nephrotoxicity.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Saudi J Biol Sci Year: 2021 Document type: Article Affiliation country: Egypt Country of publication: Saudi Arabia

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Saudi J Biol Sci Year: 2021 Document type: Article Affiliation country: Egypt Country of publication: Saudi Arabia