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ePublished: 21 Apr 2016
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J Renal Inj Prev. 2016;5(2): 74-78.
doi: 10.15171/jrip.2016.16
PMID: 27471738
PMCID: PMC4962673
  Abstract View: 4254
  PDF Download: 2472

Original Article

Tempol effects on diabetic nephropathy in male rats  

Akram Ranjbar 1, Hassan Ghasemi 2, Mahdi Hatami 2, Farahanaz Dadras 3, Tavakol Heidary Shayesteh 1, Farhad Khoshjou 4*

1 Department of Toxicology and Pharmacology, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran
2 Department of Biochemistry, Hamadan University of Medical Sciences, Hamadan, Iran
3 Department of Internal Medicine, Section of Nephrology, Iran University of Medical Sciences,Tehran, Iran
4 Urology and Nephrology Research Center, Hamadan University of Medical Sciences, Hamadan, Iran
*Corresponding Author: *Corresponding author: Farhad Khoshjou, Email:, Email: fakhoshjou@yahoo.com

Abstract

Introduction: Diabetic nephropathy (DN) is the most common cause of the chronic kidney disease in the world. Oxidative stress on the other hand has a major and well known role in its pathophysiology.

Objectives: The aim of the study is to figure out if tempol, a synthetic antioxidant agent, modifies DN and to determine its relevance to changes of serum oxidative biomarkers.

Materials and Methods: Twenty-seven male rats were equally divided in to 4 groups (7 rats for each group). Group I (control or C), group II (diabetic or D), groups III (Tempol) which were given tempol (100 mg/kg/day) by gavages for 28 days and group IV (D&T) which includes diabetic rats that also received same dose of tempol. After treatment, blood samples were isolated. Enzymatic scavengers including catalase (CAT), glutathione peroxidase (GPx) and superoxide dismutase (SOD) activities, lipid peroxidation (LPO), total antioxidant capacity (TAC) and total thiol molecules (TTM) were measured. Blood urea nitrogen (BUN), creatinine (Cr) an albumin/Cr ratio were evaluated as well. Statistical differences were assessed with one-way analysis of variance (ANOVA) by SPSS followed by Tukey t test.

Results: Oxidative stress biomarkers modified and Alb/Cr ratio increased in diabetic group (II), however, they were altered to normal in group IV (D&T) compared with diabetic group (D).

Conclusion: Tempol can modify oxidative stress biomarkers and presumably nephropathy in diabetic rats.

 



Implication for health policy/practice/research/medical education:

Diabetic nephropathy (DN) is the major etiology of chronic kidney disease. Its pathophysiology has been widely studied. Oxidative stress has been known to be involved in it extensively. Thus a couple of antioxidative agent have been studied to figure out if they can modify DN and other consequences of diabetes mellitus (DM). In current study we tried to assess a couple of oxidative biomarkers in diabetic rats, following administration of tempol, a synthetic superoxide dismutase (SOD) mimetic, to show whether it can amend their changes and reduce proteinuria as well.


Please cite this paper as:
Ranjbar A, Ghasemi H, Hatami M, Dadras F, Heidary Shayesteh T, Khoshjou F. Tempol effects on diabetic nephropathy in male rats. J Renal Inj Prev. 2016;5(2):74-78. DOI: 10.15171/jrip.2016.16.


 
 
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