International Urology and Nephrology

, Volume 49, Issue 5, pp 769–775 | Cite as

Protective impact of resveratrol in experimental rat model of hyperoxaluria

  • Taylan Oksay
  • Sedat Yunusoğlu
  • Mustafa Calapoğlu
  • İ. Aydın Candan
  • İbrahim Onaran
  • Osman Ergün
  • Alper Özorak
Urology - Original Paper
  • 216 Downloads

Abstract

Purpose

Resveratrol (RES) is a polyphenol with antioxidant, anti-inflammatory, and many other physiological effects on tissues. In the present study, the effect of resveratrol in hyperoxaluria driven nephrolithiasis/nephrocalcinosis is investigated.

Methods

Wistar-Albino rats of 250–300 g (male, n = 24) were included in the present study. The rats were randomized into three groups: Group 1 consisted of the controls (n = 8), Group 2 of hyperoxaluria (1% ethylene glycol (EG), n = 8), and Group 3 of the treatment (1% EG + 10 mg/kg of RES, n = 8) group. At the beginning and fifth week of the study, two rats from each group were placed in metabolic cages for 24 h and their urine was collected. At the end of the study, the rats were killed and their blood was collected from the vena cava inferior. The right kidneys of the rats were used for biochemical and the left ones for immunohistochemical analyzes. Malondialdehyde (MDA), catalase, urea, calcium, oxalate, and creatinine clearance were studied in the blood, urine, and kidney tissues. Moreover, routine histological evaluation, and p38-MAPK and NFkB immunohistochemical analyses were conducted.

Results

In the hyperoxaluria group, urinary oxalate levels were higher than the control group; yet, lower in the treatment group compared to hyperoxaluria group (p < 0.05). Serum MDA levels in the hyperoxaluria group were higher than the control group; but in the treatment group it is lower than the hyperoxaluria group (p < 0.05). P38 MAPK activity was higher in the hyperoxaluria group compared to the control (p < 0.05). However, in terms of p38 MAPK activity, there were no statistically significant difference between hyperoxaluria and the treatment group (p < 0.069). Whereas NFkB activity in the hyperoxaluria group is higher than the control (p < 0.001), no statistically significant difference was observed with the treatment group.

Conclusions

In the present study, resveratrol was seen to prevent hyperoxaluria. With preventing oxidative stress factors and Randall plaque formation caused by free oxygen radicals, resveratrol can be an alternative treatment option that can increase the success rate in preventing stone recurrence in the future.

Keywords

Calcium oxalate Ethylene glycol Hyperoxaluria Rat Resveratrol 

Abbreviations

EG

Ethylene glycol

RES

Resveratrol

MDA

Malondialdehyde

MAPK

Mitogen activated protein kinase

NFkB

Nuclear factor kappa B

CaOx

Calcium oxalate

SOD

Superoxide dismutase

ROS

Reactive oxygen species

TBARS

Thiobarbituric acid reactive substance

JNK

C-Jun N-terminal kinase

AP-1

Active protein-1

OPN

Osteopontin

XO

Xanthine oxidase

TNF

Tumor necrosis factor

PKC

Protein kinase C

SPSS 11.0

Statistical Package for Social Sciences 11.0

CAT

Catalase

ESWL

Extra shock wave lithotripsy

Notes

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interests.

Ethical approval

All applicable international, national, and/or institutional guidelines for the care and use of animals were followed. The study design was approved by the Süleyman Demirel University Animal Experiments Local Ethic Board, Turkey.

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Copyright information

© Springer Science+Business Media Dordrecht 2017

Authors and Affiliations

  • Taylan Oksay
    • 1
  • Sedat Yunusoğlu
    • 2
  • Mustafa Calapoğlu
    • 3
  • İ. Aydın Candan
    • 4
  • İbrahim Onaran
    • 5
  • Osman Ergün
    • 6
  • Alper Özorak
    • 1
  1. 1.Department of Urology, Medical FacultySüleyman Demirel UniversityIspartaTurkey
  2. 2.Department of UrologyAfyonkarahisar State HospitalAfyonkarahisarTurkey
  3. 3.Department of Biochemistry, Medical FacultySuleyman Demirel UniversityIspartaTurkey
  4. 4.Department of Histology and Embryology, Medical FacultySüleyman Demirel UniversityIspartaTurkey
  5. 5.Department of Medical Biology, Medical FacultySüleyman Demirel UviversityIspartaTurkey
  6. 6.Department of Urology, Urology PoliclinicKonya Training and Research HospitalMeramTurkey

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