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FUNCTION OF THE KIDNEYS UNDER CONDITIONS OF EXPERIMENTAL OXALATE NEPHROLITHIASIS

https://doi.org/10.24884/1561-6274-2008-12-1-69-74

Abstract

THE AIM of the investigation was to study kidney functions in rats under conditions of experimental oxalate nephrolithiasis. MATERIAL AND METHODS. Male Wistar rats were given drinking water with 1% solution of ethylene glycol during 3 weeks. The concentration of oxalate, calcium and phosphorus was determined in daily urine. Activity of marker enzymes lactate dehydrogenase (LDG), γ-glutamil transferase (GGT) and N-acetyl-β-D-glucosaminidase (NAG) was also determined. The presence of calcium-positive deposits on kidney slices was determined by the Koss histological method. RESULTS. Daily using ethylene glycol by rats was followed by the development of hyperoxaluria, which was due to increased formation of oxalate ions in the liver and appearance of oxalate supersaturation in tubule urine. In the experiments it was shown that enzymatic activation of urine against the background of ethylene glycol was substantially increased. Activity of NAG became 20 times higher, GGT – 3.7 times higher. LDG activity which had become 7.5 times higher by the end of the first week, then gradually returned to the initial level. These changes are evidence of injuries to the tubule cell membranes, followed by cytolysis and of pronounced impairment of the renal tubule function. Morphological investigation of kidney slices has detected numerous calcium-positive deposits localized mainly on the renal papilla surface. CONCLUSION. Experiments with continuous intake by rats of ethylene glycol have given an irrefutable proof of progression of calcium-oxalate nephrolithiasis. It points to the developed hyperoxaluria, fermenturia and the presence of calcium positive inclusions on the renal papilla surface. The above changes are signs of experimental urolithiasis in rats.

About the Authors

V. M. Bryukhanov
Алтайский государственный медицинский университет
Russian Federation


Ya. F. Zverev
Алтайский государственный медицинский университет
Russian Federation


V. V. Lampatov
Алтайский государственный медицинский университет
Russian Federation


A. Yu. Zharikov
Алтайский государственный медицинский университет
Russian Federation


O. V. Azarova
Алтайский государственный медицинский университет
Russian Federation


Yu. G. Motin
Алтайский государственный медицинский университет
Russian Federation


References

1. Тиктинский ОЛ, Александров ВП. Мочекаменная болезнь. Питер, СПб., 2000; 3-12

2. Coe FL, Evan A, Worcester E. Kidney stone disease. J Clin Invest 2005; 115 (10): 2598-2608

3. Daudon M. Epidemiology of nephrolithiasis in France. Ann Urol (Paris) 2005; 39 (6): 209-231

4. Khan SR, Hackett RL. Calcium oxalate urolithiasis in the rat: is it a model for human stone disease? A review of recent literature. Scan Electron Microsc 1985; Pt 2: 759-774

5. Kumar S, Sigmon D, Miller T et al. A new model of nephrolithiasis involving tubular dysfunction/injury. J Urol 1991; 146 (5): 1384-1389

6. Khan SR. Animal models of kidney stone formation: an analysis. World J Urol 1997; 15 (4): 236-243

7. Hennequin C, Tardivel S, Medetognon J et al. A stable animal model of diet-induced calcium oxalate crystalluria. Urol Res 1998; 26 (1): 57-63

8. Bushinsky DA, Asplin JR, Grynpas MD et al. Calcium oxalate stone formation in genetic hypercalciuric stone-forming rats. Kidney Int 2002; 61: 975-987

9. Khan SR, Glenton PA, Byer KJ. Modeling of hyperoxaluric calcium oxalate nephrolithiasis: experimental induction of hyperoxaluria by hydroxyl-L-proline.Kidney Int 2006; 70 (5): 914-923

10. Maruch D. Rapid colorimetric assay of β-galactosidase and N-acetyl-β-glucosaminidase in human urine. Clin Chim Acta 1976; 73 : 453-446

11. Thamilselvan S, Hackett RL, Khan SR. Lipid peroxidation in ethylene glycol induced hyperoxaluria and calcium oxalate nephrolithiasis. J Urol 1997; 157 (3): 1059-1063

12. Green ML, Hatch M, Freel RW. Ethylene glycol induces hyperoxaluria without metabolic acidosis in rats. Am J Physiol Renal Physiol 2005; 289: F536-F543

13. Poore RE, Hurst CH, Assimos DG, Holmes RP. Pathways of hepatic oxalate synthesis and their regulation. Am J Physiol 1997; 1: 289-294

14. Бабаева НИ, Липицкая ИЯ, Творогова МГ, Титов ВИ. Диагностическое значение исследования активности N-ацетил-β-D-глюкозаминидазы в моче (обзор литературы). Лаб дело 1991; 1: 9-16

15. Фидиркин АВ, Неймарк АИ, Звягинцев ЕН, Симонова ОГ. Экскреция оксалатов и активность некоторых ферментов мочи у лиц, страдающих мочекаменной болезнью. В: Перспективные методы функциональной диагностики. Барнаул, 1994; 132

16. de Water R, Boeve ER, van Miert PP et al. Experimental nephrolithiasis in rats: the effect of ethylene glycol and vitamin D3 on the induction of renal calcium oxalate crystals. Scanning Microsc 1996; 10 (2): 591-601

17. Bazzi C, Petrini C, Rizza V et al. Urinary N-acetyl-β-glucosaminidase excretion is a marker of tubular cell dysfunction and a predictor of outcome in primary glomerulonephritis. Nephrol Dial Transplant 2002; 17 (11): 1890-1896

18. Sikora P, Glatz S, Beck BB et al. Urinary NAG in children with urolithiasis, nephrocalcinosis, or risk of urolithiasis. Pediatr Nephrol 2003; 18 (10): 996-999

19. Yamaguchi S, Wiessner JH, Hasegawa AT et al. Study of a rat model for calcium oxalate crystal formation without severe renal damage in selected conditions. Int J Urol 2005; 12 (3): 290-298

20. Skalova S, Kutilek S. Renal tubular impairment in children with idiopathic hypercalciuria. Acta Medica (Hradec Kralove) 2006; 49 (2): 109-111

21. Muthukumar A, Selvan R. Renal injury mediated calcium oxalate nephrolithiasis: role of lipid peroxidation. Ren Fail 1997; 19 (3): 401-408

22. Veena CK, Josephine A, Preetha SP et al. Renal peroxidative changes mediated by oxalate: the protective role of fucaidan. Life Sci 2006; 79 (19): 1789-1795

23. Thamilselvan S, Hackett RL, Khan SR. Cells of proximal and distal tubular origin respond differently to challenges of oxalate and calcium oxalate crystals. J Am Soc Nephrol 1999; 10 [Suppl 14]: S452-S456

24. Thamilselvan S, Khan SR, Menon M. Oxalate and calcium oxalate mediated free radical toxicity in renal epithelial cells: effect of antioxidants. Urol Res 2003; 31 (1): 3-9

25. Rashed T, Menon M, Thamilselvan S. Molecular mechanism of oxalate-induced free radical production and glutathione redox imbalance in renal epithelial cells: effect of antioxidants. Am J Nephrol 2004; 24 (5): 557-568

26. Green ML, Freel RW, Hatch M. Lipid peroxidation is not the underlying cause of renal injury in hyperoxaluric rats. Kidney Int 2005; 68 (6): 2629-2638


Review

For citations:


Bryukhanov V.M., Zverev Ya.F., Lampatov V.V., Zharikov A.Yu., Azarova O.V., Motin Yu.G. FUNCTION OF THE KIDNEYS UNDER CONDITIONS OF EXPERIMENTAL OXALATE NEPHROLITHIASIS. Nephrology (Saint-Petersburg). 2008;12(1):69-74. (In Russ.) https://doi.org/10.24884/1561-6274-2008-12-1-69-74

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ISSN 1561-6274 (Print)
ISSN 2541-9439 (Online)