The influence of oxalate decarboxylase on the urinary oxalate excretion in swine model of nephrocalcinosis induced by hydroxyproline

Authors

  • Kateryna Pierzynowska Department of Biology, Lund University, Sölvegatan 35, 223 62 Lund, Sweden; Anara AB &SGPlus, Alfågelgranden 24, 23132 Trelleborg, Sweden https://orcid.org/0000-0002-3290-339X
  • Stefan Grzegorz Pierzynowski Department of Biology, Lund University, Sölvegatan 35, 223 62 Lund, Sweden; Anara AB &SGPlus, Alfågelgranden 24, 23132 Trelleborg, Sweden; Department of Medical Biology, Institute of Rural Health, Jaczewskiego 2, 20-950 Lublin, Poland https://orcid.org/0000-0002-2974-6557
  • Liudamyla Lozinska Department of Biology, Lund University, Sölvegatan 35, 223 62 Lund, Sweden; Anara AB &SGPlus, Alfågelgranden 24, 23132 Trelleborg, Sweden https://orcid.org/0000-0001-7211-7054
  • Sara Jarmakiewicz Department of Gastroenterology with IBD Unit of Clinical Hospital 2 Lwowska 60, Poland affiliated to the University of Rzeszow, Poland https://orcid.org/0000-0001-6896-4744
  • Paulina Świeboda Department of Biology, Lund University, Sölvegatan 35, 223 62 Lund, Sweden
  • Olexandr Fedkiv Department of Biology, Lund University, Sölvegatan 35, 223 62 Lund, Sweden https://orcid.org/0000-0003-1231-1423
  • Katarzyna Szwiec Department of Biology, Lund University, Sölvegatan 35, 223 62 Lund, Sweden
  • Jose Louis Valverde Piedra Department of Medical Biology, Institute of Rural Health, Jaczewskiego 2, 20-950 Lublin, Poland https://orcid.org/0000-0003-2916-946X
  • Rafał Filip Department of Biochemistry and Animal Physiology, University of Life Sciences, 20-950 Lublin, Poland; Department of Gastroenterology with IBD Unit of Clinical Hospital 2 Lwowska 60, Poland affiliated to the University of Rzeszow, Poland https://orcid.org/0000-0002-5954-151X

DOI:

https://doi.org/10.15584/ejcem.2017.3.4

Keywords:

Nephrocalcinosis, Oxalate decarboxylase, Hydroxyproline, Pig model

Abstract

Introduction. Kidney stone formation may be a result of increased urinary oxalate supersaturation.

Material and methods. Eighteen pigs were randomly divided into: Control group, where standard cereal-based feed was supplemented with 4% HP only, Prevention group, where treatment with OxDc slurry started at the end of the adaptation period when pigs were switched to 4% HP diet, Reduction group, where the treatment with OxDc lyo powder started after pigs were already on a 4% HP diet for 6 days.

Results. OxDc slurry prevented oxalate excretion in urine. The reduction effect of OxDc lyo feed addition was generally visible during the first two days of the therapy (p<0.05). Both dietary intake of 4% HP and OxDc preparations did not influence weight gain, water or feed intake, urine excretion and creatinine clearance.

Conclusion. The capacity of OxDc in preventing induced hyperoxaluria was moderate. Most probably, this is due to the incoherent response of animals to the HP enriched diet dependent on their gut pH, since optimum pH for OxDc is around 5-6. A higher pH essentially reduces the activity of OxDc. The capacity of OxDc in reversing the hyperoxaluria induced by a HP enriched diet was significant during the first 2 days after introducing OxDc to the diet.

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References

Khan SR. Nephrocalcinosis in animal models with and without stones. Urol Res. 2010;38(6):429-438.

Hope B, Kemper MJ, Bökenkamp A, et al. Plasma oxalate calcium supersaturation in children with primary hyperoxaluria and end stage renal failure. Kidney Int. 1999;56(1):268-274.

Knight J, Jiang J, Assimos DG, Holmes RP. Hydroxyproline ingestion and urinary oxalate and glycolate excretion. Kidney Int. 2006;70(11):1929-1934.

Mendel NS, Henderson JR, Hung LY, Wille D, Wiessner JH. A porcine model of calcium oxalate kidney stone disease. J Urol. 2004;171(3):1301-1303.

Kaplon DM, Penniston KL, Darriet C, Crenshaw TD, Nakada SY. Hydroxyproline-induced hyperoxaluria using acidified and traditional diets in the porcine model. J Endourol. 2010;24(3):355-359.

Grujic D, Salido EC, Shenoy BC, et al. Hyperoxaluria is reduced and nephrocalcinosis prevented with an oxalate-degrading enzyme in mice with hyperoxaluria. Am J Nephrol. 2009;29(2):86-93.

Hatch M, Freel RW. Alterations in intestinal transport of oxalate in disease states. Scanning Microsc. 1995;9(4):1121-1126.

Mandel NS, Henderson JR, Hung LY, Wille D, Wiessner JH. A porcine model of calcium oxalate kidney stone disease. J Urol. 2004;171:1301–1303.

Khan SR, Glenton PA, Byer KJ. Modeling of hyperoxaluric calcium oxalate nephrolithiasis: Experimental induction of hyperoxaluria by hydroxy-L-proline. Kidney Int. 2006;70:914–923.

Goncharova K, Filip R, Świeboda P, et al. Model development of hydroxyproline induced hyperoxaluria in young growing pigs. Eur J Clin Exp Med. 2017;15(1):6–11.

Bushinsky DA, Asplin JR, Grynpas MD, et al. Calcium oxalate stone formation in genetic hypercalciuric stone forming rats. Kidney Int. 2002;61:975. of patients with Rheumatoid Arthritis. Ann Acad Med Bialost. 2005;50:170-173.

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Published

2017-09-30

How to Cite

Pierzynowska, K., Pierzynowski, S. G., Lozinska, L., Jarmakiewicz, S., Świeboda, P., Fedkiv, O., Szwiec, K., Valverde Piedra, J. L., & Filip, R. (2017). The influence of oxalate decarboxylase on the urinary oxalate excretion in swine model of nephrocalcinosis induced by hydroxyproline. European Journal of Clinical and Experimental Medicine, 15(3), 206–216. https://doi.org/10.15584/ejcem.2017.3.4

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