Abstract
Urinary oxalate is supposedly derived from three sources: the diet (10–20%), ascorbate breakdown (40–50%) and endogenous metabolism (40–50%)1. Factors influencing oxalate excretion remain poorly defined. Endogenous metabolism, which appears to occur predominantly in the liver, is thought to involve amino acid catabolism1. Therefore, dietary protein as a source of amino acid may influence urinary oxalate excretion. However, studies with humans have not been conclusive. We have used a guinea pig model to further study the effects of dietary protein on urinary oxalate excretion. This animal model was chosen since the guinea pig, like humans, has a key biosynthetic enzyme, alanine-glyoxylate aminotransferase type I (AGT), located only in peroxisomes2. Guinea pigs were fed semi-purified diets containing 10, 20% or 40% of casein based protein. Urinary oxalate was monitored and hepatic AGT, glycolate oxidase (GO) and lactate dehydrogenase (LDH) levels were measured. Since glucagon is a known mediator of dietary protein metabolism, the effects of pharmacologic doses of this hormone on urinary oxalate excretion and hepatic enzyme levels were also examined.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
HE Williams and TR Wandzilak, Oxalate synthesis, transport and the hyperoxaluric syndromes, J Urol 141: 742–747 (1989).
S Hayashi and T Noguchi, Alanine: glyoxylate aminotransferase 1 is present in the peroxisomes of guinea pig kidney, Biochem Biophys Res Comm 166: 1467–1470 (1990).
MA Reid, and GM Briggs, Development of a semi-synthetic diet for young guinea pigs, J Nutr 51: 341–354 (1953).
T Noguchi and S Fujiwara, Identification of mammalian am in otransferases utilizing glyoxylate or pyruvate as amino acceptor, J Bio Chem 263: 182–186 (1988).
Y Lindquist and CI Branden, Preliminary crystallographic data for glycolate oxidase from spinach. J Biol Chem 254: 7403–7404 (1979).
RP Holmes, LJ Hart and DG Assimos, The effects of protein intake on oxalate excretion, J Urol 147: 329A (1992).
J Peret, S Foustock, M Chanez, B Bois-Joyeux and R Assan, Plasma glucagon and insulin concentrations and hepatic phosphoenolpyruvate carboxykinase and pyruvate kinase activities during and upon adaptation of rats to a high protein diet, J Nutr 111: 1173–1184 (1981).
G Boden, L Tappy, F Jadali, RD Hoeldtke, I Rezvani and OE Owen, Role of glucagon in disposal of an amino acid load, Am J Physiol 259: E225–E232 (1990).
CJ Danpure and PR Jennings, Peroxisomal alanine: glyoxylate aminotransferase deficiency in primary hyperoxaluria type I, FEBS Lett 201: 20–24 (1986).
S Hayashi, H Sakuraba and T Noguchi, Response of hepatic alanine: glyoxylate amino transferase I to hormones differs among mammalia, Biochem Biophys Res Comm 165: 372–376. (1989).
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1994 Springer Science+Business Media New York
About this chapter
Cite this chapter
Holmes, R.P., Hurst, C.H., Assimos, D.G. (1994). The Effect of Dietary Protein and Glucagon on the Urinary Excretion of Oxalate in the Guinea Pig. In: Ryall, R., Bais, R., Marshall, V.R., Rofe, A.M., Smith, L.H., Walker, V.R. (eds) Urolithiasis 2. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-2556-1_36
Download citation
DOI: https://doi.org/10.1007/978-1-4615-2556-1_36
Publisher Name: Springer, Boston, MA
Print ISBN: 978-1-4613-6091-9
Online ISBN: 978-1-4615-2556-1
eBook Packages: Springer Book Archive