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Am J Physiol Endocrinol Metab 268: E446-E452, 1995;
0193-1849/95 $5.00
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AJP - Endocrinology and Metabolism, Vol 268, Issue 3 E446-E452, Copyright © 1995 by American Physiological Society

ARTICLES

Metabolism of R-beta-hydroxypentanoate and of beta-ketopentanoate in conscious dogs

J. Leclerc, C. Des Rosiers, J. A. Montgomery, J. Brunet, L. Ste-Marie, M. W. Reider, C. A. Fernandez, L. Powers, F. David and H. Brunengraber
Department of Nutrition, Universite de Montreal, Canada.

R-beta-Hydroxypentanoate and beta-ketopentanoate are homologues of physiological ketone bodies R-beta-hydroxybutyrate and acetoacetate. They derive from the oxidation in liver of the R-moiety of R,S-1,3-pentanediol, a potential nutrient. This report documents the metabolism of R-beta-hydroxypentanoate and beta-ketopentanoate in conscious dogs. Whether administered by bolus or constant infusion, the two substrates are interconverted and rapidly metabolized. When beta-ketopentanoate was infused at a rate corresponding to 75% of the dog's caloric requirement, the steady-state total plasma concentration of the two substrates was only 1.3 mM. Because the substrates are precursors of propionyl-CoA, we assayed the urinary concentrations of markers of propionic acidemia. Their accumulation was minor compared with what is observed in patients suffering from propionic acidemia. We conclude that, at least during short-term experiments, R-beta-hydroxypentanoate and beta-ketopentanoate are well metabolized in the dog without apparent intolerance to a large supply of propionyl-CoA.


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