Issue 73, 2016, Issue in Progress

Stable isotope analysis of dietary arginine accrual and disposal efficiency in male rats fed diets with different protein content

Abstract

The administration of diets with different protein/energy ratios induce variable but distinctive responses in rats; an excessive protein content tends to decrease fat accumulation, but reversion of this ratio tends to increase adipose tissue mass. The fate of N derived from amino acid metabolism is not only dependent on energy and dietary protein; the increased excretion of urea elicited by high-protein diets contrasts with the lower urea excretion (despite excess dietary protein and energy) in rats fed a cafeteria diet. After one month of exposure to high-protein (HPD) or cafeteria (CD) diets, we administered a gavage of 15N-arginine to undisturbed adult male rats, in order to trace the utilization of this not-recyclable-N amino acid under diets with different protein/energy relationships. Rats fed a high-protein diet excreted higher amounts of N in urine and showed much lower gastrointestinal content of the label. The CD rats decreased the excretion of urine N. Both groups' N balance showed a significant proportion of N not-accounted-for (but excreted nevertheless), the proportion being especially large in the HPD group. In conclusion, the process of disposal of amino acid N through the so far unknown pathway for “non-accounted-for N” is, thus essentially dependent on excess amino acid availability; independently of urea cycle operation and diet energy content.

Graphical abstract: Stable isotope analysis of dietary arginine accrual and disposal efficiency in male rats fed diets with different protein content

Supplementary files

Article information

Article type
Paper
Submitted
28 Apr 2016
Accepted
02 Jul 2016
First published
14 Jul 2016

RSC Adv., 2016,6, 69177-69184

Stable isotope analysis of dietary arginine accrual and disposal efficiency in male rats fed diets with different protein content

F. Rotondo, T. Sanz, J. Fernández-López, M. Alemany and X. Remesar, RSC Adv., 2016, 6, 69177 DOI: 10.1039/C6RA11039H

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