Intestinal lysine metabolism is driven by the enteral availability of dietary lysine in piglets fed a bolus meal

Cécile Bos, Barbara Stoll, Hélène Fouillet, Claire Gaudichon, Xinfu Guan, Michael A. Grusak, Peter J. Reeds, Daniel Tomé, Douglas G. Burrin
2003 American Journal of Physiology. Endocrinology and Metabolism  
Intestinal lysine metabolism is driven by the enteral availability of dietary lysine in piglets fed a bolus meal. Am J Physiol Previous steady-state continuous-feeding studies have shown that the gut mucosa removes substantial amounts of both dietary and systemic amino acids. However, enteral nutrition is often given under non-steady-state conditions as a bolus meal, and this has been shown to influence systemic metabolism. Therefore, our aim was to quantify the relative metabolism of dietary
more » ... d systemic lysine by the portal-drained viscera (PDV) under non-steady-state conditions after a single bolus meal. Five 28-day-old piglets implanted with arterial, venous, and portal catheters and with an ultrasonic portal flow probe were given an oral bolus feeding of a milk formula containing a trace quantity of intrinsically 15 N-labeled soy protein and a continuous intravenous infusion of [U-13 C]lysine for 8 h. Total lysine use by the PDV was maximal 1 h after the meal (891 mol ⅐ kg Ϫ1 ⅐ h Ϫ1 ) and was predominantly of dietary origin (89%), paralleling the enteral delivery of dietary lysine. Intestinal lysine use returned to a low level after 4 h postprandially and was derived exclusively from the arterial supply until 8 h. Cumulative systemic appearance of dietary lysine reached 44 and 80% of the ingested amount 4 and 8 h after the meal, respectively, whereas the PDV first-pass use of dietary lysine was 55 and 32% of the intake for these two periods, respectively. We conclude that the first-pass utilization rate of dietary lysine by the PDV is directly increased by the enteral lysine availability and that it is higher with a bolus than with continuous oral feeding. amino acid metabolism; dietary amino acids; portal-drained viscera; nonsteady state
doi:10.1152/ajpendo.00150.2003 pmid:12851176 fatcat:gifrgmeomvedfog54hs5vbvbse