BACKGROUND: In response to injury, muscle catabolism can be extensive, and in theory, the wound consumes amino acids to support healing. The purpose of this study is to assess a technique by which in vivo protein kinetics of muscle, wound, and normal skin can be quantified in burn-injured patients. METHODS: Study protocol consisting of infusion of d5 phenylalanine; biopsies of skeletal muscle, skin, and donor-site wound on the leg; quantification of blood flow to total leg, wound, and skin; and sequential blood sampling from the femoral artery and vein. Five-compartment modeling was used to quantify the rates of protein synthesis, breakdown, and phenylalanine transport between muscle, wound, and skin. RESULTS: The study results demonstrated a net release of phenylalanine from muscle yet a net consumption of phenylalanine by the wound. Compared with skin, the wound had a substantially increased rate of protein synthesis and a reduced rate of protein breakdown (p < .01). Transport rates into and out of muscle were significantly higher than those for wound (p < .01). CONCLUSIONS: This novel methodology enables in vivo quantification of the integrated response of muscle, wound, and skin protein/amino acid metabolism and confirms the long-held theory of a net catabolism of muscle and a net anabolism of wound protein in patients after injury. This methodology can be used to assess the metabolic impact of such measures as nutrition, pharmacologic agents, and surgical procedures.
BACKGROUND: In response to injury, muscle catabolism can be extensive, and in theory, the wound consumes amino acids to support healing. The purpose of this study is to assess a technique by which in vivo protein kinetics of muscle, wound, and normal skin can be quantified in burn-injured patients. METHODS: Study protocol consisting of infusion of d5 phenylalanine; biopsies of skeletal muscle, skin, and donor-site wound on the leg; quantification of blood flow to total leg, wound, and skin; and sequential blood sampling from the femoral artery and vein. Five-compartment modeling was used to quantify the rates of protein synthesis, breakdown, and phenylalanine transport between muscle, wound, and skin. RESULTS: The study results demonstrated a net release of phenylalanine from muscle yet a net consumption of phenylalanine by the wound. Compared with skin, the wound had a substantially increased rate of protein synthesis and a reduced rate of protein breakdown (p < .01). Transport rates into and out of muscle were significantly higher than those for wound (p < .01). CONCLUSIONS: This novel methodology enables in vivo quantification of the integrated response of muscle, wound, and skin protein/amino acid metabolism and confirms the long-held theory of a net catabolism of muscle and a net anabolism of wound protein in patients after injury. This methodology can be used to assess the metabolic impact of such measures as nutrition, pharmacologic agents, and surgical procedures.
Authors: Victoria G Rontoyanni; Ioannis Malagaris; David N Herndon; Eric Rivas; Karel D Capek; Anahi D Delgadillo; Nisha Bhattarai; Armando Elizondo; Charles D Voigt; Celeste C Finnerty; Oscar E Suman; Craig Porter Journal: Shock Date: 2018-08 Impact factor: 3.454
Authors: Robert Kraft; Gabriela A Kulp; David N Herndon; Fatemah Emdad; Felicia N Williams; Hal K Hawkins; Katrina R Leonard; Marc G Jeschke Journal: Pediatr Crit Care Med Date: 2011-11 Impact factor: 3.624
Authors: Ioannis Malagaris; David N Herndon; Efstathia Polychronopoulou; Victoria G Rontoyanni; Clark R Andersen; Oscar E Suman; Craig Porter; Labros S Sidossis Journal: Clin Nutr Date: 2018-06-04 Impact factor: 7.324
Authors: Craig Porter; David N Herndon; Elisabet Børsheim; Nisha Bhattarai; Tony Chao; Paul T Reidy; Blake B Rasmussen; Clark R Andersen; Oscar E Suman; Labros S Sidossis Journal: J Burn Care Res Date: 2016 Jan-Feb Impact factor: 1.845
Authors: Craig Porter; Matthew Cotter; Eva C Diaz; Kristofer Jennings; David N Herndon; Elisabet Børsheim Journal: J Trauma Acute Care Surg Date: 2013-06 Impact factor: 3.313