Literature DB >> 7406567

Muscle and plasma amino acids following injury. Influence of intercurrent infection.

J Askanazi, Y A Carpentier, C B Michelsen, D H Elwyn, P Furst, L R Kantrowitz, F E Gump, J M Kinney.   

Abstract

The present study was undertaken to determine intracellular amino acid patterns in patients with multiple trauma, whether or not complicated by sepsis and during convalescence. A percutaneous muscle biopsy was performed three to four days following major accidental injury in ten patients and analyzed for muscle free amino acids. Venous blood was drawn at the time of the biopsy and analyzed for plasma free amino acids. Five patients developed sepsis and a repeat biopsy was performed on days 8 to 11. In five of the patients a biopsy was performed during the late convalescent period (anabolic phase). A marked depletion of nonessential amino acids in muscle occurred in both injury and sepsis due to a decrease (50%) in glutamine, which was equally marked in both states. The essential amino acids in muscle increased in injury. During sepsis, a further increase was observed with a return toward normal in the convalescent period. In injury, the most marked rise was in the branched-chain amino acids, phenylalanine, tryosine and methionine. With sepsis, a further rise in muscle branched-chain amino acids, phenylalanine and tryosine occurred, while plasma levels remain unchanged. During convalescence, muscle glutamine, arginine, histidine and plasma branched-chain amino acids were below normal, whereas muscle phenylalanine and methionine were elevated. The muscle free amino acid pattern observed after major trauma was essentially the same as earlier described following elective operation. This suggests a common response of intracellular amino acids irrespective of the degree of injury, and may indicate that the pump settings which regulate amino acid transport follow the "all or none" rule. The high intracellular levels of branched-chain amino acids in sepsis suggest that the energy deficit of this state is due to an impairment of substrate use rather than intracellular availability. The high concentrations of the aromatic amino acids and methionine may be due to altered liver function. During the late convalescent period (anabolic phase) the low levels of certain key amino acids suggests inadequate nutrition. The difficulties in nourishing the injured or septic patient are well recognized. The period following these catabolic states may be an important period for the application of an optimal, aggressive nutritional regimen.

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Year:  1980        PMID: 7406567      PMCID: PMC1344810          DOI: 10.1097/00000658-198007000-00014

Source DB:  PubMed          Journal:  Ann Surg        ISSN: 0003-4932            Impact factor:   12.969


  40 in total

1.  Plasma free aminoacid pattern in protein-calorie malnutrition. Reappraisal of its diagnostic value.

Authors:  S J Saunders; A S Truswell; G O Barbezat; W Wittman; J D Hansen
Journal:  Lancet       Date:  1967-10-14       Impact factor: 79.321

2.  Measurement of body water and intracellular electrolytes by means of muscle biopsy.

Authors:  J A Graham; J F Lamb; A L Linton
Journal:  Lancet       Date:  1967-12-02       Impact factor: 79.321

3.  Studies of tryptophan metabolism in experimental animals and man during infectious illness.

Authors:  M I Rapoport; W R Beisel
Journal:  Am J Clin Nutr       Date:  1971-07       Impact factor: 7.045

4.  Oxidation of leucine by rat skeletal muscle.

Authors:  R Odessey; A L Goldberg
Journal:  Am J Physiol       Date:  1972-12

5.  Metabolic effects of intracellular infections in man.

Authors:  W R Beisel; W D Sawyer; E D Ryll; D Crozier
Journal:  Ann Intern Med       Date:  1967-10       Impact factor: 25.391

6.  A lithium buffer system for accelerated single-column amino acid analysis in physiological fluids.

Authors:  C P Kedenburg
Journal:  Anal Biochem       Date:  1971-03       Impact factor: 3.365

7.  Tissue composition of weight loss in surgical patients. I. Elective operation.

Authors:  J M Kinney; C L Long; F E Gump; J H Duke
Journal:  Ann Surg       Date:  1968-09       Impact factor: 12.969

8.  In vivo uptake of [14C]leucine by skeletal muscle ribosomes after injury in rats fed two levels of protein.

Authors:  V R Young; P C Huang
Journal:  Br J Nutr       Date:  1969-06       Impact factor: 3.718

9.  Tissue amino acid flux after exposure of rats to Diplococcus pneumoniae.

Authors:  R W Wannemacher; M C Powanda; R S Pekarek; W R Beisel
Journal:  Infect Immun       Date:  1971-11       Impact factor: 3.441

10.  Plasma amino acids in normal humans and patients with shock.

Authors:  E H LaBrosse; J A Beech; J S McLaughlin; A R Mansberger; W D Keene; R A Cowley
Journal:  Surg Gynecol Obstet       Date:  1967-09
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  61 in total

1.  Polyamines mediate glutamine-dependent induction of the intestinal epithelial heat shock response.

Authors:  Yuji Iwashita; Toshio Sakiyama; Mark W Musch; Mark J Ropeleski; Hirohito Tsubouchi; Eugene B Chang
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2011-04-21       Impact factor: 4.052

2.  Early hemorrhage triggers metabolic responses that build up during prolonged shock.

Authors:  Angelo D'Alessandro; Hunter B Moore; Ernest E Moore; Matthew Wither; Travis Nemkov; Eduardo Gonzalez; Anne Slaughter; Miguel Fragoso; Kirk C Hansen; Christopher C Silliman; Anirban Banerjee
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2015-04-15       Impact factor: 3.619

Review 3.  Ischemia-reperfusion injury of the intestine and protective strategies against injury.

Authors:  Ismail Hameed Mallick; Wenxuan Yang; Marc C Winslet; Alexander M Seifalian
Journal:  Dig Dis Sci       Date:  2004-09       Impact factor: 3.199

4.  Branched chain amino acid uptake and muscle free amino acid concentrations predict postoperative muscle nitrogen balance.

Authors:  D J Johnson; Z M Jiang; M Colpoys; C R Kapadia; R J Smith; D W Wilmore
Journal:  Ann Surg       Date:  1986-11       Impact factor: 12.969

5.  Hypothermic anesthesia attenuates postoperative proteolysis.

Authors:  D J Johnson; D C Brooks; V M Pressler; N R Hulton; M F Colpoys; R J Smith; D W Wilmore
Journal:  Ann Surg       Date:  1986-10       Impact factor: 12.969

6.  Immunostimulating effect of oral glutamine.

Authors:  M R Gismondo; L Drago; M C Fassina; I Vaghi; R Abbiati; E Grossi
Journal:  Dig Dis Sci       Date:  1998-08       Impact factor: 3.199

7.  Glutamine Regulates Cardiac Progenitor Cell Metabolism and Proliferation.

Authors:  Joshua K Salabei; Pawel K Lorkiewicz; Candice R Holden; Qianhong Li; Kyung U Hong; Roberto Bolli; Aruni Bhatnagar; Bradford G Hill
Journal:  Stem Cells       Date:  2015-05-26       Impact factor: 6.277

8.  A randomized trial of intravenous glutamine supplementation in trauma ICU patients.

Authors:  Jon Pérez-Bárcena; Pedro Marsé; Arturo Zabalegui-Pérez; Esther Corral; Rubén Herrán-Monge; María Gero-Escapa; Mercedes Cervera; Juan Antonio Llompart-Pou; Ignacio Ayestarán; Joan Maria Raurich; Antonio Oliver; Antonio Buño; Abelardo García de Lorenzo; Guiem Frontera
Journal:  Intensive Care Med       Date:  2014-02-21       Impact factor: 17.440

Review 9.  Impact of nutrition on muscle mass, strength, and performance in older adults.

Authors:  A Mithal; J-P Bonjour; S Boonen; P Burckhardt; H Degens; G El Hajj Fuleihan; R Josse; P Lips; J Morales Torres; R Rizzoli; N Yoshimura; D A Wahl; C Cooper; B Dawson-Hughes
Journal:  Osteoporos Int       Date:  2012-12-18       Impact factor: 4.507

10.  Time course changes in blood metabolites during endotoxin fever in sheep.

Authors:  B G Southorn; J R Thompson
Journal:  Can J Vet Res       Date:  1986-07       Impact factor: 1.310

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