Effect of Infused Branched-Chain Amino Acids on Muscle and Whole-Body Amino Acid Metabolism in Man
- 1 November 1990
- journal article
- research article
- Published by Portland Press Ltd. in Clinical Science
- Vol. 79 (5) , 457-466
- https://doi.org/10.1042/cs0790457
Abstract
1. Using the forearm balance method, together with systemic infusions of L-[ring-2,6-3H]phenylalanine and L-[1-14C]leucine, we examined the effects of infused branched-chain amino acids on whole-body and skeletal muscle amino acid kinetics in 10 postabsorptive normal subjects; 10 control subjects received only saline. 2. Infusion of branched-chain amino acids caused a four-fold rise in arterial branched-chain amino acid levels and a two-fold rise in branched-chain keto acids; significant declines were observed in circulating levels of most other amino acids, including phenylalanine, which fell by 34%. Plasma insulin levels were unchanged from basal levels (8 .+-. 1 .mu.-units/ml). 3. Whole-body phenylalanine flux, an index of proteolysis, was significantly suppressed by branched-chain amino acid infusion (P < 0.002), and forearm phenylalanine production was also inhibited (P < 0.03). With branched-chain amino acid infusion total leucine flux rose, with marked increments in both oxidative and nonoxidative leucine disposal (P < 0.001). Proteolysis, as measured by endogenous leucine production, showed a modest 12% decrease, although this was not significant when compared with saline controls. The net forearm balance of leucine and other branched-chain amino acids changed from a basal net output to a marked net uptake (P < 0.001) during branched-chain amino acid infusion, with significant of local leucine disposal. Despite the rise in whole-body non-oxidative leucine disposal, and in forearm leucine uptake and disposal, forearm phenylalanine disposal, an index of muscle protein synthesis, was not stimulated by infusion of branched-chain amino acids. 4. The results suggest that in normal man branched-chain amino acid infusion suppresses skeletal muscle proteolysis independently of any rise of plasma insulin. Muscle branched-chain amino acid uptake rose dramatically in the absence of any apparent increase in muscle protein synthesis, as measured by phenylalanine disposal, or in branched-chain keto acid release. Thus, an increase in muscle branched-chain amino acid concentrations and/or local branched-chain amino acid oxidation must account for the increased disposal of branched-chain amino acids.This publication has 24 references indexed in Scilit:
- Protein Degradation in Human Skeletal Muscle Tissue: The Effect of Insulin, Leucine, Amino Acids and IonsClinical Science, 1981
- Nitrogen sparing induced by leucine compared with that induced by its keto analogue, alpha-ketoisocaproate, in fasting obese man.Journal of Clinical Investigation, 1981
- A role for leucine in regulation of protein turnover in working rat heartsAmerican Journal of Physiology-Endocrinology and Metabolism, 1980
- Influence of Leucine on Arterial Concentrations and Regional Exchange of Amino Acids in Healthy SubjectsClinical Science, 1980
- Effect of leucine and metabolites of branched chain amino acids on protein turnover in heart.Journal of Biological Chemistry, 1979
- Stapled Cystogastrostomy A Method of Treatment for Pediatric Pancreatic PseudocystAnnals of Surgery, 1979
- Infusion of the Branched Chain Amino Acids in Postoperative Patients Anticatabolic PropertiesAnnals of Surgery, 1979
- Effect of Starvation on the Turnover and Metabolic Response to LeucineJournal of Clinical Investigation, 1978
- Effect of intraarterial infusion of the ketoanalogue of leucine on amino acid release by forearm muscleMetabolism, 1977
- Studies concerning the specificity of the effect of leucine on the turnover of proteins in muscles of control and diabetic ratsBiochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis, 1977