Chronic protein deficiency differentially affects the kinetics of plasma proteins in young pigs

J Nutr. 1996 May;126(5):1489-95. doi: 10.1093/jn/126.5.1489.

Abstract

The use of plasma protein concentrations to assess protein-nutritional status has been questioned because concentrations and kinetics are affected by factors other than protein intake. To determine the effect of protein deficiency on plasma protein concentration and synthesis, two groups of four piglets consumed diets containing either 20 or 3% protein. After 8 wk, 2H3-leucine was infused intravenously to measure the fractional and absolute synthesis rates (FSR and ASR) of albumin, transferrin, retinol binding protein (RBP), transthyretin (TTR), a new peptide called TTR2, the high density apolipoprotein (HDL-apoA-1), fibrinogen, and haptoglobin. Compared with controls, protein-deficient pigs had significantly lower (P < 0.05) plasma albumin, RBP and TTR2 concentrations, significantly slower (P < 0.05) FSR of fibrinogen, HDL-apoA-1, transferring and TTR2, significantly lower (P < 0.05) ASR of albumin, fibrinogen, transferrin, and TTR2, and a significantly higher (P < 0.05) ASR of TTR. Fibrinogen and transferrin concentrations did not differ between groups, but transthyretin concentration was higher in protein-deficient pigs. These results suggest that protein-nutritional status cannot be predicted from the concentrations of all plasma proteins, that chronic protein deficiency affects the rate of synthesis of only some plasma proteins, and that the kinetic response of plasma proteins to protein restriction cannot be predicted from measurements of plasma concentrations.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aging / metabolism*
  • Aging / physiology
  • Animals
  • Apolipoprotein A-I / biosynthesis
  • Apolipoprotein A-I / metabolism
  • Blood Proteins / biosynthesis
  • Blood Proteins / metabolism*
  • Female
  • Fibrinogen / biosynthesis
  • Fibrinogen / metabolism
  • Haptoglobins / biosynthesis
  • Haptoglobins / metabolism
  • Leucine
  • Male
  • Prealbumin / biosynthesis
  • Prealbumin / metabolism
  • Protein Deficiency / metabolism*
  • Protein Deficiency / physiopathology
  • Retinol-Binding Proteins / biosynthesis
  • Retinol-Binding Proteins / metabolism
  • Retinol-Binding Proteins, Plasma
  • Serum Albumin / biosynthesis
  • Serum Albumin / metabolism
  • Swine
  • Transferrin / biosynthesis
  • Transferrin / metabolism
  • Tritium

Substances

  • Apolipoprotein A-I
  • Blood Proteins
  • Haptoglobins
  • Prealbumin
  • Retinol-Binding Proteins
  • Retinol-Binding Proteins, Plasma
  • Serum Albumin
  • Transferrin
  • Tritium
  • Fibrinogen
  • Leucine