Somatotropin-induced protein anabolism in hindquarters and portal-drained viscera of growing pigs

Am J Physiol Endocrinol Metab. 2003 Feb;284(2):E302-12. doi: 10.1152/ajpendo.00309.2002. Epub 2002 Oct 15.


To differentiate the effect of somatotropin (ST) treatment on protein metabolism in the hindquarter (HQ) and portal-drained viscera (PDV), growing swine (n = 20) treated with ST (0 or 150 microg x kg(-1) x day(-1)) for 7 days were infused intravenously with NaH(13)CO(3) and [(2)H(5)]phenylalanine and enterally with [1-(13)C]phenylalanine while in the fed state. Arterial, portal venous, and vena cava whole blood samples, breath samples, and blood flow measurements were obtained for determination of tissue and whole body phenylalanine kinetics under steady-state conditions. In the fed state, ST treatment decreased whole body phenylalanine flux, oxidation, and protein degradation without altering protein synthesis, resulting in an improvement in whole body net protein balance. Blood flow to the HQ (+80%), but not to the PDV, was increased with ST treatment. In the HQ and PDV, ST increased phenylalanine uptake (+44 and +23%, respectively) and protein synthesis (+43 and +41%, respectively), with no effect on protein degradation. In ST-treated and control pigs, phenylalanine was oxidized in the PDV (34-43% of enteral and arterial sources) but not the HQ. In both treatment groups, dietary (40%) rather than arterial (10%) extraction of phenylalanine predominated in gut amino acid metabolism, whereas localized blood flow influenced HQ amino acid metabolism. The results indicate that ST increases protein anabolism in young, growing swine by increasing protein synthesis in the HQ and PDV, with no effect on protein degradation. Differing results between the whole body and the HQ and PDV suggest that the effect of ST treatment on protein metabolism is tissue specific.

Publication types

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

MeSH terms

  • Animals
  • Body Weight / drug effects
  • Carbon Isotopes
  • Female
  • Growth Hormone / pharmacology*
  • Hindlimb
  • Intestine, Small / drug effects
  • Intestine, Small / growth & development
  • Intestine, Small / metabolism*
  • Models, Biological
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / growth & development
  • Muscle, Skeletal / metabolism*
  • Phenylalanine / pharmacokinetics
  • Portal System
  • Protein Biosynthesis*
  • Swine
  • Tritium
  • Tyrosine / metabolism
  • Viscera / drug effects
  • Viscera / growth & development
  • Viscera / metabolism


  • Carbon Isotopes
  • Tritium
  • Tyrosine
  • Phenylalanine
  • Growth Hormone