Inhibition of dipeptidyl-peptidase IV does not increase circulating IGF-1 concentrations in growing pigs

Exp Biol Med (Maywood). 2006 Sep;231(8):1373-8. doi: 10.1177/153537020623100811.

Abstract

The enzyme dipeptidyl peptidase-IV (DPP-IV) inactivates a variety of bioactive peptides, including glucagon-like peptide-1 (GLP-1) and growth hormone releasing hormone (GHRH). Inhibiting DPP-IV in order to increase circulating GLP-1 is of interest as a treatment for Type II diabetes. Inactivation of DPP-IV may also increase circulating GHRH, potentially enhancing growth in domestic animals. To test the hypothesis that inhibition of DPP-IV activity will influence the growth hormone/ IGF-1 axis, growing pigs (Sus scrofa domesticus, 78 kg) were treated with a DPP-IV inhibitor (Compound 1, the 2,5-difluor-ophenyl analog of the triazolopiperazine MK0431, sitagliptin), and plasma concentrations of IGF-1 were monitored. Pigs were administered either sterile saline (0.11 ml/kg followed by a continuous infusion at 2 ml/hr for 72 hrs, controls, n = 2), Compound 1 (2.78 mg/kg followed by a continuous infusion at 0.327 mg/kg x hr for 72 hrs, n = 4) or GHRH (0.11 ml/kg sterile saline, followed by a continuous infusion of GHRH at 2.5 microg/ kg x hr for 48 hrs, n = 4). Plasma concentrations of Compound 1 were maintained at 1 microM, which resulted in a 90% inhibition of circulating DPP-IV activity. Relative to the predose 24-hr period, area under the IGF-1 concentration curve (AUC) tended to be lower (P = 0.062) with Compound 1 (.79 +/- 130 ng/ml x hr) than controls (543 +/- 330 ng/ml x hr). GHRH treatment increased the IGF-1 AUC (1210 +/- 160 ng/ml x hr, P = 0.049 vs. controls and P = 0.001 vs. Compound 1). We conclude that inhibition of DPP-IV does not alter the circulating levels of IGF-1 in the growing pig.

MeSH terms

  • Animals
  • Area Under Curve
  • Cathepsin C / antagonists & inhibitors*
  • Cathepsin C / blood
  • Cathepsin C / drug effects
  • Enzyme Inhibitors / pharmacology
  • Growth Hormone-Releasing Hormone / drug effects
  • Growth Hormone-Releasing Hormone / metabolism*
  • Insulin-Like Growth Factor I / drug effects
  • Insulin-Like Growth Factor I / metabolism*
  • Male
  • Pyrazines / pharmacology
  • Sitagliptin Phosphate
  • Swine
  • Triazoles / pharmacology

Substances

  • Enzyme Inhibitors
  • Pyrazines
  • Triazoles
  • Insulin-Like Growth Factor I
  • Growth Hormone-Releasing Hormone
  • Cathepsin C
  • Sitagliptin Phosphate