Affiliation:
1. Department of Pharmacology, Merck Research Laboratories, Rahway, New Jersey 07065
2. Department of Metabolic Disorders, Merck Research Laboratories, Rahway, New Jersey 07065
3. Department of Medicinal Chemistry, Merck Research Laboratories, Rahway, New Jersey 07065
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-difluorophenyl 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·hr for 72 hrs, n = 4) or GHRH (0.11 ml/kg sterile saline, followed by a continuous infusion of GHRH at 2.5 μg/kg hr for 48 hrs, n = 4). Plasma concentrations of Compound 1 were maintained at 1 μM, 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 hr) than controls (543 ± 330 ng/ml hr). GHRH treatment increased the IGF-1 AUC (1210 ± 160 ng/ml 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.
Subject
General Biochemistry, Genetics and Molecular Biology
Cited by
14 articles.
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