Clinical Pharmacology & Therapeutics · 2008 · 48 citations · 20 references
MedicinePharmacokineticsPharmacologyClinical PharmacologyGeneral PharmacologyPharmacodynamicsDrug DispositionMultiple-dose PharmacokineticsClinical Pharmacology EvidenceDose Escalation EvaluationGhrelin SignalingPeptide PharmacokineticsTime-dependent Pharmacodynamic Effects
This proof-of-concept study was performed in order to establish the pharmacokinetics and pharmacodynamics of increasing oral doses of the satiety peptides glucagon-like peptide-1 (GLP-1) and peptide YY3-36 (PYY3-36). Six healthy male subjects were given oral doses of either a placebo or GLP-1 in a dose-escalating schedule (doses of 0.5, 1.0, 2.0, and 4.0 mg). Next, another group of six healthy male subjects were given oral doses of either a placebo or PYY3-36 in the same pattern of escalating doses (doses of 0.25, 0.5, 1.0, 2.0, and 4.0 mg). In healthy male volunteers, (i) oral administration of either of the peptides induced a rapid and dose-dependent increase in plasma drug concentrations; (ii) oral administration of GLP-1 induced a potent effect on insulin release; and (iii) both peptides suppressed ghrelin secretion. In conclusion, this study showed, for the first time, that satiety peptides such as GLP-1 and PYY3-36 can be orally delivered safely and effectively in humans.
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Gut hormone PYY3-36 physiologically inhibits food intake
Rachel L. Batterham, Michael A. Cowley, Caroline J. Small et al. · Nature · 2002 · 2.3K citations
Glucagon-like peptide-1: a potent regulator of food intake in humans
J-P Gutzwiller, Burkhard Göke, Jürgen Drewe et al. · Gut · 1999 · 570 citations · Full text
Effect of Peptide YY3–36 on Food Intake in Humans
Lukas Degen, Sibylle Oesch, Michel Casanova et al. · Gastroenterology · 2005 · 363 citations · Full text