Glucagon-like peptide-1: a potent regulator of food intake in humans
J-P Gutzwiller
a Division of
Gastroenterology and Department of Research, University Hospital,
CH-4031 Basel, Switzerland, b Kantonsspital Aarau, CH-5000 Aarau, Switzerland, c Clinical Research Unit for Gastrointestinal
Endocrinology, Philipps University of Marburg, D-35033 Marburg, Germany
Correspondence to: Dr C Beglinger. Accepted for publication 7 July 1998
Background/Aims Keywords:
glucagon-like peptide-1;
satiety;
food intake;
hunger and fullness score
Studies
in animals suggest a physiological role for glucagon-like
peptide-1-(7-36)-amide (GLP-1) in regulating satiety. The role of
GLP-1 in regulating food intake in man has, however, not been investigated.
Subjects
Sixteen healthy male subjects were examined in a
double blind placebo controlled fashion.
Methods
The effect of
graded intravenous doses (0, 0.375, 0.75, and 1.5 pmol/kg/min) of
synthetic human GLP-1 on food intake and feelings of hunger and satiety
was tested in healthy volunteers.
Results
Graded GLP-1
infusions resulted in a dose dependent reduction in food intake
(maximal inhibition 35%, p<0.001 v
control) and a similar reduction in calorie intake (32%; p<0.001). Fluid ingestion was also reduced by GLP-1 (18% reduction, p<0.01). No
overt side effects were produced by GLP-1, but subjects experienced less hunger and early fullness in the period before a meal during GLP-1
infusion at the highest dose (p<0.05).
Conclusions
Intravenous
infusions of GLP-1 decrease spontaneous food intake even at
physiological plasma concentrations, implying an important role for
GLP-1 in the regulation of the early satiety response in humans.
(GUT 1998;44:81-86)
© 1998 by Gut
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