GLP-1 slows solid gastric emptying and inhibits insulin, glucagon, and PYY release in humans
1 Division of Surgery, Danderyd Hospital, Karolinska Institutet, SE-182 88; Departments of 2 Gastroenterology and Hepatology, 3 Radiology, and 4 Nuclear Medicine, Karolinska Hospital, 171 76 Stockholm, Sweden; and 5 Department of Medical Physiology, University of Copenhagen, Copenhagen, DK-1017...
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Veröffentlicht in: | American journal of physiology. Regulatory, integrative and comparative physiology integrative and comparative physiology, 1999-09, Vol.277 (3), p.910-R916 |
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Sprache: | eng |
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Zusammenfassung: | 1 Division of Surgery, Danderyd
Hospital, Karolinska Institutet, SE-182 88; Departments of
2 Gastroenterology and Hepatology,
3 Radiology, and
4 Nuclear Medicine, Karolinska
Hospital, 171 76 Stockholm, Sweden; and
5 Department of Medical
Physiology, University of Copenhagen, Copenhagen, DK-1017
Denmark
The aim of
the present study was to assess the effect of glucagon-like peptide-1
(GLP-1) on solid gastric emptying and the subsequent release of
pancreatic and intestinal hormones. In eight men [age 33.6 ± 2.5 yr, body mass index 24.1 ± 0.9 (means ± SE)], scintigraphic solid gastric emptying during infusion of GLP-1 (0.75 pmol · kg 1 · min 1 )
or saline was studied for 180 min. Concomitantly, plasma concentrations of C- and N-terminal GLP-1, glucose, insulin, C-peptide, glucagon, and
peptide YY (PYY) were assessed. Infusion of GLP-1 resulted in a
profound inhibition of both the lag phase (GLP-1: 91.5, range 73.3-103.6 min vs. saline: 19.5, range 10.2-43.4 min) and
emptying rate (GLP-1: 0.34, range 0.06-0.56 %/min vs. saline:
0.84, range 0.54-1.33 %/min; P |
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ISSN: | 0363-6119 0002-9513 1522-1490 |
DOI: | 10.1152/ajpregu.1999.277.3.r910 |