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Unprecedented high insulin secretion in a healthy human subject after intravenous glucagon-like peptide-1: a case report

BACKGROUND: The gut-derived incretin hormones, glucose-dependent insulinotropic polypeptide and glucagon-like peptide-1, are released in response to ingestion of nutrients. Both hormones are highly insulinotropic in strictly glucose-dependent fashions and glucagon-like peptide-1 is often referred to...

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Autores principales: Knop, Filip K, Lund, Asger, Madsbad, Sten, Holst, Jens J, Krarup, Thure, Vilsbøll, Tina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053292/
https://www.ncbi.nlm.nih.gov/pubmed/24885055
http://dx.doi.org/10.1186/1756-0500-7-326
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author Knop, Filip K
Lund, Asger
Madsbad, Sten
Holst, Jens J
Krarup, Thure
Vilsbøll, Tina
author_facet Knop, Filip K
Lund, Asger
Madsbad, Sten
Holst, Jens J
Krarup, Thure
Vilsbøll, Tina
author_sort Knop, Filip K
collection PubMed
description BACKGROUND: The gut-derived incretin hormones, glucose-dependent insulinotropic polypeptide and glucagon-like peptide-1, are released in response to ingestion of nutrients. Both hormones are highly insulinotropic in strictly glucose-dependent fashions and glucagon-like peptide-1 is often referred to as one of the most insulinotropic substances known. CASE PRESENTATION: Plasma insulin and C-peptide concentrations were measured in a healthy Caucasian male (age: 53 years; body mass index: 28.6 kg/m(2); fasting plasma glucose: 5.7 mM; 2 h plasma glucose value following 75 g-oral glucose tolerance test: 3.5 mM; glycated haemoglobin A(1c): 5.5%) during glucagon (1 mg) and meal (2,370 kJ) tests, and during two 2 h 15 mM-hyperglycaemic clamps with continuous intravenous infusion of glucagon-like peptide-1 (1 pmol/kg/min) and glucose-dependent insulinotropic polypeptide (4 pmol/kg/min), respectively. Normal insulin and C-peptide responses were observed during meal test (peak concentrations: 300 and 3,278 pM) and glucagon test (peak concentrations: 250 and 2,483 pM). During the hyperglycaemic clamp with continuous intravenous infusion of GLP-1 the subject exhibited plasma insulin and C-peptide concentrations of 13,770 and 22,380 pM, respectively. CONCLUSIONS: To our knowledge insulin and C-peptide concentrations of these magnitudes have never been reported. Thus, the present data support the view that glucagon-like peptide-1 is one of the most insulinotropic substances known.
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spelling pubmed-40532922014-06-12 Unprecedented high insulin secretion in a healthy human subject after intravenous glucagon-like peptide-1: a case report Knop, Filip K Lund, Asger Madsbad, Sten Holst, Jens J Krarup, Thure Vilsbøll, Tina BMC Res Notes Case Report BACKGROUND: The gut-derived incretin hormones, glucose-dependent insulinotropic polypeptide and glucagon-like peptide-1, are released in response to ingestion of nutrients. Both hormones are highly insulinotropic in strictly glucose-dependent fashions and glucagon-like peptide-1 is often referred to as one of the most insulinotropic substances known. CASE PRESENTATION: Plasma insulin and C-peptide concentrations were measured in a healthy Caucasian male (age: 53 years; body mass index: 28.6 kg/m(2); fasting plasma glucose: 5.7 mM; 2 h plasma glucose value following 75 g-oral glucose tolerance test: 3.5 mM; glycated haemoglobin A(1c): 5.5%) during glucagon (1 mg) and meal (2,370 kJ) tests, and during two 2 h 15 mM-hyperglycaemic clamps with continuous intravenous infusion of glucagon-like peptide-1 (1 pmol/kg/min) and glucose-dependent insulinotropic polypeptide (4 pmol/kg/min), respectively. Normal insulin and C-peptide responses were observed during meal test (peak concentrations: 300 and 3,278 pM) and glucagon test (peak concentrations: 250 and 2,483 pM). During the hyperglycaemic clamp with continuous intravenous infusion of GLP-1 the subject exhibited plasma insulin and C-peptide concentrations of 13,770 and 22,380 pM, respectively. CONCLUSIONS: To our knowledge insulin and C-peptide concentrations of these magnitudes have never been reported. Thus, the present data support the view that glucagon-like peptide-1 is one of the most insulinotropic substances known. BioMed Central 2014-05-31 /pmc/articles/PMC4053292/ /pubmed/24885055 http://dx.doi.org/10.1186/1756-0500-7-326 Text en Copyright © 2014 Knop et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Knop, Filip K
Lund, Asger
Madsbad, Sten
Holst, Jens J
Krarup, Thure
Vilsbøll, Tina
Unprecedented high insulin secretion in a healthy human subject after intravenous glucagon-like peptide-1: a case report
title Unprecedented high insulin secretion in a healthy human subject after intravenous glucagon-like peptide-1: a case report
title_full Unprecedented high insulin secretion in a healthy human subject after intravenous glucagon-like peptide-1: a case report
title_fullStr Unprecedented high insulin secretion in a healthy human subject after intravenous glucagon-like peptide-1: a case report
title_full_unstemmed Unprecedented high insulin secretion in a healthy human subject after intravenous glucagon-like peptide-1: a case report
title_short Unprecedented high insulin secretion in a healthy human subject after intravenous glucagon-like peptide-1: a case report
title_sort unprecedented high insulin secretion in a healthy human subject after intravenous glucagon-like peptide-1: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053292/
https://www.ncbi.nlm.nih.gov/pubmed/24885055
http://dx.doi.org/10.1186/1756-0500-7-326
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