Normalization of glucose concentrations and deceleration of gastric emptying after solid meals during intravenous glucagon-like peptide 1 in patients with type 2 diabetes

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Normalization of glucose concentrations and deceleration of gastric emptying after solid meals during intravenous glucagon-like peptide 1 in patients with type 2 diabetes. / Meier, Juris J; Gallwitz, Baptist; Salmen, Stefan; Goetze, Oliver; Holst, Jens Juul; Schmidt, Wolfgang E; Nauck, Michael A.

In: The Journal of clinical endocrinology and metabolism, Vol. 88, No. 6, 06.2003, p. 2719-25.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Meier, JJ, Gallwitz, B, Salmen, S, Goetze, O, Holst, JJ, Schmidt, WE & Nauck, MA 2003, 'Normalization of glucose concentrations and deceleration of gastric emptying after solid meals during intravenous glucagon-like peptide 1 in patients with type 2 diabetes', The Journal of clinical endocrinology and metabolism, vol. 88, no. 6, pp. 2719-25. https://doi.org/10.1210/jc.2003-030049

APA

Meier, J. J., Gallwitz, B., Salmen, S., Goetze, O., Holst, J. J., Schmidt, W. E., & Nauck, M. A. (2003). Normalization of glucose concentrations and deceleration of gastric emptying after solid meals during intravenous glucagon-like peptide 1 in patients with type 2 diabetes. The Journal of clinical endocrinology and metabolism, 88(6), 2719-25. https://doi.org/10.1210/jc.2003-030049

Vancouver

Meier JJ, Gallwitz B, Salmen S, Goetze O, Holst JJ, Schmidt WE et al. Normalization of glucose concentrations and deceleration of gastric emptying after solid meals during intravenous glucagon-like peptide 1 in patients with type 2 diabetes. The Journal of clinical endocrinology and metabolism. 2003 Jun;88(6):2719-25. https://doi.org/10.1210/jc.2003-030049

Author

Meier, Juris J ; Gallwitz, Baptist ; Salmen, Stefan ; Goetze, Oliver ; Holst, Jens Juul ; Schmidt, Wolfgang E ; Nauck, Michael A. / Normalization of glucose concentrations and deceleration of gastric emptying after solid meals during intravenous glucagon-like peptide 1 in patients with type 2 diabetes. In: The Journal of clinical endocrinology and metabolism. 2003 ; Vol. 88, No. 6. pp. 2719-25.

Bibtex

@article{772afdcdddcc41f7988f59512744e724,
title = "Normalization of glucose concentrations and deceleration of gastric emptying after solid meals during intravenous glucagon-like peptide 1 in patients with type 2 diabetes",
abstract = "The effects of different i.v. doses of glucagon-like peptide 1 (GLP-1) on glucose homeostasis and gastric emptying were compared in patients with type 2 diabetes. Twelve patients with type 2 diabetes received three different infusion rates of GLP-1 (0.4, 0.8, and 1.2 pmol/kg x min) or placebo in the fasting state and after a solid test meal (containing [(13)C]octanoic acid). Blood was drawn for glucose, insulin, C-peptide, glucagon, and GLP-1 determinations. The gastric emptying rate was calculated from the (13)CO(2) excretion rates in breath samples. Statistics were determined using repeated measures ANOVA and Duncan's post hoc test. Plasma glucose concentrations were equally normalized with all GLP-1 doses (P < 0.001). Insulin and C-peptide concentrations dose-dependently rose during GLP-1 infusion in the fasting state (P < 0.05), but were dose-dependently reduced by GLP-1 after meal ingestion (P = 0.0031 and 0.0074, respectively). Glucagon secretion was suppressed with GLP-1. Gastric emptying was decelerated by GLP-1 in a dose-dependent fashion (P < 0.001). Despite a dose-dependent stimulation of insulin secretion, glucose normalization can be achieved even with 0.4 pmol GLP-1/kg x min. Due to the dose-dependent inhibition of gastric emptying, lower GLP-1 doses than previously used may be as suitable for glucose control in patients with type 2 diabetes.",
keywords = "Aged, Blood Glucose, Diabetes Mellitus, Type 2, Dose-Response Relationship, Drug, Fasting, Female, Gastric Emptying, Glucagon, Glucagon-Like Peptide 1, Humans, Injections, Intravenous, Male, Middle Aged, Osmolar Concentration, Peptide Fragments, Postprandial Period, Protein Precursors, Time Factors",
author = "Meier, {Juris J} and Baptist Gallwitz and Stefan Salmen and Oliver Goetze and Holst, {Jens Juul} and Schmidt, {Wolfgang E} and Nauck, {Michael A}",
year = "2003",
month = jun,
doi = "10.1210/jc.2003-030049",
language = "English",
volume = "88",
pages = "2719--25",
journal = "Journal of Clinical Endocrinology and Metabolism",
issn = "0021-972X",
publisher = "Oxford University Press",
number = "6",

}

RIS

TY - JOUR

T1 - Normalization of glucose concentrations and deceleration of gastric emptying after solid meals during intravenous glucagon-like peptide 1 in patients with type 2 diabetes

AU - Meier, Juris J

AU - Gallwitz, Baptist

AU - Salmen, Stefan

AU - Goetze, Oliver

AU - Holst, Jens Juul

AU - Schmidt, Wolfgang E

AU - Nauck, Michael A

PY - 2003/6

Y1 - 2003/6

N2 - The effects of different i.v. doses of glucagon-like peptide 1 (GLP-1) on glucose homeostasis and gastric emptying were compared in patients with type 2 diabetes. Twelve patients with type 2 diabetes received three different infusion rates of GLP-1 (0.4, 0.8, and 1.2 pmol/kg x min) or placebo in the fasting state and after a solid test meal (containing [(13)C]octanoic acid). Blood was drawn for glucose, insulin, C-peptide, glucagon, and GLP-1 determinations. The gastric emptying rate was calculated from the (13)CO(2) excretion rates in breath samples. Statistics were determined using repeated measures ANOVA and Duncan's post hoc test. Plasma glucose concentrations were equally normalized with all GLP-1 doses (P < 0.001). Insulin and C-peptide concentrations dose-dependently rose during GLP-1 infusion in the fasting state (P < 0.05), but were dose-dependently reduced by GLP-1 after meal ingestion (P = 0.0031 and 0.0074, respectively). Glucagon secretion was suppressed with GLP-1. Gastric emptying was decelerated by GLP-1 in a dose-dependent fashion (P < 0.001). Despite a dose-dependent stimulation of insulin secretion, glucose normalization can be achieved even with 0.4 pmol GLP-1/kg x min. Due to the dose-dependent inhibition of gastric emptying, lower GLP-1 doses than previously used may be as suitable for glucose control in patients with type 2 diabetes.

AB - The effects of different i.v. doses of glucagon-like peptide 1 (GLP-1) on glucose homeostasis and gastric emptying were compared in patients with type 2 diabetes. Twelve patients with type 2 diabetes received three different infusion rates of GLP-1 (0.4, 0.8, and 1.2 pmol/kg x min) or placebo in the fasting state and after a solid test meal (containing [(13)C]octanoic acid). Blood was drawn for glucose, insulin, C-peptide, glucagon, and GLP-1 determinations. The gastric emptying rate was calculated from the (13)CO(2) excretion rates in breath samples. Statistics were determined using repeated measures ANOVA and Duncan's post hoc test. Plasma glucose concentrations were equally normalized with all GLP-1 doses (P < 0.001). Insulin and C-peptide concentrations dose-dependently rose during GLP-1 infusion in the fasting state (P < 0.05), but were dose-dependently reduced by GLP-1 after meal ingestion (P = 0.0031 and 0.0074, respectively). Glucagon secretion was suppressed with GLP-1. Gastric emptying was decelerated by GLP-1 in a dose-dependent fashion (P < 0.001). Despite a dose-dependent stimulation of insulin secretion, glucose normalization can be achieved even with 0.4 pmol GLP-1/kg x min. Due to the dose-dependent inhibition of gastric emptying, lower GLP-1 doses than previously used may be as suitable for glucose control in patients with type 2 diabetes.

KW - Aged

KW - Blood Glucose

KW - Diabetes Mellitus, Type 2

KW - Dose-Response Relationship, Drug

KW - Fasting

KW - Female

KW - Gastric Emptying

KW - Glucagon

KW - Glucagon-Like Peptide 1

KW - Humans

KW - Injections, Intravenous

KW - Male

KW - Middle Aged

KW - Osmolar Concentration

KW - Peptide Fragments

KW - Postprandial Period

KW - Protein Precursors

KW - Time Factors

U2 - 10.1210/jc.2003-030049

DO - 10.1210/jc.2003-030049

M3 - Journal article

C2 - 12788879

VL - 88

SP - 2719

EP - 2725

JO - Journal of Clinical Endocrinology and Metabolism

JF - Journal of Clinical Endocrinology and Metabolism

SN - 0021-972X

IS - 6

ER -

ID: 132056050