Comparative Effects of Prolonged and Intermittent Stimulation of the Glucagon-Like Peptide 1 Receptor on Gastric Emptying and Glycemia

被引:146
作者
Umapathysivam, Mahesh M. [1 ]
Lee, Michael Y. [1 ]
Jones, Karen L. [2 ]
Annink, Christopher E. [3 ]
Cousins, Caroline E. [3 ]
Trahair, Laurence G. [2 ]
Rayner, Chris K. [2 ]
Chapman, Marianne J. [1 ,3 ]
Nauck, Michael A. [4 ]
Horowitz, Michael [2 ]
Deane, Adam M. [1 ,3 ]
机构
[1] Univ Adelaide, Discipline Acute Care Med, Adelaide, SA, Australia
[2] Univ Adelaide, Discipline Med, Adelaide, SA, Australia
[3] Royal Adelaide Hosp, Dept Crit Care Serv, Adelaide, SA 5000, Australia
[4] Diabet Zentrum Bad Lauterberg, Bad Lauterberg im Harz, Germany
基金
英国医学研究理事会;
关键词
DEPENDENT DIABETES-MELLITUS; POSTPRANDIAL GLYCEMIA; OPEN-LABEL; HEALTHY-SUBJECTS; EXENATIDE; HYPERGLYCEMIA; LIXISENATIDE; DECELERATION; INSULIN; WEIGHT;
D O I
10.2337/db13-0893
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Acute administration of glucagon-like peptide 1 (GLP-1) and its agonists slows gastric emptying, which represents the major mechanism underlying their attenuation of postprandial glycemic excursions. However, this effect may diminish during prolonged use. We compared the effects of prolonged and intermittent stimulation of the GLP-1 receptor on gastric emptying and glycemia. Ten healthy men received intravenous saline (placebo) or GLP-1 (0.8 pmol/kg min), as a continuous 24-h infusion (prolonged), two 4.5-h infusions separated by 20 h (intermittent), and a 4.5-h infusion (acute) in a randomized, double-blind, crossover fashion. Gastric emptying of a radiolabeled mashed potato meal was measured using scintigraphy. Acute GLP-1 markedly slowed gastric emptying. The magnitude of the slowing was attenuated with prolonged but maintained with intermittent infusions. GLP-1 potently diminished postprandial glycemia during acute and intermittent regimens. These observations suggest that short-acting GLP-1 agonists may be superior to long-acting agonists when aiming specifically to reduce postprandial glycemic excursions in the treatment of type 2 diabetes.
引用
收藏
页码:785 / 790
页数:6
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