Exenatide and weight loss

被引:53
作者
Bradley, David P. [2 ]
Kulstad, Roger [3 ]
Schoeller, Dale A. [1 ]
机构
[1] Univ Wisconsin, Dept Nutr Sci, Madison, WI 53706 USA
[2] Univ Wisconsin, Div Endocrinol, Madison, WI 53706 USA
[3] Weston Ctr, Marshfield Clin, Dept Endocrinol, Weston, WI USA
关键词
Obesity; Drug treatment; Glucagon-like peptide-1; Appetite; Energy expenditure; GLUCAGON-LIKE PEPTIDE-1; GLYCEMIC CONTROL; ENERGY-INTAKE; SUBSTRATE METABOLISM; INSULIN-SECRETION; TREATED PATIENTS; FOOD-INTAKE; 7-36; AMIDE; GLUCOSE; EXENDIN-4;
D O I
10.1016/j.nut.2009.07.008
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Objective: Glucagon-like peptide-1 (GLP-1) is a gastrointestinal hormone mainly released from the distal ileum, jejunum, and colon in response to food ingestion. It is categorized as an incretin due to its activation of GLP-1 receptors in pancreatic beta-cells leading to insulin exocytosis in a glucose-dependent manner. Exenatide (synthetic exendin-4) is a subcutaneously injected GLP-1 receptor agonist that shares 50% homology with GLP-1. It is derived from lizard venom and stimulates the GLP-1 receptor for prolonged periods. The present review aims to enumerate exenatide-instigated weight loss, summarize the known mechanisms of exenatide-induced weight loss, and elaborate on its possible application in the pharmacotherapy of obesity. Methods: A search through PubMed was performed using exenatide and weight loss as search terms. A second search was performed using exenatide and mechanisms or actions as search terms. Results: In addition to exenatide's action to increase insulin secretion in individuals with elevated levels of plasma glucose, clinical trials have reported consistent weight loss associated with exenatide treatment. Studies have found evidence that exenatide decreases energy intake and increases energy expenditure, but findings on which predominates to cause weight loss are often inconsistent and controversial. Conclusion: Further research on the effects of exenatide treatment on energy intake and expenditure are recommended to better understand the mechanisms through which exenatide causes weight loss. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:243 / 249
页数:7
相关论文
共 53 条
[41]   Glucose intolerance but normal satiety in mice with a null mutation in the glucagon-like peptide 1 receptor gene [J].
Scrocchi, LA ;
Brown, TJ ;
MacLusky, N ;
Brubaker, PL ;
Auerbach, AB ;
Joyner, AL ;
Drucker, DJ .
NATURE MEDICINE, 1996, 2 (11) :1254-1258
[42]   Effects of glucagon-like peptide 1 (7-36 amide) on whole-body protein metabolism in healthy man [J].
Shalev, A ;
Holst, JJ ;
Keller, U .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1997, 27 (01) :10-16
[43]   THE EFFECT OF LONG-TERM INTENSIFIED INSULIN-TREATMENT ON THE DEVELOPMENT OF MICROVASCULAR COMPLICATIONS OF DIABETES-MELLITUS [J].
REICHARD, P ;
NILSSON, BY ;
ROSENQVIST, U .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (05) :304-309
[44]   Glucagon-like peptide-1 receptor (GLP1-R) mRNA in the rat hypothalamus [J].
Shughrue, PJ ;
Lane, MV ;
Merchenthaler, I .
ENDOCRINOLOGY, 1996, 137 (11) :5159-5162
[45]   Association of glycaemia with macrovascular and microvascular complications of type 2 diabetes (UKPDS 35): prospective observational study [J].
Stratton, IM ;
Adler, AI ;
Neil, HAW ;
Matthews, DR ;
Manley, SE ;
Cull, CA ;
Hadden, D ;
Turner, RC ;
Holman, RR .
BMJ-BRITISH MEDICAL JOURNAL, 2000, 321 (7258) :405-412
[46]   Continuous subcutaneous infusion of glucagon-like peptide 1 lowers plasma glucose and reduces appetite in type 2 diabetic patients [J].
Toft-Nielsen, MB ;
Madsbad, S ;
Holst, JJ .
DIABETES CARE, 1999, 22 (07) :1137-1143
[47]  
TURNER RC, 1995, DIABETES, V44, P1249
[48]   CHARACTERIZATION OF HIGH-AFFINITY RECEPTORS FOR TRUNCATED GLUCAGON-LIKE PEPTIDE-1 IN RAT GASTRIC GLANDS [J].
UTTENTHAL, LO ;
BLAZQUEZ, E .
FEBS LETTERS, 1990, 262 (01) :139-141
[49]   A meta-analysis of the effect of glucagon-like peptide-1 (7-36) amide on ad libitum energy intake in humans [J].
Verdich, C ;
Flint, A ;
Gutzwiller, JP ;
Näslund, E ;
Beglinger, C ;
Hellström, PM ;
Long, SJ ;
Morgan, LM ;
Holst, JJ ;
Astrup, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (09) :4382-4389
[50]   Reduced postprandial concentrations of intact biologically active gluccagon-like peptide 1 in type 2 diabetic patients [J].
Vilsboll, T ;
Krarup, T ;
Deacon, CF ;
Madsbad, S ;
Holst, JJ .
DIABETES, 2001, 50 (03) :609-613