Literature DB >> 23562866

Acute peripheral GLP-1 receptor agonism or antagonism does not alter energy expenditure in rats after Roux-en-Y gastric bypass.

Kathrin Abegg1, Marc Schiesser, Thomas A Lutz, Marco Bueter.   

Abstract

Compared to traditional weight loss strategies, the compensatory decrease in energy expenditure in response to body weight loss is markedly attenuated after Roux-en-Y gastric bypass surgery (RYGB). Because basal and postprandial levels of glucagon-like peptide-1 (GLP-1) are increased after RYGB surgery, and because GLP-1 has been shown to increase energy expenditure, we investigated if increased GLP-1 levels are involved in the alterations in energy expenditure after RYGB. Adult male Wistar rats were randomized for RYGB (n=8) or sham surgery (n=17). Part of the sham-operated rats were food restricted and body weight-matched (n=8) to the RYGB animals. The effects of acute subcutaneous administration of the GLP-1 antagonist Exendin (9-39) (Ex-9, 30μg/kg) or the GLP-1 agonist Exendin-4 (Ex-4, 5μg/kg), respectively, on energy expenditure were tested using indirect calorimetry. We found that Ex-9 increased food intake in RYGB, but not in sham-operated rats. Energy expenditure was lower in RYGB and sham-operated body weight-matched rats compared to sham-operated ad libitum fed rats, but significantly higher in RYGB rats compared to sham-operated body weight-matched rats. There was no effect of Ex-9 treatment on energy expenditure in either group of animals. Similarly, Ex-4 decreased food intake more in RYGB than in sham-operated rats, but Ex-4 did not modulate energy expenditure in any surgical group. We conclude that acute modulation of GLP-1 signaling is not directly involved in altered energy expenditure after RYGB surgery in rats.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Energy expenditure; Glucagon-like peptide-1; Indirect calorimetry; Roux-en-Y gastric bypass

Mesh:

Substances:

Year:  2013        PMID: 23562866      PMCID: PMC3745783          DOI: 10.1016/j.physbeh.2013.03.027

Source DB:  PubMed          Journal:  Physiol Behav        ISSN: 0031-9384


  53 in total

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3.  Bariatric surgery versus intensive medical therapy in obese patients with diabetes.

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4.  Gastric bypass reduces fat intake and preference.

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5.  Changes in eating behaviour and meal pattern following Roux-en-Y gastric bypass.

Authors:  A Laurenius; I Larsson; M Bueter; K J Melanson; I Bosaeus; H Bertéus Forslund; H Lönroth; L Fändriks; T Olbers
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Authors:  Thomas A Lutz; Marco Bueter
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2014-09-24       Impact factor: 3.619

3.  Leptin deficient ob/ob mice and diet-induced obese mice responded differently to Roux-en-Y bypass surgery.

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Journal:  Int J Obes (Lond)       Date:  2014-10-28       Impact factor: 5.095

Review 4.  Ghrelin, CCK, GLP-1, and PYY(3-36): Secretory Controls and Physiological Roles in Eating and Glycemia in Health, Obesity, and After RYGB.

Authors:  Robert E Steinert; Christine Feinle-Bisset; Lori Asarian; Michael Horowitz; Christoph Beglinger; Nori Geary
Journal:  Physiol Rev       Date:  2017-01       Impact factor: 37.312

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Review 6.  Diabetes remission following metabolic surgery: is GLP-1 the culprit?

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Review 7.  Gut hormones such as amylin and GLP-1 in the control of eating and energy expenditure.

Authors:  T A Lutz
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8.  GLP-1 receptor signaling is not required for reduced body weight after RYGB in rodents.

Authors:  Jianping Ye; Zheng Hao; Michael B Mumphrey; R Leigh Townsend; Laurel M Patterson; Nicholas Stylopoulos; Heike Münzberg; Christopher D Morrison; Daniel J Drucker; Hans-Rudolf Berthoud
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9.  Roux-en-Y gastric bypass does not affect daily water intake or the drinking response to dipsogenic stimuli in rats.

Authors:  Anikó Marshall; Jessica Santollo; Caroline Corteville; Thomas A Lutz; Derek Daniels
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10.  Ileal transposition surgery produces ileal length-dependent changes in food intake, body weight, gut hormones and glucose metabolism in rats.

Authors:  A R Ramzy; S Nausheen; P K Chelikani
Journal:  Int J Obes (Lond)       Date:  2013-10-29       Impact factor: 5.095

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