The role of postprandial releases of insulin and incretin hormones in meal-induced satiety-effect of obesity and weight reduction

Previous studies have indicated that the secretion of the intestinal satiety hormone glucagon-like peptide-1 (GLP-1) is attenuated in obese subjects. To compare meal-induced response of GLP-1 and glucose-dependent insulinotropic polypeptide (GIP) in obese and lean male subjects, to investigate the e...

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Published inInternational Journal of Obesity Vol. 25; no. 8; pp. 1206 - 1214
Main Authors VERDICH, C, TOUBRO, S, BUEMANN, B, LYSGARD MADSEN, J, JUUL HOLST, J, ASTRUP, A
Format Journal Article
LanguageEnglish
Published Basingstoke Nature Publishing 01.08.2001
Nature Publishing Group
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Abstract Previous studies have indicated that the secretion of the intestinal satiety hormone glucagon-like peptide-1 (GLP-1) is attenuated in obese subjects. To compare meal-induced response of GLP-1 and glucose-dependent insulinotropic polypeptide (GIP) in obese and lean male subjects, to investigate the effect of a major weight reduction in the obese subjects, and to look for an association between these hormones and ad libitum food intake. Plasma concentrations of intestinal hormones and appetite sensations were measured prior to, and every 30 min for 180 min after, ingestion of a 2.5 MJ solid test meal. Gastric emptying was estimated scintigraphically. An ad libitum lunch was served 3 h after the test meal. Nineteen non-diabetic obese (body mass index (BMI) 34.1--43.8 kg/m(2)) and 12 lean (BMI 20.4--24.7 kg/m(2)) males. All obese subjects were re-examined after a mean stabilised weight loss of 18.8 kg (95% CI 14.4--23.2). Total area under the GLP-1 response curve (AUC(total, GLP-1)) was lower in obese before and after the weight loss compared to lean subjects (P<0.05), although weight loss improved the response from 80 to 88% of that of the lean subjects (P=0.003). The GIP response was similar in obese and lean subjects. However, after the weight loss both AUC(total, GIP) and AUC(incremental, GIP) were lowered (P<0.05). An inverse correlation was observed between AUC(incremental, GIP) and energy intake at the subsequent ad libitum meal in all groups. In lean subjects ad libitum energy intake was largely predicted by the insulin response to the preceding meal (r(2)=0.67, P=0.001). Our study confirmed previous findings of a reduced postprandial GLP-1 response in severely obese subjects. Following weight reduction, GLP-1 response in the obese subjects apparently rose to a level between that of obese and lean subjects. The data suggests that postprandial insulin and GIP responses are key players in short-term appetite regulation.
AbstractList BACKGROUND:: Previous studies have indicated that the secretion of the intestinal satiety hormone glucagon-like peptide-1 (GLP-1) is attenuated in obese subjects. OBJECTIVE:: To compare meal-induced response of GLP-1 and glucose-dependent insulinotropic polypeptide (GIP) in obese and lean male subjects, to investigate the effect of a major weight reduction in the obese subjects, and to look for an association between these hormones and ad libitum food intake. METHOD:: Plasma concentrations of intestinal hormones and appetite sensations were measured prior to, and every 30 min for 180 min after, ingestion of a 2.5 MJ solid test meal. Gastric emptying was estimated scintigraphically. An ad libitum lunch was served 3 h after the test meal. SUBJECTS:: Nineteen non-diabetic obese (body mass index (BMI) 34.1-43.8 kg/m2 ) and 12 lean (BMI 20.4-24.7 kg/m2 ) males. All obese subjects were re-examined after a mean stabilised weight loss of 18.8 kg (95% CI 14.4-23.2). RESULTS:: Total area under the GLP-1 response curve (AUCtotal, GLP-1 ) was lower in obese before and after the weight loss compared to lean subjects (P<0.05), although weight loss improved the response from 80 to 88% of that of the lean subjects (P=0.003). The GIP response was similar in obese and lean subjects. However, after the weight loss both AUCtotal, GIP and AUCincremental, GIP were lowered (P<0.05). An inverse correlation was observed between AUCincremental, GIP and energy intake at the subsequent ad libitum meal in all groups. In lean subjects ad libitum energy intake was largely predicted by the insulin response to the preceding meal (r2 =0.67, P=0.001). CONCLUSION:: Our study confirmed previous findings of a reduced postprandial GLP-1 response in severely obese subjects. Following weight reduction, GLP-1 response in the obese subjects apparently rose to a level between that of obese and lean subjects. The data suggests that postprandial insulin and GIP responses are key players in short-term appetite regulation. INTERNATIONAL JOURNAL OF OBESITY: (2001) 25, 1206-1214
Previous studies have indicated that the secretion of the intestinal satiety hormone glucagon-like peptide-1 (GLP-1) is attenuated in obese subjects. To compare meal-induced response of GLP-1 and glucose-dependent insulinotropic polypeptide (GIP) in obese and lean male subjects, to investigate the effect of a major weight reduction in the obese subjects, and to look for an association between these hormones and ad libitum food intake. Plasma concentrations of intestinal hormones and appetite sensations were measured prior to, and every 30 min for 180 min after, ingestion of a 2.5 MJ solid test meal. Gastric emptying was estimated scintigraphically. An ad libitum lunch was served 3 h after the test meal. Nineteen non-diabetic obese (body mass index (BMI) 34.1--43.8 kg/m(2)) and 12 lean (BMI 20.4--24.7 kg/m(2)) males. All obese subjects were re-examined after a mean stabilised weight loss of 18.8 kg (95% CI 14.4--23.2). Total area under the GLP-1 response curve (AUC(total, GLP-1)) was lower in obese before and after the weight loss compared to lean subjects (P<0.05), although weight loss improved the response from 80 to 88% of that of the lean subjects (P=0.003). The GIP response was similar in obese and lean subjects. However, after the weight loss both AUC(total, GIP) and AUC(incremental, GIP) were lowered (P<0.05). An inverse correlation was observed between AUC(incremental, GIP) and energy intake at the subsequent ad libitum meal in all groups. In lean subjects ad libitum energy intake was largely predicted by the insulin response to the preceding meal (r(2)=0.67, P=0.001). Our study confirmed previous findings of a reduced postprandial GLP-1 response in severely obese subjects. Following weight reduction, GLP-1 response in the obese subjects apparently rose to a level between that of obese and lean subjects. The data suggests that postprandial insulin and GIP responses are key players in short-term appetite regulation.
Author TOUBRO, S
LYSGARD MADSEN, J
VERDICH, C
BUEMANN, B
JUUL HOLST, J
ASTRUP, A
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  surname: TOUBRO
  fullname: TOUBRO, S
  organization: Research Department of Human Nutrition, Centre for Advanced Food Studies, The Royal Veterinary and Agricultural University, Frederiksberg, Denmark
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  surname: BUEMANN
  fullname: BUEMANN, B
  organization: Research Department of Human Nutrition, Centre for Advanced Food Studies, The Royal Veterinary and Agricultural University, Frederiksberg, Denmark
– sequence: 4
  givenname: J
  surname: LYSGARD MADSEN
  fullname: LYSGARD MADSEN, J
  organization: Department of Clinical Physiology and Nuclear Medicine, Hvidovre Hospital, Hvidovre, Denmark
– sequence: 5
  givenname: J
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  surname: ASTRUP
  fullname: ASTRUP, A
  organization: Research Department of Human Nutrition, Centre for Advanced Food Studies, The Royal Veterinary and Agricultural University, Frederiksberg, Denmark
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https://www.ncbi.nlm.nih.gov/pubmed/11477506$$D View this record in MEDLINE/PubMed
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crossref_primary_10_1038_ijo_2010_153
crossref_primary_10_1038_ijo_2015_172
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Issue 8
Keywords Appetite
Human
Obesity
Pathophysiology
Postprandial
Weight loss
Hormonal regulation
Satiety
Insulin
Glucagon like peptide 1
Endocrine secretion
Language English
License CC BY 4.0
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PublicationTitle International Journal of Obesity
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SHA Holt (BF0801655_CR20) 1996; 50
L Ranganath (BF0801655_CR13) 1999; 96
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MD Turton (BF0801655_CR9) 1996; 379
P Fieseler (BF0801655_CR21) 1995; 268
JJ Holst (BF0801655_CR14) 1983; 7
R Ebert (BF0801655_CR29) 1992; 26
EL Mazzaferri (BF0801655_CR32) 1984; 58
K Cunningham (BF0801655_CR34) 1991; 32
IM Chapman (BF0801655_CR38) 1998; 274
SC Woods (BF0801655_CR39) 1979; 282
DP Speechly (BF0801655_CR19) 2000; 54
L Ranganath (BF0801655_CR26) 1999; 29
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Snippet Previous studies have indicated that the secretion of the intestinal satiety hormone glucagon-like peptide-1 (GLP-1) is attenuated in obese subjects. To...
BACKGROUND:: Previous studies have indicated that the secretion of the intestinal satiety hormone glucagon-like peptide-1 (GLP-1) is attenuated in obese...
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StartPage 1206
SubjectTerms Absorptiometry, Photon
Adult
Appetite
Appetite - physiology
Area Under Curve
Biological and medical sciences
Body mass index
Diabetes
Energy Intake
Food
Gastric Emptying
Gastric Inhibitory Polypeptide
Glucagon
Glucagon-Like Peptide 1
Glucagon-Like Peptides
Glucose
Hormones
Humans
Ingestion
Insulin
Insulin - metabolism
Insulin Resistance
Insulin Secretion
Male
Medical sciences
Metabolic diseases
Middle Aged
Nutrition research
Obesity
Obesity - blood
Obesity - metabolism
Peptide Fragments - metabolism
Physiology
Polypeptides
Postprandial Period
Satiation - physiology
Weight control
Weight Loss - physiology
Title The role of postprandial releases of insulin and incretin hormones in meal-induced satiety-effect of obesity and weight reduction
URI https://www.ncbi.nlm.nih.gov/pubmed/11477506
https://www.proquest.com/docview/219289277/abstract/
Volume 25
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