The impact of Roux-en-Y gastric bypass surgery on normal metabolism in a porcine model

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The impact of Roux-en-Y gastric bypass surgery on normal metabolism in a porcine model. / Lindqvist, Andreas; Ekelund, Mikael; Garcia-Vaz, Eliana; Ståhlman, Marcus; Pierzynowski, Stefan; Gomez, Maria F; Rehfeld, Jens F; Groop, Leif; Hedenbro, Jan; Wierup, Nils; Spégel, Peter.

I: PLOS ONE, Bind 12, Nr. 3, e0173137, 03.2017.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Lindqvist, A, Ekelund, M, Garcia-Vaz, E, Ståhlman, M, Pierzynowski, S, Gomez, MF, Rehfeld, JF, Groop, L, Hedenbro, J, Wierup, N & Spégel, P 2017, 'The impact of Roux-en-Y gastric bypass surgery on normal metabolism in a porcine model', PLOS ONE, bind 12, nr. 3, e0173137. https://doi.org/10.1371/journal.pone.0173137

APA

Lindqvist, A., Ekelund, M., Garcia-Vaz, E., Ståhlman, M., Pierzynowski, S., Gomez, M. F., Rehfeld, J. F., Groop, L., Hedenbro, J., Wierup, N., & Spégel, P. (2017). The impact of Roux-en-Y gastric bypass surgery on normal metabolism in a porcine model. PLOS ONE, 12(3), [e0173137]. https://doi.org/10.1371/journal.pone.0173137

Vancouver

Lindqvist A, Ekelund M, Garcia-Vaz E, Ståhlman M, Pierzynowski S, Gomez MF o.a. The impact of Roux-en-Y gastric bypass surgery on normal metabolism in a porcine model. PLOS ONE. 2017 mar.;12(3). e0173137. https://doi.org/10.1371/journal.pone.0173137

Author

Lindqvist, Andreas ; Ekelund, Mikael ; Garcia-Vaz, Eliana ; Ståhlman, Marcus ; Pierzynowski, Stefan ; Gomez, Maria F ; Rehfeld, Jens F ; Groop, Leif ; Hedenbro, Jan ; Wierup, Nils ; Spégel, Peter. / The impact of Roux-en-Y gastric bypass surgery on normal metabolism in a porcine model. I: PLOS ONE. 2017 ; Bind 12, Nr. 3.

Bibtex

@article{20d36927941946a1aeb9f4f142ec3427,
title = "The impact of Roux-en-Y gastric bypass surgery on normal metabolism in a porcine model",
abstract = "BACKGROUND: A growing body of literature on Roux-en-Y gastric bypass surgery (RYGB) has generated inconclusive results on the mechanism underlying the beneficial effects on weight loss and glycaemia, partially due to the problems of designing clinical studies with the appropriate controls. Moreover, RYGB is only performed in obese individuals, in whom metabolism is perturbed and not completely understood.METHODS: In an attempt to isolate the effects of RYGB and its effects on normal metabolism, we investigated the effect of RYGB in lean pigs, using sham-operated pair-fed pigs as controls. Two weeks post-surgery, pigs were subjected to an intravenous glucose tolerance test (IVGTT) and circulating metabolites, hormones and lipids measured. Bile acid composition was profiled after extraction from blood, faeces and the gallbladder.RESULTS: A similar weight development in both groups of pigs validated our experimental model. Despite similar changes in fasting insulin, RYGB-pigs had lower fasting glucose levels. During an IVGTT RYGB-pigs had higher insulin and lower glucose levels. VLDL and IDL were lower in RYGB- than in sham-pigs. RYGB-pigs had increased levels of most amino acids, including branched-chain amino acids, but these were more efficiently suppressed by glucose. Levels of bile acids in the gallbladder were higher, whereas plasma and faecal bile acid levels were lower in RYGB- than in sham-pigs.CONCLUSION: In a lean model RYGB caused lower plasma lipid and bile acid levels, which were compensated for by increased plasma amino acids, suggesting a switch from lipid to protein metabolism during fasting in the immediate postoperative period.",
keywords = "Animals, Blood Glucose, Disease Models, Animal, Fasting/blood, Gastric Bypass/adverse effects, Glucose/metabolism, Glucose Tolerance Test, Humans, Insulin/metabolism, Insulin Resistance/physiology, Obesity/blood, Swine, Weight Loss/physiology",
author = "Andreas Lindqvist and Mikael Ekelund and Eliana Garcia-Vaz and Marcus St{\aa}hlman and Stefan Pierzynowski and Gomez, {Maria F} and Rehfeld, {Jens F} and Leif Groop and Jan Hedenbro and Nils Wierup and Peter Sp{\'e}gel",
year = "2017",
month = mar,
doi = "10.1371/journal.pone.0173137",
language = "English",
volume = "12",
journal = "PLoS ONE",
issn = "1932-6203",
publisher = "Public Library of Science",
number = "3",

}

RIS

TY - JOUR

T1 - The impact of Roux-en-Y gastric bypass surgery on normal metabolism in a porcine model

AU - Lindqvist, Andreas

AU - Ekelund, Mikael

AU - Garcia-Vaz, Eliana

AU - Ståhlman, Marcus

AU - Pierzynowski, Stefan

AU - Gomez, Maria F

AU - Rehfeld, Jens F

AU - Groop, Leif

AU - Hedenbro, Jan

AU - Wierup, Nils

AU - Spégel, Peter

PY - 2017/3

Y1 - 2017/3

N2 - BACKGROUND: A growing body of literature on Roux-en-Y gastric bypass surgery (RYGB) has generated inconclusive results on the mechanism underlying the beneficial effects on weight loss and glycaemia, partially due to the problems of designing clinical studies with the appropriate controls. Moreover, RYGB is only performed in obese individuals, in whom metabolism is perturbed and not completely understood.METHODS: In an attempt to isolate the effects of RYGB and its effects on normal metabolism, we investigated the effect of RYGB in lean pigs, using sham-operated pair-fed pigs as controls. Two weeks post-surgery, pigs were subjected to an intravenous glucose tolerance test (IVGTT) and circulating metabolites, hormones and lipids measured. Bile acid composition was profiled after extraction from blood, faeces and the gallbladder.RESULTS: A similar weight development in both groups of pigs validated our experimental model. Despite similar changes in fasting insulin, RYGB-pigs had lower fasting glucose levels. During an IVGTT RYGB-pigs had higher insulin and lower glucose levels. VLDL and IDL were lower in RYGB- than in sham-pigs. RYGB-pigs had increased levels of most amino acids, including branched-chain amino acids, but these were more efficiently suppressed by glucose. Levels of bile acids in the gallbladder were higher, whereas plasma and faecal bile acid levels were lower in RYGB- than in sham-pigs.CONCLUSION: In a lean model RYGB caused lower plasma lipid and bile acid levels, which were compensated for by increased plasma amino acids, suggesting a switch from lipid to protein metabolism during fasting in the immediate postoperative period.

AB - BACKGROUND: A growing body of literature on Roux-en-Y gastric bypass surgery (RYGB) has generated inconclusive results on the mechanism underlying the beneficial effects on weight loss and glycaemia, partially due to the problems of designing clinical studies with the appropriate controls. Moreover, RYGB is only performed in obese individuals, in whom metabolism is perturbed and not completely understood.METHODS: In an attempt to isolate the effects of RYGB and its effects on normal metabolism, we investigated the effect of RYGB in lean pigs, using sham-operated pair-fed pigs as controls. Two weeks post-surgery, pigs were subjected to an intravenous glucose tolerance test (IVGTT) and circulating metabolites, hormones and lipids measured. Bile acid composition was profiled after extraction from blood, faeces and the gallbladder.RESULTS: A similar weight development in both groups of pigs validated our experimental model. Despite similar changes in fasting insulin, RYGB-pigs had lower fasting glucose levels. During an IVGTT RYGB-pigs had higher insulin and lower glucose levels. VLDL and IDL were lower in RYGB- than in sham-pigs. RYGB-pigs had increased levels of most amino acids, including branched-chain amino acids, but these were more efficiently suppressed by glucose. Levels of bile acids in the gallbladder were higher, whereas plasma and faecal bile acid levels were lower in RYGB- than in sham-pigs.CONCLUSION: In a lean model RYGB caused lower plasma lipid and bile acid levels, which were compensated for by increased plasma amino acids, suggesting a switch from lipid to protein metabolism during fasting in the immediate postoperative period.

KW - Animals

KW - Blood Glucose

KW - Disease Models, Animal

KW - Fasting/blood

KW - Gastric Bypass/adverse effects

KW - Glucose/metabolism

KW - Glucose Tolerance Test

KW - Humans

KW - Insulin/metabolism

KW - Insulin Resistance/physiology

KW - Obesity/blood

KW - Swine

KW - Weight Loss/physiology

U2 - 10.1371/journal.pone.0173137

DO - 10.1371/journal.pone.0173137

M3 - Journal article

C2 - 28257455

VL - 12

JO - PLoS ONE

JF - PLoS ONE

SN - 1932-6203

IS - 3

M1 - e0173137

ER -

ID: 195966382