Gastric Bypass Improves β-Cell Function and Increases β-Cell Mass in a Porcine Model
- Andreas Lindqvist1,2,
- Peter Spégel1,
- Mikael Ekelund3,
- Eliana Garcia Vaz1,
- Stefan Pierzynowski4,5,
- Maria F. Gomez1,
- Hindrik Mulder1,
- Jan Hedenbro2,3,
- Leif Groop1 and
- Nils Wierup1⇑
- 1Department of Clinical Sciences, Lund University Diabetes Centre, Malmö, Sweden
- 2Aleris Obesity, Lund, Sweden
- 3Department of Surgery, Lund University, Lund, Sweden
- 4Department of Cell and Organism Biology, Lund University, Lund, Sweden
- 5Department of Medical Biology, Institute of Rural Health, Lublin, Poland
- Corresponding author: Nils Wierup, .
The most frequently used and effective treatment for morbid obesity is Roux-en-Y gastric bypass surgery (RYGB), which results in rapid remission of type 2 diabetes in most cases. To what extent this is accounted for by weight loss or other factors remains elusive. To gain insight into these mechanisms, we investigated the effects of RYGB on β-cell function and β-cell mass in the pig, a species highly reminiscent of the human. RYGB was performed using linear staplers during open surgery. Sham-operated pigs were used as controls. Both groups were fed a low-calorie diet for 3 weeks after surgery. Intravenous glucose tolerance tests were performed 2 weeks after surgery. Body weight in RYGB pigs and sham-operated, pair-fed control pigs developed similarly. RYGB pigs displayed improved glycemic control, which was attributed to increases in β-cell mass, islet number, and number of extraislet β-cells. Pancreatic expression of insulin and glucagon was elevated, and cells expressing the glucagon-like peptide 1 receptor were more abundant in RYGB pigs. Our data from a pig model of RYGB emphasize the key role of improved β-cell function and β-cell mass to explain the improved glucose tolerance after RYGB as food intake and body weight remained identical.
This article contains Supplementary Data online at http://diabetes.diabetesjournals.org/lookup/suppl/doi:10.2337/db13-0969/-/DC1.
- Received June 25, 2013.
- Accepted January 19, 2014.
- © 2014 by the American Diabetes Association.
Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.