Diet and Gastrointestinal Bypass-Induced Weight Loss The Roles of Ghrelin and Peptide YY

被引:103
作者
Chandarana, Keval [1 ]
Gelegen, Cigdem [1 ]
Karra, Efthimia [1 ]
Choudhury, Agharul I. [2 ]
Drew, Megan E. [1 ]
Fauveau, Veronique [3 ]
Viollet, Benoit [4 ,5 ]
Andreelli, Fabrizio [4 ]
Withers, Dominic J. [2 ]
Batterham, Rachel L. [1 ]
机构
[1] UCL, Rayne Inst, Obes Res Ctr, Dept Med, London, England
[2] Univ London Imperial Coll Sci Technol & Med, Ctr Clin Sci, MRC, Metab Signalling Grp, London, England
[3] Univ Paris 05, Inst Cochin, Fac Med Cochin, IFR Alfred Jost0, Paris, France
[4] INSERM, Paris, France
[5] CNRS, UMR 8104, Paris, France
基金
英国医学研究理事会;
关键词
GASTRIC BYPASS; PLASMA GHRELIN; GUT HORMONE; BODY-WEIGHT; POSTPRANDIAL GHRELIN; ENERGY HOMEOSTASIS; BARIATRIC SURGERY; INDUCED OBESITY; FOOD-INTAKE; APPETITE;
D O I
10.2337/db10-0566
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE-Bariatric surgery causes durable weight loss. Gut hormones are implicated in obesity pathogenesis, dietary failure, and mediating gastrointestinal bypass (GIBP) surgery weight loss. In mice, we determined the effects of diet-induced obesity (DIO), subsequent dieting, and GIBP surgery on ghrelin, peptide YY (PYY), and glucagon-like peptide-1 (GLP-1). To evaluate PYY's role in mediating weight loss post-GIBP, we undertook GIBP surgery in PyyKO mice. RESEARCH DESIGN AND METHODS-Male C57BL/6 mice randomized to a high-fat diet or control diet were killed at 4-week intervals. DIO mice underwent switch to ad libitum low-fat diet (DIO-switch) or caloric restriction (CR) for 4 weeks before being killed. PyyKO mice and their DIO wild-type (WT) littermates underwent GIBP or sham surgery and were culled 10 days post-operatively. Fasting acyl-ghrelin, total PYY, active GLP-1 concentrations, stomach ghrelin expression, and colonic Pyy and glucagon expression were determined. Fasting and postprandial PYY and GLP-1 concentrations were assessed 30 days postsurgery in GIBP and sham pair-fed (sham.PF) groups. RESULTS-DIO progressively reduced circulating fasting acyl-ghrelin, PYY, and GLP-1 levels. CR and DIO-switch caused weight loss but failed to restore circulating PYY to weight-appropriate levels. After GIBP, WT mice lost weight and exhibited increased circulating fasting PYY and colonic Pyy and glucagon expression. In contrast, the acute effects of GIBP on body weight were lost in PyyKO mice. Fasting PYY and postprandial PYY and GLP-1 levels were increased in GIBP mice compared with sham.PF mice. CONCLUSIONS-PYY plays a key role in mediating the early weight loss observed post-GIBP, whereas relative PYY deficiency during dieting may compromise weight-loss attempts. Diabetes 60:810-818, 2011
引用
收藏
页码:810 / 818
页数:9
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