Gut hormone profiles following bariatric surgery favor an anorectic state, facilitate weight loss, and improve metabolic parameters

被引:751
作者
le Roux, CW
Aylwin, SJB
Batterham, RL
Borg, CM
Coyle, F
Prasad, V
Shurey, S
Ghatei, MA
Patel, AG
Bloom, SR
机构
[1] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Dept Metab Med, London SW7 2AZ, England
[2] UCL, Rayne Inst, Dept Med, Ctr Diabet & Endocrinol, London WC1E 6BT, England
[3] Kings Coll Hosp London, Dept Endocrinol, London, England
[4] Kings Coll Hosp London, Dept Surg, London, England
[5] Northwick Pk Hosp & Clin Res Ctr, Dept Surg Res, London, England
基金
英国医学研究理事会;
关键词
D O I
10.1097/01.sla.0000183349.16877.84
中图分类号
R61 [外科手术学];
学科分类号
摘要
Objective: To study the effect of bariatric surgery on the enterohypothalamic endocrine axis of humans and rodents. Background: Bariatric surgery is the most effective obesity treatment as it achieves substantial and sustained weight loss. Glycemic control and enhanced satiation improve before substantial weight loss occurs. Gut peptides, acting both peripherally and centrally, contribute to glycemic control and regulate food intake. Methods: We examined meal-stimulated responses of insulin, ghrelin, peptide YY (PYY), glucagon-like-peptide-1 (GLP-1), and pancreatic polypeptide (PP) in humans and rodents following different bariatric surgical techniques. Results: Compared with lean and obese controls, patients following Roux-en-Y gastric bypass (RYGB) had increased postprandial plasma PYY and GLP-1 favoring enhanced satiety. Furthermore, RYGB patients had early and exaggerated insulin responses, potentially mediating improved glycemic control, None of these effects were observed in patients losing equivalent weight through gastric banding. Leptin, ghrelin, and PP were similar in both the surgical groups. Using a rodent model of jejuno-intestinal bypass (JIB), we showed elevated PYY and GLP-1 in JIB rats compared with sham-operated rats. Moreover, exogenous PYY reduced food intake and blockade of endogenous PYY increased food intake. Thus, higher plasma PYY following JIB may contribute to reduced food intake and contribute to weight loss. Conclusions: Following RYGB and JIB, a pleiotropic endocrine response may contribute to the improved glycemic control, appetite reduction, and long-term changes in body weight.
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页码:108 / 114
页数:7
相关论文
共 46 条
[1]  
ADRIAN TE, 1987, SURGERY, V101, P715
[2]   PEPTIDE-YY ABNORMALITIES IN GASTROINTESTINAL-DISEASES [J].
ADRIAN, TE ;
SAVAGE, AP ;
BACARESEHAMILTON, AJ ;
WOLFE, K ;
BESTERMAN, HS ;
BLOOM, SR .
GASTROENTEROLOGY, 1986, 90 (02) :379-384
[3]   DISTRIBUTION AND RELEASE OF HUMAN PANCREATIC POLYPEPTIDE [J].
ADRIAN, TE ;
BLOOM, SR ;
BRYANT, MG ;
POLAK, JM ;
HEITZ, P ;
BARNES, AJ .
GUT, 1976, 17 (12) :940-944
[4]   HUMAN DISTRIBUTION AND RELEASE OF A PUTATIVE NEW GUT HORMONE, PEPTIDE-YY [J].
ADRIAN, TE ;
FERRI, GL ;
BACARESEHAMILTON, AJ ;
FUESSL, HS ;
POLAK, JM ;
BLOOM, SR .
GASTROENTEROLOGY, 1985, 89 (05) :1070-1077
[5]   Characterization of the effects of pancreatic polypeptide in the regulation of energy balance [J].
Asakawa, A ;
Inui, A ;
Yuzuriha, H ;
Ueno, N ;
Katsuura, G ;
Fujimiya, M ;
Fujino, MA ;
Niijima, A ;
Meguid, MM ;
Kasuga, M .
GASTROENTEROLOGY, 2003, 124 (05) :1325-1336
[6]   APPETITE-SUPPRESSANT ACTIVITY IN PLASMA OF RATS AFTER INTESTINAL-BYPASS SURGERY [J].
ATKINSON, RL ;
BRENT, EL .
AMERICAN JOURNAL OF PHYSIOLOGY, 1982, 243 (01) :R60-R64
[7]  
AYLWIN S, 2005, CURR OPIN ENDOCRINOL, V12, P89
[8]   Gut hormone PYY3-36 physiologically inhibits food intake [J].
Batterham, RL ;
Cowley, MA ;
Small, CJ ;
Herzog, H ;
Cohen, MA ;
Dakin, CL ;
Wren, AM ;
Brynes, AE ;
Low, MJ ;
Ghatei, MA ;
Cone, RD ;
Bloom, SR .
NATURE, 2002, 418 (6898) :650-654
[9]   Inhibition of food intake in obese subjects by peptide YY3-36 [J].
Batterham, RL ;
Cohen, MA ;
Ellis, SM ;
Le Roux, CW ;
Withers, DJ ;
Frost, GS ;
Ghatei, MA ;
Bloom, SR .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (10) :941-948
[10]   Pancreatic polypeptide reduces appetite and food intake in humans [J].
Batterham, RL ;
Le Roux, CW ;
Cohen, MA ;
Park, AJ ;
Ellis, SM ;
Patterson, M ;
Frost, GS ;
Ghatei, MA ;
Bloom, SR .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (08) :3989-3992