Inhibition of food intake in obese subjects by peptide YY3-36

被引:1164
作者
Batterham, RL [1 ]
Cohen, MA [1 ]
Ellis, SM [1 ]
Le Roux, CW [1 ]
Withers, DJ [1 ]
Frost, GS [1 ]
Ghatei, MA [1 ]
Bloom, SR [1 ]
机构
[1] Univ London Imperial Coll Sci & Technol, Fac Med, Dept Metab Med, London W12 0NN, England
关键词
D O I
10.1056/NEJMoa030204
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The gut hormone fragment peptide YY3-36 (PYY) reduces appetite and food intake when infused into subjects of normal weight. In common with the adipocyte hormone leptin, PYY reduces food intake by modulating appetite circuits in the hypothalamus. However, in obesity there is a marked resistance to the action of leptin, which greatly limits its therapeutic effectiveness. We investigated whether obese subjects were also resistant to the anorectic effects of PYY. Methods: We compared the effects of PYY infusion on appetite and food intake in 12 obese and 12 lean subjects in a double-blind, placebo-controlled, crossover study. The plasma levels of PYY, ghrelin, leptin, and insulin were also determined. Results: Caloric intake during a buffet lunch offered two hours after the infusion of PYY was decreased by 30 percent in the obese subjects (P<0.001) and 31 percent in the lean subjects (P<0.001). PYY infusion also caused a significant decrease in the cumulative 24-hour caloric intake in both obese and lean subjects. PYY infusion reduced plasma levels of the appetite-stimulatory hormone ghrelin. Endogenous fasting and postprandial levels of PYY were significantly lower in obese subjects (the mean [+/-SE] fasting PYY levels were 10.2+/-0.7 pmol per liter in the obese group and 16.9+/-0.8 pmol per liter in the lean group, P<0.001). Furthermore, the fasting PYY levels correlated negatively with the body-mass index (r=-0.84, P<0.001). Conclusions: We found that obese subjects were not resistant to the anorectic effects of PYY. Endogenous PYY levels were low in the obese subjects, suggesting that PYY deficiency may contribute to the pathogenesis of obesity.
引用
收藏
页码:941 / 948
页数:8
相关论文
共 27 条
[1]  
ADRIAN TE, 1987, SURGERY, V101, P715
[2]   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
[3]   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
[4]   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
[5]   EFFECT OF DEGREE OF WEIGHT-LOSS BENEFITS [J].
BLACKBURN, G .
OBESITY RESEARCH, 1995, 3 :S211-S216
[6]   Whatever happened to leptin? [J].
Chicurel, M .
NATURE, 2000, 404 (6778) :538-540
[7]   Leptin activates anorexigenic POMC neurons through a neural network in the arcuate nucleus [J].
Cowley, MA ;
Smart, JL ;
Rubinstein, M ;
Cordán, MG ;
Diano, S ;
Horvath, TL ;
Cone, RD ;
Low, MJ .
NATURE, 2001, 411 (6836) :480-484
[8]   A preprandial rise in plasma ghrelin levels suggests a role in meal initiation in humans [J].
Cummings, DE ;
Purnell, JQ ;
Frayo, RS ;
Schmidova, K ;
Wisse, BE ;
Weigle, DS .
DIABETES, 2001, 50 (08) :1714-1719
[9]   Plasma ghrelin levels after diet-induced weight loss or gastric bypass surgery. [J].
Cummings, DE ;
Weigle, DS ;
Frayo, RS ;
Breen, PA ;
Ma, MK ;
Dellinger, EP ;
Purnell, JQ .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (21) :1623-1630
[10]   PEPTIDE-YY IN DIABETICS TREATED CHRONICALLY WITH AN INTESTINAL GLUCOSIDASE INHIBITOR [J].
FUESSL, HS ;
ADRIAN, TE ;
UTTENTHAL, LO ;
BLOOM, SR .
KLINISCHE WOCHENSCHRIFT, 1988, 66 (19) :985-989