An interaction between hypothalamic glucagon-like peptide-1 and macronutrient composition determines food intake in rats

被引:9
作者
Choi, YH [1 ]
Anderson, GH [1 ]
机构
[1] Univ Toronto, Fac Med, Dept Nutr Sci, Toronto, ON M5S 3E2, Canada
关键词
protein-free; high carbohydrate diet; high protein; low carbohydrate diet; feeding behavior; brain-gut peptide; rats;
D O I
10.1093/jn/131.6.1819
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Glucagon-like peptide-1 (GLP-1) release in response to food ingestion has been associated with decreased food intake, in the present study, we tested the hypothesis that the feeding response to GLP-1 injection into the hypothalamic paraventricular nucleus (PVN) is influenced by the macronutrient composition of the food consumed. In the first experiment, rats were injected with GLP-1 (0.2 mug) or saline (0.5 muL) in the PVN at dark onset (1800 h), and food intake from a maintenance diet (18% protein) was measured at 1, 2 and 14 h. In Experiment 2, after GLP-1 injection, rats were fed a carbohydrate (protein-free) diet for the first 2 h or gavaged with glucose (1.4 g/5 mt). In Experiment 3, after GLP-1 injection, rats were fed a protein (50%) diet for the first 2 h, or were preloaded with egg albumin (1.0 g). In the last experiment, GLP-1 was given after corn oil gavage (2.4 g). GLP-1 injection resulted in a reduced consumption of the maintenance diet from 2 to 14 h. The decreased food intake from 2 to 14 h after GLP-1 administration occurred after carbohydrate intake, either by meal or preloads, but not after protein intake, either as a meal or preload, A transient interaction of GLP-1 with a corn oil gavage was detected but only in early feeding (0-2 h), We conclude that the effect of GLP-1 injected in the PVN on food intake is influenced by the macronutrient composition of the food consumed. Carbohydrate enhances, protein blocks and corn oil has a transient effect on the suppression of food intake caused by GLP-1 in the PVN.
引用
收藏
页码:1819 / 1825
页数:7
相关论文
共 66 条
  • [1] Alvarez E, 1996, J NEUROCHEM, V66, P920
  • [2] Comparison of the postprandial release of peptide YY and proglucagon-derived peptides in the rat
    Anini, Y
    Fu-Cheng, XM
    Cuber, JC
    Kervran, A
    Chariot, J
    Rozé, C
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1999, 438 (03): : 299 - 306
  • [3] Intracerebroventricular glucagon-like peptide-1 (7-36) amide inhibits sham feeding in rats without eliciting satiety
    Asarian, L
    Corp, ES
    Hrupka, B
    Geary, N
    [J]. PHYSIOLOGY & BEHAVIOR, 1998, 64 (03) : 367 - 372
  • [4] Food for thought: A critique on the hypothesis that endogenous cholecystokinin acts as a physiological satiety factor
    Baldwin, BA
    Parrott, RF
    Ebenezer, IS
    [J]. PROGRESS IN NEUROBIOLOGY, 1998, 55 (05) : 477 - 507
  • [5] Interactions of exendin-(9-39) with the effects of glucagon-like peptide-1-(7-36) amide and of exendin-4 on arterial blood pressure and heart rate in rats
    Barragan, JM
    Rodriguez, RE
    Eng, J
    Blazquez, E
    [J]. REGULATORY PEPTIDES, 1996, 67 (01) : 63 - 68
  • [6] Neural contribution to the effect of glucagon-like peptide-1-(7-36) amide on arterial blood pressure in rats
    Barragán, JM
    Eng, J
    Rodríguez, R
    Blázquez, E
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1999, 277 (05): : E784 - E791
  • [7] BRUBAKER P, 1997, INSULINOTROPIC GUT H, V1, P65
  • [8] BUCHAN AMJ, 1999, AM J PHYSIOL-GASTR L, V277, pG1103, DOI DOI 10.1152/ajpgi.1999.277.6.G1103
  • [9] Measurement of blood-brain barrier permeability of rats with alpha-aminoisobutyric acid during microdialysis: Possible application to behavioral studies
    Choi, YH
    Fletcher, PJ
    Wong, CCS
    Anderson, GH
    [J]. PHYSIOLOGY & BEHAVIOR, 1999, 67 (04) : 587 - 598
  • [10] Peptones stimulate both the secretion of the incretin hormone glucagon-like peptide 1 and the transcription of the proglucagon gene
    Cordier-Bussat, M
    Bernard, C
    Levenez, F
    Klages, N
    Laser-Ritz, B
    Philippe, J
    Chayvialle, JA
    Cuber, JC
    [J]. DIABETES, 1998, 47 (07) : 1038 - 1045