GLP-1 and GLP-2 act in concert to inhibit fasted, but not fed, small bowel motility in the rat

被引:39
作者
Bozkurt, A
Näslund, E
Holst, JJ
Hellström, PM
机构
[1] Danderyd Hosp, Karolinska Inst, Div Surg, SE-18288 Stockholm, Sweden
[2] Marmara Univ, Dept Physiol, Istanbul, Turkey
[3] Univ Copenhagen, Dept Med Physiol, Copenhagen, Denmark
[4] Karolinska Hosp, Karolinska Inst, Dept Gastroenterol & Hepatol, S-10401 Stockholm, Sweden
关键词
glucagon-like peptides; migrating myoelectric complex; gut motility;
D O I
10.1016/S0167-0115(02)00095-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Small bowel motility was studied in rats at increasing (1-20 pmol/kg/min) intravenous doses of either glucagon-like peptide-1 (GLP-1) or glucagon-like peptide-2 (GLP-2) alone, or in combination in the fasted and fed state. There was a dose-dependent inhibitory action of GLP-1 on the migrating myoelectric complex (MMC), where the dose of 5 pmol/kg/min induced an increased MMC cycle length. No effect was seen with GLP-2 alone, but the combination of GLP-1 and GLP-2 induced a more pronounced inhibitory effect, with significant increase of the MMC cycle length from a dose of 2 pmol/kg/min. During fed motility, infusion of GLP-1 resulted in an inhibition of spiking activity compared to control. In contrast, infusion of GLP-2 only numerically increased spiking activity compared to control, while the combination of GLP-1 and GLP-2 resulted in no change compared to control. In summary, this study demonstrates an additive effect of peripheral administration of GLP-1 and GLP-2 on fasted small bowel motility. In the fed state, GLP-1 and GLP-2 seem to display counter-balancing effects on motility of the small intestine. (C) 2002 Elsevier Science B.V All rights reserved.
引用
收藏
页码:129 / 135
页数:7
相关论文
共 31 条
[1]   Characteristics of fasting and fed myoelectric activity in rat small intestine: Evaluation by computer analysis [J].
Branstrom, R ;
Hellstrom, PM .
ACTA PHYSIOLOGICA SCANDINAVICA, 1996, 158 (01) :53-62
[2]   Induction of intestinal epithelial proliferation by glucagon-like peptide 2 [J].
Drucker, DJ ;
Ehrlich, P ;
Asa, SL ;
Brubaker, PL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (15) :7911-7916
[3]   Glucagon-like peptide 1 promotes satiety and suppresses energy intake in humans [J].
Flint, A ;
Raben, A ;
Astrup, A ;
Holst, JJ .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (03) :515-520
[4]   CLONING AND FUNCTIONAL EXPRESSION OF A HUMAN GLUCAGON-LIKE PEPTIDE-1-RECEPTOR [J].
GRAZIANO, MP ;
HEY, PJ ;
BORKOWSKI, D ;
CHICCHI, GG ;
STRADER, CD .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 196 (01) :141-146
[5]   Glucagon-like peptide-1:: a potent regulator of food intake in humans [J].
Gutzwiller, JP ;
Göke, B ;
Drewe, J ;
Hildebrand, P ;
Ketterer, S ;
Handschin, D ;
Winterhalder, R ;
Conen, D ;
Beglinger, C .
GUT, 1999, 44 (01) :81-86
[6]   Glucagon-like peptide-1 promotes satiety and reduces food intake in patients with diabetes mellitus type 2 [J].
Gutzwiller, JP ;
Drewe, J ;
Göke, B ;
Schmidt, H ;
Rohrer, B ;
Lareida, J ;
Beglinger, C .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1999, 276 (05) :R1541-R1544
[7]   Structure, measurement, and secretion of human glucagon-like peptide-2 [J].
Hartmann, B ;
Johnsen, AH ;
Orskov, C ;
Adelhorst, K ;
Thim, L ;
Holst, JJ .
PEPTIDES, 2000, 21 (01) :73-80
[8]  
HELLSTROM PM, 1993, SURG RES COMMUN, V14, P51
[9]   Enteroglucagon [J].
Holst, JJ .
ANNUAL REVIEW OF PHYSIOLOGY, 1997, 59 :257-271
[10]   Glucagon-like peptide-1 inhibits gastric emptying via vagal afferent-mediated central mechanisms [J].
Imeryuz, N ;
Yegen, BC ;
Bozkurt, A ;
Coskun, T ;
VillanuevaPenacarrillo, ML ;
Ulusoy, NB .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1997, 273 (04) :G920-G927