Effect of chronic central administration of glucagon-like peptide-1 (7-36) amide on food consumption and body weight in normal and obese rats

被引:55
作者
Davis, HR [1 ]
Mullins, DE [1 ]
Pines, JM [1 ]
Hoos, LM [1 ]
France, CF [1 ]
Compton, DS [1 ]
Graziano, MP [1 ]
Sybertz, EF [1 ]
Strader, CD [1 ]
Van Heek, M [1 ]
机构
[1] Schering Plough Corp, Res Inst, Dept CNS & Cardiovasc Res, Kenilworth, NJ 07033 USA
来源
OBESITY RESEARCH | 1998年 / 6卷 / 02期
关键词
GLP-1; Zucker (fa/fa) rats; receptor desensitization; obesity;
D O I
10.1002/j.1550-8528.1998.tb00329.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Glucagon-like peptide (7-36) amide (GLP-1) acutely inhibits food and water consumption in rats after intracerebroventricular (icv) administration. To assess the potential for desensitization of these effects, we investigated the effects of chronic icy administration of GLP-1 on food consumption and body weight in Sprague-Dawley (SD) rats and Zucker (fa/fa) obese rats. In vitro functional densensitization of the GLP-1 receptor was not observed after overnight exposure of Kin m5F insulinoma cells to GLP-1 at concentrations up to 10 nM. Administration of GLP-1 to SD rats (30 mu g icv twice a day for 6 days) resulted in significant reductions in 24-hour food consumption each day (25 +/- 1%). Continuous icy infusion of GLP-1 for 7 and 14 days significantly inhibited cumulative food consumption and reduced body weight in SD rats. In the genetically obese Zucker rat, chronic dosing with GLP-1 (30 mu g icy) once a day for 6 days caused significant reductions in food consumption each day and a reduction in body weight. These results indicate that the GLP-1 pathways in the central nervous system controlling food consumption do not desensitize after chronic exposure to GLP-1 and suggest that agonists of the central GLP-1 receptor may be effective agents for the treatment of obesity.
引用
收藏
页码:147 / 156
页数:10
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