Role of intraduodenally administered enterostatin in rats: Inhibition of food

被引:23
作者
Mei, J [1 ]
ErlansonAlbertsson, C [1 ]
机构
[1] LUND UNIV, DEPT CELL & MOLEC BIOL, SECT MOLEC SIGNALLING, S-22100 LUND, SWEDEN
来源
OBESITY RESEARCH | 1996年 / 4卷 / 02期
关键词
procolipase; pentapeptide; duodenum; fat intake;
D O I
10.1002/j.1550-8528.1996.tb00528.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Central and peripheral administration of enterostatin have been reported to reduce fat or high-fat food intake in rats, Enterostatin is formed in the intestinal lumen by tryptic cleavage of pancreatic procolipase during intraluminal fat digestion, The present experiments were designed to test if enterostatin following intraintestinal infusion would affect food intake in a similar way as intracerebraventricularly or intravenously administered enterostatin. Female Sprague-Dawley rats were fitted with a duodenal catheter and adapted to a feeding schedule for 6 hours each day. After 10 days enterostatin (5.65 and 11.3 nmol/kg/min) or saline were infused into the duodenum and food intake measured, Enterostatin significantly reduced high-fat food intake during the 6 hours of feeding, but had no inhibitory effect on low-fat food intake. Addition of tetracaine to the enterostatin infusates blocked the satiating potency of intestinal enterostatin, These results support the hypothesis of a preabsorptive site of action for enterostatin.
引用
收藏
页码:161 / 165
页数:5
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