INCREASED FOOD-INTAKE AFTER TYPE-A BUT NOT TYPE-B CHOLECYSTOKININ RECEPTOR BLOCKADE

被引:77
作者
CORWIN, RL [1 ]
GIBBS, J [1 ]
SMITH, GP [1 ]
机构
[1] CORNELL UNIV,MED CTR,COLL MED,DEPT PSYCHIAT,NEW YORK,NY 10021
关键词
CCK; DEVAZEPIDE; INGESTION; L-364,718; L-365,260; MK329; SATIETY; CCK RECEPTOR ANTAGONISTS; ORAL PRELOAD; CONTROL OF FOOD INTAKE; BRAIN CHOLECYSTOKININ; PHARMACOLOGICAL CHARACTERIZATION; ANTAGONIST; CCK; RAT; SATIETY; PEPTIDE; POTENT; L-364,718; GASTRIN;
D O I
10.1016/0031-9384(91)90529-W
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
To assess the role of cholecystokinin (CCK) receptors in mediating the satiating effect of an oral preload, overnight food-deprived rats (n = 7) were given access to a high-carbohydrate liquid diet for 40 min. At the end of 40 min, food was removed and rats were injected subcutaneously (SC) with devazepide (DVZ; 1 ng/kg-1 mg/kg), an antagonist selective for the CCK-A receptor, or its vehicle, 0.5% carboxymethylcellulose (CMC). Thirty min after injection, rats were given access to the same liquid food for 60 min. DVZ increased food intake significantly. Furthermore, the effectiveness of a very low dose of DVZ (10 ng/kg) is strong evidence that the effect of DVZ was specific for CCK-A receptors. Three of the rats that increased food intake after DVZ were also tested with L-365,260, an antagonist selective for the CCK-B receptor (10 ng/kg-100-mu-g/kg). L365,260 did not increase food intake significantly. These results confirm and extend previous reports that CCK-A receptor blockade increases food intake after an oral preload. They do not, however, demonstrate a role for the CCK-B receptor in mediating the satiating effect of ingested food under the same experimental conditions.
引用
收藏
页码:255 / 258
页数:4
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