SCH-23390-INDUCED HYPOPHAGIA IS BLOCKED BY THE SELECTIVE CCK-A RECEPTOR ANTAGONIST DEVAZEPIDE, BUT NOT BY THE CCK-B GASTRIN RECEPTOR ANTAGONIST L-365,260

被引:12
|
作者
COOPER, SJ
BARBER, DJ
机构
[1] School of Psychology, University of Birmingham, Birmingham
关键词
(MK 329; Anorexia; Cholecystokinin receptors; D-1; receptor; Devazepide; Dopamine; L-364,718); L-365,260; Raclopride; SCH; 23390;
D O I
10.1016/0361-9230(90)90170-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The selective dopamine D-1 receptor antagonist SCH 23390 (30 μg/kg, SC) significantly reduced palatable food consumption by nondeprived rats in a 30-min test period. Prior administration of the selective CCK-A receptor antagonist devazepide (MK 329; L-364,718) blocked the hypophagic effect of SCH 23390. In contrast, prior administration of the selective CCK-B/gastrin receptor antagonist L-365,260 had no effect. Devazepide did not antagonize a matched hypophagic effect produced by the dopamine D-2 receptor antagonist raclopride (0.1 mg/kg, SC). These data direct attention to possible dopamine-cholecystokinin interactions in relation to the control of ingestional responses, and, more specifically, indicate possible functional relationships between D-1 and CCK-A receptor mechanisms. © 1990.
引用
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页码:631 / 633
页数:3
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