DA1 receptor activity opposes anorectic responses to amino acid-imbalanced diets

被引:4
作者
Aja, SM
Chan, P
Barrett, JA
Gietzen, DW
机构
[1] Univ Calif Davis, Dept Vet Med Anat Physiol & Cell Biol, Davis, CA 95616 USA
[2] Univ Calif Davis, Food Intake Lab, Davis, CA 95616 USA
关键词
amino acid deficiency; nutrition; food intake; tropisetron; devazepide; SCH-23390; SKF-38393; eticlopride; serotonin(3) receptor; CCKA receptor; DA(1) receptor; DA(2) receptor;
D O I
10.1016/S0091-3057(98)00213-5
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The serotonin(3) (5-HT3) receptor plays an important role in the aminoprivic feeding model. Other neurochemical systems, including cholecystokinin (CCK) and dopamine (DA), are known to affect food intake. We pretreated rats systemically with tropisetron, a 5-HT3 receptor antagonist, alone and combined with antagonists of DA(1) and DA(2) receptors, and measured intake of an amino acid-imbalanced diet (IMB). As expected, tropisetron significantly increased intake of IMB. SCH-23390, a DA(1) antagonist, increased IMB anorexia. When combined with tropisetron, DA(2) antagonism with eticlopride reduced short-term intake of both the basal diet (BAS) and IMB. In the IMB model, specificity of 5-HT3-DA(2) interactions, and of 5-HT3-CCKA interactions from previous studies, prompted investigation of CCKA-DA(2) interactions; there appeared to be none. SKF-38393, a DA(1) agonist, combined with the CCKA receptor antagonist, devazepide, increased BAS and tended to increase IMB intake. Thus, CCKA-DA(1) interactions were not specific for IMB. These data suggest that DA, receptor activity opposes IMB anorexia, possibly via an interaction with the 5-HT3 receptor. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:493 / 498
页数:6
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