Corticotropin-releasing factor as well as opioid and dopamine are involved in tail-pinch-induced food intake of rats

被引:36
作者
Samarghandian, S [1 ]
Ohata, H [1 ]
Yamauchi, N [1 ]
Shibasaki, T [1 ]
机构
[1] Nippon Med Coll, Dept Physiol, Bunkyo Ku, Tokyo 1138602, Japan
关键词
selective CRFR1 antagonist; stress; naloxone; pimozide; spiperone; feeding;
D O I
10.1016/S0306-4522(02)00712-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Several kinds of stress such as psychological stress, restraint, and foot shock inhibit feeding behavior through corticotropin-releasing factor (CRF). In contrast, a mild tail pinch increases food intake in rats. Although dopamine and opioid are thought to be involved in tail-pinch-induced food intake, it is unknown whether CRF participates in this phenomenon. Therefore, we attempted to clarify this issue using rats. A 30-s tail pinch increased food intake in 30 min after the tail pinch, and this increase was blocked by intraperitoneal injection of CRF receptor type 1 selective antagonist. CRF increased food intake in 30 min after intracerebroventricular injection at a dose of 2 or 10 ng, and this increase was also blocked by CRF receptor type 1 antagonist. Tail-pinch- or CRF-induced food intake was blocked by naloxone, pimozide, and spiperone. These results suggest that CRF, through CRF receptor type 1 as well as opioid and dopaminergic systems, are involved in the mechanism of tail-pinch-induced food intake. The results also suggest that brain CRF has dual effects on food intake, hyperphagia and anorexia, in a stress-dependent manner. (C) 2003 IBRO. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:519 / 524
页数:6
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