Department of Physiological Sciences, CCB, EEL-CTC, Federal University of Santa Catarina, 88040-900 Florianópolis SC, Brazil.
Behav Brain Res. 2009 Dec 28;205(2):396-405. doi: 10.1016/j.bbr.2009.07.017. Epub 2009 Jul 24.
This study examined the acute changes in feeding and drinking behaviours of free-feeding and free-drinking pigeons, in response to local injections of metergoline (MET, 5-HT(1/2) receptor antagonist; 7 and 20 nmol), GR46611 (GR, 5-HT(1B/1D) agonist; 2 and 6 nmol) or vehicle, into two components of the arcopallium: the nucleus taeniae of the amygdala (TnA) and the arcopallium intermedium (AI). In the TnA, the highest MET dose elicited a short-lived hyperphagy, without affecting drinking or non-ingestive behaviours during the first hour after injection. In contrast, all MET doses promptly increased drinking when injected in the AI, without affecting feeding; this effect was still evident 3 and 24 h after the treatment. When injected in the TnA, the highest GR dose promptly increased both food and water intake; these effects persisted 24 h after the treatments. GR injections in the AI evoked long-lasting increases in drinking, but not in feeding. Injections of these drugs into other arcopallial nuclei evoked no significant ingestive effects. These data indicate the presence of a tonic inhibitory influence of serotonergic inputs, partially mediated by 5-HT(1B/1D) receptors, on feeding- and drinking-related TnA circuits and on mechanisms controlling drinking in the AI. Compared to data from the rodent medial amygdala, our results suggest that a tonic inhibitory 5-HTergic control of feeding (but not drinking) behaviour, mediated by 5-HT(1/2) receptors and exerted in the medial amygdaloid area, may represent a broadly conserved functional attribute in the amniote brain, but probably involves many important taxa-specific neural mechanisms.
本研究考察了自由摄食和饮水的鸽子在眶回中两个核团(杏仁核终纹核和中间眶回)接受麦角酰二乙胺(MET,5-HT1/2 受体拮抗剂;7 和 20 nmol)、GR46611(GR,5-HT1B/1D 激动剂;2 和 6 nmol)或载体局部注射后摄食和饮水行为的急性变化。在 TnA 中,最高剂量的 MET 诱发了短暂的多食症,而在注射后 1 小时内不影响饮水或非摄食行为。相比之下,当 MET 剂量较高时,所有 MET 剂量都会迅速增加 AI 中的饮水量,而不影响摄食;这种作用在治疗后 3 和 24 小时仍然明显。当在 TnA 中注射时,最高剂量的 GR 会立即增加食物和水的摄入;这些作用在治疗后 24 小时仍然存在。GR 注射到 AI 中会引起长时间的饮水增加,但不会引起摄食增加。这些药物注射到其他眶回核中不会引起明显的摄食效应。这些数据表明,存在一种来自于 5-HT1B/1D 受体的 5-HT 能传入的紧张性抑制影响,部分介导摄食相关的 TnA 回路和控制 AI 中饮水的机制。与来自啮齿动物内侧杏仁核的数据相比,我们的结果表明,由 5-HT1/2 受体介导的紧张性抑制 5-HT 能控制摄食(但不控制饮水)行为,可能在有胎盘动物的大脑中代表一种广泛保守的功能属性,但可能涉及许多重要的特定于类群的神经机制。