Evidence for a μ-opioid-oploid connection between the paraventricular nucleus and ventral tegmental area in the rat

被引:27
作者
Quinn, JG
O'Hare, E
Levine, AS
Kim, EM
机构
[1] Univ Ulster, Sch Psychol, Newtownabbey BT37 0QB, Co Antrim, North Ireland
[2] Vet Adm Med Ctr, Res Serv 151, Minnesota Obes Ctr, Minneapolis, MN 55417 USA
基金
英国惠康基金;
关键词
opioid; DAMGO; paraventricular nucleus;
D O I
10.1016/j.brainres.2003.08.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The paraventricular nucleus (PVN) and the ventral tegmental area (VTA) have been shown to be involved in opioid mediated feeding behavior. The present study examined whether mu-opioid signalling between the PVN and VTA affected feeding behavior. Male Sprague-Dawley rats were cannulated with one cannula placed in the PVN and two cannulae placed in the VTA, which allowed for co-administration of the mu-opioid receptor agonist [D-Ala(2), NMe-Phe(4), Gly-ol(5)]-enkephalin (DAMGO) in one site and the opioid antagonist naltrexone (NTX) in the other site. Bilateral administration of DAMGO (1.2, 2.4 and 4.9 nmol) into the VTA stimulated feeding dose dependently at 2.4 and 4.9 nmol (P<0.05). The DAMGO (2.4 nmol)-induced increase of food intake following injection into the PVN was blocked by bilateral injection of NTX (6.6, 13.2 and 26.5 nmol) into the VTA at 2 and 4 h (P<0.05). In the reverse situation, the DAMGO (2.4 nmol)-induced increase of food intake following injection into the VTA was blocked by injection of NTX (13.2 and 26.5 nmol) into the PVN at 2 and 4 h (P<0.05). The present study suggests that a bidirectional mu-opioid-opioid signalling pathway exists between the PVN and the VTA which influences feeding. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:206 / 211
页数:6
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