Involvement of oxytocin and its receptor in nociceptive modulation in the central nucleus of amygdala of rats

被引:38
作者
Han, Yi [1 ,2 ,3 ]
Yu, Long-Chuan [1 ,2 ]
机构
[1] Peking Univ, Coll Life Sci, Neurobiol Lab, Beijing 100871, Peoples R China
[2] Peking Univ, Coll Life Sci, State Key Lab Biomembrane & Membrane Biotechnol, Beijing 100871, Peoples R China
[3] Kunming Med Coll, Fac Basic Med Sci, Kunming 650031, Peoples R China
基金
中国国家自然科学基金;
关键词
Anti-nociception; Oxytocin; Central nucleus of amygdala; Hindpaw withdrawal latency; OPIOID RECEPTORS; PAIN; ANTINOCICEPTION; ACCUMBENS; INTACT; MODEL;
D O I
10.1016/j.neulet.2009.02.062
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Studies have demonstrated that oxytocin plays important roles in pain modulation in the central nervous system. Oxytocin-ergic neurons are found in paraventricular nucleus and supraoptic nucleus of the hypothalamus. The oxytocin-ergic neurons send fibers from hypothalamus to amygdala and high density of oxytocin receptors are found in the central nucleus of amygdala (CeA). The present study was performed to investigate the influences of oxytocin and its receptors on nociceptive responses in the CeA of rats. Intra-CeA injection of 0.1, 0.5 or 1 nmol of oxytocin induced dose-dependent increases in the handpaw withdrawal latency induced by noxious thermal and mechanical stimulation in rats. The oxytocin-induced anti-nociception could be blocked by the selective oxytocin antagonist 1-deamino-2D-Tyr-(Oet)-4-Thr-8-Orn-oxytocin. The present study demonstrated that oxytocin and its receptors are involved in nociceptive modulation in the CeA of rats. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:101 / 104
页数:4
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