Department of Physiology, Harbin Medical University, 194 Xuefu Road, Nangang District, Harbin, Heilongjiang 150081,China.
Neurosci Lett. 2010 Aug 9;480(1):59-63. doi: 10.1016/j.neulet.2010.06.003. Epub 2010 Jun 8.
Norepinephrine (NE) participates in pain modulation of the central nervous system. The caudate putamen (CPu) is one region of the basal ganglia that has been demonstrated to be involved in nociceptive perception. Our previous work has shown that microinjection of different doses of norepinephrine into the CPu produces opposing effects in the tail-flick latency (TFL) of rats. However, the mechanism of action of NE on the pain-related neurons in the CPu remains unclear. The present study examined the effects of NE and the alpha-adrenoceptor antagonist phentolamine on the pain-evoked response of pain-excitation neurons (PENs) and pain-inhibition neurons (PINs) in the CPu of rats. Trains of electric impulses were used for noxious stimulation, and were applied to the sciatic nerve. The electrical activities of pain-related neurons in the CPu were recorded by a glass microelectrode. The results revealed that intra-CPu microinjection of NE (8microg/2microl) increased evoked firing frequency of PEN and shortened the firing latency, but decreased the evoked firing frequency of PIN and prolonged the inhibitory duration (ID). Intra-CPu administration of phentolamine (4microg/2microl) showed the opposite effects. The above results suggest that NE in the CPu modulates nociception by affecting the baseline firing rates of PENs and PINs.
去甲肾上腺素(NE)参与中枢神经系统的疼痛调制。尾状核(CPu)是基底神经节的一个区域,已被证明参与痛觉感知。我们之前的工作表明,向 CPu 中注射不同剂量的去甲肾上腺素会对大鼠的尾部闪烁潜伏期(TFL)产生相反的影响。然而,NE 对 CPu 中与疼痛相关的神经元的作用机制仍不清楚。本研究检查了 NE 和α-肾上腺素受体拮抗剂酚妥拉明对 CPu 中疼痛兴奋神经元(PENs)和疼痛抑制神经元(PINs)的疼痛诱发反应的影响。使用电脉冲串进行有害刺激,并施加到坐骨神经上。通过玻璃微电极记录 CPu 中与疼痛相关的神经元的电活动。结果表明,CPu 内微注射 NE(8μg/2μl)增加了 PEN 的诱发放电频率并缩短了放电潜伏期,但降低了 PIN 的诱发放电频率并延长了抑制持续时间(ID)。CPu 内给予酚妥拉明(4μg/2μl)则表现出相反的效果。上述结果表明,CPu 中的 NE 通过影响 PEN 和 PIN 的基线放电率来调节伤害感受。