Zhang Ying, Yang Chunxiao, Xu Xianzhang, Jiao Runsheng, Jin Hongbo, Lv Yanhong, Yang Huike, Xu Manying
Department of Physiology, Harbin Medical University, Xuefu Road, No. 174, Harbin 150081, China.
Biochem Biophys Res Commun. 2008 Jul 18;372(1):179-85. doi: 10.1016/j.bbrc.2008.05.009. Epub 2008 May 12.
Droperidol causes the blockage of the dopamine receptors in the central nervous system that are involved in pain transmission. However, the mechanism of action of droperidol in pain-related neurons is not clear, and it is still unknown whether opioids are involved in the modulation of this processing. The present study examines the effect of droperidol on the pain-evoked response of pain-excitation neurons (PENs) and pain-inhibition neurons (PINs) in the caudate nucleus (Cd) of rats. The trains of electric impulses applied to the sciatic nerve were used as noxious stimulation. Our results revealed that droperidol decreased the frequency of PEN discharge, and increased the frequency PIN discharge evoked by the noxious stimulation in the Cd of normal rats, while administration of droperidol to morphine-dependent rats produced the opposite response. Those demonstrated that droperidol is involved in the modulation of nociceptive information transmission in Cd, and there were completely opposite responses to painful stimulation between normal and morphine-dependent rats after administration of droperidol.
氟哌利多会阻断中枢神经系统中参与疼痛传递的多巴胺受体。然而,氟哌利多在疼痛相关神经元中的作用机制尚不清楚,并且阿片类药物是否参与这种过程的调节仍不明确。本研究考察了氟哌利多对大鼠尾状核中痛觉兴奋神经元(PENs)和痛觉抑制神经元(PINs)的疼痛诱发反应的影响。施加于坐骨神经的电脉冲串用作伤害性刺激。我们的结果显示,氟哌利多降低了正常大鼠尾状核中伤害性刺激诱发的PEN放电频率,并增加了PIN放电频率,而给吗啡依赖大鼠施用氟哌利多则产生相反的反应。这些结果表明氟哌利多参与了尾状核中伤害性信息传递的调节,并且在施用氟哌利多后,正常大鼠和吗啡依赖大鼠对疼痛刺激的反应完全相反。