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目的 观察静脉注射普鲁卡因及芬太尼对外侧网状核神经元伤害性反应的影响,以探讨其镇痛作用是否有脑的高级中枢的参与。方法 应用细胞外微电极记录的方法,在Wistar大鼠观察静脉注射普鲁卡因(10m g/kg)及芬太尼(1、2、5 和10μg/kg)对C强度刺激腓肠神经诱发的外侧网状核神经元伤害性反应的影响。结果 静脉注射普鲁卡因对测试的7 个单位的神经元伤害性反应均呈抑制作用,平均最大抑制为366% (P< 001),芬太尼对所有被观察的24 个神经元产生了抑制作用,平均抑制分别为290% 、756% 、639% 和718% ,均具有显著性差异,此效应并被静脉注射纳络酮(05m g/kg)完全逆转。在2 个芬太尼产生抑制的单位,静脉注射普鲁卡因也产生了抑制效应。结论 外侧网状核神经元与痛觉的传导及调制有关,脑的高级中枢也参与了静脉注射普鲁卡因及芬太尼产生的镇痛作用
Objective To observe the effect of intravenous procaine and fentanyl on the nociceptive reaction of neurons in the reticular nucleus in order to find out whether the analgesic effect involves the involvement of the higher central nervous system. Methods Extracellular microelectrode recording was used to observe the effects of intravenous injection of procaine (10 m g / kg) and fentanyl (1, 2, 5 and 10 μg / kg) on the C intensity-stimulated sural nerve in Wistar rats Of the outer reticular nucleus neurons. Results Intravenous injection of procaine inhibited neuronal nociceptive response in all seven units tested, with an average maximum inhibition of 36.6% (P <001). Fentanyl was also effective against all 24 observed The inhibitory effect of neurons was found. The average inhibition was 290%, 756%, 639% and 718%, respectively. There was a significant difference between the two groups. This effect was also induced by intravenous injection of naloxone g / kg) completely reversed. Intravenous procaine also produced an inhibitory effect in the two units where inhibition of fentanyl occurred. CONCLUSIONS: The neurons in the lateral reticular nucleus are associated with the conduction and modulation of pain sensation. The higher centers of the brain are also involved in the analgesic effect of intravenous procaine and fentanyl