Yu L C, Han J S
Department of Physiology, Beijing Medical University, P.R. China.
Int J Neurosci. 1990 Oct;54(3-4):245-51. doi: 10.3109/00207459008986640.
This study explored the possibility of a relay at habenula for the descending neural pathway of antinociception. The latency of the escape response elicited by radiant heat on the snout of the rabbit was taken as index of nociception. (1) Microinjection of 20 micrograms of morphine into nucleus accumbens resulted in a one-fold increase in nociceptive threshold 20-40 min after the injection. This effect of morphine was markedly attenuated by naloxone or met-enkephalin antiserum administered to the nucleus habenula, suggesting that the release of met-enkephalin in habenula is essential for the antinociception induced by morphine injected into nucleus accumbens. (2) Injection of 10 micrograms of morphine into habenula produced a significant increase in escape response latency 20-40 min after the injection. This antinociceptive effect of morphine was attenuated by naloxone or muscimol, and enhanced by bicuculline methochloride administered to periaqueductal grey, suggesting that morphine may act on habenula to activate a descending neural pathway extending to periaqueductal grey to induce an antinociceptive effect, which seems to utilize endogenous opioid peptides and gamma-aminobutyric acid as its mediators. Taking together, the results suggest that habenula is an important relay in the descending neural pathway from nucleus accumbens to periaqueductal grey subserving antinociception.
本研究探讨了缰核在伤害性感受下行神经通路中作为中继站的可能性。以辐射热刺激兔鼻引起逃避反应的潜伏期作为伤害性感受的指标。(1)向伏隔核微量注射20微克吗啡后20 - 40分钟,伤害性感受阈值增加了一倍。向缰核注射纳洛酮或甲硫脑啡肽抗血清可显著减弱吗啡的这种作用,这表明缰核中甲硫脑啡肽的释放对于伏隔核注射吗啡诱导的伤害性感受抑制至关重要。(2)向缰核注射10微克吗啡后20 - 40分钟,逃避反应潜伏期显著延长。吗啡的这种伤害性感受抑制作用可被纳洛酮或蝇蕈醇减弱,而向导水管周围灰质注射甲氯异嗪可增强该作用,这表明吗啡可能作用于缰核,激活一条延伸至导水管周围灰质的下行神经通路以诱导伤害性感受抑制作用,这一过程似乎以内源性阿片肽和γ - 氨基丁酸作为介质。综上所述,结果表明缰核是伏隔核至导水管周围灰质下行神经通路中一个重要的中继站,该通路参与伤害性感受抑制。