Good A J, Westbrook R F
School of Psychology, University of New South Wales, Sydney, Australia.
Behav Neurosci. 1995 Aug;109(4):631-41. doi: 10.1037//0735-7044.109.4.631.
A unilateral microinjection of morphine into the amygdala impaired the acquisition of fear and hypoalgesic responses in rats exposed to a heated floor in a hot-plate apparatus. This impairment was dose dependent, receptor specific, and not observed in rats microinjected with morphine into the caudal basolateral amygdala. A microinjection of morphine into the amygdala reduced the expression of fear responses and of naloxone-sensitive hypoalgesic responses, but did not reduce the expression of naloxone-insensitive hypoalgesic responses. The results document an involvement of opioidergic mechanisms in the amygdala in learned danger and of the amygdala in the control of opioid hypoalgesic responses. They also suggest that learned danger can activate antinociceptive mechanisms independently of the amygdala.
向大鼠杏仁核单侧微量注射吗啡,会损害其在热板装置中接触加热地板时恐惧和痛觉减退反应的习得。这种损害具有剂量依赖性、受体特异性,且在向尾侧基底外侧杏仁核微量注射吗啡的大鼠中未观察到。向杏仁核微量注射吗啡会降低恐惧反应和纳洛酮敏感的痛觉减退反应的表达,但不会降低纳洛酮不敏感的痛觉减退反应的表达。结果证明杏仁核中的阿片肽能机制参与了习得性危险,且杏仁核参与了对阿片类痛觉减退反应的控制。它们还表明,习得性危险可独立于杏仁核激活抗伤害感受机制。