Tempel A, Habas J, Paredes W, Barr G A
Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY 10461.
Brain Res. 1988 Jun 1;469(1-2):129-33. doi: 10.1016/0165-3806(88)90176-9.
Chronic administration of morphine to pre- and postnatal rats produced a marked decrease in brain mu-opioid receptor density with-out change in receptor affinity. No significant changes in delta- or kappa-receptors were observed. This downregulation was accompanied by tolerance to the analgesic actions of morphine. In neonates exposed to morphine from postnatal day one, mu-receptor number was significantly depressed until postnatal day 8, then increased gradually to control levels by day 14 of treatment. Longer treatment produced no further change in opioid receptors. These data represent the first demonstration of in vivo downregulation of brain mu-opioid receptors following morphine administration and provide evidence for a unique plasticity of the immature opioid receptor system.
对产前和产后大鼠长期给予吗啡,可使脑内μ阿片受体密度显著降低,而受体亲和力无变化。未观察到δ或κ受体有显著变化。这种下调伴随着对吗啡镇痛作用的耐受性。在出生后第1天开始接触吗啡的新生儿中,μ受体数量在出生后第8天之前显著降低,然后在治疗第14天时逐渐增加至对照水平。更长时间的治疗未使阿片受体进一步变化。这些数据首次证明了吗啡给药后体内脑μ阿片受体的下调,并为未成熟阿片受体系统的独特可塑性提供了证据。