Steece K A, Lee J M, Fields J Z, DeLeon-Jones F A, Ritzmann R F
Department of Neurobiology and Anatomy, University of Rochester, NY 14642.
Life Sci. 1989;44(20):1449-55. doi: 10.1016/0024-3205(89)90323-8.
Post-synaptic receptor modulation is thought to be one important mechanism involved in the adaptation of a neuronal system during chronic exposure to a drug. However, initial studies of opioid receptor regulation following chronic in vivo administration of narcotic agonists, such as morphine, reported no down-regulation in the number of opioid receptors in the brain. Subsequent studies, employing in vitro preparations, have reported evidence of opioid receptor down-regulation under specific conditions. It remains to be determined whether the in vitro phenomena of opioid receptor plasticity is relevant to the intact mammalian central nervous system. The data in this report shows that chronic in vivo administration the opioid peptide methionine enkephalin, results in a significant, regionally specific down-regulation of delta opioid receptors in rat brain: 30% decrease in receptor density in the striatum; no change in hypothalamus.
突触后受体调节被认为是慢性接触药物期间神经元系统适应性变化的一个重要机制。然而,最初关于麻醉激动剂(如吗啡)慢性体内给药后阿片受体调节的研究报告称,大脑中阿片受体数量没有下调。随后采用体外制剂的研究报告了在特定条件下阿片受体下调的证据。阿片受体可塑性的体外现象是否与完整的哺乳动物中枢神经系统相关仍有待确定。本报告中的数据表明,慢性体内给予阿片肽甲硫氨酸脑啡肽会导致大鼠脑中δ阿片受体显著的、区域特异性下调:纹状体中受体密度降低30%;下丘脑无变化。