Manzanares J, Lookingland K J, LaVigne S D, Moore K E
Department of Pharmacology and Toxicology, Michigan State University, East Lansing 48824.
Life Sci. 1991;48(12):1143-9. doi: 10.1016/0024-3205(91)90451-g.
The effect of the kappa opioid receptor antagonist nor-binaltorphimine (NOR-BNI) was examined on the activity of dopamine (DA) neurons comprising the nigrostriatal, mesolimbic, and tuberohypophysial systems in the male rat. DA neuronal activity was estimated by measuring: (1) the concentration of the DA metabolite 3,4-dihydroxyphenylacetic acid and, (2) the accumulation of 3,4-dihydroxyphenylalanine after administration of a decarboxylase inhibitor in brain (striatum, nucleus accumbens) and pituitary regions (intermediate lobe, neural lobe) containing terminals of these neurons. The intracerebroventricular administration of NOR-BNI produced a dose- and time-related increase in the activity of tuberohypophysial DA neurons, but failed to alter the activity of nigrostriatal or mesolimbic DA neurons. The ability of NOR-BNI to enhance the activity of tuberohypophysial DA neurons was blocked by the kappa opioid agonist U-50,488. These results indicate that NOR-BNI, acting on kappa opioid receptors, activates tuberohypophysial DA neurons projecting to the neural and intermediate lobes of the pituitary.
研究了κ阿片受体拮抗剂去甲纳曲酮(NOR - BNI)对雄性大鼠中构成黑质纹状体、中脑边缘和结节垂体系统的多巴胺(DA)神经元活性的影响。通过测量以下指标来评估DA神经元活性:(1)DA代谢物3,4 - 二羟基苯乙酸的浓度,以及(2)在含有这些神经元终末的脑区(纹状体、伏隔核)和垂体区域(中间叶、神经叶)给予脱羧酶抑制剂后3,4 - 二羟基苯丙氨酸的蓄积情况。脑室内注射NOR - BNI可使结节垂体DA神经元的活性出现剂量和时间依赖性增加,但未改变黑质纹状体或中脑边缘DA神经元的活性。κ阿片激动剂U - 50,488可阻断NOR - BNI增强结节垂体DA神经元活性的能力。这些结果表明,作用于κ阿片受体的NOR - BNI可激活投射至垂体神经叶和中间叶的结节垂体DA神经元。