Iyengar S, Kim H S, Wood P L
Neurosci Lett. 1987 Jun 15;77(2):226-30. doi: 10.1016/0304-3940(87)90591-x.
The action of butorphanol, an opiate agonist/antagonist, was studied on dopamine (DA) metabolism in several mesocortical and mesolimbic areas and compared with its effects on the nigrostriatal DA pathway. While butorphanol had a bell-shaped dose-response relationship for elevation of DA metabolites in the striatum, it had no action on DA metabolites in the entorhinal, prefrontal, pyriform and cingulate cortices and in the olfactory tubercle. In all of these areas morphine stimulated dopamine metabolism (except for the entorhinal cortex). In contrast, in the nucleus accumbens, butorphanol increased the levels of dihydroxyphenylacetic acid (DOPAC), homovanillic acid (HVA) and 3-methoxytyramine (3-MT) with no increase in DA steady state levels. This effect was reversible by both opiate antagonists, naloxone and WIN 44441-3 and appears to be mu-opioid receptor-mediated.
研究了阿片类激动剂/拮抗剂布托啡诺对几个中皮层和中脑边缘区域多巴胺(DA)代谢的作用,并将其与对黑质纹状体DA通路的影响进行了比较。虽然布托啡诺对纹状体中DA代谢产物的升高具有钟形剂量反应关系,但它对内嗅皮质、前额叶皮质、梨状皮质、扣带回皮质和嗅结节中的DA代谢产物没有作用。在所有这些区域,吗啡刺激多巴胺代谢(内嗅皮质除外)。相反,在伏隔核中,布托啡诺增加了二羟基苯乙酸(DOPAC)、高香草酸(HVA)和3-甲氧基酪胺(3-MT)的水平,而DA稳态水平没有增加。阿片类拮抗剂纳洛酮和WIN 44441-3均可逆转这种作用,且这种作用似乎是由μ-阿片受体介导的。