Morris B J, Höllt V, Herz A
Department of Neuropharmacology, Max-Planck-Institut für Psychiatrie, Planegg-Martinsried, Federal Republic of Germany.
Neuroscience. 1988 May;25(2):525-32. doi: 10.1016/0306-4522(88)90256-4.
In situ hybridization was used to measure the levels of proenkephalin mRNA and prodynorphin mRNA in regions of rat striatum and nucleus accumbens. Chronic administration of haloperidol (2.4 mg/kg/day for 7 days) increased the levels of proenkephalin mRNA in both striatum and nucleus accumbens. In contrast, the levels of prodynorphin mRNA were not significantly affected in any region. Chronic administration of the D1 antagonist SCH 23390 (2.4 mg/kg/day for 7 days) decreased the striatal content of proenkephalin mRNA. A similar effect was seen in the lateral nucleus accumbens. The levels of prodynorphin mRNA were unaffected by SCH 23390 treatment in all regions examined. These results suggest that there is no major tonic dopaminergic regulation of prodynorphin synthesis in the basal ganglia. However, it appears that there is a tonic suppression, via D2 receptors, and a tonic enhancement, via D1 receptors, of proenkephalin synthesis, in the striatum and nucleus accumbens.
采用原位杂交技术检测大鼠纹状体和伏隔核区域中脑啡肽原mRNA和强啡肽原mRNA的水平。长期给予氟哌啶醇(2.4mg/kg/天,共7天)可使纹状体和伏隔核中的脑啡肽原mRNA水平升高。相比之下,强啡肽原mRNA水平在任何区域均未受到显著影响。长期给予D1拮抗剂SCH 23390(2.4mg/kg/天,共7天)可降低纹状体中脑啡肽原mRNA的含量。在伏隔核外侧也观察到类似的效应。在所有检测区域中,强啡肽原mRNA水平均不受SCH 23390治疗的影响。这些结果表明,基底神经节中强啡肽合成不存在主要的多巴胺能紧张性调节。然而,在纹状体和伏隔核中,似乎存在通过D2受体的紧张性抑制和通过D1受体的紧张性增强来调节脑啡肽原的合成。