脑啡肽原
强啡肽
伏隔核
表号:SCH-23390
多巴胺能
内科学
纹状体
内分泌学
基底神经节
多巴胺
化学
生物
受体
脑啡肽
中枢神经系统
阿片肽
类阿片
医学
作者
Brian J. Morris,Volker Höllt,A. Herz
出处
期刊:Neuroscience
[Elsevier]
日期:1988-05-01
卷期号:25 (2): 525-532
被引量:143
标识
DOI:10.1016/0306-4522(88)90256-4
摘要
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 the 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.
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