Lindefors N, Brené S, Herrera-Marschitz M, Persson H
Department of Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Ann N Y Acad Sci. 1990;611:175-85.
NPY mRNA expression was studied in rat brain using in situ hybridization and RNA blot analysis. Transsynaptic regulation of NPY gene expression was specifically studied in caudate-putamen and frontoparietal (somatosensory) cortex of rats with unilateral lesion of midbrain dopamine neurons and in sham-injected animals. NPY mRNA expression in these two brain regions and the regulation of midbrain dopamine neurons were compared with that of SOM, PPT, CCK and GAD mRNA expression. Neurons expressing NPY and SOM mRNA showed a similar distribution and the expression of both NPY and SOM appears to be regulated by dopamine in a similar fashion. Following a unilateral dopamine deafferentation, the numerical density of both NPY and SOM mRNA expressing neurons almost doubled in the lesioned rat caudate-putamen with no change in the average grain density over positive neurons. Hence, in the intact caudate-putamen dopamine appears to normally suppress expression of these two neuropeptide genes. An activation of both NPY and SOM mRNA expression in many non- or low-expressing neurons is seen when the level of dopamine is decreased. In the frontoparietal cortex, on the other hand, dopamine appears to stimulate NPY and SOM gene expression. RNA blot analysis shows clear-cut changes of NPY mRNA levels in both caudate-putamen and frontoparietal cortex consistent with the changes observed using in situ hybridization. No evidence was found for a change in CCK mRNA expression by the dopamine deafferentation, while PPT mRNA expression decreased in the deafferented caudate-putamen. Consequently, dopamine exerts dissimilar effects on the expression of different neuropeptide genes, that in turn do not respond in the same way in different brain regions. Indirect evidence is also presented indicating that dopamine regulates NPY mRNA expression in a subpopulation of neurons that possibly also express GAD mRNA, both in caudate-putamen and in frontoparietal cortex.
利用原位杂交和RNA印迹分析研究了大鼠脑中NPY mRNA的表达。在单侧中脑多巴胺神经元损伤的大鼠和假注射动物的尾状核-壳核及额顶叶(体感)皮质中,专门研究了NPY基因表达的跨突触调节。将这两个脑区的NPY mRNA表达及中脑多巴胺神经元的调节与SOM、PPT、CCK和GAD mRNA的表达进行了比较。表达NPY和SOM mRNA的神经元显示出相似的分布,并且NPY和SOM的表达似乎以相似的方式受多巴胺调节。单侧多巴胺去传入后,在损伤的大鼠尾状核-壳核中,表达NPY和SOM mRNA的神经元的数量密度几乎增加了一倍,而阳性神经元的平均颗粒密度没有变化。因此,在完整的尾状核-壳核中,多巴胺似乎正常情况下会抑制这两种神经肽基因的表达。当多巴胺水平降低时,许多不表达或低表达的神经元中NPY和SOM mRNA的表达都会被激活。另一方面,在额顶叶皮质中,多巴胺似乎会刺激NPY和SOM基因的表达。RNA印迹分析显示,尾状核-壳核和额顶叶皮质中NPY mRNA水平有明显变化,与原位杂交观察到的变化一致。没有发现多巴胺去传入导致CCK mRNA表达发生变化的证据,而在去传入的尾状核-壳核中PPT mRNA表达下降。因此,多巴胺对不同神经肽基因的表达产生不同的影响,而这些基因在不同脑区的反应方式也不相同。还提供了间接证据表明,多巴胺在尾状核-壳核和额顶叶皮质中,在可能也表达GAD mRNA的神经元亚群中调节NPY mRNA的表达。