Brené S, Herrera-Marschitz M, Persson H, Lindefors N
Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Brain Res Mol Brain Res. 1994 Feb;21(3-4):274-82. doi: 10.1016/0169-328x(94)90258-5.
The glutamate analogue kainic acid was injected into the hippocampus of intact or 6-hydroxydopamine deafferented rats to investigate the influence of hippocampal neurons on the expression of dopamine D1 and D2 receptor mRNAs in subregions of the striatal complex and possible modulation by dopaminergic neurons. Quantitative in situ hybridization using 35S-labeled oligonucleotide probes specific for dopamine D1 and D2 receptor mRNAs, respectively, were used. It was found that an injection of kainic acid into the hippocampal formation had alone no significant effect on dopamine D1 or D2 receptor mRNA levels in any of the analyzed striatal subregions in animals analyzed 4 h after the injections. Kainic acid stimulation in the hippocampus ipsilateral to the dopamine lesion produced an increase in D1 receptor mRNA levels in the ipsilateral medial caudate-putamen, and a bilateral increase in core and shell of nucleus accumbens (ventral striatal limbic regions). A unilateral 6-hydroxydopamine lesion alone caused an increase in D2 receptor mRNA in the lateral caudate-putamen (dorsal striatal motor region) ipsilateral to the lesion and an increase in D1 receptor mRNA in the accumbens core ipsilateral to the lesion. However, in dopamine-lesioned animals, dopamine D1 receptor mRNA levels were increased bilaterally in nucleus accumbens core and shell and in the ipsilateral medial caudate-putamen following kainic acid stimulation in the hippocampus ipsilateral to the dopamine lesion. These results indicate a differential regulation of the expression of dopamine D1 and D2 receptor mRNAs by midbrain and hippocampal neurons.(ABSTRACT TRUNCATED AT 250 WORDS)
将谷氨酸类似物海藻酸注入完整大鼠或6-羟基多巴胺去传入大鼠的海马体,以研究海马神经元对纹状体复合体各亚区多巴胺D1和D2受体mRNA表达的影响以及多巴胺能神经元的可能调节作用。分别使用对多巴胺D1和D2受体mRNA特异的35S标记寡核苷酸探针进行定量原位杂交。结果发现,在注射后4小时分析的动物中,向海马结构注射海藻酸本身对任何分析的纹状体亚区的多巴胺D1或D2受体mRNA水平均无显著影响。多巴胺损伤同侧海马体的海藻酸刺激导致同侧内侧尾状核-壳核中D1受体mRNA水平升高,以及伏隔核核心和壳(腹侧纹状体边缘区)双侧升高。单侧6-羟基多巴胺损伤单独导致损伤同侧外侧尾状核-壳核(背侧纹状体运动区)中D2受体mRNA升高,以及损伤同侧伏隔核核心中D1受体mRNA升高。然而,在多巴胺损伤的动物中,多巴胺损伤同侧海马体的海藻酸刺激后,伏隔核核心和壳以及同侧内侧尾状核-壳核中的多巴胺D1受体mRNA水平双侧升高。这些结果表明中脑和海马神经元对多巴胺D1和D2受体mRNA表达有不同的调节作用。(摘要截短于250字)