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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Low levels of mRNA for dopamine D4 receptor in human cerebral cortex and striatum.
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Low levels of mRNA for dopamine D4 receptor in human cerebral cortex and striatum.

机译:人大脑皮层和纹状体中多巴胺D4受体的mRNA水平较低。

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Significant densities of mRNA for the dopamine D4 receptor in cerebral cortex, particularly in frontal lobe, have been reported in rats and monkeys, supporting the D4 hypothesis in the pathology of schizophrenia. Using northern blot analysis and the competitive reverse transcription-polymerase chain reaction (RT-PCR) method, we determined the relative levels of D4 mRNA in human brain regions to clarify whether the cortical level is also higher in humans. Northern blot analysis revealed an unexpected profile of D4 mRNA in the brain. The detected mRNA size, 1.5 kb, was quite different from the 5.3 kb reported in human neuroblastoma SK-N-MC cells. Higher levels of D4 mRNA were detected not only in the mesolimbic system but also in the corpus callosum, spinal cord, medulla, and subthalamic nucleus. It was surprising that in the cerebral cortex regions as well as the striatum, D4 mRNA was hardly detected. The competitive RT-PCR revealed these relative densities to be at least three orders of magnitude lowerthan that of the striatal D2 receptor. Our results demonstrate a remarkable difference in cortical D4 mRNA density in humans compared with that in rats and monkeys. Furthermore, the mRNA distribution suggests that the higher density of D4-like binding sites reported recently in normal human striatum is not due to the D4 receptor.
机译:在大鼠和猴子中,大脑皮层,特别是额叶中多巴胺D4受体的mRNA密度显着增加,这支持了精神分裂症病理学中的D4假说。使用Northern印迹分析和竞争性逆转录聚合酶链反应(RT-PCR)方法,我们确定了人脑区域中D4 mRNA的相对水平,以阐明人的皮质水平是否也更高。 Northern印迹分析揭示了大脑中D4 mRNA的意外状况。检测到的mRNA大小为1.5 kb,与人类神经母细胞瘤SK-N-MC细胞中报道的5.3 kb完全不同。不仅在中边缘系统中,而且在call体,脊髓,延髓和丘脑下核中也检测到较高水平的D4 mRNA。令人惊讶的是,在大脑皮层区域和纹状体中,几乎未检测到D4 mRNA。竞争性RT-PCR显示这些相对密度比纹状体D2受体低至少三个数量级。我们的结果表明,与大鼠和猴子相比,人的皮质D4 mRNA密度存在显着差异。此外,mRNA分布表明,最近在正常人纹状体中报道的更高密度的D4样结合位点不是由于D4受体引起的。

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