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体内电刺激可增加大鼠海马颗粒细胞中脑啡肽原mRNA的表达,并降低强啡肽原mRNA的表达。

Electrical stimulation in vivo increases the expression of proenkephalin mRNA and decreases the expression of prodynorphin mRNA in rat hippocampal granule cells.

作者信息

Morris B J, Feasey K J, ten Bruggencate G, Herz A, Höllt V

机构信息

Department of Neuropharmacology, Max-Planck-Institut für Psychiatrie, Planegg-Martinsried, Federal Republic of Germany.

出版信息

Proc Natl Acad Sci U S A. 1988 May;85(9):3226-30. doi: 10.1073/pnas.85.9.3226.

Abstract

In situ hybridization histochemistry in combination with RNA blot techniques was used to study the regulation of opioid gene expression in rat hippocampus. By use of a prodynorphin cDNA probe, a strong hybridization signal was identified in the granule cell layer of the hippocampus. However, experiments using a proenkephalin cDNA probe revealed that the content of proenkephalin mRNA was considerably lower than that of prodynorphin mRNA. Following five brief trains of high-frequency electrical stimulation to the dentate gyrus, the proenkephalin mRNA content of the granule cells, measured 22 hr later, was substantially increased on the stimulated side. In contrast, levels of prodynorphin mRNA were markedly decreased ipsilateral to the stimulation site. These results were confirmed by RNA blot analysis of extracted mRNA. The decrease in prodynorphin mRNA content first became apparent between 4 and 7 hr after the end of stimulation. Distinct mechanisms, therefore, regulate the expression of proenkephalin mRNA and prodynorphin mRNA in rat hippocampus.

摘要

采用原位杂交组织化学与RNA印迹技术相结合的方法,研究大鼠海马中阿片样物质基因表达的调控。使用强啡肽原cDNA探针,在海马颗粒细胞层中鉴定出强杂交信号。然而,使用脑啡肽原cDNA探针的实验表明,脑啡肽原mRNA的含量明显低于强啡肽原mRNA的含量。对齿状回进行5次高频电刺激短串刺激后,22小时后测量发现,受刺激侧颗粒细胞的脑啡肽原mRNA含量显著增加。相反,刺激部位同侧的强啡肽原mRNA水平明显降低。提取的mRNA的RNA印迹分析证实了这些结果。强啡肽原mRNA含量的降低在刺激结束后4至7小时之间首次变得明显。因此,不同的机制调节大鼠海马中脑啡肽原mRNA和强啡肽原mRNA的表达。

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