首页> 外文OA文献 >Electrical stimulation in vivo increases the expression of proenkephalin mRNA and decreases the expression of prodynorphin mRNA in rat hippocampal granule cells.
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Electrical stimulation in vivo increases the expression of proenkephalin mRNA and decreases the expression of prodynorphin mRNA in rat hippocampal granule cells.

机译:体内电刺激增加大鼠海马颗粒细胞中前脑啡肽mRNA的表达并降低前啡肽mRNA的表达。

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摘要

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.
机译:原位杂交组织化学结合RNA印迹技术用于研究大鼠海马中阿片样物质基因表达的调控。通过使用强啡肽原cDNA探针,在海马颗粒细胞层中鉴定到强杂交信号。但是,使用前脑啡肽cDNA探针进行的实验表明,前脑啡肽mRNA的含量明显低于前强啡肽mRNA的含量。在对齿状回进行了五次简短的高频电刺激训练后,在22小时后测得的颗粒细胞中的前脑啡肽mRNA含量在被刺激侧显着增加。相反,在刺激部位的同侧,前强啡肽mRNA水平显着降低。通过提取的mRNA的RNA印迹分析证实了这些结果。刺激结束后4至7小时,前强啡肽mRNA含量的下降首先变得明显。因此,不同的机制调节大鼠海马中前脑啡肽mRNA和前降啡肽mRNA的表达。

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