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首页> 外文期刊>Brain research >Dopamine receptor mRNA and protein expression in the mouse corpus striatum and cerebral cortex during pre- and postnatal development.
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Dopamine receptor mRNA and protein expression in the mouse corpus striatum and cerebral cortex during pre- and postnatal development.

机译:产前和产后发育过程中小鼠纹状体和大脑皮层中的多巴胺受体mRNA和蛋白表达。

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The outcome of dopaminergic signaling and effectiveness of dopaminergic drugs depend on the relative preponderance of each of the five dopamine receptors in a given brain region. The separate contribution of each receptor to overall dopaminergic tone is difficult to establish at a functional level due to lack of receptor subtype specific pharmacological agents. A surrogate for receptor function is receptor protein or mRNA expression. We examined dopamine receptor mRNA expression by quantitative reverse transcription real-time PCR in the striatum, globus pallidus, frontal cortex and cingulate cortex of embryonic and postnatal mice. Samples of each region were collected by laser capture microdissection. D1- and D2-receptor mRNAs were the most abundant in all the regions of the mature brain. The D1-receptor was predominant over the D2-receptor in the frontal and cingulate cortices whereas the situation was reversed in the striatum and globus pallidus. In the proliferative domains of the embryonic forebrain, D3-, D4- and D5-receptors were predominant. In the corpus striatum and cerebral cortex, the D3- and D4-receptors were the only receptors that showed marked developmental regulation. By analyzing D1 receptor protein expression, we show that developmental changes in mRNA expression reliably translate into changes in protein levels, at least for the D1-receptor.
机译:多巴胺能信号传导的结果和多巴胺能药物的有效性取决于给定大脑区域中五种多巴胺受体各自的相对优势。由于缺乏受体亚型特异的药理作用,很难在功能水平上确定每种受体对总体多巴胺能基调的单独贡献。受体功能的替代物是受体蛋白或mRNA表达。我们通过定量逆转录实时荧光定量PCR检测了胚胎和出生后小鼠纹状体,苍白球,额叶皮层和扣带状皮层中的多巴胺受体mRNA表达。通过激光捕获显微切割收集每个区域的样品。 D1和D2受体mRNA在成熟大脑的所有区域中含量最高。在额叶和扣带状皮质中,D1受体高于D2受体,而纹状体和苍白球则相反。在胚胎前脑的增殖域中,D3-,D4-和D5-受体是主要的。在纹状体和大脑皮层中,D3和D4受体是唯一显示出明显发育调节的受体。通过分析D1受体蛋白表达,我们显示出mRNA表达的发育变化可靠地转化为蛋白质水平的变化,至少对于D1受体而言。

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