首页> 外文OA文献 >Bilateral control of brain activity by dopamine D1 receptors: evidence from induction patterns of regulator of G protein signaling 2 and c-fos mRNA in D1-challenged hemiparkinsonian rats
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Bilateral control of brain activity by dopamine D1 receptors: evidence from induction patterns of regulator of G protein signaling 2 and c-fos mRNA in D1-challenged hemiparkinsonian rats

机译:多巴胺D1受体对大脑活动的双边控制:挑战D1的半帕金森病大鼠中G蛋白信号传导2和c-fos mRNA调节剂的诱导模式的证据

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摘要

Recent reports show that striatal dopamine D1-type receptors from one side of the normal rat brain can control brain activity (as measured by c-fos induction) on both sides of the brain. However, this phenomenon has not yet been studied in the presence of sensitized dopamine D1-type receptors. Here we address this issue by investigating the extent to which dopamine D1-type receptors control brain activation in rats with unilaterally sensitized dopamine D1-type receptors. Gene induction assays were used to identify activated regions from midbrain to forebrain in unilaterally 6-hydroxydopamine lesioned (hemiparkinsonian) rats challenged with the full dopamine D1-type agonist SKF82958 (3 mg/kg, 0.5 and 2 h). The genes used are c-fos, the proven neuronal activity marker, and Regulator of G protein Signaling 2, a gene we propose as a marker of signaling homeostasis. SKF82958-mediated induction of both genes is greatly enhanced in hemiparkinsonian rats compared with shams, in both the lesioned and the intact hemisphere. For example, in the denervated caudate-putamen at 2 h postinjection, this enhancement is more than 80-fold for c-fos and up to 20-fold for Regulator of G protein Signaling 2; for the intact side this is 35-fold for c-fos and 27-fold for Regulator of G protein Signaling 2. Cortical induction of c-fos and Regulator of G protein Signaling 2 was generalized to most neocortical regions and was essentially equivalent in both the denervated and intact hemispheres. Interestingly, hippocampal structures also showed strong bilateral induction of both genes. This overall pattern of brain activation can be accounted for by the basal-ganglia thalamocortical and hippocampal circuits which both contain hemisphere-crossing connections and which can be initially activated in the lesioned hemisphere. Some regions, such as the intact striatum or the CA1 region, showed relatively low c-fos induction and relatively high Regulator of G protein Signaling 2 induction, possibly indicating that these regions are engaged in unusually strong signaling regulation activities. Our results show that, besides basal ganglia-thalamocortical circuits, dopamine D1-type-mediated brain activation in hemiparkinsonian rats also involves hippocampal circuits.
机译:最近的报道表明,正常大鼠大脑一侧的纹状体多巴胺D1型受体可以控制大脑两侧的大脑活动(通过c-fos诱导测量)。但是,尚未在致敏的多巴胺D1型受体存在下研究这种现象。在这里,我们通过研究多巴胺D1型受体在单侧致敏多巴胺D1型受体大鼠中控制大脑激活的程度来解决这个问题。基因诱导试验用于鉴定单侧6-羟基多巴胺损伤(半帕金森病)大鼠的全脑多巴胺D1型激动剂SKF82958(3 mg / kg,0.5和2 h),从中脑到前脑的激活区域。所使用的基因是c-fos(已证明的神经元活性标记物)和G蛋白信号调节剂2调节剂,我们建议将其作为信号内稳态的标志物。与受损的半球和完整的半球相比,半球帕金森病大鼠中SKF82958介导的两种基因的诱导均大大增强。例如,在注射后2 h去神经支配的尾状丘脑中,这种增强作用对c-fos的作用是80倍以上,对G蛋白信号调节因子2的作用是20倍。对于完整侧,这是c-fos的35倍,G蛋白信号转导2的27倍。c-fos的皮层诱导和G蛋白信号转导2的皮质诱导被广泛应用于大多数新皮层区域,并且在两个方面都基本相同去神经和完整的半球。有趣的是,海马结构还显示出两个基因的强烈双边诱导。这种大脑激活的整体模式可以由基底神经节的丘脑皮层和海马回路来解释,它们都包含横穿半球的连接,并且可以在病变半球中最初被激活。一些区域,例如完整的纹状体或CA1区,显示出相对较低的c-fos诱导和相对较高的G蛋白信号传导2诱导调节剂,可能表明这些区域参与了异常强烈的信号传导调控活动。我们的结果表明,除了基底神经节-丘脑皮层回路外,多巴胺D1型介导的半帕金森氏病大鼠脑激活还涉及海马回路。

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