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急性给予完全多巴胺 D(1) 激动剂 SKF-82958 后,代谢型谷氨酸受体 1(mGluR1)突变小鼠纹状体中前强啡肽原(而非前脑啡肽原)的 mRNA 诱导受损。

Impaired preprodynorphin, but not preproenkephalin, mRNA induction in the striatum of mGluR1 mutant mice in response to acute administration of the full dopamine D(1) agonist SKF-82958.

作者信息

Mao Limin, Conquet François, Wang John Q

机构信息

Division of Pharmacology, School of Pharmacy, University of Missouri-Kansas City, Kansas City, Missouri 64108, USA.

出版信息

Synapse. 2002 May;44(2):86-93. doi: 10.1002/syn.10061.

Abstract

Metabotropic glutamate receptor 1 (mGluR1) is highly expressed in striatonigral projection neurons of rat striatum. To define the role of mGluR1 in the regulation of striatal gene expression, the responsiveness of the three neuropeptide gene expression to a single injection of the dopamine D(1) agonist SKF-82958 was compared between mGluR1 mutant and wild-type control mice. We found that acute injection of SKF-82958 increased preprodynorphin (PPD), substance P (SP), and preproenkephalin (PPE) mRNAs in the dorsal and ventral striatum of mutant and wild-type mice in a dose-dependent manner (0.125, 0.5, and 2 mg/kg, i.p.) as revealed by quantitative in situ hybridization. However, the induction of PPD mRNA in both the dorsal and ventral striatum of mGluR1 minus sign/minus sign mice was significantly less than that of wild-type +/+ mice in response to the two higher doses of SKF-82958. In contrast to PPD, SP and PPE in the dorsal and ventral striatum of mGluR1 mutant mice were elevated to a similar level as that of wild-type mice. There were no differences in basal levels and distribution patterns of all three mRNAs between the two genotypes of mice treated with saline. These results indicate that mGluR1 selectively participates in striatonigral PPD induction in response to D(1) receptor stimulation.

摘要

代谢型谷氨酸受体1(mGluR1)在大鼠纹状体的纹状体黑质投射神经元中高度表达。为了确定mGluR1在纹状体基因表达调控中的作用,比较了mGluR1突变小鼠和野生型对照小鼠单次注射多巴胺D(1)激动剂SKF-82958后三种神经肽基因表达的反应性。我们发现,如定量原位杂交所示,急性注射SKF-82958(腹腔注射,剂量为0.125、0.5和2mg/kg)后,突变型和野生型小鼠背侧和腹侧纹状体中的前强啡肽原(PPD)、P物质(SP)和前脑啡肽原(PPE)mRNA均呈剂量依赖性增加。然而,在两种较高剂量的SKF-82958作用下,mGluR1基因敲除小鼠背侧和腹侧纹状体中PPD mRNA的诱导明显低于野生型+/+小鼠。与PPD相反,mGluR1突变小鼠背侧和腹侧纹状体中的SP和PPE升高至与野生型小鼠相似的水平。用生理盐水处理的两种基因型小鼠的所有三种mRNA的基础水平和分布模式均无差异。这些结果表明,mGluR1在响应D(1)受体刺激时选择性地参与纹状体黑质PPD的诱导。

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