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使用核糖核酸酶保护分析法对大鼠脑中D1、D2和D3多巴胺受体mRNA进行区域定量分析。

Regional quantification of D1, D2, and D3 dopamine receptor mRNA in rat brain using a ribonuclease protection assay.

作者信息

Richtand N M, Kelsoe J R, Segal D S, Kuczenski R

机构信息

Department of Psychiatry, University of California, San Diego, La Jolla 92093-0603, USA.

出版信息

Brain Res Mol Brain Res. 1995 Oct;33(1):97-103. doi: 10.1016/0169-328x(95)00112-6.

Abstract

We describe ribonuclease protection assays for dopamine D1, D2, and D3 receptors, and regional quantitation of mRNA levels for these receptors in rat brain. Both D1 and D2 mRNA levels were highest in caudate putamen, where they were found in approximately equal levels. Of the brain regions examined, D3 mRNA was most abundant in hippocampus, hypothalamus, and nucleus accumbens. Levels of D3 mRNA were significantly lower than values for D1 and D2 mRNA in all brain regions studied. Variability was observed between animals for expression of both D1 and D2 mRNA in caudate putamen, with a significant correlation between D1 and D2 mRNA levels in neostriatum (r = 0.942, P < 0.001). This suggests a functional interaction between D1 and D2 receptor mRNA levels in this brain region. Our results are generally consistent with regional distributions previously reported using other methods. These results suggest that DA D2 receptors function both as an auto and as a postsynaptic receptor, while D1 receptors are restricted to a postsynaptic function. Our results demonstrate the utility of this method in studying possible relationships between individual animal variation in regional mRNA expression and behavioral response to pharmacological and other experimental treatments.

摘要

我们描述了用于检测大鼠脑中多巴胺D1、D2和D3受体的核糖核酸酶保护分析方法,以及这些受体mRNA水平的区域定量分析。D1和D2 mRNA水平在尾状核壳核中最高,且二者水平大致相等。在所检测的脑区中,D3 mRNA在海马体、下丘脑和伏隔核中最为丰富。在所有研究的脑区中,D3 mRNA水平均显著低于D1和D2 mRNA水平。在动物之间观察到尾状核壳核中D1和D2 mRNA表达存在变异性,新纹状体中D1和D2 mRNA水平之间存在显著相关性(r = 0.942,P < 0.001)。这表明该脑区中D1和D2受体mRNA水平之间存在功能相互作用。我们的结果总体上与先前使用其他方法报道的区域分布一致。这些结果表明,多巴胺D2受体既作为自身受体又作为突触后受体发挥作用,而D1受体则仅限于突触后功能。我们的结果证明了该方法在研究区域mRNA表达的个体动物差异与对药理学及其他实验处理的行为反应之间可能存在的关系方面的实用性。

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