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在黑质纹状体多巴胺通路存在或不存在的情况下,多巴胺D-1对尾状核神经降压素信使核糖核酸的调节作用。

Dopamine D-1 regulation of caudate neurotensin mRNA in the presence or absence of the nigrostriatal dopamine pathway.

作者信息

Hanson G R, Keefe K A

机构信息

Department of Pharmacology and Toxicology, University of Utah, 112 Skaggs Hall, Salt Lake City, UT 84112, USA.

出版信息

Brain Res Mol Brain Res. 1999 Mar 20;66(1-2):111-21. doi: 10.1016/s0169-328x(99)00033-9.

Abstract

Changes in extrapyramidal dopamine (DA) function significantly alter the activity of striatal neurotensin (NT) systems. Specifically, stimulation of DA D-1 or D-2 receptors increases or decreases striatal NT tissue levels, respectively. In contrast, removal of D-2 receptor basal activity with either an antagonist or lesion of the nigrostriatal DA projection increases striatal NT content. To understand better the significance of these changes in the levels of NT peptide, we determined the effects of treatment with the selective D-1 agonist, SKF 82958, alone or in combination with a lesion of the nigrostriatal DA pathway, on the levels of NT mRNA in various regions of the caudate nucleus. Removal of at least 90% of this DA pathway significantly increased NT mRNA in most, but not all, regions throughout the caudate nucleus. In contrast, four, but not one, administrations of SKF 82958 (2 mg kg-1 dose-1) increased NT mRNA levels in principally middle, but not rostral, caudate regions. Lesioning the nigrostriatal DA pathway enhanced the effects of SKF 82958 so that a lower, single dose (1 mg/kg) of this D-1 agonist also increased NT mRNA levels predominantly in the middle caudate sections. These findings demonstrate that DA D-1 receptors profoundly regulate the striatal expression of NT mRNA in a regionally selective fashion, which appears to be unique from that principally influenced by DA D-2 regulation.

摘要

锥体外系多巴胺(DA)功能的变化会显著改变纹状体神经降压素(NT)系统的活性。具体而言,刺激DA D-1或D-2受体分别会增加或降低纹状体NT组织水平。相反,用拮抗剂或黑质纹状体DA投射损伤去除D-2受体的基础活性会增加纹状体NT含量。为了更好地理解NT肽水平变化的意义,我们确定了单独使用选择性D-1激动剂SKF 82958或与黑质纹状体DA通路损伤联合使用,对尾状核各区域NT mRNA水平的影响。去除至少90%的该DA通路会显著增加尾状核大部分(但不是全部)区域的NT mRNA。相反,四次(而不是一次)给予SKF 82958(剂量为2 mg·kg-1)会增加主要是尾状核中部(而不是前部)区域的NT mRNA水平。损伤黑质纹状体DA通路增强了SKF 82958的作用,因此较低的单剂量(1 mg/kg)这种D-1激动剂也会主要增加尾状核中部切片的NT mRNA水平。这些发现表明,DA D-1受体以区域选择性方式深刻调节NT mRNA在纹状体中的表达,这似乎与主要受DA D-2调节的情况不同。

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