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黑质纹状体束部分损伤后酪氨酸羟化酶表达的变化。

Alterations in tyrosine hydroxylase expression following partial lesions of the nigrostriatal bundle.

作者信息

Sherman T G, Moody C A

机构信息

Department of Neuroscience, University of Pittsburgh, PA 15260, USA.

出版信息

Brain Res Mol Brain Res. 1995 Apr;29(2):285-96. doi: 10.1016/0169-328x(94)00259-h.

DOI:10.1016/0169-328x(94)00259-h
PMID:7609616
Abstract

Effects of destruction of central dopaminergic neurons on tyrosine hydroxylase gene expression were investigated. Two weeks after the unilateral injection of 6-hydroxydopamine (6-OHDA) into the medial forebrain bundle, a 67% to 99% loss of striatal dopamine (DA) content was observed ipsilateral to the injection site. Measures of tyrosine hydroxylase (TH) protein levels revealed losses in striatal content proportional to DA content. Striatal dihydroxylphenylacetic acid (DOPAC) was somewhat less affected, resulting in 2- to 4-fold increases in the striatal DOPAC/DA ratio, depending on the severity of the lesion. Morphologically, surviving TH-positive substantia nigra pars compacta (SNc) neurons were more rounded than contralateral control cells, and exhibited decreases in cross-sectional area that were proportional to the loss of striatal DA. Measures of cytoplasmic TH mRNA levels in surviving neurons by in situ hybridization autoradiography revealed a significant 23% decrease in TH content per cell that could be correlated to lesion size. The decreases in cross-sectional area and TH mRNA content resulted in a small decrease in TH mRNA density of 6%. The determination of TH transcription rate by an intron-directed in situ hybridization assay found no significant change in TH transcriptional activity as a function of lesion. We conclude that the short-term effect of partial 6-OHDA-induced lesions of the nigrostriatal dopaminergic pathway is the selective loss or shrinkage of large DA neurons of the SNc, and that the associated down-regulation of TH mRNA expression in surviving neurons is due to a post-transcriptional mechanism related either to concomitant cellular hyperactivity or is secondary to the morphological alterations.

摘要

研究了中枢多巴胺能神经元破坏对酪氨酸羟化酶基因表达的影响。在内侧前脑束单侧注射6-羟基多巴胺(6-OHDA)两周后,在注射部位同侧观察到纹状体多巴胺(DA)含量损失67%至99%。酪氨酸羟化酶(TH)蛋白水平的测量显示,纹状体含量的损失与DA含量成比例。纹状体二羟基苯乙酸(DOPAC)受影响较小,导致纹状体DOPAC/DA比值增加2至4倍,这取决于损伤的严重程度。形态学上,存活的黑质致密部(SNc)TH阳性神经元比同侧对照细胞更圆,且横截面积减小,与纹状体DA的损失成比例。通过原位杂交放射自显影术测量存活神经元中的细胞质TH mRNA水平,发现每个细胞的TH含量显著降低23%,这与损伤大小相关。横截面积和TH mRNA含量的降低导致TH mRNA密度小幅下降6%。通过内含子定向原位杂交测定法测定TH转录率,发现TH转录活性作为损伤的函数没有显著变化。我们得出结论,6-OHDA诱导的黑质纹状体多巴胺能通路部分损伤的短期效应是SNc大DA神经元的选择性丧失或萎缩,并且存活神经元中TH mRNA表达的相关下调是由于与伴随的细胞过度活跃相关的转录后机制,或者是形态学改变的继发结果。

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