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Alterations in tyrosine hydroxylase expression following partial lesions of the nigrostriatal bundle
1Department of Neuroscience, University of Pittsburgh, PA 15260, USA.
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.
Insights
Destruction of central dopaminergic neurons via 6-hydroxydopamine (6-OHDA) caused significant dopamine loss and reduced tyrosine hydroxylase (TH) mRNA in surviving neurons, indicating post-transcriptional regulation.
Area of Science:
- Neuroscience
- Molecular Biology
- Neurochemistry
Background:
- The nigrostriatal dopaminergic pathway is crucial for motor control.
- Tyrosine hydroxylase (TH) is the rate-limiting enzyme in dopamine synthesis.
- Understanding TH gene expression regulation is vital for neurodegenerative disease research.
Purpose of the Study:
- To investigate the effects of central dopaminergic neuron destruction on TH gene expression.
- To elucidate the mechanisms underlying TH down-regulation following 6-hydroxydopamine (6-OHDA) lesions.
Main Methods:
- Unilateral 6-OHDA injections into the medial forebrain bundle in rodents.
- Measurement of striatal dopamine (DA) and dihydroxyphenylacetic acid (DOPAC) content.
- Assessment of TH protein levels and TH mRNA expression in substantia nigra pars compacta (SNc) neurons using in situ hybridization.
- Determination of TH transcriptional rate via intron-directed in situ hybridization.
Main Results:
- 6-OHDA lesions caused significant loss of striatal DA (67-99%) and TH protein.
- Surviving SNc neurons showed morphological changes (shrinkage) and a 23% decrease in TH mRNA per cell.
- TH mRNA density decreased by 6%, while TH transcriptional activity remained unchanged.
- The DOPAC/DA ratio increased 2- to 4-fold, indicating altered dopamine metabolism.
Conclusions:
- Short-term 6-OHDA lesions lead to selective loss or shrinkage of SNc DA neurons.
- Down-regulation of TH mRNA in surviving neurons is primarily post-transcriptional.
- This post-transcriptional regulation may be linked to cellular hyperactivity or morphological alterations.