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Publication : Characterization of Age-dependent Behavior Deficits in the PGC-1α Knockout Mouse, in Relevance to the Parkinson's Disease Model.

First Author  Sun Z Year  2020
Journal  Neuroscience Volume  440
Pages  39-47 PubMed ID  32439544
Mgi Jnum  J:298664 Mgi Id  MGI:6478546
Doi  10.1016/j.neuroscience.2020.05.015 Citation  Sun Z, et al. (2020) Characterization of Age-dependent Behavior Deficits in the PGC-1alpha Knockout Mouse, in Relevance to the Parkinson's Disease Model. Neuroscience 440:39-47
abstractText  Parkinson's disease is a disorder of adult onset involving the progressive degeneration of selective portions of the central nervous system. It is known that mitochondrial dysfunction is involved in the pathogenesis of PD. Given that PGC-1alpha induces proliferation of mitochondria via transcription regulation, it is possible that PGC-1alpha pathway dysregulation is involved in PD pathogenesis. To determine how derangement of the PGC-1alpha pathway in age contributes to PD, in this study, we have characterized the number of dopaminergic neuron in the substantia nigra pars compacta (SNpc), motor behaviors and related expression of mitochondrial markers (CoxIV, SDHA, and Tomm20) in the ventral midbrains of PGC-1alpha null mice. We found an overall decrease in spontaneous, voluntary movements and severely impaired motor coordination in all age groups (10months and 20months) of PGC-1alpha null mice, while pole testing detected impaired motor activity in older PGC-1alpha null mice only. TH-positive neurons were significantly less in older PGC-1alpha null mice. Concentration of DA as well as its two metabolites reduced in an age-dependent manner in PGC-1alpha null mice. Expression of CoxIV, SDHA and Tomm20 also significantly decreased in the ventral midbrains of 10-month-old PGC-1alpha null mice. Thus, PGC-1alpha KO in mice induced dopaminergic neuron degeneration in the SNpc and DA deficits in the striatum in an age-dependent manner. Progressive impairment of motor coordination in an age-dependent manner was correlated to the extent of nigrostriatal dopaminergic pathway degeneration and mitochondrial dysfunction.
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