Abstract
Background: Here we aimed to evaluate: (1) Rhes mRNA expression in mouse midbrain, (2) the effect of Rhes deletion on the number of dopamine neurons, (3) nigrostriatal-sensitive behavior during aging in knockout mice. Methods: Radioactive in situ hybridization was assessed in adult mice. The beam-walking test was executed in 3-, 6- and 12-month-old mice. Immunohistochemistry of midbrain tyrosine hydroxylase (TH)-positive neurons was performed in 6- and 12-month-old mice. Results: Rhes mRNA is expressed in TH-positive neurons of SNpc and the ventral tegmental area. Moreover, lack of Rhes leads to roughly a 20% loss of nigral TH-positive neurons in both 6- and 12-month-old mutants, when compared with their age-matched controls. Finally, lack of Rhes triggers subtle alterations in motor performance and coordination during aging. Conclusions: Our findings indicate a fine-tuning role of Rhes in regulating the number of TH-positive neurons of the substantia nigra and nigrostriatal-sensitive motor behavior during aging.
Original language | English |
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Pages (from-to) | 583-589 |
Number of pages | 7 |
Journal | Movement Disorders |
Volume | 31 |
DOIs | |
Publication status | Published - 2016 |
Keywords
- Aging
- Animals
- Behavior, Animal
- Corpus Striatum
- Dopamine neurons
- Dopaminergic Neurons
- GTP-Binding Proteins
- Male
- Mice
- Mice, Inbred C57BL
- Mice, Knockout
- Midbrain
- Psychomotor Performance
- Rasd2
- Rhes
- Substantia Nigra
- TH-positive neurons
- Tyrosine 3-Monooxygenase