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Altered hippocampal doublecortin expression in Parkinson's disease
Evelini Plácido1, David J Koss2,3, Tiago Fleming Outeiro2,4,5
1Neuroscience Graduate Program, Federal University of Santa Catarina, Florianópolis, Santa Catarina, Brazil.
Journal of Neurochemistry
|March 14, 2024
Summary
Parkinson's disease (PD) may impair adult hippocampal neurogenesis, evidenced by reduced Doublecortin (DCX)-expressing cells in the hippocampus. This neurogenesis deficit could precede cognitive decline in PD patients.
Area of Science:
- Neuroscience
- Cell Biology
- Neurodegenerative Diseases
Background:
- Parkinson's disease (PD) presents with motor and non-motor symptoms, some potentially linked to hippocampal function.
- Adult hippocampal neurogenesis, the birth of new neurons in the hippocampus, may be affected in PD.
- Doublecortin (DCX) is a key protein marker for immature, migrating neurons.
Purpose of the Study:
- To investigate the role of Doublecortin (DCX) expression in adult hippocampal neurogenesis in Parkinson's disease (PD).
- To examine potential alterations in neurogenesis markers in postmortem brain tissue of PD patients compared to controls.
Main Methods:
- Utilized postmortem human brain tissue from PD patients and age-matched controls.
- Quantified the number and nuclear area of Doublecortin (DCX)-expressing cells in the subgranular zone (SGZ) of the hippocampus.
- Assessed the correlation between DCX-positive cell nuclear area and pH levels.
Main Results:
- Found a significant reduction in the number of DCX-expressing cells in the SGZ of PD brains.
- Observed a decreased nuclear area in DCX-positive cells in PD cases.
- Correlated the nuclear area of DCX-positive cells with pH levels, suggesting a link to cellular environment.
Conclusions:
- Adult hippocampal neurogenesis appears to be compromised in Parkinson's disease (PD).
- Reduced DCX expression and altered cell morphology suggest impaired neurogenesis in PD.
- These findings offer insights into the pathophysiology of PD-related neuropsychiatric symptoms and potential therapeutic targets.
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