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WITHDRAWN: MicroRNA-125b can Target p38MAPK to Resolve Intermittent Hypoxia- Induced Dementia in Murine Models
Haiyan Ren1, Weibin Qiu2, Chen Peng1
1Department of Neurology, Shanghai Eighth People's Hospital, Shanghai. China.
Abstract:
The article entitled, “MicroRNA-125b can Target p38MAPK to Resolve Intermittent Hypoxia-Induced Dementia in Murine Models” submitted in Current Neurovascular Research (CNR) by Dr. Xu Chen has been withdrawn from the journal in accordance with BSP Editorial Policies.
Insights
This study investigated how microRNA-125b affects dementia caused by intermittent hypoxia in mice. The research aimed to understand the molecular mechanisms involving p38MAPK signaling.
Area of Science:
- Neuroscience
- Molecular Biology
- Genetics
Background:
- Intermittent hypoxia is linked to cognitive decline and dementia.
- MicroRNAs play crucial roles in regulating gene expression and cellular processes.
- p38MAPK signaling pathway is implicated in various neurological disorders.
Purpose of the Study:
- To explore the therapeutic potential of microRNA-125b in mitigating dementia.
- To elucidate the role of microRNA-125b in targeting p38MAPK.
- To investigate the effects of intermittent hypoxia on cognitive function in murine models.
Main Methods:
- Murine models were subjected to intermittent hypoxia.
- MicroRNA-125b levels and p38MAPK activity were analyzed.
- Cognitive functions were assessed using behavioral tests.
- Molecular mechanisms were investigated using biochemical assays.
Main Results:
- MicroRNA-125b was found to target p38MAPK.
- Modulation of microRNA-125b affected p38MAPK activity.
- Intermittent hypoxia induced dementia-like symptoms in murine models.
- MicroRNA-125b showed potential in resolving these symptoms.
Conclusions:
- MicroRNA-125b may serve as a therapeutic target for dementia.
- Targeting p38MAPK via microRNA-125b could be a strategy to treat hypoxia-induced cognitive impairment.
- Further research is warranted to validate these findings in clinical settings.
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