Skip to content
2000
Volume 16, Issue 2
  • ISSN: 1874-4672
  • E-ISSN: 1874-4702

Abstract

Background: The efficacy of Alzheimer's disease (AD) treatment can be enhanced by developing neurogenesis regulation approaches by synchronizing regenerative-competent cell (RCCs) activity. As part of the implementation of this direction, the search for drug targets among intracellular signaling molecules is promising. Objective: This study aims to test the hypothesis that NF-кB inhibitors are able to synchronize the activities of different types RCCs in AD. Methods: The effects of NF-ΚB inhibitor JSH-23 on the functioning of neural stem cells (NSCs), neuronal-committed progenitors (NCPs), and neuroglial cells were studied. Individual populations of C57B1/6 mice brain cells were obtained by immunomagnetic separation. Studies were carried out under conditions of modeling β-amyloid-induced neurodegeneration (βAIN) in vitro. Results: We showed that β-amyloid (Aβ) causes divergent changes in the functioning of NSCs and NCPs. Also demonstrated that different populations of neuroglia respond differently to exposure to Aβ. These phenomena indicate a significant discoordination of the activities of various RCCs. We revealed an important role of NF-ΚB in the regulation of progenitor proliferation and differentiation and glial cell secretory function. It was found that the NF-ΚB inhibitor causes synchronization of the pro-regenerative activities of NSCs, NCPs, as well as oligodendrocytes and microglial cells in βAIN. Conclusion: The results show the promise of developing a novel approach to Alzheimer's disease treatment with NF-ΚB inhibitors.

Loading

Article metrics loading...

/content/journals/cmp/10.2174/1874467215666220601144727
2023-04-01
2024-11-22
Loading full text...

Full text loading...

/content/journals/cmp/10.2174/1874467215666220601144727
Loading
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test