Amyloid Beta Dynamics in Biological Fluids-Therapeutic Impact.
Thomas Gabriel Schreiner1,2,3, Bogdan Ovidiu Popescu1,4,5
1Faculty of Medicine, University of Medicine and Pharmacy "Carol Davila", 050474 Bucharest, Romania.
Journal of Clinical Medicine
|December 24, 2021
Summary
Alzheimer's disease treatments are limited. This review explores beta-amyloid (Aβ) dynamics and clearance, focusing on central nervous system (CNS) elimination strategies for potential Alzheimer's disease therapies.
Area of Science:
- Neuroscience
- Biochemistry
- Pharmacology
Background:
- Alzheimer's disease (AD) poses significant individual and socioeconomic burdens.
- Current AD treatments are inadequate, necessitating novel therapeutic strategies.
- The amyloidogenic pathway, involving beta-amyloid (Aβ), remains a key focus in AD research.
Purpose of the Study:
- To provide insights into beta-amyloid (Aβ), a critical biomarker in Alzheimer's disease.
- To detail Aβ structure, function, and dynamics in normal and pathological states.
- To review Aβ elimination mechanisms within the central nervous system (CNS) and therapeutic approaches.
Main Methods:
- Literature review focusing on Aβ structure, function, and metabolism.
- Analysis of Aβ dynamics across biological compartments.
- Examination of CNS Aβ clearance pathways, including blood-brain barrier transport.
- Review of existing and emerging therapeutic strategies for Aβ elimination.
Main Results:
- Aβ structure and function are detailed in both healthy and diseased conditions.
- Aβ dynamics are explored across various biological compartments.
- Blood-brain barrier clearance is identified as a dominant Aβ elimination route from the CNS.
- Therapeutic strategies like peripheral and cerebrospinal fluid sinks are presented.
Conclusions:
- Stimulating Aβ clearance, particularly from the cerebrospinal fluid, is crucial for AD treatment.
- A multidisciplinary approach is necessary to enhance Aβ elimination from the CNS.
- Further research into novel Aβ clearance mechanisms holds promise for future AD therapies.
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