
Journal of Neurochemistry, Journal Year: 2024, Volume and Issue: 169(1)
Published: Dec. 18, 2024
Abstract Altered energy metabolism in Alzheimer's disease (AD) is a major pathological hallmark implicated the early stages of process. Astrocytes play central role brain homeostasis and are multiple neurodegenerative diseases. Although numerous studies have investigated global changes metabolism, redox status, gene expression epigenetic markers AD, intricate interplay between different metabolic processes, particularly astrocytes, remains poorly understood. Numerous amyloid‐β precursor development progression AD. To determine effects peptides or impact protein processing on astrocyte we differentiated astrocytes from induced pluripotent stem cells derived people with onset familial AD controls. This study demonstrates that AD‐derived exhibit significantly more their including glucose uptake, glutamate uptake lactate release, increases oxidative glycolytic compared to acute exposure. In addition pathways glutamate, purine arginine citric acid cycle, demonstrate evidence gliosis highlighting potential hallmark. suggests chronic alterations may occur very process present significant risk factors for patients These findings also reveal important drivers late dementia highlights key targets diagnostic features therapeutic agents future. image
Language: Английский