Neuroscience, Год журнала: 2025, Номер unknown
Опубликована: Апрель 1, 2025
Язык: Английский
Neuroscience, Год журнала: 2025, Номер unknown
Опубликована: Апрель 1, 2025
Язык: Английский
Journal of Drug Delivery Science and Technology, Год журнала: 2025, Номер unknown, С. 106721 - 106721
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
1Cells, Год журнала: 2025, Номер 14(7), С. 525 - 525
Опубликована: Апрель 1, 2025
Alzheimer’s disease (AD) is a multifactorial neurodegenerative disorder characterized by metabolic dysregulation, oxidative stress, amyloid-β (Aβ) aggregation, metal dyshomeostasis, and mitochondrial dysfunction. Current treatments provide only symptomatic relief, highlighting the need for novel therapeutic strategies. This study investigates effects of alkaloids galantamine (GAL) lycorine (LYC) in differentiated SH-SY5Y neuroblastoma cells, an established vitro model AD, which acquire neuronal phenotype upon differentiation. Using untargeted targeted NMR-based metabolomics combined with multivariate statistical analysis, we analyzed extracellular profiles under basal conditions following Aβ42 exposure, both presence absence GAL LYC. Our findings reveal distinct responses to Aβ toxicity, significant alterations pyruvate glutamine metabolism. Both LYC contributed restoration lysine homeostasis, but had more pronounced effect, better sustaining cellular energy balance function. Unlike LYC, treatment was associated accumulation, response between two compounds. These variations may reflect mechanisms action, potentially influencing their roles counteracting Aβ-induced toxicity. highlights value profiling assessing neuroprotective agents reinforces potential natural this context.
Язык: Английский
Процитировано
0Neuroscience, Год журнала: 2025, Номер unknown
Опубликована: Апрель 1, 2025
Язык: Английский
Процитировано
0