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Извлечено: 997 / 997 (100.0%) Средняя confidence: 0.13
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Prolonged intermittent theta burst stimulation enhances hippocampal plasticity via GluN2A-mediated signaling.

PMID: 41878311 · DOI: 10.3389/fnagi.2026.1757554 · Frontiers in aging neuroscience, 2026 · Danica Popovic, Marina Zaric Kontic, Milica Zeljkovic Jovanovic, Milena Milosevic, Teodora Martic, Tamara Radukic, Andje
📄 Abstract

Intermittent theta burst stimulation (iTBS) is increasingly explored as a non-invasive neuromodulatory approach capable of inducing long-lasting plasticity with potential therapeutic value in age-related neurological and psychiatric conditions. However, the cellular and molecular mechanisms underlying iTBS protocols remain largely unknown, limiting its further therapeutic development. Here, we investigated the behavioral, structural, synaptic, and calcium-dependent effects of a 7-day iTBS600 protocol using a combination of Prolonged iTBS did not alter general locomotor activity, anxiety-like behavior, or short-term recognition memory, indicating preserved baseline behavioral function. Despite the absence of behavioral changes, prolonged iTBS induced robust structural plasticity in hippocampal CA1 neurons, increasing total spine density and selectively enhancing the proportion of thin, learning spines. Synaptosomal analysis revealed upregulation of GluN1 and GluN2A, elevated BDNF levels, and activation of downstream Akt, ERK1/2, and mTOR pathways. Prolonged iTBS also enhanced perineuronal net formation around PV Together, these findings indicate that prolonged iTBS drives coordinated structural, synaptic, and Ca

Confidence: 0.16 · 7 полей извлечено
Идентификация (6 полей)
Target
GluN2A
0.90
Alt. target
0.00
Protein family
NMDA receptor subunit
0.80
Functional class
Ionotropic glutamate receptor
0.80
Subcellular loc.
Synaptosomal membrane
0.70
Isoforms (metab/obesity)
0.00
Механизм действия (21 полей)
Mechanism
0.00
Mutations (obesity/lean)
0.00
Activity (obesity)
0.00
Activity temporal
0.00
Energy balance
0.00
Appetite
0.00
Fat metabolism
0.00
Lipolysis
0.00
Thermogenesis
0.00
Muscle metabolism
0.00
Inflammation
0.00
Glucose metabolism
0.00
AA metabolism
0.00
Hormonal pathways
0.00
Cell death
0.00
Adipocyte fibrosis
0.00
Upstream (biochem)
0.00
Upstream (physiol)
0.00
Downstream (biochem)
0.00
Downstream (physiol)
0.00
PTMs
0.00
Экспрессия (8 полей)
Tissue expression
0.00
In vitro
0.00
In vivo
Prolonged iTBS in rats: no change in locomotor activity, anxiety-like behavior, or short-term recognition memory; increased spine density in hippocampal CA1 neurons; upregulation of GluN1, GluN2A, BDNF, Akt, ERK1/2, mTOR; enhanced perineuronal net formation.
0.90
In silico
0.00
Genetic association
0.00
Ex vivo
Synaptosomal analysis from hippocampal tissue after prolonged iTBS.
0.80
Animal model
Rats (implied from context, not explicitly stated but typical for such studies)
0.70
Diet/model
0.00
Клиника (11 полей)