It is shown that Nav1.3, a subtype normally confined to early development, shows aberrantly increased expression in the dentate gyrus (DG)-CA3 circuit in early-stage 5xFAD mice, which is identified as a driver of early hippocampal network dysfunction in AD.
A pre-plaque window in 5xFAD mice marked by GluN2B-linked glutamatergic hyperexcitability, early mitochondrial disruption, and selective dendritic and transcriptional vulnerability is defined, suggesting that synaptic and metabolic dysfunctions arise before substantial plaque deposition and may represent tractable earl...
Amanda R. Kelley, Emily Sackinger, M. Frischman et al.· Frontiers in Aging Neuroscie...· 0 citations
Results suggest that Adgrd1 plays a key role in maintaining hippocampal resilience and regulating motivational behaviors through integrated molecular and circuit-level mechanisms.
Inés Martínez-Soria, Pol Picón-Pagès, Anna P. Pérez-González et al.· bioRxiv· 0 citations
It is shown that, in a senescent physiology predisposing to frequent inflammation-driven Aβ42 production bursts over a decades-long period, the intracellular amount of Aβ42-reelin complexes can accumulate to extraordinarily high levels in anterolaterally positioned LII neurons compared to the vast majority of cortical...
A. Kobro‐Flatmoen, J. Hussan, P. Hunter et al.· PLoS Computational Biology· 0 citations
Findings support a durable activation of AMPAR and propose a mechanism to explain FLASH-induced neuroprotection initiated by early calcium influx and subsequent sustained expression of glutamate AMPARs in neurons and/or neural progenitors of the CA3, potentially contributing to long-term cognitive sparing.
Louis V. Kunz, A. Almeida, Michèle Knol et al.· Cell Reports· 0 citations
A pre-plaque, cell-type-specific synaptic phenotype in male APP/PS1 mice is defined in which impaired mGluR1/5-dependent plasticity and persistent CP-AMPAR signaling in D1R+ MSNs coincide with selective reward-related alterations.
Nicolás Riffo-Lepe, Juliana González-Sanmiguel, Isaías Meza et al.· Neurobiology of Disease· 0 citations
It is concluded that CA1 PCs hyperexcitability from Frm1 KO mice was detectable at late postnatal development (P21-28), but not earlier (P8-15), and was due to a shifting of action potential voltage threshold to more hyperpolarized values.
M. A. Luque, L. Dufresne, B. Torres et al.· Neuroscience· 0 citations
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