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@ARTICLE{Khanzada:280245,
author = {Khanzada, Shahrukh and Hu, Xin and Emery, Brett Addison and
Średniawa, Władysław and Wójcik, Daniel K and
Kempermann, Gerd and Amin, Hayder},
title = {{D}ynamic mapping of network-level {LTP} in the hippocampus
via high-resolution bioelectrical sensing.},
journal = {APL bioengineering},
volume = {9},
number = {3},
issn = {2473-2877},
address = {Melville, NY},
publisher = {AIP Publishing},
reportid = {DZNE-2025-00923},
pages = {036109},
year = {2025},
abstract = {Understanding the complexity of neural network dynamics
demands advanced biosensing technologies capable of
capturing large-scale interactions with high spatial and
temporal precision. Traditional approaches, such as
patch-clamp and field recordings, are inherently limited in
resolving network-wide synaptic connections, particularly
long-term potentiation (LTP), due to their localized scope
and indirect access to hippocampal subfields. To address
these challenges, we introduce EvoNES, a CMOS-based
high-definition 4096 microelectrode array platform that
leverages bidirectional stimulus-responsive biosensing
functionality. By coupling precise external electrode
stimulation targeting the Schaffer collateral and medial
perforant pathways with simultaneous on-chip bioelectrical
recordings, EvoNES enables the first real-time
quantification of evoked responses and LTP dynamics across
the entire hippocampal circuit. This system bridges critical
gaps in traditional techniques, providing a mesoscopic-scale
view of cell assemblies interplay and delivering
unprecedented insights into the distributed mechanisms
underlying memory encoding and learning processes. Advanced
computational analyses generate variation maps revealing
distinct voltage fluctuation patterns and differential
sensitivity across hippocampal subregions during synaptic
potentiation. Our findings identify four distinct waveform
classes within the CA1-CA3 network and three unique evoked
firing patterns in the dentate gyrus (DG). Post-tetanic
responses show faster induction, expanded activated zones,
and the activation of previously silent cell assemblies,
indicating significant network restructuring. Applied in
aged mice, EvoNES demonstrates age-dependent changes in
network LTP, both quantitatively and qualitatively. This
high-resolution biosensing platform in a live neural context
provides unprecedented insights into hippocampal memory
formation and offers a powerful tool for investigating
neural plasticity and network interactions in both health
and disease states.},
cin = {AG Amin / AG Kempermann},
ddc = {570},
cid = {I:(DE-2719)1710010 / I:(DE-2719)1710001},
pnm = {351 - Brain Function (POF4-351) / 352 - Disease Mechanisms
(POF4-352)},
pid = {G:(DE-HGF)POF4-351 / G:(DE-HGF)POF4-352},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:40740280},
pmc = {pmc:PMC12310272},
doi = {10.1063/5.0258985},
url = {https://pub.dzne.de/record/280245},
}