<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Diachenko M</submitter><funding>European Union Joint Programme – Neurodegenerative Disease Research</funding><funding>Dutch National Epilepsy Foundation</funding><funding>Netherlands Organization for Health and Development</funding><funding>REBALANCE</funding><funding>ZonMw</funding><pagination>fcaf443</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12641122</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(6)</volume><pubmed_abstract>Early stages of Alzheimer's disease are marked by brain hyperexcitability, evidenced by subclinical epileptiform features suggesting an excitation-inhibition imbalance. Clinically translatable biomarkers for early detection of excitation-inhibition changes at the network level, however, are lacking. We investigated the functional excitation-inhibition ratio, theta-gamma phase-amplitude coupling and epileptiform features in hippocampal and cortical local field potentials recorded weekly in freely behaving male APPswe/PS1dE9 (APP/PS1) mice (&lt;i>n&lt;/i> = 10) and wild-type controls (&lt;i>n&lt;/i> = 10) between 3 and up to and including 11 months of age. APP/PS1 mice exhibited a shift towards increased excitation, reflected in the elevated functional excitation-inhibition ratio emerging most prominently in the hippocampus at 6 months. Additionally, elevated population spiking activity and age-related impairments in theta-gamma phase-amplitude coupling were observed in the local field potentials of APP/PS1 mice in both the hippocampus and the cortex. Importantly, the functional excitation-inhibition ratio correlated positively with elevated population spiking activity in both brain regions in APP/PS1 mice. Our findings highlight the functional excitation-inhibition ratio as a promising biomarker of hippocampal and cortical network disinhibition and hyperexcitability in APP/PS1 mice, with potential value as an early disease marker in Alzheimer's disease.</pubmed_abstract><journal>Brain communications</journal><pubmed_title>Hippocampal and cortical activities reflect early hyperexcitability in an Alzheimer's mouse model.</pubmed_title><pmcid>PMC12641122</pmcid><funding_grant_id>2022-10</funding_grant_id><funding_grant_id>10510062210003</funding_grant_id><funding_grant_id>2019/01724/ZONMW</funding_grant_id><pubmed_authors>Tolner EA</pubmed_authors><pubmed_authors>Krivoshein G</pubmed_authors><pubmed_authors>Diachenko M</pubmed_authors><pubmed_authors>van Kesteren RE</pubmed_authors><pubmed_authors>Linkenkaer-Hansen K</pubmed_authors><pubmed_authors>Mansvelder HD</pubmed_authors><pubmed_authors>van den Maagdenberg AMJM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hippocampal and cortical activities reflect early hyperexcitability in an Alzheimer's mouse model.</name><description>Early stages of Alzheimer's disease are marked by brain hyperexcitability, evidenced by subclinical epileptiform features suggesting an excitation-inhibition imbalance. Clinically translatable biomarkers for early detection of excitation-inhibition changes at the network level, however, are lacking. We investigated the functional excitation-inhibition ratio, theta-gamma phase-amplitude coupling and epileptiform features in hippocampal and cortical local field potentials recorded weekly in freely behaving male APPswe/PS1dE9 (APP/PS1) mice (&lt;i>n&lt;/i> = 10) and wild-type controls (&lt;i>n&lt;/i> = 10) between 3 and up to and including 11 months of age. APP/PS1 mice exhibited a shift towards increased excitation, reflected in the elevated functional excitation-inhibition ratio emerging most prominently in the hippocampus at 6 months. Additionally, elevated population spiking activity and age-related impairments in theta-gamma phase-amplitude coupling were observed in the local field potentials of APP/PS1 mice in both the hippocampus and the cortex. Importantly, the functional excitation-inhibition ratio correlated positively with elevated population spiking activity in both brain regions in APP/PS1 mice. Our findings highlight the functional excitation-inhibition ratio as a promising biomarker of hippocampal and cortical network disinhibition and hyperexcitability in APP/PS1 mice, with potential value as an early disease marker in Alzheimer's disease.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2026-05-31T03:15:03.424Z</modification><creation>2026-05-31T03:10:06.088Z</creation></dates><accession>S-EPMC12641122</accession><cross_references><pubmed>41293234</pubmed><doi>10.1093/braincomms/fcaf443</doi></cross_references></HashMap>