<HashMap><database>biostudies-literature</database><scores/><additional><submitter>You Z</submitter><funding>Heilongjiang Postdoctoral Grant</funding><funding>China Postdoctoral Science Foundation</funding><funding>National Natural Science Foundation of China</funding><pagination>77</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11852879</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>31(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The pathogenesis of epilepsy is complex, and current antiepileptic drugs do not effectively control the seizures. Cytoplasmic polyadenylation element-binding protein 3 (CPEB3) regulates neuronal excitability, but its mechanism of action in epilepsy is not clear. In this paper, we investigated the effect of CPEB3 on seizures and elucidated its underlying molecular mechanism.&lt;h4>Methods&lt;/h4>Bioinformatics-based search for genes closely associated with epilepsy. Changes in expression and cellular localization of CPEB3 in epilepsy were verified by western blotting (WB) and Immunofluorescence staining. Subsequently, The adeno-associated virus was employed to overexpress or knockdown in mice. Behavioral experiments verified the effect of CPEB3 on epileptic phenotype, and the m</pubmed_abstract><journal>Molecular medicine (Cambridge, Mass.)</journal><pubmed_title>CPEB3 can regulate seizure susceptibility by inhibiting the transcriptional activity of STAT3 on NMDARs expression.</pubmed_title><pmcid>PMC11852879</pmcid><funding_grant_id>LBH-Q20045</funding_grant_id><funding_grant_id>LBH-Q21132</funding_grant_id><funding_grant_id>2018M640306</funding_grant_id><funding_grant_id>81871016</funding_grant_id><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Huang C</pubmed_authors><pubmed_authors>You Z</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Fan Z</pubmed_authors><pubmed_authors>Wei F</pubmed_authors><pubmed_authors>Gao X</pubmed_authors><pubmed_authors>Sun J</pubmed_authors></additional><is_claimable>false</is_claimable><name>CPEB3 can regulate seizure susceptibility by inhibiting the transcriptional activity of STAT3 on NMDARs expression.</name><description>&lt;h4>Background&lt;/h4>The pathogenesis of epilepsy is complex, and current antiepileptic drugs do not effectively control the seizures. Cytoplasmic polyadenylation element-binding protein 3 (CPEB3) regulates neuronal excitability, but its mechanism of action in epilepsy is not clear. In this paper, we investigated the effect of CPEB3 on seizures and elucidated its underlying molecular mechanism.&lt;h4>Methods&lt;/h4>Bioinformatics-based search for genes closely associated with epilepsy. Changes in expression and cellular localization of CPEB3 in epilepsy were verified by western blotting (WB) and Immunofluorescence staining. Subsequently, The adeno-associated virus was employed to overexpress or knockdown in mice. Behavioral experiments verified the effect of CPEB3 on epileptic phenotype, and the m</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2025-04-18T13:06:05.552Z</modification><creation>2025-04-06T22:36:18.449Z</creation></dates><accession>S-EPMC11852879</accession><cross_references><pubmed>39994587</pubmed><doi>10.1186/s10020-025-01136-2</doi></cross_references></HashMap>