<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16</volume><submitter>Ismail FS</submitter><pubmed_abstract>Implications of glia in the pathophysiology of epilepsy raise the question of how these cells besides neurons are responsive to antiseizure medications (ASMs). Understanding ASM effects on glia and glia-mediated inflammation may help to explore astrocytes and microglia as potential targets for alternative anti-epileptogenic therapies. The aim of this study was to investigate the effects of the new generation ASM brivaracetam (BRV) in an astrocyte-microglia co-culture model of inflammation. Primary rat astrocytes co-cultures containing 5%-10% (M5, "physiological" conditions) or 30%-40% (M30, "pathological inflammatory" conditions) of microglia were treated with different concentrations of BRV (0.5, 2, 10, and 20 μg/ml) for 24 h. Glial cell viability was measured by MTT assay. Microglial act</pubmed_abstract><journal>Frontiers in cellular neuroscience</journal><pagination>995861</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9670320</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Brivaracetam exhibits mild pro-inflammatory features in an &lt;i>in vitro&lt;/i> astrocyte-microglia co-culture model of inflammation.</pubmed_title><pmcid>PMC9670320</pmcid><pubmed_authors>Kummel ML</pubmed_authors><pubmed_authors>Faustmann PM</pubmed_authors><pubmed_authors>Forster E</pubmed_authors><pubmed_authors>Faustmann TJ</pubmed_authors><pubmed_authors>Corvace F</pubmed_authors><pubmed_authors>Ismail FS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Brivaracetam exhibits mild pro-inflammatory features in an &lt;i>in vitro&lt;/i> astrocyte-microglia co-culture model of inflammation.</name><description>Implications of glia in the pathophysiology of epilepsy raise the question of how these cells besides neurons are responsive to antiseizure medications (ASMs). Understanding ASM effects on glia and glia-mediated inflammation may help to explore astrocytes and microglia as potential targets for alternative anti-epileptogenic therapies. The aim of this study was to investigate the effects of the new generation ASM brivaracetam (BRV) in an astrocyte-microglia co-culture model of inflammation. Primary rat astrocytes co-cultures containing 5%-10% (M5, "physiological" conditions) or 30%-40% (M30, "pathological inflammatory" conditions) of microglia were treated with different concentrations of BRV (0.5, 2, 10, and 20 μg/ml) for 24 h. Glial cell viability was measured by MTT assay. Microglial act</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-21T14:13:02.858Z</modification><creation>2025-04-21T14:13:02.858Z</creation></dates><accession>S-EPMC9670320</accession><cross_references><pubmed>36406753</pubmed><doi>10.3389/fncel.2022.995861</doi></cross_references></HashMap>