Sertraline modulates hippocampal plasticity via sigma 1 receptors, cellular stress and neurosteroids.
Ontology highlight
ABSTRACT: In addition to modulating serotonin transport, selective serotonin reuptake inhibitors (SSRIs) have multiple other mechanisms that may contribute to clinical effects, and some of these latter actions prompt repurposing of SSRIs for non-psychiatric indications. In a recent study of the SSRIs fluvoxamine, fluoxetine and sertraline we found that, unlike the other two SSRIs, sertraline acutely inhibited LTP at a low micromolar concentration through inverse agonism of sigma 1 receptors (S1Rs). In the present studies, we pursued mechanisms contributing to sertraline modulation of LTP in rat hippocampal slices. We found that sertraline partially inhibits synaptic responses mediated by N-methyl-D-aspartate receptors (NMDARs) via effects on NMDARs that contain GluN2B subunits. A selective S1R antag
SUBMITTER: Izumi Y
PROVIDER: S-EPMC11582653 | biostudies-literature | 2024 Nov
REPOSITORIES: biostudies-literature
ACCESS DATA