<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Deyama S</submitter><funding>Takeda Science Foundation</funding><funding>Japan Agency for Medical Research and Development</funding><funding>Uehara Memorial Foundation</funding><funding>Mochida Memorial Foundation for Medical and Pharmaceutical Research</funding><funding>YOKOYAMA Foundation for Clinical Pharmacology</funding><funding>Hokkoku Cancer Foundation</funding><funding>Japan Society for the Promotion of Science</funding><pagination>484-501</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10121976</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(2)</volume><pubmed_abstract>Intracerebroventricular infusion of resolvin E1 (RvE1), a bioactive metabolite derived from eicosapentaenoic acid, exerts antidepressant-like effects in a mouse model of lipopolysaccharide (LPS)-induced depression; these effects are blocked by systemic injection of rapamycin, a mechanistic target of rapamycin complex 1 (mTORC1) inhibitor. Additionally, local infusion of RvE1 into the medial prefrontal cortex (mPFC) or dorsal hippocampal dentate gyrus (DG) produces antidepressant-like effects. To evaluate the potential of RvE1 for clinical use, the present study examined whether treatment with RvE1 via intranasal (i.n.) route, a non-invasive route for effective drug delivery to the brain, produces antidepressant-like effects in LPS-challenged mice using tail suspension and forced swim tests</pubmed_abstract><journal>Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics</journal><pubmed_title>Intranasal Administration of Resolvin E1 Produces Antidepressant-Like Effects via BDNF/VEGF-mTORC1 Signaling in the Medial Prefrontal Cortex.</pubmed_title><pmcid>PMC10121976</pmcid><funding_grant_id>YRY-1903</funding_grant_id><funding_grant_id>JP17K08360</funding_grant_id><funding_grant_id>21gm0910012h0004</funding_grant_id><funding_grant_id>JP19K07120</funding_grant_id><funding_grant_id>JP19H01014</funding_grant_id><pubmed_authors>Kaneda K</pubmed_authors><pubmed_authors>Aoki S</pubmed_authors><pubmed_authors>Deyama S</pubmed_authors><pubmed_authors>Shuto S</pubmed_authors><pubmed_authors>Sugie R</pubmed_authors><pubmed_authors>Fukuda H</pubmed_authors><pubmed_authors>Minami M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Intranasal Administration of Resolvin E1 Produces Antidepressant-Like Effects via BDNF/VEGF-mTORC1 Signaling in the Medial Prefrontal Cortex.</name><description>Intracerebroventricular infusion of resolvin E1 (RvE1), a bioactive metabolite derived from eicosapentaenoic acid, exerts antidepressant-like effects in a mouse model of lipopolysaccharide (LPS)-induced depression; these effects are blocked by systemic injection of rapamycin, a mechanistic target of rapamycin complex 1 (mTORC1) inhibitor. Additionally, local infusion of RvE1 into the medial prefrontal cortex (mPFC) or dorsal hippocampal dentate gyrus (DG) produces antidepressant-like effects. To evaluate the potential of RvE1 for clinical use, the present study examined whether treatment with RvE1 via intranasal (i.n.) route, a non-invasive route for effective drug delivery to the brain, produces antidepressant-like effects in LPS-challenged mice using tail suspension and forced swim tests</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2026-06-02T19:25:40.176Z</modification><creation>2025-04-04T20:40:53.043Z</creation></dates><accession>S-EPMC10121976</accession><cross_references><pubmed>36622634</pubmed><doi>10.1007/s13311-022-01337-1</doi></cross_references></HashMap>