<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Emre C</submitter><funding>Vetenskapsrådet</funding><funding>Gun och Bertil Stohnes Stiftelse</funding><funding>Stiftelsen för Gamla tjänarinnor; Gun och Bertil Stohnes Stiftelse; Hållstens Forskninsstiftelse; Torsten Söderbergs Stiftelse; EENT Foundation of New Orleans</funding><funding>Stockholms Läns Landsting</funding><funding>Alzheimerfonden</funding><pagination>245</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8938447</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5(1)</volume><pubmed_abstract>Sustained microglial activation and increased pro-inflammatory signalling cause chronic inflammation and neuronal damage in Alzheimer's disease (AD). Resolution of inflammation follows neutralization of pathogens and is a response to limit damage and promote healing, mediated by pro-resolving lipid mediators (LMs). Since resolution is impaired in AD brains, we decided to test if intranasal administration of pro-resolving LMs in the App&lt;sup>NL-G-F/NL-G-F&lt;/sup> mouse model for AD could resolve inflammation and ameliorate pathology in the brain. A mixture of the pro-resolving LMs resolvin (Rv) E1, RvD1, RvD2, maresin 1 (MaR1) and neuroprotectin D1 (NPD1) was administered to stimulate their respective receptors. We examined amyloid load, cognition, neuronal network oscillations, glial activati</pubmed_abstract><journal>Communications biology</journal><pubmed_title>Intranasal delivery of pro-resolving lipid mediators rescues memory and gamma oscillation impairment in App&lt;sup>NL-G-F/NL-G-F&lt;/sup> mice.</pubmed_title><pmcid>PMC8938447</pmcid><funding_grant_id>2018-02601</funding_grant_id><pubmed_authors>Alcalde SG</pubmed_authors><pubmed_authors>Ohshima M</pubmed_authors><pubmed_authors>Jun B</pubmed_authors><pubmed_authors>Emre C</pubmed_authors><pubmed_authors>Do KV</pubmed_authors><pubmed_authors>Hjorth E</pubmed_authors><pubmed_authors>Bazan NG</pubmed_authors><pubmed_authors>Maioli S</pubmed_authors><pubmed_authors>Cothern ML</pubmed_authors><pubmed_authors>Nilsson P</pubmed_authors><pubmed_authors>Schultzberg M</pubmed_authors><pubmed_authors>Fisahn A</pubmed_authors><pubmed_authors>Arroyo-Garcia LE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Intranasal delivery of pro-resolving lipid mediators rescues memory and gamma oscillation impairment in App&lt;sup>NL-G-F/NL-G-F&lt;/sup> mice.</name><description>Sustained microglial activation and increased pro-inflammatory signalling cause chronic inflammation and neuronal damage in Alzheimer's disease (AD). Resolution of inflammation follows neutralization of pathogens and is a response to limit damage and promote healing, mediated by pro-resolving lipid mediators (LMs). Since resolution is impaired in AD brains, we decided to test if intranasal administration of pro-resolving LMs in the App&lt;sup>NL-G-F/NL-G-F&lt;/sup> mouse model for AD could resolve inflammation and ameliorate pathology in the brain. A mixture of the pro-resolving LMs resolvin (Rv) E1, RvD1, RvD2, maresin 1 (MaR1) and neuroprotectin D1 (NPD1) was administered to stimulate their respective receptors. We examined amyloid load, cognition, neuronal network oscillations, glial activati</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-04T08:24:20.519Z</modification><creation>2025-04-04T08:24:20.519Z</creation></dates><accession>S-EPMC8938447</accession><cross_references><pubmed>35314851</pubmed><doi>10.1038/s42003-022-03169-3</doi></cross_references></HashMap>