<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/CINECAstyle.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-22T16:21:43Z</responseDate><request verb="GetRecord" identifier="oai:iris.unica.it:11584/447170" metadataPrefix="oai_dc">https://iris.unica.it/oai/request</request><GetRecord><record><header><identifier>oai:iris.unica.it:11584/447170</identifier><datestamp>2025-06-20T00:13:26Z</datestamp><setSpec>com_11584_207615</setSpec><setSpec>com_11584_111066</setSpec><setSpec>col_11584_207612</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
<dc:title>Conjugated linoleic acid isomers anti-neuroinflammatory effects on activated microglial cells</dc:title>
<dc:creator>PORCEDDA, CLARA</dc:creator>
<dc:contributor>SOGOS, VALERIA</dc:contributor>
<dc:subject>Settore BIO/17 - Istologia</dc:subject>
<dc:description>Conjugated linoleic acid (CLA) isomers display anti-inflammatory effects within the central nervous system (CNS). This research examined how CLA isomers c9,t11 and t10,c12 influence fatty acid (FA) and N-acylethanolamine (NAE) profiles, along with their relationship with the expression of pro-inflammatory molecules in the BV-2 microglia cell line, which are the resident immune cells in the CNS that play a key role in sustaining neuronal activity and immune balance. BV-2 cells were exposed to 25 μM of c9,t11-CLA, t10,c12-CLA, or oleic acid (OA) for 24 hours, after which they were stimulated with lipopolysaccharide (LPS). Following the treatment, the fatty acid and N-acylethanolamine profiles, as well as the expression of pro-inflammatory molecules, were assessed. Our findings showed that CLA isomers lessen the morphological alterations caused by LPS in BV-2 cells and decrease both the gene expression and protein levels of inflammatory markers. This impact was associated with an increase in acyl-CoA oxidase 1, an important enzyme involved in the anti-inflammatory peroxisomal beta-oxidation pathway that effectively processes CLA isomers. Importantly, t10,c12-CLA markedly inhibited stearoyl-CoA desaturase 1, which influenced the production of monounsaturated fatty acids. The profile of NAEs was significantly modified by CLA isomers, leading to a notable increase in the release of the anti-neuroinflammatory mediator known as docosahexaenoic acid (DHA)-derived N-acylethanolamine (DHAEA). In summary, our research indicates that the anti-neuroinflammatory properties of CLA isomers can be attributed to their effects on fatty acid metabolism and modulation of bioactive fatty acid-derived N-acylethanolamines, emphasizing a potential approach for nutritional interventions in conditions marked by neuroinflammation.</dc:description>
<dc:date>2025-02-12T00:00:00+01:00</dc:date>
<dc:type>info:eu-repo/semantics/doctoralThesis</dc:type>
<dc:identifier>https://hdl.handle.net/11584/447170</dc:identifier>
<dc:language>ita</dc:language>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:publisher>Università degli Studi di Cagliari</dc:publisher>
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