<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.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>2026-06-02T09:05:54Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/33874" metadataPrefix="qdc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/33874</identifier><datestamp>2026-05-11T08:07:47Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37953</setSpec></header><metadata><qdc:qualifieddc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>The Sponge-Derived Brominated Compound Aeroplysinin-1 Impairs the Endothelial Inflammatory Response through Inhibition of the NF-κB Pathway</dc:title>
   <dc:creator>Vidal-Valenzuela, Isabel</dc:creator>
   <dc:creator>Castilla-Ruiz, Laura</dc:creator>
   <dc:creator>Marrero-Capitán, Ana Dácil</dc:creator>
   <dc:creator>Bravo-Ruiz, Inés</dc:creator>
   <dc:creator>Bernal-Muñoz, Manuel</dc:creator>
   <dc:creator>Manrique-Poyato, María Inmaculada</dc:creator>
   <dc:creator>Rodríguez-Quesada, Ana María</dc:creator>
   <dc:creator>Medina-Torres, Miguel Ángel</dc:creator>
   <dc:creator>Martínez-Poveda, Beatriz Amparo</dc:creator>
   <dc:subject>Inflamación</dc:subject>
   <dcterms:abstract>Aeroplysinin-1 (Apl-1) is a brominated compound isolated from the marine sponge&#xd;
Aplysina aerophoba that exhibits pleiotropic bioactive effects, impairing cell growth in cancer cells,&#xd;
inhibiting angiogenesis in vitro and in vivo and modulating the redox status of different cell types,&#xd;
among other reported activities. In addition to the aforementioned effects, the anti-inflammatory po-&#xd;
tential of this natural compound was explored in previous work of our laboratory, but the mechanism&#xd;
of action underlying this effect was not described. In this work, we delve into the anti-inflammatory&#xd;
effect of Apl-1 in the context of vascular endothelial cells in vitro, providing new data regarding&#xd;
the molecular mechanism underlying this activity. The characterization of the mechanism of action&#xd;
points to an inhibitory effect of Apl-1 on the NF-κB pathway, one of the main axes involved in&#xd;
endothelial response during inflammatory events. Our results show that Apl-1 can inhibit the ex-&#xd;
pression of pro-inflammatory genes in tumor necrosis factor alpha (TNF-α)- and lipopolysaccharide&#xd;
(LPS)-stimulated human umbilical vein endothelial cells (HUVECs), targeting the nuclear factor&#xd;
kappa B subunit (NF-κB) pathway through a mechanism of action involving the inhibition of I kappa&#xd;
B kinase (IKK) complex phosphorylation and RelA/p65 nuclear import. In addition, Apl-1 prevented&#xd;
the phosphorylation of Akt induced by TNF-α in HUVECs, probably supporting the inhibitory effect&#xd;
of this compound in the NF-κB pathway. Experimental evidence reported in this work opens the door&#xd;
to the potential pharmacological use of this compound as an anti-inflammatory agent in diseases that&#xd;
course with a pathological endothelial response to inflammation, such as atherosclerosis.</dcterms:abstract>
   <dcterms:dateAccepted>2024-09-28T17:55:02Z</dcterms:dateAccepted>
   <dcterms:available>2024-09-28T17:55:02Z</dcterms:available>
   <dcterms:created>2024-09-28T17:55:02Z</dcterms:created>
   <dcterms:issued>2022</dcterms:issued>
   <dc:type>journal article</dc:type>
   <dc:identifier>Vidal, I.; Castilla, L.; Marrero, A.D.; Bravo-Ruiz, I.; Bernal, M.; Manrique, I.; R. Quesada, A.; Medina, M.Á.; Martínez-Poveda, B. The Sponge-Derived Brominated Compound Aeroplysinin-1 Impairs the Endothelial Inflammatory Response through Inhibition of the NF-κB Pathway. Mar. Drugs 2022, 20, 605. https://doi.org/10.3390/md20100605</dc:identifier>
   <dc:identifier>https://hdl.handle.net/10630/33874</dc:identifier>
   <dc:identifier>10.3390/md20100605</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:rights>open access</dc:rights>
   <dc:publisher>MDPI</dc:publisher>
</qdc:qualifieddc>
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