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<dc:creator>Romero Sanz, Silvia</dc:creator>
<dc:creator>Caldero Escudero, Elena</dc:creator>
<dc:creator>Álvarez Illera, María Pilar</dc:creator>
<dc:creator>Santo Domingo Mayoral, Jaime</dc:creator>
<dc:creator>Fonteriz García, Rosalba Inés</dc:creator>
<dc:creator>Montero Zoccola, María Teresa</dc:creator>
<dc:creator>Álvarez Martín, Javier</dc:creator>
<dc:date>2023</dc:date>
<dc:description>Producción Científica</dc:description>
<dc:description>Introduction: The high prevalence of neurodegenerative diseases in our&#xd;
population and the lack of effective treatments encourage the search for new&#xd;
therapeutic targets for these pathologies. We have recently described that&#xd;
submaximal inhibition of the Sarco-Endoplasmic Reticulum Ca2+ ATPase&#xd;
(SERCA), the main responsible for ER calcium storage, is able to increase&#xd;
lifespan in Caenorhabditis elegans worms by mechanisms involving&#xd;
mitochondrial metabolism and nutrient-sensitive pathways.&#xd;
Methods: We have studied here the effects of submaximal SERCA inhibition in a&#xd;
chemicalmodel of Parkinson’s disease (PD) induced in C. elegansworms by treatment&#xd;
with themitochondrial complex I inhibitor rotenone. For specific SERCA inhibition,we&#xd;
treated worms with RNAi against sca-1, the sole orthologue of SERCA in C. elegans.&#xd;
Results and Discussion: Our results show that rotenone produces alterations in&#xd;
worms that include decreased lifespan, smaller size, reduced fertility, decreased&#xd;
motility, defecation and pumping rate, increased mitochondrial ROS production,&#xd;
reduced mitochondrial membrane potential and oxygen consumption rate, altered&#xd;
mitochondrial structure, and altered ethanol preference in behavioral studies. Most of&#xd;
these alterations were either fully or partially reversed in worms treated with sca-1&#xd;
RNAi, suggesting that SERCA inhibition could be a novel pharmacological target in the&#xd;
prevention or treatment of neurodegeneration.</dc:description>
<dc:format>application/pdf</dc:format>
<dc:identifier>https://uvadoc.uva.es/handle/10324/66076</dc:identifier>
<dc:language>eng</dc:language>
<dc:publisher>Frontiers</dc:publisher>
<dc:subject>2411.99 Otras</dc:subject>
<dc:subject>3209.99 Otras</dc:subject>
<dc:title>SERCA inhibition improves lifespan and healthspan in a chemical model of Parkinson disease in Caenorhabditis elegans</dc:title>
<dc:type>info:eu-repo/semantics/article</dc:type>
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<edm:dataProvider>UVaDOC. Repositorio Documental de la Universidad de Valladolid</edm:dataProvider>
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