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<title>Medium and long-term effects of low doses of Chlorpyrifos during the postnatal, preweaning developmental stage on sociability, dominance, gut microbiota and plasma metabolites</title>
<creator>Pérez Fernández, Cristian</creator>
<creator>Morales Navas, Miguel</creator>
<creator>Aguilera Sáez, Luis Manuel</creator>
<creator>Abreu, Ana Cristina</creator>
<creator>Guardia Escote, Laia</creator>
<creator>Fernández, Ignacio</creator>
<creator>Garrido Cárdenas, José Antonio</creator>
<creator>Colomina, María Teresa</creator>
<creator>Giménez, Estela</creator>
<creator>Sánchez Santed, Fernando</creator>
<subject>Chlorpyrifos</subject>
<subject>Development</subject>
<subject>ASD</subject>
<subject>Sociability</subject>
<subject>Dominance</subject>
<subject>Gut microbiota</subject>
<subject>Metabolomics</subject>
<subject>Evidence of approval (animals)</subject>
<description>Autism spectrum disorder (ASD) is a complex neurodevelopmental pathology characterized by altered verbalizations, reduced social interaction behavior, and stereotypies. Environmental factors have been associated with&#xd;
its development. Some researchers have focused on pesticide exposure. Chlorpyrifos (CPF) is the most used&#xd;
Organophosphate. Previous developmental studies with CPF showed decreased, enhanced or no effect on social&#xd;
outcomes eminently in mice. The study of CPF exposure during preweaning stages on social behavior is sparse in&#xd;
mice and non-existent in rats. d stressors could be at the basis of ASD development, and around postnatal day 10&#xd;
in the rat is equivalent to the human birthday in neurodevelopmental terms. We explored the effects of exposure&#xd;
to low doses (1mg/kg/mL/day) of CPF during this stage regarding: sociability, dominance gut microbiome and&#xd;
plasma metabolomic profile, since alterations in these systems have also been linked to ASD. There was a modest&#xd;
influence of CPF on social behavior in adulthood, with null effects during adolescence. Dominance and hierarchical status were not affected by exposure. Dominance status explained the significant reduction in reaction&#xd;
to social novelty observed on the sociability test. CPF induced a significant gut microbiome dysbiosis and&#xd;
triggered a hyperlipidemic, hypoglycemic/hypogluconeogenesis and a general altered cell energy production in&#xd;
females. These behavioral results in rats extend and complement previous studies with mice and show novel&#xd;
influences on gut metagenomics and plasma lipid profile and metabolomics, but do not stablish a relation between the exposure to CPF and the ASD phenotype. The effects of dominance status on reaction to social novelty&#xd;
have an important methodological meaning for future research on sociability.</description>
<date>2024-02-08</date>
<date>2024-02-08</date>
<date>2020-05</date>
<type>info:eu-repo/semantics/article</type>
<identifier>0013-9351</identifier>
<identifier>http://hdl.handle.net/10259/8633</identifier>
<identifier>10.1016/j.envres.2020.109341</identifier>
<language>eng</language>
<relation>Environmental Research. 2020, V. 184, 109341</relation>
<relation>https://doi.org/10.1016/j.envres.2020.109341</relation>
<rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</rights>
<rights>info:eu-repo/semantics/openAccess</rights>
<rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</rights>
<publisher>Elsevier</publisher>
</thesis></metadata></record></GetRecord></OAI-PMH>