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<mods:namePart>Pérez Fernández, Cristian</mods:namePart>
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<mods:namePart>Morales Navas, Miguel</mods:namePart>
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<mods:namePart>Aguilera Sáez, Luis Manuel</mods:namePart>
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<mods:namePart>Abreu, Ana Cristina</mods:namePart>
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<mods:namePart>Guardia Escote, Laia</mods:namePart>
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<mods:namePart>Fernández, Ignacio</mods:namePart>
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<mods:namePart>Garrido Cárdenas, José Antonio</mods:namePart>
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<mods:namePart>Colomina, María Teresa</mods:namePart>
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<mods:namePart>Giménez, Estela</mods:namePart>
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<mods:namePart>Sánchez Santed, Fernando</mods:namePart>
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<mods:dateAccessioned encoding="iso8601">2024-02-08T11:39:42Z</mods:dateAccessioned>
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<mods:dateIssued encoding="iso8601">2020-05</mods:dateIssued>
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<mods:identifier type="issn">0013-9351</mods:identifier>
<mods:identifier type="uri">http://hdl.handle.net/10259/8633</mods:identifier>
<mods:identifier type="doi">10.1016/j.envres.2020.109341</mods:identifier>
<mods:abstract>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.</mods:abstract>
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<mods:accessCondition type="useAndReproduction">Attribution-NonCommercial-NoDerivatives 4.0 Internacional</mods:accessCondition>
<mods:subject>
<mods:topic>Chlorpyrifos</mods:topic>
</mods:subject>
<mods:subject>
<mods:topic>Development</mods:topic>
</mods:subject>
<mods:subject>
<mods:topic>ASD</mods:topic>
</mods:subject>
<mods:subject>
<mods:topic>Sociability</mods:topic>
</mods:subject>
<mods:subject>
<mods:topic>Dominance</mods:topic>
</mods:subject>
<mods:subject>
<mods:topic>Gut microbiota</mods:topic>
</mods:subject>
<mods:subject>
<mods:topic>Metabolomics</mods:topic>
</mods:subject>
<mods:subject>
<mods:topic>Evidence of approval (animals)</mods:topic>
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<mods:titleInfo>
<mods: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</mods:title>
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