<?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>2026-06-19T12:55:05Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/8632" metadataPrefix="marc">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/8632</identifier><datestamp>2025-01-23T01:05:15Z</datestamp><setSpec>com_10259_9895</setSpec><setSpec>com_10259_3989</setSpec><setSpec>com_10259.4_106</setSpec><setSpec>com_10259_2604</setSpec><setSpec>col_10259_9896</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dcterms="http://purl.org/dc/terms/" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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<subfield code="a">Pérez Fernández, Cristian</subfield>
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<subfield code="a">Morales Navas, Miguel</subfield>
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<subfield code="a">Guardia Escote, Laia</subfield>
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<subfield code="a">Garrido Cárdenas, José Antonio</subfield>
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<subfield code="a">Colomina, María Teresa</subfield>
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<subfield code="a">Giménez, Estela</subfield>
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<subfield code="a">Sánchez Santed, Fernando</subfield>
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<subfield code="a">Development is especially sensitive to Chlorpyrifos (CPF) toxicity, associated with several neurodegenerative&#xd;
and neurodevelopmental disorders where motor function dysfunction is a core symptom. Amongst the alternative molecular targets to cholinesterases inhibition, developmental CPF alters different components in the&#xd;
most important neurotransmitter systems, although this depends on the exposure period. Exposure during the&#xd;
late postnatal preweaning stage is the least studied by far. This period includes essential neurodevelopmental&#xd;
processes and has an important translational meaning. The present study analyzed the influence of low doses of&#xd;
CPF on this developmental window on locomotor activity and the state of the different neurotransmitter systems&#xd;
by pharmacological challenges. Brain gene expression and microbiome modulation following CPF were also&#xd;
analyzed. CPF exposure long-term increased spontaneous vertical activity, female's activity following acute&#xd;
stress, hyposensitized the cholinergic system and hypersensitized the GABAergic system, up-regulated both&#xd;
muscarinic 2 receptor and GABA-A-α2 receptor subunit in the dorsal striatum and the frontal cortex, respectively&#xd;
and induced gut microbiota dysbiosis at both genus and species levels. The present study supports alternative&#xd;
molecular targets than the ChEs following late postnatal, preweaning exposure to low doses of CPF, focusing on&#xd;
both cholinergic and GABAergic systems and the gut microbiome as an important factor.</subfield>
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<subfield code="a">http://hdl.handle.net/10259/8632</subfield>
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<subfield code="a">10.1016/j.fct.2019.110865</subfield>
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<subfield code="a">Chlorpyrifos</subfield>
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<subfield code="a">Long-term effects of low doses of Chlorpyrifos exposure at the preweaning developmental stage: A locomotor, pharmacological, brain gene expression and gut microbiome analysis</subfield>
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