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<title>Long-term effects of low doses of Chlorpyrifos exposure at the preweaning developmental stage: A locomotor, pharmacological, brain gene expression and gut microbiome analysis</title>
<creator>Pérez Fernández, Cristian</creator>
<creator>Morales Navas, Miguel</creator>
<creator>Guardia Escote, Laia</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>Locomotor</subject>
<subject>Cholinergic system</subject>
<subject>GABAergic system</subject>
<subject>Gene expression</subject>
<subject>Gut microbiome</subject>
<description>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.</description>
<date>2024-02-08</date>
<date>2024-02-08</date>
<date>2020-01</date>
<type>info:eu-repo/semantics/article</type>
<identifier>0278-6915</identifier>
<identifier>http://hdl.handle.net/10259/8632</identifier>
<identifier>10.1016/j.fct.2019.110865</identifier>
<language>eng</language>
<relation>Food and Chemical Toxicology. 2020, V. 135, 110865</relation>
<relation>https://doi.org/10.1016/j.fct.2019.110865</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>