<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mar AC</submitter><funding>Medical Research Council and Wellcome Trust</funding><funding>IMI-NEWMEDS</funding><funding>Medical Research Council</funding><funding>Begona Gamallo-Lana</funding><funding>Ming Lei</funding><funding>Johan Alsio</funding><funding>Wellcome Trust</funding><pagination>2837-2857</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5591806</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>234(19)</volume><pubmed_abstract>&lt;h4>Rationale&lt;/h4>Impairments in attention and inhibitory control are endophenotypic markers of neuropsychiatric disorders such as schizophrenia and represent key targets for therapeutic management. Robust preclinical models and assays sensitive to clinically relevant treatments are crucial for improving cognitive enhancement strategies.&lt;h4>Objectives&lt;/h4>We assessed a rodent model with neural and behavioral features relevant to schizophrenia (gestational day 17 methylazoxymethanol acetate treatment (MAM-E17)) on a novel test of attention and executive function, and examined the impact of putative nootropic drugs.&lt;h4>Methods&lt;/h4>MAM-E17 and sham control rats were trained on a novel touchscreen-based rodent continuous performance test (rCPT) designed to closely mimic the human CPT paradigm.</pubmed_abstract><journal>Psychopharmacology</journal><pubmed_title>MAM-E17 rat model impairments on a novel continuous performance task: effects of potential cognitive enhancing drugs.</pubmed_title><pmcid>PMC5591806</pmcid><funding_grant_id>Ming Lei was supported by the Chinese Scholarship</funding_grant_id><funding_grant_id>n° 115008 of which resources are composed of EFPI</funding_grant_id><funding_grant_id>G0001354</funding_grant_id><funding_grant_id>The Behavioural and Clinical Neuroscience Institut</funding_grant_id><funding_grant_id>350-2012-230 Johan Alsio was supported by the Swed</funding_grant_id><funding_grant_id>Begona Gamallo-Lana was supported by La Caixa Fell</funding_grant_id><funding_grant_id>G1000183</funding_grant_id><pubmed_authors>Bussey TJ</pubmed_authors><pubmed_authors>Lei M</pubmed_authors><pubmed_authors>Saksida LM</pubmed_authors><pubmed_authors>Mar AC</pubmed_authors><pubmed_authors>Gamallo-Lana B</pubmed_authors><pubmed_authors>Robbins TW</pubmed_authors><pubmed_authors>Nilsson SRO</pubmed_authors><pubmed_authors>Alsio J</pubmed_authors><pubmed_authors>Dourado T</pubmed_authors></additional><is_claimable>false</is_claimable><name>MAM-E17 rat model impairments on a novel continuous performance task: effects of potential cognitive enhancing drugs.</name><description>&lt;h4>Rationale&lt;/h4>Impairments in attention and inhibitory control are endophenotypic markers of neuropsychiatric disorders such as schizophrenia and represent key targets for therapeutic management. Robust preclinical models and assays sensitive to clinically relevant treatments are crucial for improving cognitive enhancement strategies.&lt;h4>Objectives&lt;/h4>We assessed a rodent model with neural and behavioral features relevant to schizophrenia (gestational day 17 methylazoxymethanol acetate treatment (MAM-E17)) on a novel test of attention and executive function, and examined the impact of putative nootropic drugs.&lt;h4>Methods&lt;/h4>MAM-E17 and sham control rats were trained on a novel touchscreen-based rodent continuous performance test (rCPT) designed to closely mimic the human CPT paradigm.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Oct</publication><modification>2026-07-15T18:32:33.529Z</modification><creation>2019-03-27T02:55:56Z</creation></dates><accession>S-EPMC5591806</accession><cross_references><pubmed>28744563</pubmed><doi>10.1007/s00213-017-4679-5</doi></cross_references></HashMap>