<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Maddock RJ</submitter><funding>NICHD NIH HHS</funding><funding>Intellectual and Developmental Disabilities Research Center, School of Medicine, Washington University in St. Louis</funding><funding>NCRR NIH HHS</funding><funding>NIMH NIH HHS</funding><funding>Yerkes National Primate Research Center, Emory University</funding><funding>National Institute of Mental Health</funding><funding>University of California, Davis</funding><funding>National Institute of Child Health and Human Development</funding><pagination>280-290</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11809764</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>121</volume><pubmed_abstract>Converging data show that exposure to maternal immune activation (MIA) in utero alters brain development in animals and increases the risk of neurodevelopmental disorders in humans. A recently developed non-human primate MIA model affords opportunities for studies with uniquely strong translational relevance to human neurodevelopment. The current longitudinal study used 1H-MRS to investigate the developmental trajectory of prefrontal cortex metabolites in male rhesus monkey offspring of dams (n = 14) exposed to a modified form of the inflammatory viral mimic, polyinosinic:polycytidylic acid (Poly IC), in the late first trimester. Brain metabolites in these animals were compared to offspring of dams that received saline (n = 10) or no injection (n = 4). N-acetylaspartate (NAA), glutamate, c</pubmed_abstract><journal>Brain, behavior, and immunity</journal><pubmed_title>Altered brain metabolites in male nonhuman primate offspring exposed to maternal immune activation.</pubmed_title><pmcid>PMC11809764</pmcid><funding_grant_id>RR00169</funding_grant_id><funding_grant_id>P50 HD103526</funding_grant_id><funding_grant_id>P50 MH106438</funding_grant_id><funding_grant_id>P51 RR000169</funding_grant_id><funding_grant_id>T32MH073124</funding_grant_id><funding_grant_id>P50HD103526</funding_grant_id><funding_grant_id>T32 MH073124</funding_grant_id><funding_grant_id>P50MH106438</funding_grant_id><pubmed_authors>Schumann CD</pubmed_authors><pubmed_authors>Van de Water J</pubmed_authors><pubmed_authors>Maddock RJ</pubmed_authors><pubmed_authors>Kimberley McAllister A</pubmed_authors><pubmed_authors>Hogrefe CE</pubmed_authors><pubmed_authors>Lesh TA</pubmed_authors><pubmed_authors>Bauman MD</pubmed_authors><pubmed_authors>Bennett J</pubmed_authors><pubmed_authors>Styner MA</pubmed_authors><pubmed_authors>Carter CS</pubmed_authors><pubmed_authors>Tanase C</pubmed_authors><pubmed_authors>Amaral DG</pubmed_authors><pubmed_authors>Vlasova RM</pubmed_authors><pubmed_authors>Ryan AM</pubmed_authors><pubmed_authors>Chen S</pubmed_authors><pubmed_authors>Murai T</pubmed_authors><pubmed_authors>Geschwind DH</pubmed_authors><pubmed_authors>Iosif AM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Altered brain metabolites in male nonhuman primate offspring exposed to maternal immune activation.</name><description>Converging data show that exposure to maternal immune activation (MIA) in utero alters brain development in animals and increases the risk of neurodevelopmental disorders in humans. A recently developed non-human primate MIA model affords opportunities for studies with uniquely strong translational relevance to human neurodevelopment. The current longitudinal study used 1H-MRS to investigate the developmental trajectory of prefrontal cortex metabolites in male rhesus monkey offspring of dams (n = 14) exposed to a modified form of the inflammatory viral mimic, polyinosinic:polycytidylic acid (Poly IC), in the late first trimester. Brain metabolites in these animals were compared to offspring of dams that received saline (n = 10) or no injection (n = 4). N-acetylaspartate (NAA), glutamate, c</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2025-04-04T02:39:09.614Z</modification><creation>2025-04-04T02:39:09.614Z</creation></dates><accession>S-EPMC11809764</accession><cross_references><pubmed>39032543</pubmed><doi>10.1016/j.bbi.2024.07.011</doi></cross_references></HashMap>