Maternal choline supplementation modulates cognition and induces anti-inflammatory signaling in the prefrontal cortex of adolescent rats exposed to maternal immune activation

dc.contributor.authorKing, Cole J.
dc.date.accessioned2024-04-12T17:33:03Z
dc.date.graduationmonthMay
dc.date.issued2024
dc.description.abstractMaternal infection has long been described as a risk factor for neurodevelopmental disorders, especially autism spectrum disorders (ASD) and schizophrenia. Although many pathogens do not cross the placenta and infect the developing fetus directly, the maternal immune response to them is sufficient to alter fetal neurodevelopment, a phenomenon termed maternal immune activation (MIA). Low maternal choline is also a risk factor for neurodevelopmental disorders, and most pregnant people do not receive enough of it. In addition to its role in neurodevelopment, choline is capable of inducing anti-inflammatory signaling through a nicotinic pathway. Therefore, it was hypothesized that maternal choline supplementation would blunt the neurodevelopmental impact of MIA in offspring through long- term instigation of cholinergic anti-inflammatory signaling. To model MIA in rats, the viral mimetic polyinosinic:polycytidylic acid (poly(I:C)) was used to elicit a maternal antiviral innate immune response in dams both with and without choline supplementation. Offspring were reared to both early and late adolescent stages (postnatal days 28 and 50, respectively), where cognition and anxiety-related behaviors were examined. After behavioral testing, animals were euthanized, and their prefrontal cortices (PFCs) were collected for analysis. MIA offspring demonstrated sex-specific patterns of altered cognition and repetitive behaviors, which were modulated by maternal choline supplementation. Choline supplementation also bolstered anti-inflammatory signaling in the PFCs of MIA animals at both early and late adolescent stages. These findings suggest that maternal choline supplementation may be sufficient to blunt some of the behavioral and neurobiological impacts of inflammatory exposures in utero, indicating that it may be a cheap, safe, and effective intervention for neurodevelopmental disorders.
dc.description.advisorBethany Plakke Anderson
dc.description.degreeMaster of Public Health
dc.description.departmentPublic Health Interdepartmental Program
dc.description.levelMasters
dc.description.sponsorshipUniversity Small Research Grant (USRG) Startup funds to Dr. Plakke from KSU Master of Public Health program funding
dc.identifier.urihttps://hdl.handle.net/2097/44249
dc.language.isoen_US
dc.publisherKansas State University
dc.rights© the author. This Item is protected by copyright and/or related rights. You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s).
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.subjectMaternal immune activation
dc.subjectNeurodevelopmental disorders
dc.subjectCholine
dc.subjectPrefrontal cortex
dc.subjectBehavior
dc.subjectCognition
dc.titleMaternal choline supplementation modulates cognition and induces anti-inflammatory signaling in the prefrontal cortex of adolescent rats exposed to maternal immune activation
dc.typeThesis
local.embargo.terms2025-05-10

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