Prefrontal Cortex Response to Prenatal Insult and Postnatal Opioid Exposure

The influence of proinflammatory challenges, such as maternal immune activation (MIA) or postnatal exposure to drugs of abuse, on brain molecular pathways has been reported. On the other hand, the simultaneous effects of MIA and drugs of abuse have been less studied and sometimes offered inconsisten...

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Main Authors: Haley E. Rymut, Laurie A. Rund, Bruce R. Southey, Rodney W. Johnson, Jonathan V. Sweedler, Sandra L. Rodriguez-Zas
Format: Article
Language:English
Published: MDPI AG 2022-07-01
Series:Genes
Subjects:
Online Access:https://www.mdpi.com/2073-4425/13/8/1371
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author Haley E. Rymut
Laurie A. Rund
Bruce R. Southey
Rodney W. Johnson
Jonathan V. Sweedler
Sandra L. Rodriguez-Zas
author_facet Haley E. Rymut
Laurie A. Rund
Bruce R. Southey
Rodney W. Johnson
Jonathan V. Sweedler
Sandra L. Rodriguez-Zas
author_sort Haley E. Rymut
collection DOAJ
description The influence of proinflammatory challenges, such as maternal immune activation (MIA) or postnatal exposure to drugs of abuse, on brain molecular pathways has been reported. On the other hand, the simultaneous effects of MIA and drugs of abuse have been less studied and sometimes offered inconsistent results. The effects of morphine exposure on a pig model of viral-elicited MIA were characterized in the prefrontal cortex of males and females using RNA-sequencing and gene network analysis. Interacting and main effects of morphine, MIA, and sex were detected in approximately 2000 genes (false discovery rate-adjusted <i>p</i>-value < 0.05). Among the enriched molecular categories (false discovery rate-adjusted <i>p</i>-value < 0.05 and −1.5 > normalized enrichment score > 1.5) were the cell adhesion molecule pathways associated with inflammation and neuronal development and the long-term depression pathway associated with synaptic strength. Gene networks that integrate gene connectivity and expression profiles displayed the impact of morphine-by-MIA interaction effects on the pathways. The cell adhesion molecules and long-term depression networks presented an antagonistic effect between morphine and MIA. The differential expression between the double-challenged group and the baseline saline-treated Controls was less extreme than the individual challenges. The previous findings advance the knowledge about the effects of prenatal MIA and postnatal morphine exposure on the prefrontal cortex pathways.
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spelling doaj.art-02c7d6a355084381ae235d2141da846c2023-12-03T13:42:46ZengMDPI AGGenes2073-44252022-07-01138137110.3390/genes13081371Prefrontal Cortex Response to Prenatal Insult and Postnatal Opioid ExposureHaley E. Rymut0Laurie A. Rund1Bruce R. Southey2Rodney W. Johnson3Jonathan V. Sweedler4Sandra L. Rodriguez-Zas5Department of Animal Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USADepartment of Animal Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USADepartment of Animal Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USADepartment of Animal Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USANeuroscience Program, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USADepartment of Animal Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USAThe influence of proinflammatory challenges, such as maternal immune activation (MIA) or postnatal exposure to drugs of abuse, on brain molecular pathways has been reported. On the other hand, the simultaneous effects of MIA and drugs of abuse have been less studied and sometimes offered inconsistent results. The effects of morphine exposure on a pig model of viral-elicited MIA were characterized in the prefrontal cortex of males and females using RNA-sequencing and gene network analysis. Interacting and main effects of morphine, MIA, and sex were detected in approximately 2000 genes (false discovery rate-adjusted <i>p</i>-value < 0.05). Among the enriched molecular categories (false discovery rate-adjusted <i>p</i>-value < 0.05 and −1.5 > normalized enrichment score > 1.5) were the cell adhesion molecule pathways associated with inflammation and neuronal development and the long-term depression pathway associated with synaptic strength. Gene networks that integrate gene connectivity and expression profiles displayed the impact of morphine-by-MIA interaction effects on the pathways. The cell adhesion molecules and long-term depression networks presented an antagonistic effect between morphine and MIA. The differential expression between the double-challenged group and the baseline saline-treated Controls was less extreme than the individual challenges. The previous findings advance the knowledge about the effects of prenatal MIA and postnatal morphine exposure on the prefrontal cortex pathways.https://www.mdpi.com/2073-4425/13/8/1371RNA-seqopioidinfectionpathways
spellingShingle Haley E. Rymut
Laurie A. Rund
Bruce R. Southey
Rodney W. Johnson
Jonathan V. Sweedler
Sandra L. Rodriguez-Zas
Prefrontal Cortex Response to Prenatal Insult and Postnatal Opioid Exposure
Genes
RNA-seq
opioid
infection
pathways
title Prefrontal Cortex Response to Prenatal Insult and Postnatal Opioid Exposure
title_full Prefrontal Cortex Response to Prenatal Insult and Postnatal Opioid Exposure
title_fullStr Prefrontal Cortex Response to Prenatal Insult and Postnatal Opioid Exposure
title_full_unstemmed Prefrontal Cortex Response to Prenatal Insult and Postnatal Opioid Exposure
title_short Prefrontal Cortex Response to Prenatal Insult and Postnatal Opioid Exposure
title_sort prefrontal cortex response to prenatal insult and postnatal opioid exposure
topic RNA-seq
opioid
infection
pathways
url https://www.mdpi.com/2073-4425/13/8/1371
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AT rodneywjohnson prefrontalcortexresponsetoprenatalinsultandpostnatalopioidexposure
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