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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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Autores principales: Rymut, Haley E., Rund, Laurie A., Southey, Bruce R., Johnson, Rodney W., Sweedler, Jonathan V., Rodriguez-Zas, Sandra L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9407090/
https://www.ncbi.nlm.nih.gov/pubmed/36011282
http://dx.doi.org/10.3390/genes13081371
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author Rymut, Haley E.
Rund, Laurie A.
Southey, Bruce R.
Johnson, Rodney W.
Sweedler, Jonathan V.
Rodriguez-Zas, Sandra L.
author_facet Rymut, Haley E.
Rund, Laurie A.
Southey, Bruce R.
Johnson, Rodney W.
Sweedler, Jonathan V.
Rodriguez-Zas, Sandra L.
author_sort Rymut, Haley E.
collection PubMed
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 p-value < 0.05). Among the enriched molecular categories (false discovery rate-adjusted p-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 pubmed-94070902022-08-26 Prefrontal Cortex Response to Prenatal Insult and Postnatal Opioid Exposure Rymut, Haley E. Rund, Laurie A. Southey, Bruce R. Johnson, Rodney W. Sweedler, Jonathan V. Rodriguez-Zas, Sandra L. Genes (Basel) Article 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 p-value < 0.05). Among the enriched molecular categories (false discovery rate-adjusted p-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. MDPI 2022-07-30 /pmc/articles/PMC9407090/ /pubmed/36011282 http://dx.doi.org/10.3390/genes13081371 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rymut, Haley E.
Rund, Laurie A.
Southey, Bruce R.
Johnson, Rodney W.
Sweedler, Jonathan V.
Rodriguez-Zas, Sandra L.
Prefrontal Cortex Response to Prenatal Insult and Postnatal Opioid Exposure
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 Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9407090/
https://www.ncbi.nlm.nih.gov/pubmed/36011282
http://dx.doi.org/10.3390/genes13081371
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