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Transcriptional Alterations in Dorsolateral Prefrontal Cortex and Nucleus Accumbens Implicate Neuroinflammation and Synaptic Remodeling in Opioid Use Disorder.
Seney, Marianne L; Kim, Sam-Moon; Glausier, Jill R; Hildebrand, Mariah A; Xue, Xiangning; Zong, Wei; Wang, Jiebiao; Shelton, Micah A; Phan, BaDoi N; Srinivasan, Chaitanya; Pfenning, Andreas R; Tseng, George C; Lewis, David A; Freyberg, Zachary; Logan, Ryan W.
Affiliation
  • Seney ML; Translational Neuroscience Program, Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania; Center for Adolescent Reward, Rhythms, and Sleep, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Kim SM; Translational Neuroscience Program, Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania; Center for Adolescent Reward, Rhythms, and Sleep, University of Pittsburgh, Pittsburgh, Pennsylvania; Center for Systems Neurogenetics of Addiction, The Jackson Labora
  • Glausier JR; Translational Neuroscience Program, Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Hildebrand MA; Translational Neuroscience Program, Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Xue X; Department of Biostatistics, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Zong W; Department of Biostatistics, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Wang J; Department of Biostatistics, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Shelton MA; Translational Neuroscience Program, Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Phan BN; Department of Computational Biology, Carnegie Mellon University, Pittsburgh, Pennsylvania.
  • Srinivasan C; Department of Computational Biology, Carnegie Mellon University, Pittsburgh, Pennsylvania.
  • Pfenning AR; Department of Computational Biology, Carnegie Mellon University, Pittsburgh, Pennsylvania; Neuroscience Institute, Carnegie Mellon University, Pittsburgh, Pennsylvania.
  • Tseng GC; Department of Biostatistics, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Lewis DA; Translational Neuroscience Program, Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Freyberg Z; Translational Neuroscience Program, Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania; Department of Cell Biology, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Logan RW; Center for Systems Neurogenetics of Addiction, The Jackson Laboratory, Bar Harbor, Maine; Department of Pharmacology and Experimental Therapeutics, Boston University School of Medicine, Boston, Massachusetts; Center for Systems Neuroscience, Boston University, Boston, Massachusetts. Electronic addre
Biol Psychiatry ; 90(8): 550-562, 2021 10 15.
Article in En | MEDLINE | ID: mdl-34380600
ABSTRACT

BACKGROUND:

Prevalence rates of opioid use disorder (OUD) have increased dramatically, accompanied by a surge of overdose deaths. While opioid dependence has been extensively studied in preclinical models, an understanding of the biological alterations that occur in the brains of people who chronically use opioids and who are diagnosed with OUD remains limited. To address this limitation, RNA sequencing was conducted on the dorsolateral prefrontal cortex and nucleus accumbens, regions heavily implicated in OUD, from postmortem brains in subjects with OUD.

METHODS:

We performed RNA sequencing on the dorsolateral prefrontal cortex and nucleus accumbens from unaffected comparison subjects (n = 20) and subjects diagnosed with OUD (n = 20). Our transcriptomic analyses identified differentially expressed transcripts and investigated the transcriptional coherence between brain regions using rank-rank hypergeometric orderlap. Weighted gene coexpression analyses identified OUD-specific modules and gene networks. Integrative analyses between differentially expressed transcripts and genome-wide association study datasets using linkage disequilibrium scores assessed the genetic liability of psychiatric-related phenotypes in OUD.

RESULTS:

Rank-rank hypergeometric overlap analyses revealed extensive overlap in transcripts between the dorsolateral prefrontal cortex and nucleus accumbens in OUD, related to synaptic remodeling and neuroinflammation. Identified transcripts were enriched for factors that control proinflammatory cytokine, chondroitin sulfate, and extracellular matrix signaling. Cell-type deconvolution implicated a role for microglia as a potential driver for opioid-induced neuroplasticity. Linkage disequilibrium score analysis suggested genetic liabilities for risky behavior, attention-deficit/hyperactivity disorder, and depression in subjects with OUD.

CONCLUSIONS:

Overall, our findings suggest connections between the brain's immune system and opioid dependence in the human brain.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Opioid-Related Disorders / Nucleus Accumbens Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Biol Psychiatry Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Opioid-Related Disorders / Nucleus Accumbens Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Biol Psychiatry Year: 2021 Document type: Article
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