Chronic stress and antidepressant treatment alter purine metabolism and beta oxidation within mouse brain and serum

Peter J. Hamilton, Emily Y. Chen, Vladimir Tolstikov, Catherine J. Peña, Joseph A. Picone, Punit Shah, Kiki Panagopoulos, Ana N. Strat, Deena M. Walker, Zachary S. Lorsch, Hannah L. Robinson, Nicholas L. Mervosh, Drew D. Kiraly, Rangaprasad Sarangarajan, Niven R. Narain, Michael A. Kiebish, Eric J. Nestler

Research output: Contribution to journalArticlepeer-review

Abstract

Major depressive disorder (MDD) is a complex condition with unclear pathophysiology. Molecular disruptions within limbic brain regions and the periphery contribute to depression symptomatology and a more complete understanding the diversity of molecular changes that occur in these tissues may guide the development of more efficacious antidepressant treatments. Here, we utilized a mouse chronic social stress model for the study of MDD and performed metabolomic, lipidomic, and proteomic profiling on serum plus several brain regions (ventral hippocampus, nucleus accumbens, and medial prefrontal cortex) of susceptible, resilient, and unstressed control mice. To identify how commonly used tricyclic antidepressants impact the molecular composition in these tissues, we treated stress-exposed mice with imipramine and repeated our multi-OMIC analyses. Proteomic analysis identified three serum proteins reduced in susceptible animals; lipidomic analysis detected differences in lipid species between resilient and susceptible animals in serum and brain; and metabolomic analysis revealed dysfunction of purine metabolism, beta oxidation, and antioxidants, which were differentially associated with stress susceptibility vs resilience by brain region. Antidepressant treatment ameliorated stress-induced behavioral abnormalities and affected key metabolites within outlined networks, most dramatically in the ventral hippocampus. This work presents a resource for chronic social stress-induced, tissue-specific changes in proteins, lipids, and metabolites and illuminates how molecular dysfunctions contribute to individual differences in stress sensitivity.

Original languageEnglish (US)
Article number18134
JournalScientific reports
Volume10
Issue number1
DOIs
StatePublished - Dec 1 2020
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • General

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