Ppar‐α hypermethylation in the hippocampus of mice exposed to social isolation stress is associated with enhanced neuroinflammation and aggressive behavior

Abstract

Social behavioral changes, including social isolation or loneliness, increase the risk for stress‐related disorders, such as major depressive disorder, posttraumatic stress disorder (PTSD), and suicide, which share a strong neuroinflammatory etiopathogenetic component. The peroxi-some‐proliferator activated receptor (PPAR)‐α, a newly discovered target involved in emotional behavior regulation, is a ligand‐activated nuclear receptor and a transcription factor that, following stimulation by endogenous or synthetic ligands, may induce neuroprotective effects by modulating neuroinflammation, and improve anxiety and depression‐like behaviors by enhancing neurosteroid biosynthesis. How stress affects epigenetic mechanisms with downstream effects on inflammation and emotional behavior remains poorly understood. We studied the effects of 4‐week social isola-tion, using a mouse model of PTSD/suicide‐like behavior, on hippocampal PPAR‐α epigenetic mod-ification. Decreased PPAR‐α expression in the hippocampus of socially isolated mice was associated with increased levels of methylated cytosines of PPAR‐α gene CpG‐rich fragments and deficient neurosteroid biosynthesis. This effect was associated with increased histone deacetylases (HDAC)1, methyl‐cytosine binding protein (MeCP)2 and decreased ten‐eleven translocator (TET)2 expression, which favor hypermethylation. These alterations were associated with increased TLR‐4 and pro-inflammatory markers (e.g., TNF‐α,), mediated by NF‐κB signaling in the hippocampus of aggressive mice. This study contributes the first evidence of stress‐induced brain PPAR‐α epigenetic reg-ulation. Social isolation stress may constitute a risk factor for inflammatory‐based psychiatric disorders associated with neurosteroid deficits, and targeting epigenetic marks linked to PPAR‐α downregulation may offer a valid therapeutic approach.