Wheel running reduces ethanol seeking by increasing neuronal activation and reducing oligodendroglial/neuroinflammatory factors in the medial prefrontal cortex

• Published in: Brain, behavior, and immunity Vol. 58; pp. 357 - 368
• Main Authors: Somkuwar, Sucharita S., Fannon-Pavlich, McKenzie J., Ghofranian, Atoosa, Quigley, Jacqueline A., Dutta, Rahul R., Galinato, Melissa H., Mandyam, Chitra D.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 01.11.2016
• Subjects: Alcohol; Allergy and Immunology; Animals; BrdU; Cues; Drug-Seeking Behavior; Encephalitis - metabolism; Ethanol - administration & dosage; Extinction, Psychological - drug effects; Male; MBP; Medial prefrontal cortex; MOG; Motor Activity - drug effects; Neurons - drug effects; Neurons - metabolism; NG2; Olig2; Oligodendroglia - drug effects; Oligodendroglia - metabolism; PECAM-1; Platelet Endothelial Cell Adhesion Molecule-1 - metabolism; Prefrontal Cortex - drug effects; Prefrontal Cortex - metabolism; Psychiatry; Rats, Wistar; Reinstatement; Wheel running; Wheel running; Medial prefrontal cortex; PECAM-1; MOG; Reinstatement; NG2; Alcohol; MBP; Olig2; BrdU
• ISSN: 0889-1591; 1090-2139; 1090-2139
• DOI: 10.1016/j.bbi.2016.08.006

•Protracted abstinence enhances ethanol seeking triggered by contexual cues.•Enhanced ethanol seeking is associated with oligodendrogenesis and neuroinflammatory responses in the mPFC.•Wheel running during abstinence prevents ethanol seeking triggered by contexual cues.•Reduced seeking is associated with reduced oligodendrogenesis and neuroinflammatory responses in the mPFC. The therapeutic effects of wheel running (WR) during abstinence on reinstatement of ethanol seeking behaviors in rats that self-administered ethanol only (ethanol drinking, ED) or ED with concurrent chronic intermittent ethanol vapor experience (CIE-ED) were investigated. Neuronal activation as well as oligodendroglial and neuroinflammatory factors were measured in the medial prefrontal cortex (mPFC) tissue to determine cellular correlates associated with enhanced ethanol seeking. CIE-ED rats demonstrated escalated and unregulated intake of ethanol and maintained higher drinking than ED rats during abstinence. CIE-ED rats were more resistant to extinction from ethanol self-administration, however, demonstrated similar ethanol seeking triggered by ethanol contextual cues compared to ED rats. Enhanced seeking was associated with reduced neuronal activation, and increased number of myelinating oligodendrocyte progenitors and PECAM-1 expression in the mPFC, indicating enhanced oligodendroglial and neuroinflammatory response during abstinence. WR during abstinence enhanced self-administration in ED rats, indicating a deprivation effect. WR reduced reinstatement of ethanol seeking in CIE-ED and ED rats, indicating protection against relapse. The reduced ethanol seeking was associated with enhanced neuronal activation, reduced number of myelinating oligodendrocyte progenitors, and reduced PECAM-1 expression. The current findings demonstrate a protective role of WR during abstinence in reducing ethanol seeking triggered by ethanol contextual cues and establish a role for oligodendroglia-neuroinflammatory response in ethanol seeking. Taken together, enhanced oligodendroglia-neuroinflammatory response during abstinence may contribute to brain trauma in chronic alcohol drinking subjects and be a risk factor for enhanced propensity for alcohol relapse.