Susceptible, but not resilient, mice exhibited reduced permissive acetylation at the Rac1 promoter and its 2000-bp upstream region. Resilient mice showed reduced methylation within the Rac1 promoter whereas susceptible mice showed enhanced methylation in the 1000-bp upstream region. Chronic intra-NAc administration of an HDAC inhibitor reversed social avoidance behavior and rescued Rac1 expression in susceptible mice. Collectively, these results suggest that

epigenetic mechanisms maintain Rac1 Selleckchem LDN193189 expression in resilient mice, promoting adaptive behavioral response to stress, but have the opposite effect in susceptible mice. Analysis of human postmortem NAc tissue samples C59 cell line from depressed patients corroborated these animal findings. Rac1 expression was strongly reduced in unmedicated patients compared to controls, and depressed patients showed decreased acetylation in regions ∼200-bp upstream and downstream of the transcription start site (TSS) accompanied by increased methylation in the gene region ∼200-bp upstream of the TSS. Rac1 likely promotes resilient responses to CSDS via its effects on MSN spine structure. Viral-mediated overexpression of Rac1 reduced the CSDS-induced enhancement in dendritic stubby (immature) spine density whereas Cre-mediated Rac1 genetic deletion had the opposite effect. A

robust neurophysiological correlate of susceptibility to CSDS is the enhanced excitability of VTA dopamine neurons following stress (Krishnan et al., 2008 and Cao et al.,

2010). CSDS increases the spontaneous firing STK38 rate of VTA dopamine neurons and the percentage of neurons demonstrating burst firing events in susceptible, but not resilient, mice (Cao et al., 2010). These physiological changes correlate inversely with social interaction score and can be reversed with chronic antidepressant treatment, suggesting an involvement of stress-induced changes to neuronal excitability in depression-like behavior. One mechanism underlying enhanced excitability in susceptible mice is the Ih (hyperpolarization-activated cation) current (Cao et al., 2010). The Ih current regulates tonic firing of dopamine neurons as well as the transition from single-spike to burst firing, and is robustly increased only in susceptible mice following CSDS. Ih inhibitor infusion reverses social avoidance behavior, and chronic antidepressant treatment reduces the stress-induced increase in Ih current. Enhanced neuronal excitability is also mediated by reduced activation of AKT (thymoma-viral proto-oncogene) in the VTA, which likely produces a subsequent reduction in inhibitory tone (Krishnan et al., 2008). Phosphorylated AKT is reduced in the VTA of susceptible mice following CSDS, and this reduction is necessary and sufficient to produce social avoidance behavior.