, 2008) Collectively, this suggests that the amygdala plays an a

, 2008). Collectively, this suggests that the amygdala plays an active role in extinction learning by modulating fear expression in the presence o f an extinguished CS by way of functionally MAPK Inhibitor Library distinct neuronal populations. However, extinction learning also involves

reciprocal interactions between the amygdala and the PL and IL subregions of the vmPFC, which can differentially influence fear expression (see Herry et al., 2010 and Milad and Quirk, 2012, for recent reviews). The PL promotes fear expression through reciprocal connections with the (BLA) amygdala, which provides signals regarding the presence of a threat. These signals are thought to become amplified within the PL before projecting back to amygdala nuclei that then relay these signals to output regions that engender fear expression (Milad and Quirk, 2012). Consistent with this, Protease Inhibitor Library firing rates of PL neurons intensify in the presence of an aversive CS in a manner related to assays of fear expression (i.e., freezing) (Burgos-Robles et al., 2009). Stimulation of the PL subregion enhances fear expression to CSs and slows extinction learning (Vidal-Gonzalez et al., 2006), while inactivation the PL leads to reduced fear expression to an aversive CS (Corcoran and Quirk, 2007 and Sierra-Mercado

et al., 2011). Conversely, the IL plays a critical role in fear inhibition and regulation. Recent research in rodents has suggested that during extinction learning, these functionally distinct cell populations in the LA and BA may signal the presence of

a ‘safe’ CS to the IL region of the vmPFC, which can then feedback to this same population of neurons (Repa et al., 2001, Herry et al., 2008 and Burgos-Robles et al., 2009). The IL can then suppress fear expression by inhibiting the CE directly (Quirk et al., 2003) or indirectly through the ITCs that surround the BA and LA and project heavily to the CE (Pare et al., 2004, Millhouse, 1986, McDonald, 1998 and Vertes, 2004). The IL can also activate local inhibitory interneurons in the LA to gate fear expression (Rosenkranz et al., 2003). Finally, Oxymatrine the hippocampus also plays an important role by providing contextual modulation of extinction learning (Milad and Quirk, 2012). Although extinction training serves as a useful paradigm to model safety learning, the viability of extinction training as a therapeutic option for treating affective disorders depends critically on the extent to which this learning is retained and later utilized when cues are again encountered. Research across species has demonstrated a critical role for the IL of the vmPFC in the retention and retrieval of extinction learning (Akirav and Maroun, 2007, Quirk and Mueller, 2008, Holmes and Wellman, 2009, Sotres-Bayon and Quirk, 2010 and Milad and Quirk, 2012).

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