In this review, we will discuss the role of NPY in stress-related behaviors and its relevance to select psychiatric disorders. NPY immunopositive cell bodies and fibers are generally found in cortical, limbic, hypothalamic, and brainstem regions (Allen et al., 1983). Expression of NPY in the human

and rodent brain is similar, with abundant NPY mRNA or immunoreactivity located in the neocortex, amygdala, hippocampus, basal ganglia, hypothalamus, periaqueductal grey, dorsal raphe nucleus, and the A1-3 and A6 noradrenergic cells groups in the brainstem (Adrian and et al, 1983, Allen and et al, 1983, Caberlotto et al., 2000, Wahlestedt et al., 1989, Yamazoe and et al, 1985, de Quidt and Emson, 1986a and de Quidt and Emson, 1986b). The effects of NPY are mediated by at least four subtypes of G-protein coupled receptors termed DAPT manufacturer Y1, Y2, Y4, and Y5. Y6 receptors are expressed in the mouse brain, but this isoform is absent in the rat and nonfunctional in human and non-human primates (Larhammar and Salaneck, 2004). Autoradiographic and immunohistochemical examinations indicate that Y1 and

Y2 receptors (Y1R and Y2R) exhibit the greatest expression in the brain, whereas lower levels of Y4 and Y5 receptors (Y4R and Y5R) are also present (Dumont and et al, 1993, Stanic and et al, 2006, Stanic and Selleck Talazoparib et al, 2011, Dumont and et al, 1998, Kask and et al, 2002 and Wolak and et al, 2003). Significant differences in the distribution of NPY receptors are detectable between the rodent and human brain, warranting caution in the generalization of the role of NPY receptors from preclinical animal models to humans

(Dumont et al., 1998). NPY receptors can couple to various effectors systems by associating with inhibitory Gi/o proteins (see review (Sah and Geracioti, 2013)). NPY receptors inhibit adenylyl cyclase and the accumulation of cAMP, mobilize calcium through phospholipase C and phosphatidylinositol 3-kinase activity, and have effects on multiple ion Calpain channels (Sah and Geracioti, 2013). Within stress responsive brain regions such as the cortex, amygdala, hypothalamus, and locus coeruleus, NPY receptors are localized on or impact the function of neurons expressing GABA, glutamate, corticotropin-releasing factor (CRF), and norepinephrine (NE) (Grove and et al, 2000, Dimitrov and et al, 2007, Giesbrecht and et al, 2010, Rostkowski and et al, 2009, Illes et al., 1993 and Eaton et al., 2007). It has been hypothesized that NPY serves as a functional “brake” to tone down the excitatory effects of pro-stress neurotransmitters such as CRF and NE (Sah and Geracioti, 2013, Eaton et al., 2007 and Heilig and et al, 1994).