, 2007). Y1R knockout mice display increased immobility in the forced swim test, indicative of a depression-like phenotype Venetoclax in vivo (Karlsson et al., 2008). Both Y2R and Y4R

knockout mice exhibit reduced depression-like behavior in the tail suspension test, another common screening assay for antidepressant potential (Tasan and et al, 2009, Painsipp et al., 2008 and Painsipp and et al, 2008). Knockout of both Y2R and Y4R results in augmented anti-depressant effects compared to single-knockout of either receptor (Tasan et al., 2009). Anti-depressant strategies including imipramine and electroconvulsive stimuli increase NPY immunoreactivity or receptor mRNA and binding sites, respectively (Heilig and et al, 1988 and Madsen and et al, 2000). The anti-depressant LY294002 price properties of NPY may be mediated through interactions

with the serotonin system, as administration of a tryptophan hydroxylase inhibitor blocked the anti-depressant effects of NPY in the forced swim test (Redrobe et al., 2005). The Flinders-sensitive line (FSL) is a transgenic model of depression in which abnormalities in NPY, serotonin, and catecholaminergic systems have been identified (Overstreet and et al, 2005 and Serova and et al, 1998). Depression-like behavior has been associated with impaired hippocampal neurogenesis, and enhanced NPY and serotonin activities been shown to increase cell proliferation in the dentate gyrus of the hippocampus (Husum et al., 2006). Hippocampal and amygdalar NPY immunoreactivity is lower in FSL rats compared to Flinders-resistant controls (Jimenez Vasquez and et al, 2000, Jimenez-Vasquez et al., 2000 and Zambello and et al, 2008), and aging is associated during with exacerbated loss of hippocampal NPY immunoreactivity in the FSL line (Husum et al., 2006). In FSL rats, Y5R antagonism produces anti-depressant effects in the forced swim test (Walker et al., 2009). Electroconvulsive stimuli and the selective serotonin

reuptake inhibitor fluoxetine increase NPY mRNA or immunoreactivity in the hippocampus and hypothalamus, and upregulate amygdalar Y1R binding sites in FSL rats (Caberlotto and et al, 1998 and Caberlotto and et al, 1999). Exercise and escitalopram are associated with similar alterations in hippocampal NPY and Y1 receptor mRNA (Bjornebekk et al., 2010). NPY has also been examined in olfactory bulbectomized rats (OBX), which are utilized as a rodent model due to depression-like disruptions in behavior, physiology, and neurochemistry (Song and Leonard, 2005 and Kelly et al., 1997). Anti-depressant effects are observed following chronic treatment with NPY, a Y1R agonist, and a Y2R antagonist in OBX rats (Goyal and et al, 2009 and Morales-Medina and et al, 2012a). In contrast, chronic administration of a Y2R agonist enhanced depression-like behavior in OBX rats in the forced swim test (Morales-Medina et al., 2012).