, 2008 and Hart, 1988). Microbial invasion is sensed by cells of the innate immune system through selleck kinase inhibitor activation of pattern-recognition receptors (PRRs), following the recognition of molecular structures specific for pathogens, termed pathogen-associated molecular patterns (PAMPs) (Kawai and Akira, 2011). The first identified and best characterized PRRs belong to the family of Toll-like receptors (TLRs); however, other PRRs such as the nuclear-binding domain (NOD)-like receptors (NLRs)

represent a further group of PRRs playing important roles in PAMP recognition and immunity (Franchi et al., 2009 and Kawai and Akira, 2011). Unlike NLRs which are intracellular PRRs, TLRs are associated with the cell membrane. Lipopolysaccharide (LPS) is a major component of the outer membrane of Gram-negative bacteria and acts as a predominant TLR4 agonist (Poltorak et al., 1998 and Kawai and Akira, 2011). After binding to TLR4 it leads to NF-κB and mitogen-activated protein (MAP) kinase activation and induces a strong cytokine response (Poltorak et al., 1998 and Kawai

and Akira, 2011). Thus, LPS is one of the most widely studied PAMPs triggering acute sickness behavior, as well as delayed depression-like behavior in rodents (Frenois et al., 2007 and Yirmiya, 1996) and elicits similar effects to that of the injection of specific cytokines such as

IL-1β (Anisman et al., 2008) and TNF-α (Bluthe et either al., 1991). The behavioral effects of peripheral see more immune activation are mediated via an afferent neural and an endocrine pathway. As part of the endocrine pathway, cytokines and circulating PAMPs reach the brain at the level of the choroid plexus and the circumventricular organs and induce the expression of cytokines within the brain (Dantzer et al., 2000). The peripheral and central effects of immune activation can be assessed by means of several parameters. First, immune activation induces c-Fos-like immunoreactivity, an indicator of neuronal activation, within the brain and can provide insights into the neural networks that subserve sickness symptoms (Gaykema and Goehler, 2011 and Sagar et al., 1995). Second, immune activation leads to an increase of circulating corticosterone levels indicating a stimulation of the hypothalamic–pituitary–adrenal (HPA) axis (Lenczowski et al., 1997). Third, the tryptophan catabolite kynurenine, which is generated by indoleamine-2,3-dioxygenase (IDO) upon activation by cytokines, has emerged as a key mediator for the induction of anhedonic and anxiety-like behavior (Haroon et al., 2012, O’connor et al., 2009 and Salazar et al., 2012).