, 2000). Interestingly, HAB mice

exhibit a lower rate of adult hippocampal neurogenesis along with impaired functional integration of newly-born neurons when compared with their normal anxiety/depression-related behaviour (NAB) counterparts (Sah et al., 2012). However, Selleckchem MLN8237 the ability of chronic treatment with fluoxetine to alleviate depression-like behaviour in HAB mice is dissociated from changes in adult hippocampal neurogenesis (Sah et al., 2012). The use of knockout animals helps to determine the importance of some factors, such as brain-derived neurotrophic factor – BDNF, on the stress response. Deficiency in BDNF makes male mice susceptible to acute and subchronic mild stress (induced by intraperitoneal injection) and increases behavioural despair and plasma corticosterone levels (Advani et al., 2009), and this is coupled with reduced adult hippocampal neurogenesis (Taliaz et al., 2010). Moreover, BDNF

Selleck Pfizer Licensed Compound Library is required for antidepressant-induced increases in the survival of newly-born neurons and antidepressant-related behaviour in mice (Sairanen et al., 2005). Thus, BDNF seems to play a role in stress susceptibility, adult hippocampal neurogenesis and antidepressant-induced changes in behaviour. Similarly, mice lacking the cannabinoid receptor, CB1, are greatly susceptible to the anhedonic effects of chronic stress (Martin et al., 2002), and exhibit 50% lower basal cell proliferation in the subgranular zone of the dentate gyrus of the hippocampus (Jin et al., 2004), as well as depressive-like responses (Steiner et al., 2008) in basal conditions. On the other hand, mice lacking the fatty acid amide hydrolase enzyme, which results in increased availability of anandamide (which acts at CB receptors), exhibit an antidepressant-like phenotype (Bambico et al., 2010) as well as increased hippocampal cell proliferation (Aguado et al., 2005). Taken together, it is clear that genetic background Thiamine-diphosphate kinase is an important determinant of stress-induced changes

in adult hippocampal neurogenesis and stress resilience, and that certain factors that regulate adult hippocampal neurogenesis such as BDNF and cannabinoid signalling are also important determinants of stress resilience. Such factors may be important therapeutic targets for the development of drugs that promote stress resilience (Karatsoreos and McEwen, 2013 and Hill and Gorzalka, 2005). Perhaps the most definitive approach to determine whether adult hippocampal neurogenesis contributes to differential stress susceptibility is to interrogate whether ablation of neurogenesis exacerbates or attenuates the physiological and behavioural responses to stress. Ablation of adult neurogenesis can be achieved by chemical (i.e. methylazoxymethanol – MAM) (Jayatissa et al., 2009 and Mateus-Pinheiro et al., 2013), genetic (Schloesser et al., 2010, Snyder et al., 2011 and Yu et al., 2008) and irradiation-based methods (Santarelli et al., 2003 and Wu and Hen, 2014).