This type of temporally restricted feeding (RF) schedule synchronises circadian oscillators in the limbic forebrain (Amir et al., 2004; Lamont et al., 2005; Waddington Lamont et al., 2007) and can induce a diurnal rhythm of clock gene protein expression in the dorsomedial nucleus of the hypothalamus (DMH; (Verwey et al., 2007). Ghrelin is a stomach peptide that acts in the brain to regulate energy balance (Kojima et al., 1999; Tschop et al., 2000; Toshinai et al., 2001). Ghrelin is secreted in response to fasting and hypoglycemia, and causes feeding when administered either peripherally or centrally (Tschop et al., 2000; Toshinai et al., 2001). Importantly, plasma ghrelin levels increase

before, and are rapidly reduced following, a meal, suggesting click here a role in meal initiation (Cummings et al., 2001; Toshinai et al., 2001; Sanchez et al., 2004; Drazen et al., 2006). The effects Talazoparib in vitro of ghrelin are mediated through the growth hormone secretagogue receptor (GHSR), found in brain regions associated with feeding and the regulation of circadian rhythms. For example, the message for GHSR is found in the SCN of rats, primates and, to a lesser extent, mice (Guan et al., 1997; Mitchell et al., 2001; Zigman et al., 2006). Ghrelin receptors are also found in brain regions stimulated in anticipation of scheduled

meals (Angeles-Castellanos et al., 2004). These data suggest that ghrelin may play a role in circadian timing mechanisms, particularly entrainment to food availability. The latter hypothesis has been supported by studies showing

that GHSR-knockout (KO) mice show attenuated anticipatory locomotor activity on an RF schedule (Blum et al., 2009; LeSauter et al., 2009), and cFOS expression is reduced in many brain areas in response to RF (Blum et al., 2009; Lamont et al., 2012). Moreover, and in spite of evidence for the presence of the ghrelin receptor in the circadian system, the role of ghrelin on circadian rhythms remains to be studied in detail. Here we looked for the presence ID-8 of GHSR in the circadian system of mice using GHSR-KO mice with a LacZ reporter inserted into the promoter of the GHSR gene. To further investigate the circadian phenotype of animals lacking the ghrelin receptor, analyses of running wheel activity and neuronal activation were performed under various lighting conditions. KO and WT mice were placed under a 12 : 12 h light : dark schedule (LD), constant darkness (DD) or constant light (LL); they were killed at different intervals to observe circadian rhythms of cFos expression. We also examined circadian rhythms of GHSR-KO and WT mice under conditions of DD and LL, and the ability of these animals to entrain to scheduled meals under these lighting conditions. Mice with targeted mutations to the ghrelin receptor gene (GHSR-KO) and their WT littermates were bred at the Carleton University Department of Neuroscience animal facilities.