There was no effect of age on the number of orexin/Fos-ir cells in the LHL, nor was there an effect of swab or age × swab interaction on any measure in LHM and LHL. Plasma testosterone measures revealed a main effect of age in both Experiment 1a (F1,35 = 30.164, P < 0.01) and Experiment 2 (F1,26 = 40.52, P < 0.01), such that adult hamsters had greater testosterone concentrations

than juvenile hamsters (Table 3). In addition in Experiment 2, a main effect of swab was observed (F1,26 = 5.16, P = 0.03), in which hamsters exposed to VS had greater testosterone concentrations than those exposed to blank swabs. This main effect appears to be driven solely by an increase in testosterone in VS-exposed Quizartinib supplier adults, although no statistically significant age × swab interaction was detected. This report provides the first demonstration that adolescent maturation of social information processing includes a transformation of a species-specific, socially relevant sensory signal from a neutral stimulus to an unconditioned reward in the absence of social see more experience. This perceptual shift is accompanied by a gain in the ability of the social stimulus to activate midbrain, ventral striatal and prefrontal components of the mesocorticolimbic reward pathway, indicating that these particular regions are recruited to mediate the adolescent gain in the perception

of VS as rewarding (Fig. 7). Juvenile male hamsters failed to show a CPP for VS. However, they did show a CPP to cocaine, demonstrating a pre-adolescent ability to show a place preference for a pharmacological reward. This is consistent with previous reports that demonstrate enhanced sensitivity to cocaine, nicotine and ethanol reward during adolescence (Doremus-Fitzwater et al., 2010). As expected, adult males did form a CPP for VS, leading to the conclusion that adult, but not prepubertal, male hamsters perceive VS as rewarding. These results provide

strong evidence that in the absence of sexual experience, a species-specific social stimulus that is a relatively weak reward or neutral in valence to juveniles becomes a potent unconditioned reward as a consequence of adolescent maturation. This report also extends earlier studies on the development of hamsters’ attraction Sitaxentan to VS, where adults, but not juveniles, spend significantly more time investigating VS than control stimuli. Preferences for VS are present only after males reach 40 days of age, by which time circulating levels of testosterone are elevated as a result of puberty onset (Johnston & Coplin, 1979). Whether elevated testosterone levels influence the perception of VS as rewarding is an open and testable question. However, it appears that organizational effects of testosterone are not necessary for the rewarding interpretations of VS, as hamsters that are gonadectomized prior to the onset of puberty and given replacement testosterone in adulthood still show a CPP to VS (De Lorme et al., 2012).