, 1990, Schmidt et al., 1992 and Bedford et al., 1979). We will focus here on the voluntary exercise model. Several weeks of wheel running has indeed a major effect on body composition, but not really on

body weight (Droste et al., 2003 and Droste et al., 2007). Exercising rats and mice have substantially less abdominal fat and more muscle tissue. Long-term voluntary exercise has a major impact on physiological system like the HPA axis, the sympathetic nervous system and sleep regulation. Wheel running for several weeks evokes major changes in HPA axis regulation (Droste et al., 2003 and Droste et al., 2007). These were associated with increased activity of the sympatho-adrenomedullary system, i.e. enhanced synthesis and release of adrenaline from the adrenal medulla, which is under sympathetic control (Droste et al., 2003 and Droste et al., 2007). Exercising rats and mice show increases in Selumetinib purchase adrenal weight (relative to the body weight; Reul and Droste, 2005, Droste et al., 2003 and Droste et al., 2007). The adrenal medulla of the runners presented increased levels of CX-5461 price tyrosine hydroxylase (TH; the rate-limiting enzyme in adrenaline synthesis) mRNA indicating a rise in the activity of sympatho-adrenomedullary system (Reul and Droste, 2005, Droste et al., 2003 and Droste et al., 2007). These changes in adrenal size and adrenomedullary activity

can be regarded as a direct consequence of long-term enhanced physical activity. Baseline early morning plasma ACTH levels were decreased in exercising mice suggesting a reduced hypothalamic-pituitary found drive at this time of the day (Droste et al., 2003). Furthermore, evening plasma corticosterone values were higher in the running mice which may be an adaptive response to increased metabolic demand due to running during this time of the day/night cycle (Droste et al., 2003). In vivo microdialysis in exercising rats showed that free glucocorticoid hormone levels were increased at this time of the day as well (Droste et al., 2009b). There were distinct

changes in the HPA axis responses to different stressful challenges. Exposure to a novel environment, which is regarded as a mild psychological stressor, resulted in a lower plasma glucocorticoid hormone response in exercising rats and mice than in sedentary animals (Droste et al., 2003 and Droste et al., 2007). In contrast, subjecting rats and mice to forced swimming (this involves a substantial physical stress component) led to a significantly higher glucocorticoid response in the exercising animals (Droste et al., 2003 and Droste et al., 2007). As plasma ACTH responses were not different to either stressor, it appears that mechanisms at the level of the adrenal gland are predominantly responsible for the distinct glucocorticoid responses to the novelty challenge and the forced swim stress.