e. in nonstressed females), prolonged exposure to chronic stress results in an attenuated CORT response to stimuli, which predisposes to higher susceptibility to pathogenic autoimmunity. A comprehensive and widely accepted biological model linking stress, CORT and autoimmune diseases is currently lacking. Although numerous studies demonstrated that CORT suppresses autoimmune diseases in humans and in animal models [15, 35, 36], other studies indicate that low levels of CORT or certain stress

paradigms may skew to proinflammatory conditions [14, 18, 19, 37-42]. In the present study we found that CVS exacerbated EAE in female mice despite the overall stress-induced increase in CORT levels, which was also reported previously [32, 43, 44]. The elevated urine CORT levels Galunisertib cost in females were, however, significantly lower on the fourth week of stress and reached those of nonstressed females. In addition, CORT selleck chemicals levels failed to increase toward disease onset (9 days postimmunization) in stressed as compared with nonstressed mice. Following the disease onset (14 and 21 days postimmunization) CORT levels in stressed mice markedly increased to levels higher than those observed during stress, and remained similar to those observed in nonstressed mice throughout the course of the disease. These results suggest that the temporarily decreased functionality of the HPA axis in stressed female mice, which resulted in a

delayed CORT response to MOG35-55 immunization, could at least partially account for the initial exacerbation of the disease over that induced in nonstressed mice. An important N-acetylglucosamine-1-phosphate transferase finding in our study was that although stressed male mice demonstrated decreased weight gain and increased

anxiety index similar to females, they showed significantly lower levels of urine CORT under basal, stress and EAE conditions. Although to a less extent, blood CORT levels were also lower in male than in female mice. However, whereas primarily free CORT was observed in the urine, only a small fraction (less than 10%) of the blood CORT was free, with levels similar between male and female mice, while the rest was presumably bound to CORT-binding globulin [45]. Higher CORT levels were previously documented in female compared with male Sprague–Dawley rats [46]. Furthermore, CORT secretion has been previously shown to attenuate EAE severity, suggesting that the HPA axis suppresses autoimmune disease progression [47-49]. Taking together, it is reasonable to assume that although similar levels of free CORT were observed in male and female mice, the overall higher basal levels of CORT in nonstressed females attenuated their EAE severity. The role of free versus bound CORT in gender-related EAE susceptibility should be further investigated. Given the antiinflammatory properties of CORT, we asked why CVS generally exacerbated EAE in female mice.