The EAE-associated behavioral syndrome: I. Temporal correlation with inflammatory mediators

• Published in: Journal of neuroimmunology 2003-04, Vol.137 (1), p.94-99
• Main Authors: Pollak, Y., Ovadia, H., Orion, E., Weidenfeld, J., Yirmiya, R.
• Format: Article
• Language: English
• Subjects: Animals; Behavior, Animal - physiology; Brain - immunology; Brain - metabolism; Cytokines - biosynthesis; Dinoprostone - biosynthesis; EAE; Encephalomyelitis, Autoimmune, Experimental - immunology; Encephalomyelitis, Autoimmune, Experimental - metabolism; Encephalomyelitis, Autoimmune, Experimental - psychology; Female; Gene Expression Regulation - physiology; Infiltration; Interleukin 1β (IL-1β); Interleukin-1 - biosynthesis; Mice; Prostaglandin E 2; RNA, Messenger - biosynthesis; Sickness behavior; TNF-α
• ISSN: 0165-5728; 1872-8421
• DOI: 10.1016/S0165-5728(03)00075-4

To elucidate the mechanisms underlying the EAE-associated behavioral syndrome (EBS), we examined the temporal correlation between the behavioral alterations and inflammatory processes. Onset of the behavioral syndrome was associated with the onset of brain infiltration, as well as mRNA expression of interleukin 1β (IL-1β) and tumor necrosis factor α (TNF-α) and elevated production of interleukin 1β protein and prostaglandin E 2 (PGE 2). Sickness behavior symptoms coincided with peak cytokine expression. Behavioral recovery was associated with a reduction of cytokine expression, but not infiltration, PGE 2 production or motor disturbances. These results suggest that inflammatory processes in general, and the production of pro-inflammatory cytokines in particular, are involved in mediating EAE-associated sickness behavior.