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. 2013 Nov 21;4:400. doi: 10.3389/fimmu.2013.00400

Table 1.

Previous studies characterizing behavioral changes in mouse models of EAE.

Pollak et al. (25) Peruga et al. (26) Rodrigues et al. (24) Haji et al. (27) Acharjee et al. (28)
Animals Female SJL/J mice Female C57BL/6 mice Female C57BL/6 mice Female C57BL/6 mice Female C57BL/6 mice
EAE protocol 150 μg of PLP139–151 15–20 × 106 activated lymph node cells i.p. 50 μg of MOG35–55 100 ng of PTX i.p. 100 μg of MOG35–55 300 ng of PTX i.p. 200 μg of MOG35–55 500 ng of PTX i.p. 100 μg of MOG35–55 800 ng of PTX i.p.
Onset of motor deficits (days) Not specified Signs of tail weakness at 60 dpi Clinical signs of disease at 11 dpi Expected at 10–11 dpi [according to Ref. (29)] Limp tails at 9–13 dpi
Behavioral parameters/paradigms Food and sucrose intake; social exploration Open field; rotarod; light/dark box; startle response and pre-pulse inhibition; learned helplessness paradigm Elevated plus maze; inhibitory avoidance task; object recognition task Open field; elevated plus maze Open field; elevated plus maze; forced swim test; tail suspension; sociability test; fear conditioning
Cytokine levels IL-1β expression/level (RT-PCR/ELISA) and TNF-α expression (RT-PCR); PGE2 production (RIA assay); brain (cerebellum, hypothalamus, hippocampus, brain stem) IL-6 and TNF-α expression (RT-PCR); brain (hippocampus); 15, 29, 41, 59 dpi TNF-α levels (ELISA); Brain (striatum); 10 dpi IL-1β and TNF-α expression (RT-PCR); brain (hippocampus, hypothalamus, amygdala) 7 dpi
Main results Transient sickness behavior episodes associated with EAE attacks; Increased pro-inflammatory cytokine levels before the onset of motor impairment; decrease in pro-inflammatory cytokines at the peak of the neurological symptoms Anxiety- and depression-like behavior before the occurrence of motor deficits; Increased TNF-α and neuronal loss in the hippocampus No differences in anxiety-like behavior and memory in animals induced with EAE Anxiety-like behavior before the occurrence of motor deficits; Increased TNF-α levels and activated microglia in the striatum Anxiety- and depression-like behavior, memory loss and conditioned learning deficits in early stage of EAE; elevated levels of IL-1β and TNF-α in the hypothalamus and increased basal plasma corticosterone levels