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. 2020 May 5;17(3):1160–1169. doi: 10.1007/s13311-020-00866-x

Fig. 2.

Fig. 2

(A) Fever burden in TLR4fl/fl SAH mice was compared with the fever burden of global TLR4−/− SAH mice. The lack of TLR4 completely inhibited the SAHiP response. Statistical significance was determined by student’s t test (p < 0.0001; n = 3 F, n = 3 M). (B) Prostaglandin pathway involvement in SAHiP was determined by performing SAH in NestinCre: ptger3fl/fl mice, which yielded the same fever burden as observed for TLR4fl/fl SAH and ptger3fl/fl + 100 μg meloxicam SAH mice. The SAHiP response was unaffected by the total lack of prostaglandin EP3 receptors in neurons, and the inhibition of the cyclo-oxygenase enzyme by meloxicam. Statistical significance was determined by two-way ANOVA and showed no differences (n = 6 per group, equally divided between the genders)