Figure 5From: Erythropoietin improves motor and cognitive deficit, axonal pathology, and neuroinflammation in a combined model of diffuse traumatic brain injury and hypoxia, in association with upregulation of the erythropoietin receptor Erythropoietin (EPO) attenuates axonal pathology in the pyramidal tracts of the brainstem. (A) Axonal bulbs in the pyramidal tracts of the brainstem in traumatic axonal injury (TAI) rats with/without EPO treatment at 1, 7 or 14 d. No statistical difference was observed at any time point amongst the treatment groups, however there was a spontaneous decrease in the number of axonal bulbs at 7 d in TAI rats only. (B) Number of swollen axons in the pyramidal tracts of TAI and TAI + EPO rats at 1, 7 and 14 d. EPO treatment failed to reduce axonal swelling, however there was an overall decrease in the number of swollen axons in TAI rats at 7 d. TAI + Hx rats had a strikingly more axonal bulbs (C) and swollen axons (D) in the pyramidal tracts of the brainstem, with both substantially (though not significantly) reduced at 1 d by treatment with EPO. Data shown as mean ± SEM, n = 6 per group per time point.(*P <0.05, 2-way ANOVA with post-hoc Bonferroni test).Back to article page