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. Author manuscript; available in PMC: 2014 Nov 1.
Published in final edited form as: Neurobiol Dis. 2013 Jul 13;59:26–37. doi: 10.1016/j.nbd.2013.07.001

Figure 1. Ro3206145 inhibits p38 MAPK activity ex vivo.

Figure 1

(A) Example western blot of phosphorylated activating transcription factor 2 (p-ATF2) following a kinase reaction with phosphorylated p38 MAPK that was immuno-precipitated from rat retinal explants. Explants were exposed to ultra-violet (UV) light to activate p38 MAPK. Increasing concentrations of Ro3206145 were effective at inhibiting p38 MAPK activation of ATF2. (B) Densitometer quantification (of the ATF2 assay (n≥3 for each condition) shows significant increase in p38 MAPK activity with UV exposure relative to naïve controls (* p = 0.01). Ro3206145 (in DMSO) reduces activity, reaching significance compared to UV exposure alone for 10 μM and higher (** p ≤ 0.003).