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. Author manuscript; available in PMC: 2013 Nov 1.
Published in final edited form as: J Neurochem. 2012 Sep 28;123(4):555–567. doi: 10.1111/j.1471-4159.2012.07955.x

Figure 7.

Figure 7

Changes in the phosphorylation state of MAPK p38, JNK and ERK1/2 in BV-2 microglia stimulated for 0.5, 1, 2 and 4 hr with LPS 6.25 ng/ml with and without 12 mM sodium acetate. Panel A shows representative images of the Western blots from the 4 hr experiment. Panels B, C and D show the optical densities of phosphorylated MAPK p38, JNK and ERK1/2 normalized to the loading controls MAPK p38, JNK and ERK1/2, respectively (n = 6). The data represent the means ± SD where statistical significance (* = compared to NaCl) was set at p ≤ 0.05, as determined by One Way ANOVA followed by Tukey’s post-hoc test.