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. 2019 Jun 7;9(31):17988–17994. doi: 10.1039/c9ra03023a

Fig. 7. RAW 264.7 cells were incubated with PSP (400 μg mL−1) or LPS (1 μg mL−1) for 30 min. PSP induced phosphorylation of p38 MAPK and the phosphorylation of p38 MAPK was determined by Western blot. PSP induced degradation of IκB-α for 30 min and increased iNOS, COX-2 and NF-κB expression for 6 h. These results were expressed as mean ± SD, n = 3. *p < 0.05, **p < 0.01, compared to the control group.

Fig. 7