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Resolution: standard / high Figure 8.
Effects of Bay 11-7082 and LLnL onC. crepidioides-induced iNOS expression and NO production in RAW264.7 cells. (A) iNOS reporter gene analysis. RAW264.7 cells were transfected with the indicated
luciferase reporter plasmids. After transfection, the cells were incubated in a medium
containing Bay 11-7082 (20 μM) or LLnL (20 μM) for 1 h and then treated with C. crepidioides (500 μg/ml) for 6 h. Thereafter, luciferase activities were measured. The activities
are expressed relative to that of cells transfected with pGL3 iNOS without further
treatment, which was defined as 1. LUC, luciferase. Data are mean ± SD of three independent
experiments. (B) RAW264.7 cells were pretreated with Bay 11-7082 (20 μM) or LLnL (10 μM) for 1 h
before stimulation with C. crepidioides (500 μg/ml) for another 6 h. The iNOS mRNA expression was determined by RT-PCR. (C) RAW264.7 cells were pretreated with the indicated concentrations of Bay 11-7082
or LLnL for 1 h before stimulation with the indicated concentrations of C. crepidioides for another 48 h. The nitrite content in the culture media was analyzed. Data are
mean ± SD of triplicate cultures. C. c., C. crepidioides.
Tomimori et al. BMC Complementary and Alternative Medicine 2012 12:78 doi:10.1186/1472-6882-12-78 |