Close
  Indian J Med Microbiol
 

Figure 4: (a) Effect of Moringa oleifera hydroethanolic bioactive leaves extract on lipopolysaccharide-induced inducible nitric oxide synthase, cyclooxygenase-2, and nuclear factor kappa-light-chain-enhancer of activated B-cells p65 expression in RAW264.7 cells. Cells were stimulated with lipopolysaccharide (1 µg/ml) in the presence of Moringa oleifera hydroethanolic leaves extract (125 µg/ml, 250 µg/ml) and dexamethasone (0.5 µg/ml) for 24 h at 37°C. Cell lysates were extracted, and protein expression levels were analyzed by Western blot. β-actin was used as the loading control. (b) The level of each protein was measured and normalized to β-actin. The values are reported as the mean ± standard deviation percentage of three independent experiments. Statistical analysis using one-way analysis of variance with Tukey's post-hoc test. It shows a significant difference with lipopolysaccharide treated group (*P < 0.05)

Figure 4: (a) Effect of <i>Moringa oleifera</i> hydroethanolic bioactive leaves extract on lipopolysaccharide-induced inducible nitric oxide synthase, cyclooxygenase-2, and nuclear factor kappa-light-chain-enhancer of activated B-cells p65 expression in RAW264.7 cells. Cells were stimulated with lipopolysaccharide (1 µg/ml) in the presence of <i>Moringa oleifera</i> hydroethanolic leaves extract (125 µg/ml, 250 µg/ml) and dexamethasone (0.5 µg/ml) for 24 h at 37°C. Cell lysates were extracted, and protein expression levels were analyzed by Western blot. β-actin was used as the loading control. (b) The level of each protein was measured and normalized to β-actin. The values are reported as the mean ± standard deviation percentage of three independent experiments. Statistical analysis using one-way analysis of variance with Tukey's <i>post-hoc</i> test. It shows a significant difference with lipopolysaccharide treated group (*<i>P</i> < 0.05)