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Fig
ure
3.
(A) The NO radical scavenging ability of bromelain. The NO radical scavenging ability of bromelain was calculated as (%) = (1 – sample A
420nm
/control A
420nm
) x 100. All data are expressed as mean ± standard deviation (n = 3).
P
< 0.05, compared to the control.(B) Effect of bromelain on inflammatory gene expression (iNOS and COX-2) in LPS-stimulated RAW 264.7 macrophage cells. (C) Effect of bromelain on the phosphorylation of MAP kinases. (D) Effect of bromelain on AP–1 expression. RAW 264.7 macrophages were treated for 24 h with the indicated concentrations of bromelain before treatment with LPS (1 μg/mL for 30 min). Following this, cell lysates were analyzed by western blotting using the indicated antibodies. β-actin was used as the control. The protein bands are representative of experiments, and the % expression level indicates the level relative to LPS treated cells which were set as 100%. All data are expressed as mean ± standard deviation (n = 3).
P
< 0.05, compared to the control
From
Medicinal Effects of Bromelain (
Ananas comosus
) Targeting Oral Environment as an Anti-oxidant and Anti-inflammatory Agent
Jung-Ha Lee, Jae-Bong Lee, Jin-Tae Lee, Hae-Ryoun Park, Jin-Bom Kim
Journal of Food and Nutrition Research
.
2018
, 6(12), 773-784 doi:10.12691/jfnr-6-12-8
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