TY - JOUR
T1 - Inhibitory effect of sulforaphane on secretory group IIA phospholipase A2
AU - Lee, Yuri
AU - Lee, Wonhwa
AU - Kim, Jaehong
AU - Bae, Jong Sup
N1 - Publisher Copyright:
© 2018 Yuri Lee et al.
PY - 2018
Y1 - 2018
N2 - Background and Objective: The expression of secretory group IIA phospholipase A2 (sPLA2-IIA) has been shown to be elevated in various inflammatory diseases and Lipopolysaccharide (LPS) up-regulates the expression of sPLA2-IIA in Human umbilical vein endothelial cells (HUVECs). Sulforaphane (SFN), a natural isothiocyanate present in cruciferous vegetables such as broccoli and cabbage, is effective in preventing carcinogenesis, diabetes and inflammatory responses. Here, SFN was examined for its effects on the expression and activity of sPLA2-IIA in HUVECs and in mouse models of sepsis. Materials and Methods: After HUVECs were activated with LPS, cells were post-treated with SFN. In vivo, LPS-injected or Cecal ligation and puncture (CLP) operated mice were administrated SFN. Then, the effects of SFN on the activity and expression of sPLA2-IIA were determined by Enzyme-linked immunosorbent assay (ELISA). The effects of SFN on the activities of cytosolic phospholipase A2 (cPLA2) and Extracellular signal-regulated kinase (ERK)1/2 were monitored. Statistical relevance was determined by one-way analysis of variance (ANOVA). p<0.05 were considered to indicate significance Results: Post-treatment of cells or mice with SFN inhibited LPS- or CLP-induced expression and activity of sPLA2-IIA. SFN also suppressed the activation of cPLA2 and ERK1/2 by LPS. Conclusion: It is concluded that, SFN inhibited LPS-mediated expression of sPLA2-IIA by suppression of cPLA2 and ERK1/2.
AB - Background and Objective: The expression of secretory group IIA phospholipase A2 (sPLA2-IIA) has been shown to be elevated in various inflammatory diseases and Lipopolysaccharide (LPS) up-regulates the expression of sPLA2-IIA in Human umbilical vein endothelial cells (HUVECs). Sulforaphane (SFN), a natural isothiocyanate present in cruciferous vegetables such as broccoli and cabbage, is effective in preventing carcinogenesis, diabetes and inflammatory responses. Here, SFN was examined for its effects on the expression and activity of sPLA2-IIA in HUVECs and in mouse models of sepsis. Materials and Methods: After HUVECs were activated with LPS, cells were post-treated with SFN. In vivo, LPS-injected or Cecal ligation and puncture (CLP) operated mice were administrated SFN. Then, the effects of SFN on the activity and expression of sPLA2-IIA were determined by Enzyme-linked immunosorbent assay (ELISA). The effects of SFN on the activities of cytosolic phospholipase A2 (cPLA2) and Extracellular signal-regulated kinase (ERK)1/2 were monitored. Statistical relevance was determined by one-way analysis of variance (ANOVA). p<0.05 were considered to indicate significance Results: Post-treatment of cells or mice with SFN inhibited LPS- or CLP-induced expression and activity of sPLA2-IIA. SFN also suppressed the activation of cPLA2 and ERK1/2 by LPS. Conclusion: It is concluded that, SFN inhibited LPS-mediated expression of sPLA2-IIA by suppression of cPLA2 and ERK1/2.
KW - Cecal ligation and puncture
KW - HUVEC
KW - Inflammatory diseases
KW - Lipopolysaccharide
KW - Secretory group IIA phospholipase A2
KW - Sulforaphane
UR - http://www.scopus.com/inward/record.url?scp=85041341866&partnerID=8YFLogxK
U2 - 10.3923/ijp.2018.187.193
DO - 10.3923/ijp.2018.187.193
M3 - Article
AN - SCOPUS:85041341866
SN - 1811-7775
VL - 14
SP - 187
EP - 193
JO - International Journal of Pharmacology
JF - International Journal of Pharmacology
IS - 2
ER -