Abstract | AIM AND OBJECTIVE: METHODS: The anti-inflammatory activities of vicenin-2 and scolymoside were determined by measuring permeability,monocytes adhesion and migration, and activation of pro-inflammatory proteins in LPS-activated HUVECs and mice. RESULTS: We found that post-treatment of each compound inhibited LPS-induced barrier disruption, expression of cell adhesion molecules (CAMs), and adhesion/transendothelial migration of human neutrophils to human endothelial cells. Each compound induced potent inhibition of phorbol-12-myristate 13-acetate (PMA) and LPS-induced endothelial cell protein C receptor ( EPCR)shedding. It also suppressed LPS-induced hyperpermeability and leukocytes migration in vivo. Furthermore,each compound suppressed the production of tumor necrosis factor-α (TNF-α) or Interleukin (IL)-6 and the activation of nuclear factor-κB (NF-κB) or extracellular regulated kinases (ERK) 1/2 by LPS. Moreover, posttreatment with each compound resulted in reduced LPS-induced lethal endotoxemia. CONCLUSION:
Vicenin-2 and scolymoside possess anti-inflammatory functions by inhibiting hyperpermeability,expression of CAMs, and adhesion and migration of leukocytes, thereby endorsing its usefulness as a therapy for vascular inflammatory diseases.
|
Authors | Hyejin Kang, Sae-Kwang Ku, Byeongjin Jung, Jong-Sup Bae |
Journal | Inflammation research : official journal of the European Histamine Research Society ... [et al.]
(Inflamm Res)
Vol. 64
Issue 12
Pg. 1005-21
(Dec 2015)
ISSN: 1420-908X [Electronic] Switzerland |
PMID | 26482935
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Anti-Inflammatory Agents
- Glucosides
- Interleukin-6
- Lipopolysaccharides
- apigenin-6,8-di-C-glycopyranoside
- interleukin-6, mouse
- scolymoside
- Apigenin
- ADAM Proteins
- ADAM17 Protein
- Luteolin
- Tetradecanoylphorbol Acetate
|
Topics |
- ADAM Proteins
(biosynthesis, genetics)
- ADAM17 Protein
- Animals
- Anti-Inflammatory Agents
(pharmacology)
- Apigenin
(pharmacology)
- Cell Adhesion
(drug effects)
- Cell Membrane Permeability
(drug effects)
- Cell Movement
(drug effects)
- Glucosides
(pharmacology)
- Human Umbilical Vein Endothelial Cells
(drug effects)
- Humans
- Interleukin-6
(biosynthesis)
- Lipopolysaccharides
(antagonists & inhibitors, pharmacology)
- Luteolin
(pharmacology)
- Macrophage Activation
(drug effects)
- Male
- Mice
- Mice, Inbred C57BL
- Monocytes
(drug effects)
- Tetradecanoylphorbol Acetate
(antagonists & inhibitors)
|