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Ameliorative Effect of Vicenin-2 and Scolymoside on TGFBIp-Induced Septic Responses.

Abstract
Transforming growth factor β-induced protein (TGFBIp) is an extracellular matrix protein whose expression in several cell types is greatly increased by TGF-β. TGFBIp is released by the human umbilical vein endothelial cells (HUVECs) and functions as a mediator of experimental sepsis. Cyclopia subternata is a medicinal plant commonly used in traditional medicine to relieve pain in biological processes. In this study, we investigated the antiseptic effects and underlying mechanisms of vicenin-2 and scolymoside, two active compounds in C. subternata against TGFBIp-mediated septic responses in HUVECs and mice. The anti-inflammatory activities of vicenin-2 or scolymoside were determined by measuring permeability, human neutrophils adhesion and migration, and activation of pro-inflammatory proteins in TGFBIp-activated HUVECs and mice. According to the results, vicenin-2 or scolymoside effectively inhibited lipopolysaccharide-induced release of TGFBIp and suppressed TGFBIp-mediated septic responses, such as hyperpermeability, adhesion and migration of leukocytes, and expression of cell adhesion molecules. In addition, vicenin-2 or scolymoside suppressed the production of tumor necrosis factor-α and interleukin 6 and activation of nuclear factor-κB and extracellular regulated kinases 1/2 by TGFBIp. Vicenin-2 or scolymoside reduced cecal ligation and puncture (CLP)-induced septic mortality and pulmonary injury. Collectively, these results indicate that vicenin-2 and scolymoside could be a potential therapeutic agent for treatment of various severe vascular inflammatory diseases via inhibition of the TGFBIp signaling pathway.
AuthorsWonhwa Lee, Sae-Kwang Ku, Jong-Sup Bae
JournalInflammation (Inflammation) Vol. 38 Issue 6 Pg. 2166-77 (Dec 2015) ISSN: 1573-2576 [Electronic] United States
PMID26084452 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Anti-Inflammatory Agents
  • Cell Adhesion Molecules
  • Extracellular Matrix Proteins
  • Glucosides
  • Inflammation Mediators
  • Plant Extracts
  • Transforming Growth Factor beta
  • apigenin-6,8-di-C-glycopyranoside
  • scolymoside
  • betaIG-H3 protein
  • Apigenin
  • Extracellular Signal-Regulated MAP Kinases
  • Luteolin
Topics
  • Animals
  • Anti-Inflammatory Agents (isolation & purification, pharmacology)
  • Apigenin (isolation & purification, pharmacology)
  • Capillary Permeability (drug effects)
  • Cell Adhesion (drug effects)
  • Cell Adhesion Molecules (metabolism)
  • Cells, Cultured
  • Chemotaxis, Leukocyte (drug effects)
  • Cyclopia Plant (chemistry)
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Enzyme Activation
  • Extracellular Matrix Proteins (immunology, metabolism)
  • Extracellular Signal-Regulated MAP Kinases (metabolism)
  • Glucosides (isolation & purification, pharmacology)
  • Human Umbilical Vein Endothelial Cells (drug effects, immunology, metabolism)
  • Inflammation Mediators (metabolism)
  • Luteolin (isolation & purification, pharmacology)
  • Male
  • Mice, Inbred C57BL
  • Neutrophils (drug effects, immunology, metabolism)
  • Phytotherapy
  • Plant Extracts (isolation & purification, pharmacology)
  • Plants, Medicinal
  • Pulmonary Edema (immunology, prevention & control)
  • Sepsis (immunology, metabolism, microbiology, prevention & control)
  • Time Factors
  • Transforming Growth Factor beta (immunology, metabolism)

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