HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Anti-angiogenic effect of tetraacetyl-phytosphingosine.

Abstract
In a search for the wound healing accelerators, we found that tetraacetyl-phytosphingosine (TAPS), a sphingolipid metabolite produced by phytosphingosine acetylation, has significant inhibitory potential on healing of rabbit ear wound. As angiogenesis is fundamental to proper wound healing, we examined the effect of TAPS on angiogenesis using human umbilical vein endothelial cells cultured in vitro. TAPS markedly decreased vascular endothelial growth factor (VEGF)-induced chemotactic migration and capillary-like tube formation. Recognizing its inhibitory potential on angiogenesis, we further investigated the action mechanism of TAPS. TAPS significantly inhibited VEGF-induced proteolytic enzyme production, including matrix metalloproteinase-2, urokinase-type plasminogen activator and plasminogen activator inhibitor-1. TAPS also suppressed VEGF-induced phosphorylation of p42/44 extracellular signal-regulated kinase and c-Jun N-terminal kinase. In addition, TAPS abolished VEGF-induced intracellular calcium increase, measured using laser scanning confocal microscopy. Together, these results suggest that TAPS exerts its inhibitory action on angiogenesis through the inhibition of mitogen-activated protein kinase activation and intracellular calcium increase, thereby affecting the process of wound healing negatively.
AuthorsYoo Bin Kwon, Chang Deok Kim, Bo Joong Kim, Min-Young Kim, Chang Seo Park, Tae-Jin Yoon, Young-Joon Seo, Ki-Beom Suhr, Jang-Kyu Park, Jeung-Hoon Lee
JournalExperimental dermatology (Exp Dermatol) Vol. 16 Issue 4 Pg. 311-7 (Apr 2007) ISSN: 0906-6705 [Print] Denmark
PMID17359337 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Plasminogen Activator Inhibitor 1
  • Vascular Endothelial Growth Factor A
  • tetraacetyl-phytosphingosine
  • Extracellular Signal-Regulated MAP Kinases
  • JNK Mitogen-Activated Protein Kinases
  • Urokinase-Type Plasminogen Activator
  • Matrix Metalloproteinase 2
  • phytosphingosine
  • Sphingosine
  • Calcium
Topics
  • Acetylation
  • Animals
  • Calcium (metabolism)
  • Cell Movement
  • Cells, Cultured
  • Endothelial Cells (cytology, drug effects, enzymology)
  • Extracellular Signal-Regulated MAP Kinases (metabolism)
  • Humans
  • JNK Mitogen-Activated Protein Kinases (metabolism)
  • Matrix Metalloproteinase 2 (metabolism)
  • Neovascularization, Physiologic (drug effects)
  • Phosphorylation (drug effects)
  • Plasminogen Activator Inhibitor 1 (metabolism)
  • Rabbits
  • Signal Transduction (drug effects)
  • Sphingosine (analogs & derivatives, chemistry, pharmacology)
  • Umbilical Veins (cytology)
  • Urokinase-Type Plasminogen Activator (metabolism)
  • Vascular Endothelial Growth Factor A (pharmacology)
  • Wound Healing (drug effects)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: