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Piperlonguminine downregulates endothelial protein C receptor shedding in vitro and in vivo.

Abstract
Endothelial cell protein C receptor (EPCR) plays an important role in coagulation and inflammation. EPCR can be shed from the cell surface, and this is mediated by tumor necrosis factor-α-converting enzyme (TACE). Piperlonguminine (PL), an important component of Piper longum fruits, is known to exhibit antihyperlipidemic, antiplatelet, and antimelanogenesis activities. However, little is known about the effects of PL on EPCR shedding. Here, we investigated this issue by monitoring the effects of PL on phorbol-12-myristate 13-acetate (PMA) and on cecal ligation and puncture (CLP)-mediated EPCR shedding and underlying mechanisms. PL induced potent inhibition of PMA, and CLP induced EPCR shedding through suppression of TACE expression. And treatment with PL resulted in reduced PMA-stimulated phosphorylation of p38, extracellular regulated kinases (ERK) 1/2, and c-Jun N-terminal kinase (JNK). Given these results, PL might have potential as an anti-sEPCR shedding reagent against PMA- and CLP-mediated EPCR shedding.
AuthorsSae-Kwang Ku, Jeong Ah Kim, Jong-Sup Bae
JournalInflammation (Inflammation) Vol. 37 Issue 2 Pg. 435-42 (Apr 2014) ISSN: 1573-2576 [Electronic] United States
PMID24127121 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Anti-Inflammatory Agents
  • Antigens, CD
  • Dioxolanes
  • Endothelial Protein C Receptor
  • Interleukin-6
  • PROCR protein, human
  • Plant Extracts
  • Procr protein, mouse
  • Receptors, Cell Surface
  • Tumor Necrosis Factor-alpha
  • Extracellular Signal-Regulated MAP Kinases
  • JNK Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • ADAM Proteins
  • ADAM17 Protein
  • ADAM17 protein, human
  • Adam17 protein, mouse
  • piperlongumine
  • Tetradecanoylphorbol Acetate
Topics
  • ADAM Proteins (metabolism)
  • ADAM17 Protein
  • Animals
  • Anti-Inflammatory Agents (pharmacology)
  • Antigens, CD (drug effects, metabolism)
  • Cells, Cultured
  • Dioxolanes (pharmacology)
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Endothelial Protein C Receptor
  • Enzyme Activation
  • Extracellular Signal-Regulated MAP Kinases (metabolism)
  • Fruit
  • Human Umbilical Vein Endothelial Cells (drug effects, metabolism)
  • Humans
  • Interleukin-6 (metabolism)
  • JNK Mitogen-Activated Protein Kinases (metabolism)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Phosphorylation
  • Phytotherapy
  • Piper
  • Plant Extracts (pharmacology)
  • Plants, Medicinal
  • Receptors, Cell Surface (drug effects, metabolism)
  • Sepsis (drug therapy, metabolism, microbiology)
  • Tetradecanoylphorbol Acetate (pharmacology)
  • Time Factors
  • Tumor Necrosis Factor-alpha (metabolism)
  • p38 Mitogen-Activated Protein Kinases (metabolism)

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