Inhibitive effect of purple sweet potato leaf extract and its components on cell adhesion and inflammatory response in human aortic endothelial cells

Cell Adh Migr. 2013 Mar-Apr;7(2):237-45. doi: 10.4161/cam.23649.

Abstract

This study investigated the effects of purple sweet potato leaf extract (PSPLE) and its components, cyanidin and quercetin, on human aortic endothelial cells (HAECs) during the inflammatory process. HAECs were pretreated with 100 μg/mL PSPLE or 10 μM quercetin, cyanidin or aspirin for 18 h followed by TNF-α (2 ng/mL) for 6 h, and U937 cell adhesion was determined. Adhesion molecule expression and CD40 were evaluated; NFκB p65 protein localization and DNA binding were assessed. PSPLE, aspirin, cyanidin and quercetin significantly inhibited TNF-α-induced monocyte-endothelial cell adhesion (p < 0.05). Cyanidin, quercetin and PSPLE also significantly attenuated VCAM-1, IL-8 and CD40 expression, and quercetin significantly attenuated ICAM-1 and E-selectin expression (p < 0.05). Significant reductions in NFκB expression and DNA binding by aspirin, cyanidin and quercetin were also observed in addition to decreased expression of ERK1, ERK2 and p38 MAPK (p < 0.05). Thus, PSPLE and its components, cyanidin and quercetin, have anti-inflammatory effects through modulation of NFκB and MAPK signaling. Further in vivo studies are necessary to explore the possible therapeutic effects of PSPLE on atherosclerosis.

Keywords: NFκB; adhesion molecules; human aortic endothelial cells; phytochemicals; pro-inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anthocyanins / pharmacology
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Antioxidants / pharmacology
  • Aorta / drug effects
  • Aspirin / pharmacology
  • CD40 Antigens / biosynthesis
  • Cell Adhesion / drug effects*
  • Cell Adhesion Molecules / biosynthesis
  • Cell Line
  • E-Selectin / biosynthesis
  • Endothelial Cells / drug effects*
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / metabolism
  • Humans
  • Inflammation / drug therapy*
  • Intercellular Adhesion Molecule-1 / biosynthesis
  • Interleukin-8 / biosynthesis
  • Ipomoea batatas / chemistry*
  • Mitogen-Activated Protein Kinase 1 / biosynthesis
  • Mitogen-Activated Protein Kinase 3 / biosynthesis
  • NF-kappa B / biosynthesis
  • Plant Extracts / pharmacology*
  • Plant Leaves / chemistry
  • Quercetin / pharmacology
  • Transcription Factor RelA / drug effects
  • Transcription Factor RelA / metabolism
  • Tumor Necrosis Factor-alpha / pharmacology
  • U937 Cells
  • Vascular Cell Adhesion Molecule-1 / biosynthesis
  • p38 Mitogen-Activated Protein Kinases / biosynthesis

Substances

  • Anthocyanins
  • Anti-Inflammatory Agents, Non-Steroidal
  • Antioxidants
  • CD40 Antigens
  • Cell Adhesion Molecules
  • E-Selectin
  • Interleukin-8
  • NF-kappa B
  • Plant Extracts
  • Transcription Factor RelA
  • Tumor Necrosis Factor-alpha
  • Vascular Cell Adhesion Molecule-1
  • Intercellular Adhesion Molecule-1
  • cyanidin
  • Quercetin
  • MAPK1 protein, human
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • p38 Mitogen-Activated Protein Kinases
  • Aspirin