Capsaicin-Induced Death of Human Haematological Malignant Cell Lines Is Independent of TRPV1 Activation

Pharmacology. 2016;98(1-2):79-86. doi: 10.1159/000445437. Epub 2016 May 4.

Abstract

The effect of the plant-derived vanilloid, capsaicin (CAP), on the metabolic activity of THP-1, U266B1 and U937 hematological malignancy cells was determined. CAP reduced metabolic activity in a concentration-dependent manner in the three cell lines. A biphasic effect was observed on THP-1 cells (EC50: IC50 (95% CI) 32.9 (19.9-54.3)/219 (144-246) µmol/l). U266B1 cells were more resistant to CAP than THP-1 and U937. Metabolic activity was significantly inhibited by CAP in U937 compared to U266B1 cells (IC50: 197 versus 431 µmol/l, respectively, p < 0.008). Transient receptor potential vanilloid-1 (TRPV1) and CB1 antagonists (SB452533 and AM251, respectively) suppressed the CAP-induced increase in THP-1 cell metabolic activity (p < 0.001). AM251 and SB452533 appeared to act as partial agonists and displayed a synergistic effect with CAP in U937 cells. CAP inhibits the metabolic activity of malignant hematological cells through non-TRPV1-dependent mechanisms.

MeSH terms

  • Cannabinoid Receptor Antagonists / pharmacology
  • Capsaicin / pharmacology*
  • Cell Death / drug effects
  • Cell Line, Tumor
  • Hematologic Neoplasms / metabolism*
  • Humans
  • Indoles / pharmacology
  • Oxazines / metabolism
  • Piperidines / pharmacology
  • Pyrazoles / pharmacology
  • TRPV Cation Channels / antagonists & inhibitors
  • Xanthenes / metabolism

Substances

  • Cannabinoid Receptor Antagonists
  • Indoles
  • Oxazines
  • Piperidines
  • Pyrazoles
  • TRPV Cation Channels
  • TRPV1 protein, human
  • Xanthenes
  • resazurin
  • AM 251
  • Capsaicin
  • iodopravadoline