Evaluation of anti-proliferative and anti-inflammatory activities of Pelagia noctiluca venom in Lipopolysaccharide/Interferon-γ stimulated RAW264.7 macrophages

Biomed Pharmacother. 2016 Dec:84:1986-1991. doi: 10.1016/j.biopha.2016.11.010. Epub 2016 Nov 18.

Abstract

Components of Pelagia noctiluca (P. noctiluca) venom were evaluated for their anticancer and nitric Oxide (NO) inhibition activities. Three fractions, out of four, obtained by gel filtration on Sephadex G75 of P. noctiluca venom revealed an important selective anti-proliferative activity on several cell lines such as human bladder carcinoma (RT112), human glioblastoma (U87), and human myelogenous leukemia (K562) but not on mitogen-stimulated peripheral blood mononuclear cells. Interestingly, P. noctiluca components showed an important dose-dependent anti-inflammatory activity, through inhibition of NO production via transcriptional regulation of Inducible NO Synthase (iNOS), in IFN-γ/LPS stimulated RAW 264.7 macrophages. These data strongly suggest that P. noctiluca venom could be used as a natural inhibitor of cancer cell lines and a potent anti-inflammatory agent for the treatment of anti-inflammatory diseases.

Keywords: Anti-inflammatory activity; Cell proliferation; MTT assay; Nitric oxide; Pelagia noctiluca; Venom.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / isolation & purification
  • Anti-Inflammatory Agents / pharmacology*
  • Cell Line
  • Cell Proliferation / drug effects*
  • Cell Proliferation / physiology
  • Cell Survival / drug effects
  • Cell Survival / physiology
  • Cnidarian Venoms / isolation & purification
  • Cnidarian Venoms / pharmacology*
  • Dose-Response Relationship, Drug
  • Drug Evaluation, Preclinical / methods
  • Humans
  • Interferon-gamma / toxicity*
  • K562 Cells
  • Leukocytes, Mononuclear / drug effects
  • Leukocytes, Mononuclear / metabolism
  • Lipopolysaccharides / toxicity*
  • Macrophages / drug effects*
  • Macrophages / metabolism
  • Mice
  • Nitric Oxide Synthase Type II / antagonists & inhibitors
  • Nitric Oxide Synthase Type II / metabolism

Substances

  • Anti-Inflammatory Agents
  • Cnidarian Venoms
  • Lipopolysaccharides
  • Interferon-gamma
  • Nitric Oxide Synthase Type II