Pacific ciguatoxin 1B-induced modulation of inflammatory mediators in a murine macrophage cell line

Toxicon. 2010 Oct;56(5):776-84. doi: 10.1016/j.toxicon.2009.05.039. Epub 2009 Jun 9.

Abstract

Ciguatoxins, potent marine neurotoxins responsible for ciguatera, exert their numerous damaging effects through primary binding to the voltage-sensitive sodium channels of excitable cells. Using RAW 264.7 murine macrophages, we report the first experimental study presenting evidence that P-CTX-1B (the most potent congener from the Pacific) could modulate mRNA expression of pro- and anti-inflammatory cytokines as well as of inducible nitric oxide synthase (iNOS). P-CTX-1B, unlike other less potent marine polyether toxins, P-CTX-3C and PbTx-3, induced the overexpression of interleukin (IL)-1beta, IL-6, IL-10, tumor necrosis factor-alpha and iNOS with different magnitude and kinetic profiles, as compared to bacterial lipopolysaccharide (LPS). Unlike LPS, P-CTX-1B did not modulate IL-11 expression. In this report, we provide new evidence of the P-CTX-1B iNOS- and cytokines-inducing ability and shed new light on host response to potent neurotoxins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Ciguatoxins / toxicity*
  • Enzyme Induction
  • Inflammation Mediators / metabolism*
  • Lipopolysaccharides / pharmacology
  • Macrophages / drug effects*
  • Macrophages / metabolism
  • Mice
  • Nitric Oxide Synthase Type II / biosynthesis
  • Polymerase Chain Reaction
  • RNA, Messenger / genetics

Substances

  • Inflammation Mediators
  • Lipopolysaccharides
  • RNA, Messenger
  • ciguatoxin 1B (CTX 1B)
  • Ciguatoxins
  • Nitric Oxide Synthase Type II