Suppression of proinflammatory cytokines in monocytes by a tetravalent guanylhydrazone

J Exp Med. 1996 Mar 1;183(3):927-36. doi: 10.1084/jem.183.3.927.

Abstract

An overproduction of proinflammatory cytokines by activated macrophages/monocytes mediates the injurious sequelae of inflammation, septic shock, tissue injury, and cachexia. We recently synthesized a tetravalent guanylhydrazone compound (CNI-1493) that inhibits cytokine-inducible arginine transport and nitric oxide (NO) production in macrophages, and protects mice against lethal endotoxemia and carrageenan-induced inflammation. During these investigations we noticed that CNI-1493 effectively prevented lipopolysaccharide (LPS)-induced NO production, even when added in concentrations 10-fold less than required to competitively inhibit L-arginine uptake, suggesting that the suppressive effects of this guanylhydrazone compound might extend to other LPS-induced responses. Here, we report that CNI-1493 suppressed the LPS-stimulated production of proinflammatory cytokines (tumor necrosis factor [TNF], interleukins 1beta and 6, macrophage inflammatory proteins 1alpha and 1beta) from human peripheral blood mononuclear cells. Cytokine suppression was specific, in that CNI-1493 did not inhibit either the constitutive synthesis of transforming growth factor beta or the upregulation of major histocompatibility complex class II by interferon gamma (IFN-gamma). In contrast to the macrophage suppressive actions of dexamethasone, which are overridden in the presence of IFN-gamma, CNI-1493 retained its suppressive effects even in the presence of IFN-gamma. The mechanism of cytokine-suppressive action by CNI-1493 was independent of extracellular L-arginine content and NO production and is not restricted to induction by LPS. As a selective inhibitor of macrophage activation that prevents TNF production, this tetravalent guanylhydrazone could be useful in the development of cytokine-suppressive agents for the treatment of diseases mediated by overproduction of cytokines.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cell Line
  • Chemokine CCL4
  • Cytokines / antagonists & inhibitors
  • Cytokines / biosynthesis*
  • Dose-Response Relationship, Drug
  • Enzyme Induction
  • Humans
  • Hydrazones / pharmacology*
  • Inflammation*
  • Interferon-gamma / biosynthesis
  • Interleukin-1 / biosynthesis
  • Interleukin-6 / biosynthesis
  • Kinetics
  • Lipopolysaccharides / antagonists & inhibitors
  • Lipopolysaccharides / pharmacology
  • Macrophage Inflammatory Proteins
  • Macrophages / drug effects
  • Macrophages / immunology*
  • Mice
  • Monocytes / drug effects
  • Monocytes / immunology*
  • Monokines / biosynthesis
  • Nitric Oxide / biosynthesis
  • Nitric Oxide Synthase / antagonists & inhibitors
  • Nitric Oxide Synthase / biosynthesis*
  • Tumor Necrosis Factor-alpha / biosynthesis

Substances

  • Chemokine CCL4
  • Cytokines
  • Hydrazones
  • Interleukin-1
  • Interleukin-6
  • Lipopolysaccharides
  • Macrophage Inflammatory Proteins
  • Monokines
  • Tumor Necrosis Factor-alpha
  • Nitric Oxide
  • Interferon-gamma
  • semapimod
  • Nitric Oxide Synthase