Nitric oxide (NO) and cartilage metabolism: NO effects are modulated by superoxide in response to IL-1

Biorheology. 2002;39(1-2):201-14.

Abstract

Nitric oxide (NO) is thought to mediate most effects of interleukin-1 (IL-1) on cartilage. In vitro evidence includes the decreased synthesis of extracellular matrix components, the abnormal cell renewal, the decreased production of IL-1 receptor antagonist, the induction of apoptosis and the enhanced sensitivity of chondrocytes to oxidative stress. Studies in NOS2(-/-) mice or administration of NO synthase inhibitors in animal models of joint disorders have confirmed its potent pathophysiological role in cartilage. Using L-NMMA (1 mM), as a NO synthase inhibitor, and CuDips (10 microM), as a SOD mimetic, we provide evidence that the inhibitory potency of IL-1beta on proteoglycan synthesis and its stimulating effect on COX-2 activity depend both on NO and O2-* production. Peroxynitrite formation is further demonstrated by the occurrence of 3-nitrotyrosines in chondrocytes stimulated in vitro with 2.5 ng/ml IL-1 and in femoral condyles of rats injected locally with 1 microg IL-1. Preliminary data suggest that such contribution of reactive oxygen species is not shared in common by IL-17, another NO-producing cytokine. We conclude that superoxide is a key modulator of NO-mediated effects in chondrocyte stimulated with IL-1 and that a combined therapy with NO synthase inhibitors and antioxidants may be promising for a full cartilage protection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cartilage Diseases / immunology
  • Cartilage Diseases / metabolism
  • Cartilage, Articular / metabolism*
  • Cells, Cultured
  • Chondrocytes / drug effects
  • Chondrocytes / metabolism*
  • Depression, Chemical
  • Enzyme Inhibitors / pharmacology
  • Free Radical Scavengers / pharmacology
  • Humans
  • Interleukin-1 / pharmacology*
  • Interleukin-17 / pharmacology
  • Male
  • Models, Animal
  • Nitric Oxide / metabolism*
  • Nitric Oxide Synthase / antagonists & inhibitors
  • Proteoglycans / biosynthesis*
  • Rats
  • Rats, Wistar
  • Salicylates / pharmacology
  • omega-N-Methylarginine / pharmacology

Substances

  • Enzyme Inhibitors
  • Free Radical Scavengers
  • Interleukin-1
  • Interleukin-17
  • Proteoglycans
  • Salicylates
  • copper bis(3,5-diisopropylsalicylate)
  • omega-N-Methylarginine
  • Nitric Oxide
  • Nitric Oxide Synthase