Therapeutic strategies for the inhibition of inducible nitric oxide synthase--potential for a novel class of anti-inflammatory agents

Cell Biol Int. 1996 Jan;20(1):51-8. doi: 10.1006/cbir.1996.0008.

Abstract

In recent years, NO, a gas previously considered a potentially toxic chemical, has become established as a diffusible universal messenger mediating cell-cell communication throughout the body. In mammals, NO is a recognized mediator of blood vessel relaxation that helps to maintain blood pressure. In the central nervous system NO acts as a non-conventional neurotransmitter and participates in the establishment of long-term plasticity required for memory formation. In addition, NO is responsible for some parts of the host response to sepsis and inflammation and contributes to certain disease states. A number of strategies have emerged with regard to a pharmacological control of pathological NO overproductions. This review will discuss these novel therapeutic approaches that may provide new means for clinical medicine.

Publication types

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

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / therapeutic use*
  • Arginine / metabolism
  • Biopterins / analogs & derivatives
  • Biopterins / metabolism
  • Enzyme Inhibitors / therapeutic use*
  • Gene Expression Regulation, Enzymologic
  • Glucocorticoids / pharmacology
  • Humans
  • Immunosuppressive Agents / pharmacology
  • Nitric Oxide / biosynthesis
  • Nitric Oxide / physiology
  • Nitric Oxide Synthase / antagonists & inhibitors*
  • Nitric Oxide Synthase / genetics
  • Transcription Factors / therapeutic use

Substances

  • Anti-Inflammatory Agents
  • Enzyme Inhibitors
  • Glucocorticoids
  • Immunosuppressive Agents
  • Transcription Factors
  • Biopterins
  • Nitric Oxide
  • Arginine
  • Nitric Oxide Synthase
  • sapropterin