Inhibition of rat liver arginase by an intermediate in NO biosynthesis, NG-hydroxy-L-arginine: implications for the regulation of nitric oxide biosynthesis by arginase

Biochem Biophys Res Commun. 1994 Jul 15;202(1):174-80. doi: 10.1006/bbrc.1994.1909.

Abstract

NG-hydroxy-L-arginine, an intermediate in the biosynthesis of nitric oxide (NO), has been found to be a uniquely potent competitive inhibitor of rat liver arginase. Among previously reported inhibitors of arginase and the eight arginine analogs tested herein, only NG-hydroxy-L-arginine was found to be strongly inhibitory. Significantly, the Ki (42 microM) for inhibition of rat liver arginase by NG-hydroxy-L-arginine was found to be 20-40-fold lower than the KM (1-1.7 mM) for its natural substrate, L-arginine. Since NG-hydroxy-L-arginine is the only known intermediate in the biosynthesis of NO from L-arginine, this finding may have significant implications for the regulation of NO levels in tissues or cells, such as liver or macrophages, which synthesize both NO and contain arginase.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Arginase / antagonists & inhibitors
  • Arginase / isolation & purification
  • Arginase / metabolism*
  • Arginine / analogs & derivatives*
  • Arginine / metabolism
  • Arginine / pharmacology*
  • Homeostasis
  • Liver / enzymology*
  • Molecular Structure
  • Nitric Oxide / biosynthesis*
  • Rats
  • Structure-Activity Relationship

Substances

  • Nitric Oxide
  • N(omega)-hydroxyarginine
  • Arginine
  • Arginase