Activation of nitric oxide synthase from cultured aortic endothelial cells by phospholipids

Biochem Biophys Res Commun. 1993 Sep 30;195(3):1314-20. doi: 10.1006/bbrc.1993.2187.

Abstract

Nitric oxide is a recently discovered biomolecule with a broad range of actions and synthesized by nitric oxide synthases. We investigated effects of lipids on particulate nitric oxide synthase purified from cultured bovine aortic endothelial cells by monitoring the conversion of L-[3H]arginine to L-[3H]citrulline. Phosphatidylcholine, lysophosphatidylcholine, and phosphatidylethanolamine dose-dependently enhanced the enzyme activity up to 3 fold in the presence of Ca2+, calmodulin, NADPH, FAD, and (6R)-5,6,7,8-tetrahydrobiopterin. These phospholipids increased the Vmax of nitric oxide synthase without altering the Km for L-arginine and the affinities for Ca2+ and calmodulin. These findings suggest that phospholipids play an important role in modulating endothelial nitric oxide synthase activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Oxidoreductases / drug effects*
  • Animals
  • Aorta / cytology
  • Arachidonic Acid / pharmacology
  • Arginine / pharmacology
  • Cattle
  • Dose-Response Relationship, Drug
  • Endothelium, Vascular / enzymology*
  • Enzyme Activation
  • Lysophosphatidylcholines / pharmacology
  • Lysophospholipids / pharmacology
  • Nitric Oxide Synthase
  • Phosphatidylcholines / pharmacology
  • Phosphatidylserines / pharmacology
  • Phospholipids / pharmacology*

Substances

  • Lysophosphatidylcholines
  • Lysophospholipids
  • Phosphatidylcholines
  • Phosphatidylserines
  • Phospholipids
  • lysophosphatidylethanolamine
  • Arachidonic Acid
  • Arginine
  • Nitric Oxide Synthase
  • Amino Acid Oxidoreductases