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PMID: 3495737 Published · ppublish English Journal Article

Nitric oxide release accounts for the biological activity of endothelium-derived relaxing factor.

Nature ·Vol. 327 ·No. 6122 ·1987-00-00 ·Pages 524-6

Palmer RM, Ferrige AG, Moncada S

Abstract

Endothelium-derived relaxing factor (EDRF) is a labile humoral agent which mediates the action of some vasodilators. Nitrovasodilators, which may act by releasing nitric oxide (NO), mimic the effect of EDRF and it has recently been suggested by Furchgott that EDRF may be NO. We have examined this suggestion by studying the release of EDRF and NO from endothelial cells in culture. No was determined as the chemiluminescent product of its reaction with ozone. The biological activity of EDRF and of NO was measured by bioassay. The relaxation of the bioassay tissues induced by EDRF was indistinguishable from that induced by NO. Both substances were equally unstable. Bradykinin caused concentration-dependent release of NO from the cells in amounts sufficient to account for the biological activity of EDRF. The relaxations induced by EDRF and NO were inhibited by haemoglobin and enhanced by superoxide dismutase to a similar degree. Thus NO released from endothelial cells is indistinguishable from EDRF in terms of biological activity, stability, and susceptibility to an inhibitor and to a potentiator. We suggest that EDRF and NO are identical.

MeSH Terms
Animals Aorta/drug effects,physiology Bradykinin/pharmacology Endothelium/drug effects,physiology Hemoglobins/pharmacology Humans In Vitro Techniques Kinetics Muscle Relaxation/drug effects Muscle, Smooth, Vascular/drug effects,physiology Nitric Oxide/pharmacology Rabbits Swine Vasodilator Agents/metabolism,pharmacology
Chemicals
Hemoglobins Vasodilator Agents Nitric Oxide Bradykinin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Palmer R M
Ferrige A G
Moncada S
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1987-00-00
Pages
524-6
Language
English
Region
England
NLM ID
0410462
Subset
IM
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