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PMID: 1382421 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

The non specificity of specific nitric oxide synthase inhibitors.

Biochemical and biophysical research communications ·Vol. 187 ·No. 2 ·1992-09-16 ·Pages 797-801

Peterson DA, Peterson DC, Archer S, Weir EK

Abstract

L-NAME (Nw-Nitro-L-arginine methylester) and L-NMMA (NG- Monomethyl-L-arginine, monoacetate) are used widely as nitric oxide (NO) synthase inhibitors. Because of their functional groups (alcohols, amines and carboxylates), it appeared that they could interact with iron in a variety of systems. Using three in vitro models we observed these two compounds had inhibitory effects on cytochrome C reduction by ferrous iron, by ferrous iron accelerated by an unsaturated fatty acid or by epinephrine. This suggests that L-NAME and L-NMMA could have effects in iron containing systems found intracellularly apart from their inhibition of (NO) synthesis.

MeSH Terms
Amino Acid Oxidoreductases/antagonists & inhibitors Arginine/analogs & derivatives,pharmacology Cytochrome c Group/metabolism Epinephrine/pharmacology Fatty Acids, Unsaturated/pharmacology Ferrous Compounds/metabolism NG-Nitroarginine Methyl Ester Nitric Oxide Synthase Oxidation-Reduction omega-N-Methylarginine
Chemicals
Cytochrome c Group Fatty Acids, Unsaturated Ferrous Compounds omega-N-Methylarginine Arginine Nitric Oxide Synthase Amino Acid Oxidoreductases NG-Nitroarginine Methyl Ester Epinephrine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Peterson D A
Department of Medicine, VA Medical Center, Minneapolis, MN.
Peterson D C
Archer S
Weir E K
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1992-09-16
Pages
797-801
Language
English
Region
United States
NLM ID
0372516
Subset
IM
Grants
NHLBI NIH HHS · 1R29-HL45735-1 · United States
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