Scavenging of superoxide anion by phosphorylethanolamine: studies in human neutrophils and in a cell free system. 1991

L I Gordon, and D Weiss, and S Prachand, and S A Weitzman
Northwestern University Medical School, Department of Medicine, Chicago, Ill. 60611.

On the basis of previous observations, we attempted to characterize the effects of various products of phospholipid hydrolysis on neutrophil (PMN) respiratory burst activity. We studied the effects of phosphorylcholine (PC) and phosphorylethanoline (PE) on superoxide anion production in PMN and in cell free system. We found that PE but not PC inhibited measured superoxide anion, but that this was not due to inhibition of cellular superoxide generation but to scavenging of generated superoxide anion. Further, utilizing a system based upon the photo-oxidation of O-dianisidine sensitized by riboflavin, we were able to determine that the scavenging effect of PE was not superoxide dismutase (SOD)-like but rather a general scavenging or glutathione (GSH)-like effect. These data underscore the importance of identifying the mechanism of inhibition of superoxide generation by putative inhibitors as being due to a direct cellular effect or to a scavenging property.

UI MeSH Term Description Entries
D009240 N-Formylmethionine Leucyl-Phenylalanine A formylated tripeptide originally isolated from bacterial filtrates that is positively chemotactic to polymorphonuclear leucocytes, and causes them to release lysosomal enzymes and become metabolically activated. F-Met-Leu-Phe,N-Formyl-Methionyl-Leucyl-Phenylalanine,Formylmet-Leu-Phe,Formylmethionyl Peptide,Formylmethionyl-Leucyl-Phenylalanine,Formylmethionylleucylphenylalanine,N-Formylated Peptide,N-formylmethionyl-leucyl-phenylalanine,fMet-Leu-Phe,F Met Leu Phe,Formylmet Leu Phe,Formylmethionyl Leucyl Phenylalanine,Leucyl-Phenylalanine, N-Formylmethionine,N Formyl Methionyl Leucyl Phenylalanine,N Formylated Peptide,N Formylmethionine Leucyl Phenylalanine,N formylmethionyl leucyl phenylalanine,Peptide, Formylmethionyl,Peptide, N-Formylated,fMet Leu Phe
D009504 Neutrophils Granular leukocytes having a nucleus with three to five lobes connected by slender threads of chromatin, and cytoplasm containing fine inconspicuous granules and stainable by neutral dyes. LE Cells,Leukocytes, Polymorphonuclear,Polymorphonuclear Leukocytes,Polymorphonuclear Neutrophils,Neutrophil Band Cells,Band Cell, Neutrophil,Cell, LE,LE Cell,Leukocyte, Polymorphonuclear,Neutrophil,Neutrophil Band Cell,Neutrophil, Polymorphonuclear,Polymorphonuclear Leukocyte,Polymorphonuclear Neutrophil
D010100 Oxygen An element with atomic symbol O, atomic number 8, and atomic weight [15.99903; 15.99977]. It is the most abundant element on earth and essential for respiration. Dioxygen,Oxygen-16,Oxygen 16
D010767 Phosphorylcholine Calcium and magnesium salts used therapeutically in hepatobiliary dysfunction. Choline Chloride Dihydrogen Phosphate,Choline Phosphate Chloride,Phosphorylcholine Chloride,Choline Phosphate,Phosphocholine,Chloride, Choline Phosphate,Chloride, Phosphorylcholine,Phosphate Chloride, Choline,Phosphate, Choline
D010777 Photochemistry A branch of physical chemistry which studies chemical reactions, isomerization and physical behavior that may occur under the influence of visible and/or ultraviolet light. Photochemistries
D002474 Cell-Free System A fractionated cell extract that maintains a biological function. A subcellular fraction isolated by ultracentrifugation or other separation techniques must first be isolated so that a process can be studied free from all of the complex side reactions that occur in a cell. The cell-free system is therefore widely used in cell biology. (From Alberts et al., Molecular Biology of the Cell, 2d ed, p166) Cellfree System,Cell Free System,Cell-Free Systems,Cellfree Systems,System, Cell-Free,System, Cellfree,Systems, Cell-Free,Systems, Cellfree
D003962 Dianisidine Highly toxic compound which can cause skin irritation and sensitization. It is used in manufacture of azo dyes. 3,3'-Dimethoxybenzidine,Dianisidine Dihydrochloride,Dianisidine Hydrochloride,Dianisidine Sulfate,O-Dianisidine,3,3' Dimethoxybenzidine,Dihydrochloride, Dianisidine,Hydrochloride, Dianisidine,O Dianisidine,Sulfate, Dianisidine
D004983 Ethanolamines AMINO ALCOHOLS containing the ETHANOLAMINE; (-NH2CH2CHOH) group and its derivatives. Aminoethanols
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D006868 Hydrolysis The process of cleaving a chemical compound by the addition of a molecule of water.

Related Publications

L I Gordon, and D Weiss, and S Prachand, and S A Weitzman
December 1986, Toxicology and applied pharmacology,
L I Gordon, and D Weiss, and S Prachand, and S A Weitzman
April 1988, Thrombosis and haemostasis,
L I Gordon, and D Weiss, and S Prachand, and S A Weitzman
January 1982, Clinical immunology and immunopathology,
L I Gordon, and D Weiss, and S Prachand, and S A Weitzman
June 1999, Molecular and cellular biochemistry,
L I Gordon, and D Weiss, and S Prachand, and S A Weitzman
April 1996, International journal of andrology,
L I Gordon, and D Weiss, and S Prachand, and S A Weitzman
September 1987, The Biochemical journal,
L I Gordon, and D Weiss, and S Prachand, and S A Weitzman
September 1994, Biochemical and biophysical research communications,
L I Gordon, and D Weiss, and S Prachand, and S A Weitzman
October 1983, The Journal of experimental medicine,
L I Gordon, and D Weiss, and S Prachand, and S A Weitzman
August 2013, The Korean journal of parasitology,
L I Gordon, and D Weiss, and S Prachand, and S A Weitzman
September 1999, The Journal of antimicrobial chemotherapy,
Copied contents to your clipboard!