Iron-catalyzed lipid peroxidation in aortic cells in vitro: protective effect of extracellular magnesium
Low serum Mg 2+ has been associated with an increased incidence of cardiovascular pathology in human populations. We investigated the effect of extracellular Mg 2+ on Fe-catalyzed lipid peroxidation in rat aortic segments and in human aortic smooth muscle cells. Products of phospholipid oxidation [m...
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Published in | Atherosclerosis Vol. 175; no. 1; pp. 15 - 22 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier Ireland Ltd
01.07.2004
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Low serum Mg
2+ has been associated with an increased incidence of cardiovascular pathology in human populations. We investigated the effect of extracellular Mg
2+ on Fe-catalyzed lipid peroxidation in rat aortic segments and in human aortic smooth muscle cells. Products of phospholipid oxidation [malonaldehyde (MDA) and 4-hydroxyalkenals (4-HA)], loss of fatty acyl double bonds (by proton-NMR) and glutathione levels indicated that exogenous ferric ions were several-fold more effective than ferrous ions in causing lipid peroxidation. Increased peroxidation was detectable at <1.0
μM Fe
3+. Exogenous ferric iron-ionophore, 8-hydroxyquinoline, did not increase peroxidation by ferric ion, suggesting that Fe-catalyzed lipid peroxidation occurred at the cell surface. As ionized serum [Mg
2+]
o was lowered from the physiological (0.7–0.96
mM) into the pathophysiological range (0.3–0.5
mM) in Fe
3+-containing medium, MDA/4-HA levels increased two to three-fold, with a concomitant loss of fatty acyl double bonds and decreased extracellular glutathione. Conversely, MDA/4-HA decreased as ionized Mg
2+ was increased, accompanied by a rise in extracellular glutathione. The results indicate that Mg
2+ protects aortic cell plasma membranes from ferric iron-catalyzed lipid peroxidation and that this is a contributing factor in the protective action of ionized Mg
2+ on the cardiovascular system. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0021-9150 1879-1484 |
DOI: | 10.1016/j.atherosclerosis.2004.01.040 |