These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: Glutathione-dependent inhibition of lipid peroxidation by a soluble, heat-labile factor not glutathione peroxidase.
    Author: McCay PB, Gibson DD, Hornbrook KR.
    Journal: Fed Proc; 1981 Feb; 40(2):199-205. PubMed ID: 7461144.
    Abstract:
    Both enzymic and nonenzymic lipid peroxidation in membranes are inhibited by a)certain chelating compounds, b)some metal ion (Mn2+, Co2+, and Ce3+), and c)lipid soluble antioxidants. The commonalities suggest that the processes of oxidative lipid degradation in the two types of systems may be similar, differing only in the mechanism of initiation. This is further borne out by studies with a glutathione-dependent, heat-labile cytosolic factor that inhibits malondialdehyde formation (a product of lipid peroxidation) in both systems. Studies in the authors' laboratory, however, have demonstrated that the cytosolic factor protects membranous organelles from oxidative damage to the lipids by preventing peroxidation from occurring at all. Analyses of the fatty acid composition of the membranes demonstrate that the polyunsaturated fatty acid content remains stable when the membranes are subjected to peroxidizing conditions in the presence of the cytosolic factor and GSH. Both the cytosolic factor and GSH are required for the protective action since neither can provide this marked stabilizing effects by itself. High concentrations of GSH reduce lipid peroxidation to some extent, but low concentrations are not effective without the addition of the cytosolic factor. The mechanism of this inhibition of peroxidative attack is unknown. Partial purification of rat liver cytosolic glutathione peroxidase demonstrated that the heat-labile cytosolic factor was not glutathione peroxidase. The cytosolic factor may be a glutathione transferase, but that is not known with certainty. Possibly more than one cytosolic protein possesses this GSH-dependent property for inhibiting lipid peroxidation under conditions of oxidative stress. The conditions for the functioning of this protective system in intact cells appear to be optimum and it may constitute a ubiquitous membrane-stabilizing system in that it is also present in other tissues (heart and lung, for example).
    [Abstract] [Full Text] [Related] [New Search]