Rehncrona, Stig;
Smith, David S.;
Åkesson, Björn;
Westerberg, Eva;
Siesjö, Bo K.
Peroxidative Changes in Brain Cortical Fatty Acids and Phospholipids, as Characterized During Fe2+‐ and Ascorbic Acid‐Stimulated Lipid Peroxidation In Vitro
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Media type:
E-Article
Title:
Peroxidative Changes in Brain Cortical Fatty Acids and Phospholipids, as Characterized During Fe2+‐ and Ascorbic Acid‐Stimulated Lipid Peroxidation In Vitro
Contributor:
Rehncrona, Stig;
Smith, David S.;
Åkesson, Björn;
Westerberg, Eva;
Siesjö, Bo K.
Published:
Wiley, 1980
Published in:
Journal of Neurochemistry, 34 (1980) 6, Seite 1630-1638
Language:
English
DOI:
10.1111/j.1471-4159.1980.tb11254.x
ISSN:
0022-3042;
1471-4159
Origination:
Footnote:
Description:
Abstract: The occurrence of peroxidative damage, as distinguished from anaerobic damage, to brain fatty acids and phospholipids was characterized in vitro. Fe2+ and ascorbic acid were used to stimulate peroxidation in cortical homogenates from rat brain incubated with or without oxygen. Lipid peroxidation was established in samples incubated with oxygen by increased diene conjugation, accumulation of thiobarbituric acid‐reactive material (TBAR) and of lipid‐soluble fluorescent products. No peroxidation occurred in samples incubated in the absence of oxygen (100% N2). Lipid peroxidation was characterized by a selective loss of arachidonic acid and docosahexaenoic acid and by degradation of ethanolamine phosphoglyceride, while choline phosphoglyceride did not change. During the course of peroxidation there were parallel increases in products of lipid peroxidation concomitant with the decrease in polyenoic fatty acids. The maximal changes in diene conjugation and TBAR occurred earlier than the maximal changes in fluorescent material and fatty acids. It is concluded that measurements of changes in brain fatty acid and phospholipid composition may be a useful tool to establishment of whether peroxidative damage is important in vivo in situations with a critically reduced oxygen supply. Estimation of lipid‐soluble fluorescence in vivo may also be useful, since it is considered to reflect the accumulation of stable end products of peroxidation.