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Open AccessJournal ArticleDOI

Lipid peroxide formation in microsomes. General considerations

Eric D. Wills
- 01 Jun 1969 - 
- Vol. 113, Iss: 2, pp 315-324
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TLDR
It is considered that lipid peroxide formation occurs as a result of the operation of the microsomal electron-transport chain switching from hydroxylation to oxidize unsaturated lipids of the endoplasmic reticulum.
Abstract: 
1. Liver microsomes form lipid peroxide when incubated with ascorbate or NADPH, but not with NADH. Increasing the concentration of ascorbate beyond the optimum (0.5mm) decreases the rate of lipid peroxide formation, but this effect does not occur with NADPH. Other reducing agents such as p-phenylenediamine or ferricyanide were not able to replace ascorbate and induce lipid peroxide formation. 2. The rate of ascorbate-induced peroxidation is optimum at pH6.0 whereas the rate of the NADPH system is optimum at pH7.0. Both systems require phosphate for maximum activity. 3. Lipid peroxide formation occurs at the maximum specific rate in very dilute microsome suspensions (0.15mg. of protein/ml.). 4. Treatment of microsomes with deoxycholate and other detergents causes membrane disintegration and inhibits lipid peroxide formation. 5. Lipid peroxide formation is accompanied by a rapid uptake of oxygen and there is a large excess of oxygen utilized for each molecule of malonaldehyde measured in the peroxide method. 6. Boiled microsomes form lipid peroxide in the presence of ascorbate, but not if NADPH is added. 7. Lipid peroxide formation induced by NADPH is strongly inhibited by p-chloromercuribenzoate, weakly inhibited by N-ethylmaleimide and unaffected by iodoacetamide. Ascorbate-induced peroxidation in untreated microsomes is unaffected by p-chloromercuribenzoate, but inhibited if boiled microsomes are used. These experiments may be interpreted on the basis that a ferredoxin-type protein forms part of the system in which NADPH induces lipid peroxide formation. 8. Most heavy-metal ions, with the exception of inorganic iron (Fe(2+) or Fe(3+)), which activates, inhibit both ascorbate-induced and NADPH-induced peroxidation. Mg(2+) increases the rate of peroxidation whereas Ca(2+) inhibits it. 9. Lipid peroxide formation is inhibited strongly by GSH and weakly by cysteine. Ascorbate-induced peroxidation is much more sensitive than NADPH-induced peroxidation. 10. Peroxidation is strongly inhibited by addition of low concentrations (0.01-0.1mm) of cytochrome c or of haemoglobin. 11. It is considered that lipid peroxide formation occurs as a result of the operation of the microsomal electron-transport chain switching from hydroxylation to oxidize unsaturated lipids of the endoplasmic reticulum.

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Book ChapterDOI

Microsomal lipid peroxidation.

John A. Buege, +1 more
- 01 Jan 1978 - 
TL;DR: This chapter discusses microsomal lipid peroxidation, a complex process known to occur in both plants and animals that involves the formation and propagation of lipid radicals, the uptake of oxygen, a rearrangement of the double bonds in unsaturated lipids, and the eventual destruction of membrane lipids.
Journal ArticleDOI

Catalytic metals, ascorbate and free radicals: combinations to avoid.

TL;DR: This presentation discusses the role of catalytic metals in free radical-mediated oxidations, ascorbate as both a pro-oxidant and an antioxidant, use of asCorbate to determine adventitious catalytic metal concentrations, and uses of ascorBate radical as a marker of oxidative stress.
Journal ArticleDOI

Carbon tetrachloride hepatotoxicity: an example of lethal cleavage

TL;DR: In this paper, an example of Lethal Cleavage is presented. But it is based on Carbon Tetrachloride Hepatotoxicity (CTH) and it does not consider the effect of carbon dioxide.
Journal ArticleDOI

Effects of calmodulin antagonists on radiation-induced lipid peroxidation in microsomes.

TL;DR: Rat liver microsomes were irradiated with gamma-rays at a dose rate of 1.31 Gys-1.31 and calmodulin antagonists considerably inhibited radiation-induced lipid peroxidation in the presence of ferric (Fe3+) ions, which decreased the cytochrome P-450 content of microsome.
Journal ArticleDOI

Evidence for the participation of cytochrome b5 in hepatic microsomal mixed-function oxidation reactions

TL;DR: It is concluded that the DPNH enhancement of the overall hydroxylation reaction is dependent on the presence of an apparent rate-limiting step in the TPNH-dependent reaction as demonstrated by modifying this step with cations.
References
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Journal Article

Protein Measurement with the Folin Phenol Reagent

TL;DR: Procedures are described for measuring protein in solution or after precipitation with acids or other agents, and for the determination of as little as 0.2 gamma of protein.
Journal ArticleDOI

Mechanisms of lipid peroxide formation in animal tissues.

Wills Ed
- 01 Jun 1966 - 
TL;DR: Catalysis of peroxidation of unsaturated fatty acids by the mitochondrial and microsomal fractions of liver is inhibited by ascorbic acid at pH7.4 but the activity of the supernatant fraction is enhanced.
Journal ArticleDOI

The thiobarbituric acid reaction and the autoxidations of polyunsaturated fatty acid methyl esters.

TL;DR: The mechanism of oxidation of methylene-interrupted trienes, tetraenes, pentaenes, and hexaenes postulates an additional step in chain propagation involving intramolecular rearrangement of the hydroperoxy free radical to a free radical bearing a closed five-membered ring peroxide.
Journal ArticleDOI

Adp-activated lipid peroxidation coupled to the tpnh oxidase system of microsomes.

TL;DR: The occurrence of a TPNH-induced peroxidation of lipids in rat-liver microsomes is reported and the reaction requires activation by ADP or other pyrophosphates, and appears to be coupled to the TPNh oxidase system of the microsome.
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