Literature DB >> 4390101

Lipid peroxide formation in microsomes. General considerations.

E D Wills.   

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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Year:  1969        PMID: 4390101      PMCID: PMC1184638          DOI: 10.1042/bj1130315

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  21 in total

1.  Inhibition of the autoxidation of unsaturated fatty acids by haematin proteins.

Authors:  S E LEWIS; E D WILLS
Journal:  Biochim Biophys Acta       Date:  1963-06-18

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

Authors:  L K DAHLE; E G HILL; R T HOLMAN
Journal:  Arch Biochem Biophys       Date:  1962-08       Impact factor: 4.013

3.  Studies of the mechanism of vitamin E action. IV. Lipide peroxidation in the vitamin E-deficient rabbit.

Authors:  H ZALKIN; A L TAPPEL
Journal:  Arch Biochem Biophys       Date:  1960-05       Impact factor: 4.013

4.  Liver and brain mitochondria.

Authors:  W N ALDRIDGE
Journal:  Biochem J       Date:  1957-11       Impact factor: 3.857

5.  Lipid peroxide formation in regenerating rat liver.

Authors:  N WOLFSON; K M WILBUR; F BERNHEIM
Journal:  Exp Cell Res       Date:  1956-04       Impact factor: 3.905

6.  The reduction of dehydroascorbic acid in plant extracts.

Authors:  E M Crook; E J Morgan
Journal:  Biochem J       Date:  1944       Impact factor: 3.857

7.  The thiobarbituric acid reagent as a test for the oxidation of unsaturated fatty acids by various agents.

Authors:  K M WILBUR; F BERNHEIM; O W SHAPIRO
Journal:  Arch Biochem       Date:  1949-12

8.  Reduced triphosphopyridine nucleotide oxidase-catalyzed alterations of membrane phospholipids. I. Nature of the lipid alterations.

Authors:  H E May; P B McCay
Journal:  J Biol Chem       Date:  1968-05-10       Impact factor: 5.157

9.  Lipid peroxide formation in microsomes. Relationship of hydroxylation to lipid peroxide formation.

Authors:  E D Wills
Journal:  Biochem J       Date:  1969-06       Impact factor: 3.857

10.  The inhibitory effect of reduced glutathione on the lipid peroxidation of the microsomal fraction and mitochondria.

Authors:  B O Christophersen
Journal:  Biochem J       Date:  1968-01       Impact factor: 3.857

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  70 in total

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Authors:  R Marín; A J Rodríguez; T Proverbio
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5.  Lipid peroxide formation in microsomes. Relationship of hydroxylation to lipid peroxide formation.

Authors:  E D Wills
Journal:  Biochem J       Date:  1969-06       Impact factor: 3.857

6.  The stimulatory effects of carbon tetrachloride and other halogenoalkanes on peroxidative reactions in rat liver fractions in vitro. General features of the systems used.

Authors:  T F Slater; B C Sawyer
Journal:  Biochem J       Date:  1971-08       Impact factor: 3.857

7.  Lipid peroxide formation in microsomes. The role of non-haem iron.

Authors:  E D Wills
Journal:  Biochem J       Date:  1969-06       Impact factor: 3.857

8.  Effects of lipid peroxidation on membrane-bound enzymes of the endoplasmic reticulum.

Authors:  E D Wills
Journal:  Biochem J       Date:  1971-08       Impact factor: 3.857

9.  Acute hexachlorocyclohexane-induced oxidative stress in rat cerebral hemisphere.

Authors:  A Sahoo; G B Chainy
Journal:  Neurochem Res       Date:  1998-08       Impact factor: 3.996

10.  Stimulation of 5-lipoxygenase activity under conditions which promote lipid peroxidation.

Authors:  D Riendeau; D Denis; L Y Choo; D J Nathaniel
Journal:  Biochem J       Date:  1989-10-15       Impact factor: 3.857

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