Stimulation of synaptosomal free radical production by fatty acids: Relation to esterification and to degree of unsaturation
Open Access
- 13 November 1995
- journal article
- research article
- Published by Wiley in FEBS Letters
- Vol. 375 (1-2) , 53-55
- https://doi.org/10.1016/0014-5793(95)01173-c
Abstract
The ability of three fatty acids and their respective ethyl esters, to promote generation of reactive oxygen species (ROS), was compared in a preparation of rat brain synaptosomes. Arachidonic but not palmitic or linoleic acids promoted ROS generation. Ethyl esterification of each fatty acid significantly enhanced ROS production and also levels of lipid peroxidation. Pro-oxidant activity was enhanced by fatty acids, proportionally to their degree of unsaturation. Since ethanol consumption is known to lead to esterification of membrane lipids, this transformation may in part account for the ROS-promoting potential of alcohol.Keywords
This publication has 16 references indexed in Scilit:
- The effect of fatty acid unsaturation on the antioxidant activity of β-carotene and α-tocopherol in hexane solutionsFree Radical Biology & Medicine, 1995
- Molecular Mechanism of Ethanol Metabolism by Human Brain to Fatty Acid Ethyl EstersAlcohol, Clinical and Experimental Research, 1993
- Ethanol toxicity and oxidative stressToxicology Letters, 1992
- Evaluation of the probe 2',7'-dichlorofluorescin as an indicator of reactive oxygen species formation and oxidative stressChemical Research in Toxicology, 1992
- Ethanol-induced fatty acid ethyl ester formation in vivo and in vitro in rat lungToxicology, 1991
- Introduction: Role of lipid peroxidation and oxidative stress in alcohol toxicityFree Radical Biology & Medicine, 1989
- Polyunsaturated Fatty Acids and EthanolAdvances in Alcohol & Substance Abuse, 1988
- Presence of Nonoxidative Ethanol Metabolism in Human Organs Commonly Damaged by Ethanol AbuseScience, 1986
- Myocardial metabolites of ethanol.Circulation Research, 1983
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976