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Free Radical Chain Reactions and Polyunsaturated Fatty Acids in Brain Lipids
[Image: see text] Polyunsaturated fatty acyl chains (PUFAs) concentrate in the brain and give rise to numerous oxidative chemical degradation products. It is widely assumed that these products are the result of free radical chain reactions, and reactions of this type have been demonstrated in prepar...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330197/ https://www.ncbi.nlm.nih.gov/pubmed/35910174 http://dx.doi.org/10.1021/acsomega.2c02285 |
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author | Ng, Sharon C. W. Furman, Ran Axelsen, Paul H. Shchepinov, Mikhail S. |
author_facet | Ng, Sharon C. W. Furman, Ran Axelsen, Paul H. Shchepinov, Mikhail S. |
author_sort | Ng, Sharon C. W. |
collection | PubMed |
description | [Image: see text] Polyunsaturated fatty acyl chains (PUFAs) concentrate in the brain and give rise to numerous oxidative chemical degradation products. It is widely assumed that these products are the result of free radical chain reactions, and reactions of this type have been demonstrated in preparations where a single PUFA substrate species predominates. However, it is unclear whether such reactions can occur in the biologically complex milieu of lipid membranes where PUFA substrates are a minority species, and where diverse free radical scavengers or other quenching mechanisms are present. It is of particular interest to know whether they occur in brain, where PUFAs are concentrated and where PUFA oxidation products have been implicated in the pathogenesis of neurodegenerative disorders. To ascertain whether free radical chain reactions can occur in a complex brain lipid mixture, mouse brain lipids were extracted, formed into vesicles, and treated with a fixed number of hydroxyl radicals under conditions wherein the concentrations and types of PUFA-containing phospholipids were varied. Specific phospholipid species in the mixture were assayed by tandem mass spectrometry to quantify the oxidative losses of endogenous PUFA-containing phospholipids. Results reveal crosstalk between the oxidative degradation of ω3 and ω6 PUFAs that can only be explained by the occurrence of free radical chain reactions. These results demonstrate that PUFAs in a complex brain lipid mixture can participate in free radical chain reactions wherein the extent of oxidative degradation is not limited by the number of reactive oxygen species available to initiate such reactions. These reactions may help explain otherwise puzzling in vivo interactions between ω3 and ω6 PUFAs in mouse brain. |
format | Online Article Text |
id | pubmed-9330197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-93301972022-07-29 Free Radical Chain Reactions and Polyunsaturated Fatty Acids in Brain Lipids Ng, Sharon C. W. Furman, Ran Axelsen, Paul H. Shchepinov, Mikhail S. ACS Omega [Image: see text] Polyunsaturated fatty acyl chains (PUFAs) concentrate in the brain and give rise to numerous oxidative chemical degradation products. It is widely assumed that these products are the result of free radical chain reactions, and reactions of this type have been demonstrated in preparations where a single PUFA substrate species predominates. However, it is unclear whether such reactions can occur in the biologically complex milieu of lipid membranes where PUFA substrates are a minority species, and where diverse free radical scavengers or other quenching mechanisms are present. It is of particular interest to know whether they occur in brain, where PUFAs are concentrated and where PUFA oxidation products have been implicated in the pathogenesis of neurodegenerative disorders. To ascertain whether free radical chain reactions can occur in a complex brain lipid mixture, mouse brain lipids were extracted, formed into vesicles, and treated with a fixed number of hydroxyl radicals under conditions wherein the concentrations and types of PUFA-containing phospholipids were varied. Specific phospholipid species in the mixture were assayed by tandem mass spectrometry to quantify the oxidative losses of endogenous PUFA-containing phospholipids. Results reveal crosstalk between the oxidative degradation of ω3 and ω6 PUFAs that can only be explained by the occurrence of free radical chain reactions. These results demonstrate that PUFAs in a complex brain lipid mixture can participate in free radical chain reactions wherein the extent of oxidative degradation is not limited by the number of reactive oxygen species available to initiate such reactions. These reactions may help explain otherwise puzzling in vivo interactions between ω3 and ω6 PUFAs in mouse brain. American Chemical Society 2022-07-14 /pmc/articles/PMC9330197/ /pubmed/35910174 http://dx.doi.org/10.1021/acsomega.2c02285 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Ng, Sharon C. W. Furman, Ran Axelsen, Paul H. Shchepinov, Mikhail S. Free Radical Chain Reactions and Polyunsaturated Fatty Acids in Brain Lipids |
title | Free Radical Chain Reactions and Polyunsaturated Fatty
Acids in Brain Lipids |
title_full | Free Radical Chain Reactions and Polyunsaturated Fatty
Acids in Brain Lipids |
title_fullStr | Free Radical Chain Reactions and Polyunsaturated Fatty
Acids in Brain Lipids |
title_full_unstemmed | Free Radical Chain Reactions and Polyunsaturated Fatty
Acids in Brain Lipids |
title_short | Free Radical Chain Reactions and Polyunsaturated Fatty
Acids in Brain Lipids |
title_sort | free radical chain reactions and polyunsaturated fatty
acids in brain lipids |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330197/ https://www.ncbi.nlm.nih.gov/pubmed/35910174 http://dx.doi.org/10.1021/acsomega.2c02285 |
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