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NMR protocol for determination of oxidation susceptibility of serum lipids and application of the protocol to a chocolate study
A protocol for determination of oxidation susceptibility of serum lipids based on proton nuclear magnetic resonance ((1)H NMR) spectroscopy is presented and compared to the commonly used spectrophotometric method. Even though there are methodological differences between these two methods, the NMR-ba...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3351613/ https://www.ncbi.nlm.nih.gov/pubmed/22661918 http://dx.doi.org/10.1007/s11306-011-0323-2 |
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author | Tynkkynen, Tuulia Mursu, Jaakko Nurmi, Tarja Tuppurainen, Kari Laatikainen, Reino Soininen, Pasi |
author_facet | Tynkkynen, Tuulia Mursu, Jaakko Nurmi, Tarja Tuppurainen, Kari Laatikainen, Reino Soininen, Pasi |
author_sort | Tynkkynen, Tuulia |
collection | PubMed |
description | A protocol for determination of oxidation susceptibility of serum lipids based on proton nuclear magnetic resonance ((1)H NMR) spectroscopy is presented and compared to the commonly used spectrophotometric method. Even though there are methodological differences between these two methods, the NMR-based oxidation susceptibility correlates well (r (2) = 0.73) with the lag time determined spectrophotometrically. In addition to the oxidizability of serum lipids, the NMR method provides also information about the lipid profile. The NMR oxidation assay was applied to the chocolate study including fasting serum samples (n = 45) from subjects who had consumed white (WC), dark (DC) or high-polyphenol chocolate (HPC) daily for 3 weeks. The oxidation susceptibility of serum lipids decreased in the HPC group, and there was a significant difference between the WC and HPC groups (P = 0.031). According to the random forest analysis, the consumption of the HPC chocolate induced changes to the amounts of HDL, phosphatidylcholine, sphingomyelin, and nervonic, docosahexaenoic and myristic acids. Furthermore, arachidonic, docosahexaenoic, docosapentaenoic and palmitic acids, gamma-glutamyl transferase, hemoglobin, HDL, phosphatidylcholine and choline containing phospholipids explained about 60% of the oxidation susceptibility values. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11306-011-0323-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-3351613 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-33516132012-05-31 NMR protocol for determination of oxidation susceptibility of serum lipids and application of the protocol to a chocolate study Tynkkynen, Tuulia Mursu, Jaakko Nurmi, Tarja Tuppurainen, Kari Laatikainen, Reino Soininen, Pasi Metabolomics Original Article A protocol for determination of oxidation susceptibility of serum lipids based on proton nuclear magnetic resonance ((1)H NMR) spectroscopy is presented and compared to the commonly used spectrophotometric method. Even though there are methodological differences between these two methods, the NMR-based oxidation susceptibility correlates well (r (2) = 0.73) with the lag time determined spectrophotometrically. In addition to the oxidizability of serum lipids, the NMR method provides also information about the lipid profile. The NMR oxidation assay was applied to the chocolate study including fasting serum samples (n = 45) from subjects who had consumed white (WC), dark (DC) or high-polyphenol chocolate (HPC) daily for 3 weeks. The oxidation susceptibility of serum lipids decreased in the HPC group, and there was a significant difference between the WC and HPC groups (P = 0.031). According to the random forest analysis, the consumption of the HPC chocolate induced changes to the amounts of HDL, phosphatidylcholine, sphingomyelin, and nervonic, docosahexaenoic and myristic acids. Furthermore, arachidonic, docosahexaenoic, docosapentaenoic and palmitic acids, gamma-glutamyl transferase, hemoglobin, HDL, phosphatidylcholine and choline containing phospholipids explained about 60% of the oxidation susceptibility values. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11306-011-0323-2) contains supplementary material, which is available to authorized users. Springer US 2011-06-03 2012 /pmc/articles/PMC3351613/ /pubmed/22661918 http://dx.doi.org/10.1007/s11306-011-0323-2 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Article Tynkkynen, Tuulia Mursu, Jaakko Nurmi, Tarja Tuppurainen, Kari Laatikainen, Reino Soininen, Pasi NMR protocol for determination of oxidation susceptibility of serum lipids and application of the protocol to a chocolate study |
title | NMR protocol for determination of oxidation susceptibility of serum lipids and application of the protocol to a chocolate study |
title_full | NMR protocol for determination of oxidation susceptibility of serum lipids and application of the protocol to a chocolate study |
title_fullStr | NMR protocol for determination of oxidation susceptibility of serum lipids and application of the protocol to a chocolate study |
title_full_unstemmed | NMR protocol for determination of oxidation susceptibility of serum lipids and application of the protocol to a chocolate study |
title_short | NMR protocol for determination of oxidation susceptibility of serum lipids and application of the protocol to a chocolate study |
title_sort | nmr protocol for determination of oxidation susceptibility of serum lipids and application of the protocol to a chocolate study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3351613/ https://www.ncbi.nlm.nih.gov/pubmed/22661918 http://dx.doi.org/10.1007/s11306-011-0323-2 |
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