Dietary hydroxy fatty acids are absorbed in humans: implications for the measurement of ‘oxidative stress’ in vivo
Lipid peroxidation products formed in vivo or originating from the diet may lead to atherosclerosis. However, little is known about the absorption of these products in man. We studied the absorption of fat (30 g) containing 14–15 mg [U- 13C]-labeled hydroxy or dihydroxy triglycerides in two groups o...
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Veröffentlicht in: | Free radical biology & medicine 2002-01, Vol.32 (2), p.162-168 |
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creator | Wilson, Robert Lyall, Karin Smyth, Louise Fernie, Claire E Riemersma, Rudolph A |
description | Lipid peroxidation products formed in vivo or originating from the diet may lead to atherosclerosis. However, little is known about the absorption of these products in man. We studied the absorption of fat (30 g) containing 14–15 mg [U-
13C]-labeled hydroxy or dihydroxy triglycerides in two groups of six apparently healthy women aged 40 ± 2 years. Post-prandial
13C-labeled hydroxy fatty acid concentration increased in a pattern somewhat different from that of plasma triglycerides, with peak levels being reached between 4 and 6 h. However, the amount of
13C-labeled oxidized fat absorbed (area under the curve of plasma concentrations from 0 to 8 h) was related to that of plasma triglycerides:
13C hydroxy vs TG (r = 0.88,
p < .02), and
13C dihydroxy vs TG (r = 0.85,
p < .05).
13C monohydroxy triglycerides appeared to be absorbed to a greater extent than those of
13C dihydroxy triglycerides. Although low levels of
13C hydroxy lipids could be detected in fasting plasma after 24 h, concentrations were very low. Dietary lipid oxidation products are absorbed. The measurement of hydroxy fatty acids in plasma total lipids may not be a valid marker of lipid peroxidation in vivo when subjects are not fasting. |
doi_str_mv | 10.1016/S0891-5849(01)00780-8 |
format | Article |
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13C]-labeled hydroxy or dihydroxy triglycerides in two groups of six apparently healthy women aged 40 ± 2 years. Post-prandial
13C-labeled hydroxy fatty acid concentration increased in a pattern somewhat different from that of plasma triglycerides, with peak levels being reached between 4 and 6 h. However, the amount of
13C-labeled oxidized fat absorbed (area under the curve of plasma concentrations from 0 to 8 h) was related to that of plasma triglycerides:
13C hydroxy vs TG (r = 0.88,
p < .02), and
13C dihydroxy vs TG (r = 0.85,
p < .05).
13C monohydroxy triglycerides appeared to be absorbed to a greater extent than those of
13C dihydroxy triglycerides. Although low levels of
13C hydroxy lipids could be detected in fasting plasma after 24 h, concentrations were very low. Dietary lipid oxidation products are absorbed. The measurement of hydroxy fatty acids in plasma total lipids may not be a valid marker of lipid peroxidation in vivo when subjects are not fasting.</description><identifier>ISSN: 0891-5849</identifier><identifier>EISSN: 1873-4596</identifier><identifier>DOI: 10.1016/S0891-5849(01)00780-8</identifier><identifier>PMID: 11796205</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Bio-marker ; Biomarkers - analysis ; Carbon Isotopes - chemistry ; Dietary Fats - pharmacokinetics ; Fatty Acids - pharmacokinetics ; Female ; Free radicals ; Humans ; Hydroxy Acids - analysis ; Hydroxy Acids - pharmacokinetics ; Hydroxy fatty acids ; Isotope Labeling ; Lipid Peroxidation ; Lipid Peroxides - analysis ; Lipid Peroxides - pharmacokinetics ; Mass Spectrometry ; Oxidative stress ; Oxidative Stress - physiology ; Post-prandial lipaemia ; Stable isotope ; Triglycerides - blood ; Woman</subject><ispartof>Free radical biology & medicine, 2002-01, Vol.32 (2), p.162-168</ispartof><rights>2002 Elsevier Science Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c361t-4ca4591c493da50fd104075ef49259cbe24cce7afd6f28cff0449f280900124f3</citedby><cites>FETCH-LOGICAL-c361t-4ca4591c493da50fd104075ef49259cbe24cce7afd6f28cff0449f280900124f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0891-5849(01)00780-8$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3549,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11796205$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wilson, Robert</creatorcontrib><creatorcontrib>Lyall, Karin</creatorcontrib><creatorcontrib>Smyth, Louise</creatorcontrib><creatorcontrib>Fernie, Claire E</creatorcontrib><creatorcontrib>Riemersma, Rudolph A</creatorcontrib><title>Dietary hydroxy fatty acids are absorbed in humans: implications for the measurement of ‘oxidative stress’ in vivo</title><title>Free radical biology & medicine</title><addtitle>Free Radic Biol Med</addtitle><description>Lipid peroxidation products formed in vivo or originating from the diet may lead to atherosclerosis. However, little is known about the absorption of these products in man. We studied the absorption of fat (30 g) containing 14–15 mg [U-
13C]-labeled hydroxy or dihydroxy triglycerides in two groups of six apparently healthy women aged 40 ± 2 years. Post-prandial
13C-labeled hydroxy fatty acid concentration increased in a pattern somewhat different from that of plasma triglycerides, with peak levels being reached between 4 and 6 h. However, the amount of
13C-labeled oxidized fat absorbed (area under the curve of plasma concentrations from 0 to 8 h) was related to that of plasma triglycerides:
13C hydroxy vs TG (r = 0.88,
p < .02), and
13C dihydroxy vs TG (r = 0.85,
p < .05).
13C monohydroxy triglycerides appeared to be absorbed to a greater extent than those of
13C dihydroxy triglycerides. Although low levels of
13C hydroxy lipids could be detected in fasting plasma after 24 h, concentrations were very low. Dietary lipid oxidation products are absorbed. The measurement of hydroxy fatty acids in plasma total lipids may not be a valid marker of lipid peroxidation in vivo when subjects are not fasting.</description><subject>Adult</subject><subject>Bio-marker</subject><subject>Biomarkers - analysis</subject><subject>Carbon Isotopes - chemistry</subject><subject>Dietary Fats - pharmacokinetics</subject><subject>Fatty Acids - pharmacokinetics</subject><subject>Female</subject><subject>Free radicals</subject><subject>Humans</subject><subject>Hydroxy Acids - analysis</subject><subject>Hydroxy Acids - pharmacokinetics</subject><subject>Hydroxy fatty acids</subject><subject>Isotope Labeling</subject><subject>Lipid Peroxidation</subject><subject>Lipid Peroxides - analysis</subject><subject>Lipid Peroxides - pharmacokinetics</subject><subject>Mass Spectrometry</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - physiology</subject><subject>Post-prandial lipaemia</subject><subject>Stable isotope</subject><subject>Triglycerides - blood</subject><subject>Woman</subject><issn>0891-5849</issn><issn>1873-4596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM9uEzEQhy1ERdPAI4B8QnBYGO96_5hLhUqhSJU4AGfLsceKUXYdPN5Vc-tj0Nfrk7BponLkNHP4fr_RfIy9FPBOgGjef4dOiaLupHoD4i1A20HRPWEL0bVVIWvVPGWLR-SUnRH9AgBZV90zdipEq5oS6gWbPgXMJu34eudSvNlxb3LecWODI24ScrOimFboeBj4euzNQB946LebYE0OcSDuY-J5jbxHQ2PCHofMo-f3t3_iTXAzNCGnnJDo_vZu3zKFKT5nJ95sCF8c55L9_Hz54-KquP725evFx-vCVo3IhbRmfkVYqSpnavBOgIS2Ri9VWSu7wlJai63xrvFlZ70HKdW8gQIQpfTVkr0-9G5T_D0iZd0HsrjZmAHjSLoVUkA51y9ZfQBtikQJvd6m0M9itAC9F64fhOu9TQ1CPwjX3Zx7dTwwrnp0_1JHwzNwfgBwfnMKmDTZgINFFxLarF0M_znxF_Lnk_A</recordid><startdate>20020115</startdate><enddate>20020115</enddate><creator>Wilson, Robert</creator><creator>Lyall, Karin</creator><creator>Smyth, Louise</creator><creator>Fernie, Claire E</creator><creator>Riemersma, Rudolph A</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20020115</creationdate><title>Dietary hydroxy fatty acids are absorbed in humans: implications for the measurement of ‘oxidative stress’ in vivo</title><author>Wilson, Robert ; Lyall, Karin ; Smyth, Louise ; Fernie, Claire E ; Riemersma, Rudolph A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c361t-4ca4591c493da50fd104075ef49259cbe24cce7afd6f28cff0449f280900124f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adult</topic><topic>Bio-marker</topic><topic>Biomarkers - analysis</topic><topic>Carbon Isotopes - chemistry</topic><topic>Dietary Fats - pharmacokinetics</topic><topic>Fatty Acids - pharmacokinetics</topic><topic>Female</topic><topic>Free radicals</topic><topic>Humans</topic><topic>Hydroxy Acids - analysis</topic><topic>Hydroxy Acids - pharmacokinetics</topic><topic>Hydroxy fatty acids</topic><topic>Isotope Labeling</topic><topic>Lipid Peroxidation</topic><topic>Lipid Peroxides - analysis</topic><topic>Lipid Peroxides - pharmacokinetics</topic><topic>Mass Spectrometry</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - physiology</topic><topic>Post-prandial lipaemia</topic><topic>Stable isotope</topic><topic>Triglycerides - blood</topic><topic>Woman</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wilson, Robert</creatorcontrib><creatorcontrib>Lyall, Karin</creatorcontrib><creatorcontrib>Smyth, Louise</creatorcontrib><creatorcontrib>Fernie, Claire E</creatorcontrib><creatorcontrib>Riemersma, Rudolph A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Free radical biology & medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wilson, Robert</au><au>Lyall, Karin</au><au>Smyth, Louise</au><au>Fernie, Claire E</au><au>Riemersma, Rudolph A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dietary hydroxy fatty acids are absorbed in humans: implications for the measurement of ‘oxidative stress’ in vivo</atitle><jtitle>Free radical biology & medicine</jtitle><addtitle>Free Radic Biol Med</addtitle><date>2002-01-15</date><risdate>2002</risdate><volume>32</volume><issue>2</issue><spage>162</spage><epage>168</epage><pages>162-168</pages><issn>0891-5849</issn><eissn>1873-4596</eissn><abstract>Lipid peroxidation products formed in vivo or originating from the diet may lead to atherosclerosis. However, little is known about the absorption of these products in man. We studied the absorption of fat (30 g) containing 14–15 mg [U-
13C]-labeled hydroxy or dihydroxy triglycerides in two groups of six apparently healthy women aged 40 ± 2 years. Post-prandial
13C-labeled hydroxy fatty acid concentration increased in a pattern somewhat different from that of plasma triglycerides, with peak levels being reached between 4 and 6 h. However, the amount of
13C-labeled oxidized fat absorbed (area under the curve of plasma concentrations from 0 to 8 h) was related to that of plasma triglycerides:
13C hydroxy vs TG (r = 0.88,
p < .02), and
13C dihydroxy vs TG (r = 0.85,
p < .05).
13C monohydroxy triglycerides appeared to be absorbed to a greater extent than those of
13C dihydroxy triglycerides. Although low levels of
13C hydroxy lipids could be detected in fasting plasma after 24 h, concentrations were very low. Dietary lipid oxidation products are absorbed. The measurement of hydroxy fatty acids in plasma total lipids may not be a valid marker of lipid peroxidation in vivo when subjects are not fasting.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11796205</pmid><doi>10.1016/S0891-5849(01)00780-8</doi><tpages>7</tpages></addata></record> |
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source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | Adult Bio-marker Biomarkers - analysis Carbon Isotopes - chemistry Dietary Fats - pharmacokinetics Fatty Acids - pharmacokinetics Female Free radicals Humans Hydroxy Acids - analysis Hydroxy Acids - pharmacokinetics Hydroxy fatty acids Isotope Labeling Lipid Peroxidation Lipid Peroxides - analysis Lipid Peroxides - pharmacokinetics Mass Spectrometry Oxidative stress Oxidative Stress - physiology Post-prandial lipaemia Stable isotope Triglycerides - blood Woman |
title | Dietary hydroxy fatty acids are absorbed in humans: implications for the measurement of ‘oxidative stress’ in vivo |
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