Evidence map›Paper›PMID 23543770›Full record

ArticleJournal of lipid research2013

Plasma oxylipin profiling identifies polyunsaturated vicinal diols as responsive to arachidonic acid and docosahexaenoic acid intake in growing piglets.

Maaike J Bruins, Adrie D Dane, Katrin Strassburg, Rob J Vreeken, John W Newman, Norman Salem, Cynthia Tyburczy, J Thomas Brenna

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 29 citations in OpenAlex.

  1. Trial
  2. Eicosanoid profiles in an arthritis model: Effects of a soluble epoxide hydrolase inhibitor.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 2 countries.

Maaike J BruinsDSM Biotechnology Center, Delft, The Netherlands.
Adrie D DaneNetherlands Metabolomics Centre (NMC), Leiden/Amsterdam Center for Drug Research (LACDR), Leiden University, Leiden, The Netherlands.
Katrin StrassburgNetherlands Metabolomics Centre (NMC), Leiden/Amsterdam Center for Drug Research (LACDR), Leiden University, Leiden, The Netherlands.
Rob J VreekenNetherlands Metabolomics Centre (NMC), Leiden/Amsterdam Center for Drug Research (LACDR), Leiden University, Leiden, The Netherlands.
John W NewmanObesity and Metabolism Research Unit, US Department of Agriculture (USDA), Agricultural Research Service (ARS), Western Human Nutrition Research Center, Davis, CA.
Norman SalemDSM Nutritional Lipids, Columbia, MD; and.
Cynthia TyburczyDivision of Nutritional Sciences, Cornell University, Ithaca, NY.
J Thomas BrennaDivision of Nutritional Sciences, Cornell University, Ithaca, NY. Electronic address: jtb4@cornell.edu.
Cornell University · USDSM (Netherlands) · NLNetherlands Metabolomics Centre · NLLeiden University · NLWestern Human Nutrition Research Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The dose-responsiveness of plasma oxylipins to incremental dietary intake of arachidonic acid (20:4n-6; ARA) and docosahexaenoic acid (22:6n-3; DHA) was determined in piglets. Piglets randomly received one of six formulas (n = 8 per group) from days 3 to 27 postnatally. Diets contained incremental ARA or incremental DHA levels as follows (% fatty acid, ARA/DHA): (A1) 0.1/1.0; (A2) 0.53/1.0; (A3-D3) 0.69/1.0; (A4) 1.1/1.0; (D1) 0.66/0.33; and (D2) 0.67/0.62, resulting in incremental intake (g/kg BW/day) of ARA: 0.07 ± 0.01, 0.43 ± 0.03, 0.55 ± 0.03, and 0.82 ± 0.05 at constant DHA intake (0.82 ± 0.05), or incremental intake of DHA: 0.27 ± 0.02, 0.49 ± 0.03, and 0.81 ± 0.05 at constant ARA intake (0.54 ± 0.04). Plasma oxylipin concentrations and free plasma PUFA levels were determined at day 28 using LC-MS/MS. Incremental dietary ARA intake dose-dependently increased plasma ARA levels. In parallel, ARA intake dose-dependently increased ARA-derived diols 5,6- and 14,15-dihydroxyeicosatrienoic acid (DiHETrE) and linoleic acid-derived 12,13-dihydroxyoctadecenoic acid (DiHOME), downstream metabolites of cytochrome P450 expoxygenase (CYP). The ARA epoxide products from CYP are important in vascular homeostatic maintenance. Incremental DHA intake increased plasma DHA and most markedly raised the eicosapentaenoic acid (EPA) metabolite 17,18-dihydroxyeicosatetraenoic acid (DiHETE) and the DHA metabolite 19,20-dihydroxydocosapentaenoic acid (DiHDPE). In conclusion, increasing ARA and DHA intake dose-dependently influenced endogenous n-6 and n-3 oxylipin plasma concentrations in growing piglets, although the biological relevance of these findings remains to be determined.

Indexed as

Arachidonic AcidDocosahexaenoic AcidsAnimalsCytochrome P-450 Enzyme SystemDietary FatsDose-Response Relationship, DrugFatty Acids, UnsaturatedOxylipinsSwine19,20-dihydroxydocosapentaenoic acidArachidonic AcidCytochrome P-450 Enzyme SystemDietary FatsDocosahexaenoic AcidsFatty Acids, UnsaturatedOxylipinseicosanoidlipidomicsmetabolomicsomega-3omega-6 polyunsaturated fatty acidprostaglandin

Identifiers

PMID23543770
PMCPMC3646461
OpenAlexW2128828271

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.