Evidence map›Paper›PMID 31179494›Full record

ArticleThe Journal of nutrition2019

Developmental Accretion of Docosahexaenoic Acid Is Independent of Fatty Acid Transporter Expression in Brain and Lung Tissues of C57BL/6 and Fat1 Mice.

William Yakah, Pratibha Singh, George Perides, Joanne Brown, Steven D Freedman, Camilia R Martin

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of nutrition, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

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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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

William YakahDepartment of Neuroscience, Michigan State University, East Lansing, MI.
Pratibha SinghDivision of Gastroenterology, Boston, MA.
George PeridesDivision of Gastroenterology, Boston, MA.
Joanne BrownDivision of Gastroenterology, Boston, MA.
Steven D FreedmanDivision of Gastroenterology, Boston, MA.
Camilia R MartinDivision of Translational Research, Boston, MA.
Beth Israel Deaconess Medical Center · USMichigan State University · US

Funding

Impact of fatty acid imbalance in intestinal health and disease in prematurityR01DK104346 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI MARTIN, CAMILIA R · 2014 to 2017
$2.8M
NIDDK NIH HHS R01 DK104346
6 · The paper itself

Abstract

backgroundDevelopmental expression of fatty acid transporters and their role in polyunsaturated fatty acid concentrations in the postnatal period have not been evaluated.

objectiveWe hypothesized that transporter expression is developmentally regulated, tissue-specific, and that expression can modulate fatty acid accretion independently of diet.

methodsBrain and lung transporter expression were quantified in C57BL/6 wild-type (WT) and Fat1 mice. Pups were dam-fed until day 21. Dams were fed AIN-76A 10% corn oil to represent a typical North American/European diet. After weaning, mice were fed the same diet as dams. Gene expression of Fatp1, Fatp4, Fabp5, and Fat/cd36 was quantified by quantitative reverse transcriptase-polymerase chain reaction. Fatty acid concentrations were measured by GC-MS.

resultsBrain docosahexaenoic acid (DHA) concentrations increased from day 3 to day 28 in both genotypes, with higher concentrations at days 3 and 14 in Fat1 than in WT mice [median (IQR)]: 10.7 (10.6-11.2) mol% compared with 6.6 (6.4-7.2) mol% and 12.5 (12.4-12.9) mol% compared with 8.9 (8.7-9.1) mol%, respectively; P < 0.05). During DHA accrual, transporter expression decreased. Fold changes in brain Fatp4, Fabp5, and Fat/cd36 were inversely correlated with fold changes in brain DHA concentrations in Fat1 relative to WT mice (ρ = -0.85, -0.75, and -0.78, respectively; P ≤ 0.001). Lung DHA concentrations were unchanged across the 3 time points for both genotypes. Despite unchanging DHA concentrations, there was increased expression of Fatp1 at days 14 and 28 (5-fold), Fatp4 at day 14 (2.3-fold), and Fabp5 at day 14 (3.8-fold) relative to day 3 in Fat1 mice. In WT mice, Fatp1 increased almost 5-fold at day 28 relative to day 3. There was no correlation between lung transporters and DHA concentrations in Fat1 relative to WT mice.

conclusionsDevelopment of fatty acid transporter expression in C57BL/6 WT and Fat1 mice is genotype and tissue specific. Further, postnatal accretion of brain DHA appears independent of transporter status, with tissue concentrations representing dietary contributions.

Indexed as

AnimalsBrainCorn OilDietary FatsDocosahexaenoic AcidsFatty AcidsFatty Acid Transport ProteinsFemaleGene Expression RegulationGenotypeLungMaleMiceMice, Inbred C57BLMice, TransgenicRNA, MessengerCorn OilDietary FatsDocosahexaenoic AcidsFatty AcidsFatty Acid Transport ProteinsRNA, MessengerSlc27a1 protein, mousearachidonic aciddocosahexaenoic acidfatty acid accretionfatty acid transportersnewborn development

Identifiers

PMID31179494
PMCPMC6768804
OpenAlexW2952334850

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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.