Evidence map›Paper›PMID 27513579›Full record

ArticlePloS one2016

DHA but Not EPA Emulsions Preserve Neurological and Mitochondrial Function after Brain Hypoxia-Ischemia in Neonatal Mice.

Korapat Mayurasakorn, Zoya V Niatsetskaya, Sergey A Sosunov, Jill J Williams, Hylde Zirpoli, Iliyan Vlasakov, Richard J Deckelbaum, Vadim S Ten

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
6.7field-weighted citation impact, top 3% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

  1. Pooled it
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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 2 institutions in 1 country.

Korapat MayurasakornInstitute of Human Nutrition, Columbia University, New York, New York, United States of America.
Zoya V NiatsetskayaDepartment of Pediatrics, Columbia University, New York, New York, United States of America.
Sergey A SosunovDepartment of Pediatrics, Columbia University, New York, New York, United States of America.
Jill J WilliamsInstitute of Human Nutrition, Columbia University, New York, New York, United States of America.
Hylde ZirpoliInstitute of Human Nutrition, Columbia University, New York, New York, United States of America.
Iliyan VlasakovCenter for Experimental Therapeutics and Reperfusion Injury, Department of Anesthesiology, Perioperative and Pain Medicine, Harvard Institutes of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, United States of America.
Richard J DeckelbaumInstitute of Human Nutrition, Columbia University, New York, New York, United States of America.
Vadim S TenDepartment of Pediatrics, Columbia University, New York, New York, United States of America.
Columbia University · USHarvard University · US

Funding

Resolution Mechanisms in Acute Inflammation: Resolution PharmacologyP01GM095467 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI SERHAN, CHARLES NICHOLAS · 2011 to 2020
$14.8M
Omega 3 Fatty Acids, Acute Neuroprotection Via MitochondriaR01NS088197 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHANG, CHUCHUN LIZ, TEN, VADIM S · 2015 to 2025
$4.6M
METABOLISM OF INTRAVENOUS LIPID EMULSIONSR01HL040404 · NHLBI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI DECKELBAUM, RICHARD JOSEPH · 1988 to 2008
$2.9M
NHLBI NIH HHS R01 HL040404NIGMS NIH HHS P01 GM095467NINDS NIH HHS R01 NS088197
6 · The paper itself

Abstract

background and purposeTreatment with triglyceride emulsions of docosahexaenoic acid (tri-DHA) protected neonatal mice against hypoxia-ischemia (HI) brain injury. The mechanism of this neuroprotection remains unclear. We hypothesized that administration of tri-DHA enriches HI-brains with DHA/DHA metabolites. This reduces Ca2+-induced mitochondrial membrane permeabilization and attenuates brain injury.

methods10-day-old C57BL/6J mice following HI-brain injury received tri-DHA, tri-EPA or vehicle. At 4-5 hours of reperfusion, mitochondrial fatty acid composition and Ca2+ buffering capacity were analyzed. At 24 hours and at 8-9 weeks of recovery, oxidative injury, neurofunctional and neuropathological outcomes were evaluated. In vitro, hyperoxia-induced mitochondrial generation of reactive oxygen species (ROS) and Ca2+ buffering capacity were measured in the presence or absence of DHA or EPA.

resultsOnly post-treatment with tri-DHA reduced oxidative damage and improved short- and long-term neurological outcomes. This was associated with increased content of DHA in brain mitochondria and DHA-derived bioactive metabolites in cerebral tissue. After tri-DHA administration HI mitochondria were resistant to Ca2+-induced membrane permeabilization. In vitro, hyperoxia increased mitochondrial ROS production and reduced Ca2+ buffering capacity; DHA, but not EPA, significantly attenuated these effects of hyperoxia.

conclusionsPost-treatment with tri-DHA resulted in significant accumulation of DHA and DHA derived bioactive metabolites in the HI-brain. This was associated with improved mitochondrial tolerance to Ca2+-induced permeabilization, reduced oxidative brain injury and permanent neuroprotection. Interaction of DHA with mitochondria alters ROS release and improves Ca2+ buffering capacity. This may account for neuroprotective action of post-HI administration of tri-DHA.

Indexed as

AnimalsCalciumDocosahexaenoic AcidsEicosapentaenoic AcidEmulsionsHypoxia-Ischemia, BrainMiceMice, Inbred C57BLMitochondriaNeuroprotective AgentsOxidative StressReactive Oxygen SpeciesCalciumDocosahexaenoic AcidsEicosapentaenoic AcidEmulsionsNeuroprotective AgentsReactive Oxygen Species

Identifiers

PMID27513579
PMCPMC4981459
OpenAlexW2515134490

What OpenQuestion holds

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LicenceCC BY
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.