Evidence map›Paper›PMID 29986724›Full record

ArticleJournal of neuroinflammation2018

Unveiling anti-oxidative and anti-inflammatory effects of docosahexaenoic acid and its lipid peroxidation product on lipopolysaccharide-stimulated BV-2 microglial cells.

Bo Yang, Runting Li, C Michael Greenlief, Kevin L Fritsche, Zezong Gu, Jiankun Cui, James C Lee, David Q Beversdorf, Grace Y Sun

Open access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

40 citing papers in PubMed, 63 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Bo YangChemistry Department, University of Missouri, Columbia, MO, USA.
Runting LiBiochemistry Department, University of Missouri, 117 Schweitzer Hall, Columbia, MO, 65211, USA.
C Michael GreenliefChemistry Department, University of Missouri, Columbia, MO, USA.
Kevin L FritscheDepartment of Nutrition and Exercise Physiology, University of Missouri, Columbia, MO, USA.
Zezong GuDepartment of Pathology and Anatomical Sciences, University of Missouri, Columbia, MO, USA.
Jiankun CuiDepartment of Pathology and Anatomical Sciences, University of Missouri, Columbia, MO, USA.
James C LeeDepartment of Bioengineering, University of Illinois at Chicago, Chicago, IL, USA.
David Q BeversdorfDepartments of Radiology, Neurology and Psychological Sciences, University of Missouri, Columbia, MO, USA.
Grace Y SunBiochemistry Department, University of Missouri, 117 Schweitzer Hall, Columbia, MO, 65211, USA. sung@missouri.edu.ORCID http://orcid.org/0000-0003-4303-0317
University of Missouri · USUniversity of Illinois Chicago · US

Funding

Roles of Tau Oligomers in Alzheimer's VasculopathyR01AG044404 · NIA · UNIVERSITY OF MISSOURI-COLUMBIA · PI LEE, JAMES C · 2014 to 2024
$3.5M
NIA NIH HHS R01 AG044404Research Council Grant, University of Missouri 17-009
6 · The paper itself

Abstract

backgroundPhospholipids in the central nervous system are enriched in n-3 and n-6 polyunsaturated fatty acids (PUFA), especially docosahexaenoic acid (DHA) and arachidonic acid (ARA). These PUFA can undergo enzymatic reactions to produce lipid mediators, as well as reaction with oxygen free radicals to produce 4-hydroxyhexenal (4-HHE) from DHA and 4-hydroxynonenal (4-HNE) from ARA. Recent studies demonstrated pleiotropic properties of these peroxidation products through interaction with oxidative and anti-oxidant response pathways. In this study, BV-2 microglial cells were used to investigate ability for DHA, 4-HHE, and 4-HNE to stimulate the anti-oxidant stress responses involving the nuclear factor erythroid-2-related factor 2 (Nrf2) pathway and synthesis of heme oxygenase (HO-1), as well as to mitigate lipopolysaccharide (LPS)-induced nitric oxide (NO), reactive oxygen species (ROS), and cytosolic phospholipase A

methodsEffects of DHA, 4-HHE, and 4-HNE on LPS-induced NO production was determined using the Griess reagent. LPS-induced ROS production was measured using CM-H

resultsDHA (12.5-100 μM), 4-HHE (1.25-10 μM), and 4-HNE (1.25-10 μM) dose dependently suppressed LPS-induced production of NO, ROS, and as p-cPLA

conclusionsThis study demonstrated the ability of DHA and its lipid peroxidation products, namely, 4-HHE and 4-HNE at 1.25-10 μM, to enhance Nrf2/HO-1 and mitigate LPS-induced NO, ROS, and p-cPLA

Indexed as

AldehydesAnimalsAnti-Inflammatory AgentsCell Line, TransformedCell SurvivalCytokinesDocosahexaenoic AcidsDose-Response Relationship, DrugLipid PeroxidationLipopolysaccharidesMiceMicrogliaNitric Oxide Synthase Type IIPhospholipases A2Prostaglandin-Endoperoxide SynthasesReactive Oxygen Species4-hydroxy-2-hexenal4-hydroxy-2-nonenalAldehydesAnti-Inflammatory AgentsCytokinesDocosahexaenoic AcidsLipopolysaccharidesNitric Oxide Synthase Type IIPhospholipases A2Prostaglandin-Endoperoxide SynthasesReactive Oxygen Species4-Hydroxyhexenal (4-HHE)4-Hydroxynonenal (4-HNE)cPLA2Docosahexaenoic acid (DHA)HO-1iPLA2Lipopolysaccharide (LPS)MicrogliaNONrf2ROS

Identifiers

PMID29986724
PMCPMC6038194
OpenAlexW2880141166

What OpenQuestion holds

Textmetadata
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.