Evidence map›Paper›PMID 19487688›Full record

ArticleThe Journal of biological chemistry2009

Lipidomic analysis of dynamic eicosanoid responses during the induction and resolution of Lyme arthritis.

Victoria A Blaho, Matthew W Buczynski, Charles R Brown, Edward A Dennis

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 1 pooled it
7.9field-weighted citation impact, top 2% 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

66 citing papers in PubMed, 1 synthesis or guideline pooled it, 105 citations in OpenAlex.

  1. Metabolites of prostaglandin synthases as potential biomarkers of Lyme disease severity and symptom resolution.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2019
    Pooled it
  2. Inflammation and resolution in obesity.Nature reviews. Endocrinology · 2025 · on this map
    Review
  3. Impact ofFrontiers in immunology · 2024
    Article
  4. Article
  5. Redox Imbalance and Its Metabolic Consequences in Tick-Borne Diseases.Frontiers in cellular and infection microbiology · 2022
    Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Host Metabolic Response in Early Lyme Disease.Journal of proteome research · 2020
    Article
  12. Macrophage polarization is linked to CaJournal of lipid research · 2020
    Article
  13. Lyme Disease Frontiers: ReconcilingPathogens (Basel, Switzerland) · 2019
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Macrophage LTBJournal of lipid research · 2017
    Article

6 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Victoria A BlahoDepartment of Veterinary Pathobiology, University of Missouri, Columbia, Missouri 65211, USA.
Matthew W Buczynski
Charles R Brown
Edward A Dennis
University of California, San Diego · USUniversity of Missouri · US

Funding

STEROL LIPIDSU54GM069338 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DENNIS, EDWARD A · 2003 to 2013
$72.2M
Training Grant in GastroenterologyT32DK007202 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GHOSH, PRADIPTA · 1985 to 2022
$7.7M
Eicosanoid regulation of experimental Lyme arthritisR01AR052748 · NIAMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI BROWN, CHARLES R. · 2006 to 2010
$1.3M
NIAMS NIH HHS R01 AR052748NIAMS NIH HHS R01-AR052748NIDDK NIH HHS T32 DK007202NIDDK NIH HHS T32 DK07202NIGMS NIH HHS GM069338NIGMS NIH HHS U54 GM069338
6 · The paper itself

Abstract

Eicosanoids and other bioactive lipid mediators are indispensable regulators of biological processes, as demonstrated by the numerous inflammatory diseases resulting from their dysregulation, including cancer, hyperalgesia, atherosclerosis, and arthritis. Despite their importance, a robust strategy comparable with gene or protein array technology for comprehensively analyzing the eicosanoid metabolome has not been forthcoming. We have developed liquid chromatography-tandem mass spectrometry methodology that quantitatively and comprehensively analyzes the eicosanoid metabolome and utilized this approach to characterize eicosanoid production during experimental Lyme arthritis in mice infected with the bacterium Borrelia burgdorferi. Eicosanoids were extracted throughout infection from the joints of Lyme arthritis-resistant and -susceptible mice and subjected to lipidomic profiling. We identified temporal and quantitative differences between these mouse strains in the production of eicosanoids, which correlated with differences in arthritis development. The eicosanoid biosynthetic enzyme cyclooxygenase (COX)-2 has been implicated in the regulation of Lyme arthritis pathology, and subsequent lipidomic profiling of B. burgdorferi-infected COX-2(-/-) mice identified reductions not only in COX-2 products but, surprisingly, also significant off-target reductions in 5-lipoxygenase metabolites. Our results demonstrate the utility of a comprehensive lipidomic approach for identifying potential contributors to disease pathology and may facilitate the development of more precisely targeted treatment strategies.

Indexed as

Gene Expression RegulationAnimalsArachidonate 5-LipoxygenaseBorrelia burgdorferiChromatography, LiquidEicosanoidsFemaleLipidsLyme DiseaseMass SpectrometryMiceMice, Inbred C3HMice, Inbred DBAMice, TransgenicModels, BiologicalArachidonate 5-LipoxygenaseEicosanoidsLipids

Identifiers

PMID19487688
PMCPMC2755884
OpenAlexW2007613321

What OpenQuestion holds

Textmetadata
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.