Evidence map›Paper›PMID 29589254›Full record

ArticleInflammation2018

Juniperonic Acid Incorporation into the Phospholipids of Murine Macrophage Cells Modulates Pro-Inflammatory Mediator Production.

Po-Jung Tsai, Wen-Cheng Huang, Shao-Wei Lin, Sung-Nien Chen, Hung-Jing Shen, Hsiang Chang, Lu-Te Chuang

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Trial
  2. Biosynthesis of Sciadonic Acid Derived from Gymnosperms with Anti-Colitis Activity.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. Sulfated heteropolysaccharides fromFood chemistry: X · 2022
    Article
  4. Article
  5. Article
  6. Red Arils ofMolecules (Basel, Switzerland) · 2021
    Article
  7. Article
  8. Article
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

7 authors at 2 institutions in 1 country.

Po-Jung TsaiDepartment of Human Development and Family Studies, National Taiwan Normal University, Taipei, Taiwan.
Wen-Cheng HuangDepartment of Human Development and Family Studies, National Taiwan Normal University, Taipei, Taiwan.
Shao-Wei LinDepartment of Biotechnology and Pharmaceutical Technology, Yuanpei University of Medical Technology, 306 Yuanpei Street, Hsinchu, 300, Taiwan.
Sung-Nien ChenDepartment of Biotechnology and Pharmaceutical Technology, Yuanpei University of Medical Technology, 306 Yuanpei Street, Hsinchu, 300, Taiwan.
Hung-Jing ShenDepartment of Human Development and Family Studies, National Taiwan Normal University, Taipei, Taiwan.
Hsiang ChangDepartment of Biotechnology and Pharmaceutical Technology, Yuanpei University of Medical Technology, 306 Yuanpei Street, Hsinchu, 300, Taiwan.
Lu-Te ChuangDepartment of Biotechnology and Pharmaceutical Technology, Yuanpei University of Medical Technology, 306 Yuanpei Street, Hsinchu, 300, Taiwan. ltchuang@mail.ypu.edu.tw.ORCID http://orcid.org/0000-0002-0318-0030
Yuanpei University · TWNational Taiwan Normal University · TW

Funding

Ministry of Science and Technology, Executive Yuan, Taiwan MOSC103-2313-B-264-001-Ministry of Science and Technology, Executive Yuan, Taiwan MOST104-2320-B-264-002-
6 · The paper itself

Abstract

Juniperonic acid (JPA; Δ5,11,14,17-20:4), originally identified in certain gymnosperm seeds, is a rare n-3 polyunsaturated fatty acid (PUFA) with lipid-modulating effects on rats and anti-proliferative effects on fibroblast cell proliferation. However, little is known how JPA exerted its immunosuppressive effect. The objective of this study was to investigate whether JPA inhibited the production of inflammatory mediators through the modulation of cellular phospholipid fatty acid compositions. Using standard lipid chemistry techniques in conjunction with argentated column chromatography, high-purity JPA (> 98%) was extracted, isolated, and purified from Biota kernels. When murine RAW264.7 macrophages were incubated with increasing concentrations of JPA, amounts of cellular phospholipid total PUFA, JPA, and Δ7-docosatetraenoic acid (Δ7-DTA; elongation product of JPA) increased in a dose-dependent manner; however, the proportions of total monounsaturated fatty acid (MUFA) and arachidonic acid (AA) decreased. JPA suppressed the production of nitric oxide (NO), interleukin-6 (IL-6), and tumor necrosis factor-α (TNF-α) and the expression of inducible nitric oxide synthase (iNOS) up to 21, 75, 30, and 44%, respectively. The induction of cyclooxygenase-2 (COX-2) over-expression by JPA could account for the doubling of the PGE

Indexed as

AnimalsCyclooxygenase 2EdemaFatty Acids, MonounsaturatedFatty Acids, UnsaturatedInflammationMacrophagesMiceMitogen-Activated Protein KinasesNitric Oxide Synthase Type IIPhospholipidsRAW 264.7 CellsCyclooxygenase 2Fatty Acids, MonounsaturatedFatty Acids, Unsaturatedjuniperonic acidMitogen-Activated Protein KinasesNitric Oxide Synthase Type IIPhospholipidsArachidonic acid (AA)Juniperonic acid (JPA)MacrophageProstaglandin E2 (PGE2)Type-2 cyclooxygenase (COX-2)

Identifiers

PMID29589254
OpenAlexW2794640526

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.