Evidence map›Paper›PMID 27338466›Full record

ArticleNutrients2016

Anti-Inflammatory Effects of Spirulina platensis Extract via the Modulation of Histone Deacetylases.

Tho X Pham, Young-Ki Park, Ji-Young Lee

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 41 citations in OpenAlex.

  1. The histone deacetylase family in health and disease.Signal transduction and targeted therapy · 2026
    Review
  2. Indian journal of clinical biochemistry : IJCB · 2025
    Article
  3. Review
  4. Review
  5. Effect ofInternational journal of molecular sciences · 2024
    Article
  6. Review
  7. Frontiers in endocrinology · 2024
    Article
  8. Supplementation withMarine drugs · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Role of Epigenetics in the Regulation of Immune Functions of the Skin.The Journal of investigative dermatology · 2021
    Review
  14. Article
  15. Article
  16. Influence of Spirulina platensis and ascorbic acid on amikacin-induced nephrotoxicity in rabbits.Environmental science and pollution research international · 2019
    Article
  17. Article
  18. Article
  19. 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

3 authors at 1 institution in 1 country.

Tho X PhamDepartment of Nutritional Sciences, University of Connecticut, Storrs, CT 06269, USA. tho.pham@uconn.edu.
Young-Ki ParkDepartment of Nutritional Sciences, University of Connecticut, Storrs, CT 06269, USA. young-ki.park@uconn.edu.
Ji-Young LeeDepartment of Nutritional Sciences, University of Connecticut, Storrs, CT 06269, USA. ji-young.lee@uconn.edu.
University of Connecticut · US

Funding

Evaluation of athero-protective role of blue-green algaeR21AT005152 · NCCIH · UNIVERSITY OF NEBRASKA LINCOLN · PI LEE, JI-YOUNG · 2009 to 2010
$387k
NCCIH NIH HHS R21 AT005152
6 · The paper itself

Abstract

We previously demonstrated that the organic extract of Spirulina platensis (SPE), an edible blue-green alga, possesses potent anti-inflammatory effects. In this study, we investigated if the regulation of histone deacetylases (HDACs) play a role in the anti-inflammatory effect of SPE in macrophages. Treatment of macrophages with SPE rapidly and dose-dependently reduced HDAC2, 3, and 4 proteins which preceded decreases in their mRNA levels. Degradation of HDAC4 protein was attenuated in the presence of inhibitors of calpain proteases, lysosomal acidification, and Ca(2+)/calmodulin-dependent protein kinase II, respectively, but not a proteasome inhibitor. Acetylated histone H3 was increased in SPE-treated macrophages to a similar level as macrophages treated with a pan-HDAC inhibitor, with concomitant inhibition of inflammatory gene expression upon LPS stimulation. Knockdown of HDAC3 increased basal and LPS-induced pro-inflammatory gene expression, while HDAC4 knockdown increased basal expression of interleukin-1β (IL-1β), but attenuated LPS-induced inflammatory gene expression. Chromatin immunoprecipitation showed that SPE decreased p65 binding and H3K9/K14 acetylation at the Il-1β and tumor necrosis factor α (Tnfα) promoters. Our results suggest that SPE increased global histone H3 acetylation by facilitating HDAC protein degradation, but decreases histone H3K9/K14 acetylation and p65 binding at the promoters of Il-1β and Tnfα to exert its anti-inflammatory effect.

Indexed as

AcetylationAnimalsAnti-Inflammatory AgentsCalcium-Calmodulin-Dependent Protein Kinase Type 2Chromatin ImmunoprecipitationDose-Response Relationship, DrugGene ExpressionHistone Deacetylase InhibitorsHistone DeacetylasesHistonesInterleukin-1betaLysosomesMacrophagesMiceMice, Inbred C57BLPromoter Regions, GeneticAnti-Inflammatory AgentsCalcium-Calmodulin-Dependent Protein Kinase Type 2Histone Deacetylase InhibitorsHistone DeacetylasesHistonesInterleukin-1betaTumor Necrosis Factor-alphaanti-inflammatoryepigeneticshistone deacetylasesinflammationSpirulina platensis

Identifiers

PMID27338466
PMCPMC4924221
OpenAlexW2473894594

What OpenQuestion holds

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LicenceCC BY
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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.