Evidence map›Paper›PMID 25873160›Full record

ArticleInternational journal of molecular medicine2015

Hydrogen sulfide attenuates cytokine production through the modulation of chromatin remodeling.

Ester C S Rios, Bartosz Szczesny, Francisco G Soriano, Gabor Olah, Csaba Szabo

Open access · bronzeAbstract read
In one paragraph

Article in International journal of molecular medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.7field-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

32 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
  2. Black gas, bright future: HNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Review
  3. Slow HBiomolecules · 2024
    Article
  4. Review
  5. Article
  6. Article
  7. Biological Functions of Hydrogen Sulfide in Plants.International journal of molecular sciences · 2022
    Review
  8. The Role of Hydrogen Sulfide in Plaque Stability.Antioxidants (Basel, Switzerland) · 2022
    Review
  9. Article
  10. Article
  11. Review
  12. CSE/HFrontiers in immunology · 2022
    Article
  13. Hydrogen Sulfide Actions in the Vasculature.Comprehensive Physiology · 2021
    Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Review
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

5 authors at 2 institutions in 2 countries.

Ester C S RiosDepartment of Anesthesiology, University of Texas Medical Branch, Galveston, TX, USA.
Bartosz SzczesnyDepartment of Anesthesiology, University of Texas Medical Branch, Galveston, TX, USA.
Francisco G SorianoDepartment of Emergency Medicine, University of São Paulo Medical School, São Paulo, Brazil.
Gabor OlahDepartment of Anesthesiology, University of Texas Medical Branch, Galveston, TX, USA.
Csaba SzaboDepartment of Anesthesiology, University of Texas Medical Branch, Galveston, TX, USA.
The University of Texas Medical Branch at Galveston · USUniversidade de São Paulo · BR

Funding

Regulation of cellular bioenergetics by hydrogen sulfideR01GM107846 · NIGMS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI SZABO, CSABA · 2014 to 2017
$1.2M
NIGMS NIH HHS R01 GM107846NIGMS NIH HHS R01GM107846
6 · The paper itself

Abstract

Hydrogen sulfide (H2S) is an endogenous gaseous biological mediator, which regulates, among others, the oxidative balance of cells under normal physiological conditions, as well as in various diseases. Several previous studies have reported that H2S attenuates inflammatory mediator production. In this study, we investigated the role of H2S in chromatin modulation in an in vitro model of lipopolysaccharide (LPS)-induced inflammation and evaluated its effects on inflammatory cytokine production. Tamm-Horsfall protein 1 (THP-1) differentiated macrophages were pre-treated with sodium hydrosulfide (NaHS) (an H2S donor) at 0.01, 0.1, 0.5 or 1 mM for 30 min. To stimulate cytokine production, the cells were challenged with bacterial LPS (1 µg/ml) for 1, 4, 8 or 24 h. Histone H3 acetylation was analyzed by chromatin immunoprecipitation (ChIP), cytokine production was measured by ELISA and histone deacetylase (HDAC) activity was analyzed using a standard biochemical assay. H2S inhibited the production of interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) in a concentration-dependent manner; it was most effective at the two highest concentrations used. This effect was associated with a decrease in histone H3 acetylation at the IL-6 and TNF-α promoters in the cells exposed to H2S or H2S + LPS. The findings of the present study suggest that H2S suppresses histone acetylation, which, in turn, inhibits chromatin openness, leading to a decrease in the gene transcription of various pro-inflammatory cytokines. Therefore, this mechanism may contribute to the previously demonstrated anti-inflammatory effects of H2S and various H2S donors.

Indexed as

AcetylationCell Line, TumorChromatin Assembly and DisassemblyDose-Response Relationship, DrugHistone DeacetylasesHistonesHumansHydrogen SulfideInterleukin-6MacrophagesTumor Necrosis Factor-alphaHistone DeacetylasesHistonesHydrogen SulfideIL6 protein, humanInterleukin-6Tumor Necrosis Factor-alpha

Identifiers

PMID25873160
PMCPMC4432924
OpenAlexW1968924850

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Registered trials

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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.