Evidence map›Paper›PMID 40887477›Full record

ArticleScientific reports2025

Bioactive compounds in the modulation of oxidative stress in monocytes and macrophages.

Renu Kushwaha, Phaniendra Alugoju, Naga Venkata Anusha Anthikapalli, Richa Sharma, Michaela Sedlářová, Pavel Pospíšil, Gabriella Tamasi, Claudia Bonechi, Claudio Rossi, Ankush Prasad

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. 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

10 authors.

Renu KushwahaDepartment of Biophysics, Faculty of Science, Palacký University, Šlechtitelů 27, 779 00, Olomouc, Czech Republic.ORCID https://orcid.org/0009-0000-0541-004X
Phaniendra AlugojuDepartment of Biophysics, Faculty of Science, Palacký University, Šlechtitelů 27, 779 00, Olomouc, Czech Republic.ORCID https://orcid.org/0000-0002-4964-446X
Naga Venkata Anusha AnthikapalliDepartment of Biophysics, Faculty of Science, Palacký University, Šlechtitelů 27, 779 00, Olomouc, Czech Republic.ORCID https://orcid.org/0009-0006-9565-9503
Richa SharmaDepartment of Biophysics, Faculty of Science, Palacký University, Šlechtitelů 27, 779 00, Olomouc, Czech Republic.ORCID https://orcid.org/0009-0004-3127-874X
Michaela SedlářováDepartment of Botany, Faculty of Science, Palacký University, Šlechtitelů 27, 779 00, Olomouc, Czech Republic.ORCID https://orcid.org/0000-0003-2319-1033
Pavel PospíšilDepartment of Biophysics, Faculty of Science, Palacký University, Šlechtitelů 27, 779 00, Olomouc, Czech Republic.ORCID https://orcid.org/0000-0001-9126-2011
Gabriella TamasiDepartment of Biotechnology, Chemistry and Pharmacy, University of Siena, Via Aldo Moro 2, 53100, Siena, Italy.ORCID https://orcid.org/0000-0002-6796-8863
Claudia BonechiDepartment of Biotechnology, Chemistry and Pharmacy, University of Siena, Via Aldo Moro 2, 53100, Siena, Italy.
Claudio RossiDepartment of Biotechnology, Chemistry and Pharmacy, University of Siena, Via Aldo Moro 2, 53100, Siena, Italy. claudio.rossi@unisi.it.ORCID https://orcid.org/0000-0001-6032-1015
Ankush PrasadDepartment of Biophysics, Faculty of Science, Palacký University, Šlechtitelů 27, 779 00, Olomouc, Czech Republic. ankush.prasad@upol.cz.ORCID https://orcid.org/0000-0002-2009-8987

Funding

''Current research topics in molecular and general biophysics" of Palacký University. IGA_PrF_2025_028
6 · The paper itself

Abstract

Human immunity involves both innate and adaptive defence mechanisms, with inflammation playing a central role in responding to cellular injury, pathogenic infections, and allergic stimuli. Reactive oxygen species (ROS) are closely associated with the onset and progression of inflammation. While moderate ROS levels function as crucial signalling molecules, excessive ROS can damage cellular components. This study aimed to evaluate the anti-inflammatory and antioxidant potential of plant-derived bioactive compounds including chlorogenic acid, oleuropein, tomatine, and tyrosol using human monocytic cell models (U-937 and THP-1). Differentiation of U-937 and THP-1 cells was induced prior to treatment with the selected bioactive compounds. Cell morphology and integrity were examined utilizing confocal microscopy. Gene expression stability was evaluated using reference genes β-actin and glyceraldehyde 3-phosphate dehydrogenase (GAPDH). Protein expression levels of key inflammatory markers were determined by Western blot analysis. In addition, molecular docking studies were conducted to assess the binding affinity of the compounds to human target proteins [Interleukin-4 (IL-4), 5-Lipoxygenase (LOX-5), Myeloperoxidase (MPO), and Tumor necrosis factor-alpha ( TNF-α)]. No cytotoxic effects were observed in treated cells, and GAPDH was confirmed as a stable reference gene under all experimental conditions. In U-937 cells, treatment with the bioactive compounds led to increased expression of the anti-inflammatory cytokine IL-4 and decreased expression of MPO. Notably, exposure to chlorogenic acid and tyrosol reduced MPO activity. Oleuropein and tyrosol demonstrated a strong suppressive effect on the expression of LOX-5, an enzyme responsible for leukotriene production. All tested bioactive compounds significantly reduced the phorbol 12-myristate 13-acetate (PMA) induced increase in LOX-5 activity. Molecular docking supported the potential of these compounds to interact with key inflammatory proteins, contributing to reduced oxidative stress. The plant-derived compounds, particularly oleuropein and tyrosol from olives, exhibit promising anti-inflammatory and antioxidant effects by modulating ROS-associated signalling pathways and downregulating inflammatory markers. These findings support the therapeutic potential of agricultural waste-derived bioactive in inflammation management and oxidative stress regulation.

Indexed as

Anti-Inflammatory AgentsMacrophagesMonocytesOxidative StressAntioxidantsArachidonate 5-LipoxygenaseChlorogenic AcidHumansIridoid GlucosidesIridoidsMolecular Docking SimulationPeroxidasePhenylethyl AlcoholReactive Oxygen SpeciesTHP-1 CellsTumor Necrosis Factor-alpha4-hydroxyphenylethanolAnti-Inflammatory AgentsAntioxidantsArachidonate 5-LipoxygenaseChlorogenic AcidIridoid GlucosidesIridoidsoleuropeinPeroxidasePhenylethyl AlcoholReactive Oxygen SpeciesTumor Necrosis Factor-alphaAntioxidantsBioactive compoundFree radicalsInflammationInterleukin-4LOX-5MacrophagesMonocytesReactive oxygen species

Identifiers

PMID40887477
PMCPMC12399750

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.