Evidence map›Paper›PMID 42543442›Full record

ArticleLasers in medical science2026

Effects of photobiomodulation, alone or combined with dexamethasone, on cellular metabolic activity and inflammatory markers in LPS/IFN-γ-stimulated J774 macrophages.

Rosani Tereza de Siqueira E Silva, Alessandra Lima da Silva Martins, Tainá Caroline Dos Santos Malavazzi, Mohammadhossein Shaker, Natalia Cristina Cova de Souza, Aline Silva Souza, José Antonio Silva Junior, Sandra Kalil Bussadori, Anna Carolina Ratto Tempestini Horliana, Kristianne Porta Santos Fernandes and 2 more

Abstract read
In one paragraph

Article in Lasers in medical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Rosani Tereza de Siqueira E SilvaPostgraduate Program in Biophotonics-Medicine, Universidade Nove de Julho, São Paulo, Brazil.
Alessandra Lima da Silva MartinsPostgraduate Program in Biophotonics-Medicine, Universidade Nove de Julho, São Paulo, Brazil.
Tainá Caroline Dos Santos MalavazziDepartment of Oral Pathology, School of Dentistry, Universidade de São Paulo, São Paulo, Brazil.
Mohammadhossein ShakerPostgraduate Program in Biophotonics-Medicine, Universidade Nove de Julho, São Paulo, Brazil.
Natalia Cristina Cova de SouzaPostgraduate Program in Biophotonics-Medicine, Universidade Nove de Julho, São Paulo, Brazil.
Aline Silva SouzaPostgraduate Program in Biophotonics-Medicine, Universidade Nove de Julho, São Paulo, Brazil.
José Antonio Silva JuniorPostgraduate Program in Biophotonics-Medicine, Universidade Nove de Julho, São Paulo, Brazil.
Sandra Kalil BussadoriPostgraduate Program in Biophotonics-Medicine, Universidade Nove de Julho, São Paulo, Brazil.
Anna Carolina Ratto Tempestini HorlianaPostgraduate Program in Biophotonics-Medicine, Universidade Nove de Julho, São Paulo, Brazil.
Kristianne Porta Santos FernandesPostgraduate Program in Biophotonics-Medicine, Universidade Nove de Julho, São Paulo, Brazil.
Raquel Agnelli Mesquita-FerrariPostgraduate Program in Biophotonics-Medicine, Universidade Nove de Julho, São Paulo, Brazil. raquel.mesquita@gmail.com.
Cinthya Cosme Gutierrez DuranPostgraduate Program in Biophotonics-Medicine, Universidade Nove de Julho, São Paulo, Brazil. cinthya.cgduran@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the present study was to investigate the effects of photobiomodulation (PBM), dexamethasone (DEXA), and their combination on cellular metabolic activity and inflammatory cytokines in LPS/IFN-γ-stimulated J774 macrophages.Cells were stimulated with lipopolysaccharide (LPS) and interferon-gamma (IFN-γ) and treated with PBM (780 nm) and/or DEXA (2 or 4 μM). Cellmorphology, metabolic activity assessed by the 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) assay, and total protein, tumornecrosis factor-alpha (TNF-α), and interleukin-6 (IL-6) levels measured by enzyme-linked immunosorbent assay (ELISA) were analyzed at 24 and 48hours. PBM combined with DEXA at 2 μM increased MTT metabolic activity at 24 hours and was associated with preserved morphology and maintainedhigher total protein levels, with consistent superiority over DEXA alone. PBM + DEXA 2 μM produced the strongest reduction in TNF-α and IL-6 at 24hours, and IL-6 levels remained lower at 48 hours compared to the M1 + PBM group. The 4 μM dose demonstrated lower efficacy and signs of functionalimpairment, which were partially mitigated by PBM. These findings indicate that PBM may enhance the anti-inflammatory effects of low-dose DEXA while supporting a favorable cellular metabolic response, suggesting its potential as an adjunct strategy to optimize the glucocorticoid-based modulation ofinflammatory responses.

Indexed as

Anti-Inflammatory AgentsDexamethasoneLow-Level Light TherapyMacrophagesAnimalsBiomarkersCell LineInflammationInterferon-gammaInterleukin-6LipopolysaccharidesMiceTumor Necrosis Factor-alphaAnti-Inflammatory AgentsBiomarkersDexamethasoneInterferon-gammaInterleukin-6LipopolysaccharidesTumor Necrosis Factor-alphaCytokinesDexamethasoneInflammationMacrophages, activatedPhotobiomodulation therapy

Identifiers

PMID42543442
PMCPMC13429541

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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.