Evidence map›Paper›PMID 41477277›Full record

ArticleJournal of pharmacopuncture2025

Anti-Inflammatory Effect of

Carla Marrassini, María Laura Barreiro Arcos, Laura Cogoi, María Rosario Alonso, Claudia Anesini

Abstract read
In one paragraph

Article in Journal of pharmacopuncture, 2025. 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

5 authors.

Carla MarrassiniPharmacognosy, Faculty of Pharmacy and Biochemistry, IQUIMEFA UBA CONICET, University of Buenos Aires, Buenos Aires, Argentina.ORCID https://orcid.org/0000-0002-1237-1330
María Laura Barreiro ArcosFaculty of Engineering and Agricultural Sciences, BIOMED UCA CONICET, Argentine Catholic University, Buenos Aires, Argentina.ORCID https://orcid.org/0000-0002-7976-9183
Laura CogoiPharmacognosy, Faculty of Pharmacy and Biochemistry, IQUIMEFA UBA CONICET, University of Buenos Aires, Buenos Aires, Argentina.ORCID https://orcid.org/0000-0002-2800-3751
María Rosario AlonsoPharmacognosy, Faculty of Pharmacy and Biochemistry, IQUIMEFA UBA CONICET, University of Buenos Aires, Buenos Aires, Argentina.ORCID https://orcid.org/0000-0002-6041-7153
Claudia AnesiniPharmacognosy, Faculty of Pharmacy and Biochemistry, IQUIMEFA UBA CONICET, University of Buenos Aires, Buenos Aires, Argentina.ORCID https://orcid.org/0000-0002-7338-9761

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Keratinocytes, the predominant cells in the uppermost layer of the skin, serve as theprimary protection against environmental threats. These cells exhibit activation in the presence of physical trauma, ultraviolet radiation, chemical agents, or allergenic substances. Once activated, keratinocytes release a variety of immunomodulatory soluble mediators that initiate and propagate the inflammatory response. However, dysregulation of this response and the consequent overactivation of pro-inflammatory mediators within the skin may contribute to the pathogenesis of diverse conditions, including cancer, psoriasis, chronic inflammation, autoimmune diseases, hyperpigmentation, and skin aging. Thus, downregulating pro-inflammatory mediators and recovering the physiological balance between factors that promote and those that counteract inflammation represent crucial steps in managing inflammatory skin disorders. Valued in folk medicine for its anti-inflammatory effects, Methods: This investigation sought to determine the anti-inflammatory properties of an ethanolic extract of Results: The extract's analysis revealed the presence of polyphenols and flavonoids, with chlorogenic acid identified as the predominant polyphenol. Notably, it effectively counteracted the LPS-induced elevation in NO production and also reduced release of pro-inflammatory cytokines such as IL-6, TNF-α, and IL-1β. Additionally, the extract exhibited the potential to accelerate wound closure in an Conclusion: The present findings suggest that

Indexed as

cytokinesinflammationnatural compoundsRT-PCRskinwound healing

Identifiers

PMID41477277
PMCPMC12745363

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.