Evidence map›Paper›PMID 41918372›Full record

ArticleChemistry & biodiversity2026

In Vitro Antimicrobial Activity and In Vivo Intestinal Barrier Regulation by Commiphora leptophloeos Bark Extract in 5-Fluorouracil-Induced Mucositis.

Stphannie Jamyla de Araújo Barbosa, Renato Dantas-Medeiros, Susana Barbosa Ribeiro, Amanda Silveira da Silva, Lucas Vinicius Souza de Carvalho, Rafaela Torres Dantas da Silva, Gerlane Coelho Bernardo Guerra, Raimundo Fernandes de Araújo Júnior, Nizyara Costa da Silva, Raphael Victor Silva Andrade and 8 more

Abstract read
In one paragraph

Article in Chemistry & biodiversity, 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

18 authors.

Stphannie Jamyla de Araújo BarbosaPostgraduate Program in Pharmaceutical Science, Federal University of Rio Grande Norte, Natal, Brazil.
Renato Dantas-MedeirosDepartment of Pharmaceutical Sciences, Federal University of Rio Grande Norte, Natal, Brazil.
Susana Barbosa RibeiroPostgraduate Program in Pharmaceutical Science, Federal University of Rio Grande Norte, Natal, Brazil.
Amanda Silveira da SilvaDepartment of Pharmaceutical Sciences, Federal University of Rio Grande Norte, Natal, Brazil.
Lucas Vinicius Souza de CarvalhoDepartment of Pharmaceutical Sciences, Federal University of Rio Grande Norte, Natal, Brazil.
Rafaela Torres Dantas da SilvaDepartment of Biomedicine, Federal University of Rio Grande Norte, Natal, Brazil.
Gerlane Coelho Bernardo GuerraPostgraduate Program in Pharmaceutical Science, Department biophysical and Pharmacology, Federal University of Rio Grande Norte, Natal, Brazil.
Raimundo Fernandes de Araújo JúniorPostgraduate Program in Health Sciences, Postgraduate Program in Functional and Structural Biology UFRN, Department of Morphology, Federal University of Rio Grande Norte, Natal, Brazil.
Nizyara Costa da SilvaPostgraduate Program in Oral Science, Department of Dentistry, Federal University of Rio Grande Norte, Natal, Brazil.
Raphael Victor Silva AndradePostgraduate Program in Oral Science, Department of Dentistry, Federal University of Rio Grande Norte, Natal, Brazil.
Gabrielle Marques de PaivaPostgraduate Program in Oral Science, Department of Dentistry, Federal University of Rio Grande Norte, Natal, Brazil.
Silvana Maria ZucolottoPostgraduate Program in Pharmaceutical Science, Postgraduate Program in PPgDITM Department of Pharmaceutical Sciences, Federal University of Rio Grande Norte, Natal, Brazil.
Rafaela Alcindo Silva de Sousa FéPostgraduate Program in Oral Science, Department of Dentistry, Federal University of Rio Grande Norte, Natal, Brazil.
Maria Laura de Souza LimaPostgraduate Program in Oral Science, Department of Dentistry, Federal University of Rio Grande Norte, Natal, Brazil.
Raphaël GrougnetFaculté de Pharmacie, Université Paris Cité, Paris, France.
Sergio OrtizUMR 7200 Therapeutic Innovation Laboratory, CNRS, Strasbourg Institute for Drug Discovery and Development (IMS), Strasbourg University, Strasbourg, France.
Ana Caroline ZanattaDepartment of Pharmaceutical Sciences, Faculty of Pharmacy, São Paulo University, Ribeirão Preto, Brazil.
Aurigena Antunes de AraújoPostgraduate Program in Pharmaceutical Science, Postgraduate Program in Oral Science, Department of Biophysical and Pharmacology Federal University of Rio Grande Norte, Natal, Brazil.ORCID https://orcid.org/0000-0001-9264-4695

Funding

Federal University of Rio Grande do Norte 151486/2024-7INCT-BIOFOTO BUCAL CNPq 408830/2024-7INCT iCEIS 406264/2022-8Instituto Nacional de Ciência e Tecnologia para o Controle das Intoxicações por Plantas 408830/2024-7Silvana Maria Zucolotto 313727/2020-1
6 · The paper itself

Abstract

This study evaluated the phytochemical composition, antimicrobial activity, and in vivo protective effects of the hydroethanolic extract from Commiphora leptophloeos stem bark (HECL) against 5-fluorouracil (5-FU)-induced intestinal mucositis. Despite the extensive traditional use of C. leptophloeos in gastrointestinal disorders, its stem bark extract has not yet been chemically characterized nor systematically investigated in experimental models of chemotherapy-induced intestinal injury. Phytochemical analysis by mass spectrometry identified 21 metabolites, mainly procyanidins and flavonoids. Antimicrobial screening against 90 bacterial strains showed selective inhibition of Gram-positive bacteria at 40-80 µg/mL. In vivo, mucositis was induced in female Swiss mice with 5-FU (450 mg/kg, i.p.). Treatment with HECL (10 mg/kg) significantly preserved villus and crypt architecture (p < 0.05) and reduced IL-6 levels (p < 0.05). HECL also increased MUC-2 expression (p < 0.05), while maintaining intestinal barrier integrity, as indicated by occludin immunostaining. Additionally, the extract modulated oxidative stress (malondialdehyde) and acetylcholinesterase activity. Overall, HECL demonstrated bioactive potential with broad-spectrum antimicrobial activity and protective effects against chemotherapy-induced intestinal injury, supporting its role as a therapeutic adjuvant in intestinal disorders.

Indexed as

Anti-Bacterial AgentsCommiphoraMucositisPlant ExtractsAnimalsFemaleFluorouracilGram-Positive BacteriaIntestinal Barrier FunctionIntestinal MucosaMiceMicrobial Sensitivity TestsOxidative StressPlant BarkAnti-Bacterial AgentsFluorouracilPlant Extracts5‐fluorouracilchemotherapyCommiphoramucositis

Identifiers

PMID41918372
PMCPMC13040120

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.