Evidence map›Paper›PMID 31182753›Full record

ArticleScientific reports2019

Development of a Novel Ex-vivo 3D Model to Screen Amoebicidal Activity on Infected Tissue.

Nancy Elena Guzmán-Delgado, Irma Edith Carranza-Torres, Sara García-Davis, Gildardo Rivera, Javier Morán-Martínez, Nadia Denys Betancourt-Martínez, G M M Groothuis, I A M de Graaf, Pilar Carranza-Rosales

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Host-parasite interactions duringFrontiers in cellular and infection microbiology · 2026
    Article
  2. Review
  3. 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

9 authors at 5 institutions in 2 countries.

Nancy Elena Guzmán-DelgadoDivisión de Investigación en Salud, UMAE, Hospital de Cardiología #34, Instituto Mexicano del Seguro Social, Monterrey, Nuevo León, Mexico.
Irma Edith Carranza-TorresCentro de Investigación Biomédica del Noreste, Instituto Mexicano del Seguro Social, Monterrey, Nuevo León, Mexico.
Sara García-DavisFacultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León, San Nicolás de los Garza, Nuevo León, Mexico.
Gildardo RiveraLaboratorio de Biotecnología Farmacéutica, Centro de Biotecnología Genómica, Instituto Politécnico Nacional, Reynosa, 88710, Tamaulipas, Mexico.
Javier Morán-MartínezCentro de Investigación Biomédica, Facultad de Medicina, Universidad Autónoma de Coahuila, Torreón, Coahuila, Mexico.
Nadia Denys Betancourt-MartínezCentro de Investigación Biomédica, Facultad de Medicina, Universidad Autónoma de Coahuila, Torreón, Coahuila, Mexico.
G M M GroothuisGroningen Research Institute of Pharmacy, University of Groningen, Groningen, The Netherlands.
I A M de GraafGroningen Research Institute of Pharmacy, University of Groningen, Groningen, The Netherlands.
Pilar Carranza-RosalesCentro de Investigación Biomédica del Noreste, Instituto Mexicano del Seguro Social, Monterrey, Nuevo León, Mexico. carranza60@yahoo.com.mx.ORCID http://orcid.org/0000-0002-8944-9298
Mexican Social Security Institute · MXUniversidad Autónoma de Coahuila · MXUniversity of Groningen · NLInstituto Politécnico Nacional · MXUniversidad Autónoma de Nuevo León · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amoebiasis is a parasitic disease that causes thousands of deaths every year, its adverse effects and resistance to conventional treatments have led to the search of new treatment options, as well as the development of novel screening methods. In this work, we implemented a 3D model of intestine and liver slices from hamsters that were infected ex vivo with virulent E. histolytica trophozoites. Results show preserved histology in both uninfected tissues as well as ulcerations, destruction of the epithelial cells, and inflammatory reaction in intestine slices and formation of micro abscesses, and the presence of amoebae in the sinusoidal spaces and in the interior of central veins in liver slices. The three chemically synthetized compounds T-001, T-011, and T-016, which act as amoebicides in vitro, were active in both infected tissues, as they decreased the number of trophozoites, and provoked death by disintegration of the amoeba, similar to metronidazole. However, compound T-011 induced signs of cytotoxicity to liver slices. Our results suggest that ex vivo cultures of precision-cut intestinal and liver slices represent a reliable 3D approach to evaluate novel amoebicidal compounds, and to simultaneously detect their toxicity, while reducing the number of experimental animals commonly required by other model systems.

Indexed as

Drug Evaluation, PreclinicalModels, MolecularAmebicidesAnimalsCell DeathCricetinaeEntamoeba histolyticaEntamoebiasisIntestinesLiverMaleAmebicides

Identifiers

PMID31182753
PMCPMC6557822
OpenAlexW2949436852

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.