Evidence map›Paper›PMID 38077413›Full record

ArticlePeerJ2023

Cytogenotoxic potential and toxicity in adult

Carla Letícia Gediel Rivero-Wendt, Ana Luisa Miranda Vilela, Luana GarciaFernandes, Andreza Negreli Santos, Igor Leal, Jeandre Jaques, Carlos Eurico Fernandes

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 1 institution in 1 country.

Carla Letícia Gediel Rivero-WendtInstitute of Bioscience, Federal University of Mato Grosso do Sul, Laboratory of Experimental Pathology, Campo Grande, Mato Grosso do Sul, Brazil.
Ana Luisa Miranda VilelaIndependent Research, Brasilia, Distrito Federal, Brazil.
Luana GarciaFernandesInstitute of Bioscience, Federal University of Mato Grosso do Sul, Laboratory of Experimental Pathology, Campo Grande, Mato Grosso do Sul, Brazil.
Andreza Negreli SantosInstitute of Bioscience, Federal University of Mato Grosso do Sul, Multicenter Graduate Program in Biochemistry and Molecular Biology, Campo Grande, Mato Grosso do Sul, Brazil.
Igor LealInstitute of Bioscience, Federal University of Mato Grosso do Sul, Multicenter Graduate Program in Biochemistry and Molecular Biology, Campo Grande, Mato Grosso do Sul, Brazil.
Jeandre JaquesInstitute of Bioscience, Federal University of Mato Grosso do Sul, Multicenter Graduate Program in Biochemistry and Molecular Biology, Campo Grande, Mato Grosso do Sul, Brazil.
Carlos Eurico FernandesInstitute of Bioscience, Federal University of Mato Grosso do Sul, Laboratory of Experimental Pathology, Campo Grande, Mato Grosso do Sul, Brazil.
Universidade Federal de Mato Grosso do Sul · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Chloramine-T (CL-T) is a synthetic sodium salt used as a disinfectant in fish farms to combat bacterial infections in fish gills and skin. While its efficacy in pathogen control is well-established, its reactivity with various functional groups has raised concerns. However, limited research exists on the toxicity of disinfection by-products to aquatic organisms. Therefore, this study aims to assess the sublethal effects of CL-T on adult zebrafish by examining biomarkers of nucleus cytotoxicity and genotoxicity, acetylcholinesterase (AChE) inhibition, and histopathological changes. Methods: Male and female adult zebrafish (wildtype AB lineage) specimens were exposed to 70, 140, and 200 mg/L of CL-T and evaluated after 96 h. Cytotoxic and genotoxic effects were evaluated by estimating the frequencies of nuclear abnormalities (NA), micronuclei (MN), and integrated optical density (IOD) of nuclear erythrocytes. Histopathological changes in the gills and liver were assessed using the degree of tissue changes (DTC). AChE activity was measured in brain samples. Results and conclusions: At a concentration of 200 mg/L, NA increased, indicating the cytogenotoxic potential of CL-T in adult zebrafish. Morphological alterations in the nuclei were observed at both 70 and 200 mg/L concentrations. Distinct IOD profiles were identified across the three concentrations. There were no changes in AChE activity in adult zebrafish. The DTC scores were high in all concentrations, and histological alterations suggested low to moderate toxicity of CL-T for adult zebrafish.

Indexed as

PerciformesZebrafishAcetylcholinesteraseAnimalsChloraminesFemaleMaleTosyl CompoundsAcetylcholinesteraseChloramineschloramine-TTosyl CompoundsAcetylcholinesterase activityGill and liver histopathologyIntegrated optical density (IOD)Micronucleus testNuclear abnormalities

Identifiers

PMID38077413
PMCPMC10702335
OpenAlexW4389300766

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.