Evidence map›Paper›PMID 30560060›Full record

ArticleToxicology reports2019

An imazamox-based herbicide causes apoptotic changes in rat liver and pancreas.

Çiğdem Sevim, Selim Çomaklı, Ali Taghizadehghalehjoughi, Mustafa Özkaraca, Robin Mesnage, Leda Kovatsi, Tatyana I Burykina, Alexandra Kalogeraki, Michael N Antoniou, Aristidis Tsatsakis

Open access · goldAbstract read
In one paragraph

Article in Toxicology reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

7 citing papers in PubMed, 34 citations in OpenAlex.

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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

10 authors at 5 institutions in 4 countries.

Çiğdem SevimDepartment of Veterinary Pharmacology and Toxicology, Faculty of Veterinary Medicine, Ataturk University, Erzurum, Turkey.
Selim ÇomaklıDepartment of Veterinary Pathology, Faculty of Veterinary Medicine, Ataturk University, Erzurum, Turkey.
Ali TaghizadehghalehjoughiDepartment of Veterinary Pharmacology and Toxicology, Faculty of Veterinary Medicine, Ataturk University, Erzurum, Turkey.
Mustafa ÖzkaracaDepartment of Veterinary Pathology, Faculty of Veterinary Medicine, Ataturk University, Erzurum, Turkey.
Robin MesnageDepartment of Medical and Molecular Genetics, King's College London, London, United Kingdom.
Leda KovatsiLaboratory of Forensic Medicine and Toxicology, School of Medicine, Aristotle University of Thessaloniki, Greece.
Tatyana I BurykinaDepartment of Analytical and Forensic Medical Toxicology, Sechenov University, 2-4 Bolshaya Pirogovskaya st., 119991 Moscow, Russia.
Alexandra KalogerakiDepartment of Pathology-Cytopathology, Medical School, University of Crete, Heraklion, Greece.
Michael N AntoniouDepartment of Medical and Molecular Genetics, King's College London, London, United Kingdom.
Aristidis TsatsakisDepartment of Toxicology & Forensic Sciences, Faculty Medicine, University of Crete, Heraklion, Greece.
Atatürk University · TRKing's College London · GBUniversity of Crete · GRAristotle University of Thessaloniki · GRSechenov University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We studied the acute toxicity of an imazamox-based herbicide at 12, 24 and 36 mg/kg body (bw) weight imazamox equivalent dose on the liver and pancreatic tissue in Sprague Dawley rats. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities, glucose, calcium as well as creatinine, were determined in blood samples, which were collected after 24, 48 and 72 h exposure. Caspase 3 and anti-insulin expression and immunopositivity were evaluated using in situ hybridization and immunohistochemistry, respectively. The imazamox-based herbicide evaluated in this study induced toxic effects even from the lowest dose tested (12 mg/kg bw). The two highest doses caused a statistically significant cytotoxicity on the Langerhans islet cells. Necrotic and degenerative changes were detected in hepatocytes at the two highest doses. Imazamox is considered to be poorly toxic to the liver. Nevertheless, the imazamox-based herbicide formulation tested here reduced the size of the β-islet cells, induced an elevation in serum glucose and calcium. Our data shows that commercial formulations of imazamox containing various co-formulants can have hepatic and pancreatic toxic effects.

Indexed as

Anti-insulinCaspase 3ImazamoxImmunohistochemistryIn situ hybridization

Identifiers

PMID30560060
PMCPMC6289906
OpenAlexW2901019328

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.