Evidence map›Paper›PMID 33266415›Full record

ArticleToxins2020

Effects of Single and Repeated Oral Doses of Ochratoxin A on the Lipid Peroxidation and Antioxidant Defense Systems in Mouse Kidneys.

Szilamér Ferenczi, Dániel Kuti, Mátyás Cserháti, Csilla Krifaton, Sándor Szoboszlay, József Kukolya, Zsuzsanna Szőke, Mihály Albert, Balázs Kriszt, Krisztina J Kovács and 2 more

Open access · goldAbstract read
In one paragraph

Article in Toxins, 2020. 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
0.7field-weighted citation impact, top 32% 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, 14 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

12 authors at 4 institutions in 1 country.

Szilamér FerencziInstitute of Experimental Medicine, Laboratory of Molecular Neuroendocrinology, 43. Szigony Street, Budapest 1083, Hungary.
Dániel KutiInstitute of Experimental Medicine, Laboratory of Molecular Neuroendocrinology, 43. Szigony Street, Budapest 1083, Hungary.
Mátyás CserhátiSzent István University, Department of Environmental Protection & Safety, 1. Páter K. Street, Gödöllő 2100, Hungary.
Csilla KrifatonSzent István University, Department of Environmental Protection & Safety, 1. Páter K. Street, Gödöllő 2100, Hungary.
Sándor SzoboszlaySzent István University, Department of Environmental Protection & Safety, 1. Páter K. Street, Gödöllő 2100, Hungary.
József KukolyaCentral Environmental and Food Science Research Institute, Department of Microbiology, 15. Herman O. Street, Budapest 1022, Hungary.
Zsuzsanna SzőkeNational Agricultural Research and Innovation Center, Agricultural Biotechnology Institute, Reproduction Biology and Toxicology Research Group, 4. Szent-Györgyi A. Street, Gödöllő 2100, Hungary.
Mihály AlbertCEVA Phylaxia Ltd, 5. Szállás Street, Budapest 1107, Hungary.
Balázs KrisztSzent István University, Department of Environmental Protection & Safety, 1. Páter K. Street, Gödöllő 2100, Hungary.
Krisztina J KovácsInstitute of Experimental Medicine, Laboratory of Molecular Neuroendocrinology, 43. Szigony Street, Budapest 1083, Hungary.
Miklós MézesSzent István University, Department of Nutrition, 1. Páter K. Street, Gödöllő 2100, Hungary.ORCID 0000-0003-2323-833X
Krisztián BaloghSzent István University, Department of Nutrition, 1. Páter K. Street, Gödöllő 2100, Hungary.ORCID 0000-0002-9435-4568
Magyar Agrár- és Élettudományi Egyetem · HUHUN-REN Institute of Experimental Medicine · HUAgricultural Biotechnology Institute · HUCentral Environmental and Food Science Research Institute · HU

Funding

European Union and the European Social Fund EFOP-3.6.3-VEKOP-16-2017-00008Hungarian Research Fund OTKA 109622Hungarian Research Fund OTKA 109744NVKP NVKP- 16-1-2016-0009
6 · The paper itself

Abstract

Ochratoxin-A (OTA) is a carcinogenic and nephrotoxic mycotoxin, which may cause health problems in humans and animals, and it is a contaminant in foods and feeds. The purpose of the present study is to evaluate the effect of oral OTA exposure on the antioxidant defense and lipid peroxidation in the kidney. In vivo administration of OTA in CD1, male mice (1 or 10 mg/kg body weight in a single oral dose for 24 h and repeated daily oral dose for 72 h or repeated daily oral dose of 0.5 mg/kg bodyweight for 21 days) resulted in a significant elevation of OTA levels in blood plasma. Some histopathological alterations, transcriptional changes in the glutathione system, and oxidative stress response-related genes were also found. In the renal cortex, the activity of the glutathione-system-related enzymes and certain metabolites of the lipid peroxidation (conjugated dienes, trienes, and thiobarbituric reactive substances) also changed.

Indexed as

AnimalsGlutathioneKelch-Like ECH-Associated Protein 1KidneyLipid PeroxidationMaleMiceOchratoxinsOxidative StressOxidoreductasesGlutathioneKeap1 protein, mouseKelch-Like ECH-Associated Protein 1ochratoxin AOchratoxinsOxidoreductasesgene expressionglutathionekidneyochratoxin-Aoxidative stress

Identifiers

PMID33266415
PMCPMC7700583
OpenAlexW3106627542

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.