Animal performance and biochemical parameters are sex-dependent in peripubertal rats exposed to deoxynivalenol.


Journal

Toxicon : official journal of the International Society on Toxinology
ISSN: 1879-3150
Titre abrégé: Toxicon
Pays: England
ID NLM: 1307333

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 21 09 2022
accepted: 12 10 2022
pubmed: 23 10 2022
medline: 22 11 2022
entrez: 22 10 2022
Statut: ppublish

Résumé

Deoxynivalenol (DON), a mycotoxin produced mainly by Fusarium graminearum and F. culmorum commonly contaminates food commodities across the globe. Due to this, exposure to DON might pose potential health hazards to humans and animals. Biological factors like sex and age can influence the toxicity of DON. However, in toxicological studies involving DON, the sex and age-dependent response has been often overlooked. Thereby, the objective of this study was to evaluate if sex differences are evident in DON's systemic effects in peripubertal rats. Juvenile animals (n = 24) with 28 days postnatal day were randomly assigned to two experimental groups: Control group (n = 12, 6 females and 6 males, mycotoxin-free diet) and DON group (n = 12, 6 females and 6 males, diet containing 10 mg DON/kg of feed). During 28 days of treatment, the animals were weighed weekly and body weight gain and food intake were calculated for each week. After the experimental period, blood samples, intestine, liver, and kidney were collected and destined for biochemical, hematological, histopathological, and oxidative stress analyses. Greater anorectic responses were seen in males, while only females showed increased levels of creatinine and triglycerides. Regardless of sex, DON induces an increased number of white blood cells, particularly lymphocytes and a significant reduction in the levels of hemoglobin, hematocrit, mean corpuscular hemoglobin, and neutrophils. In males and females fed a DON-contaminated diet, histological lesions were observed in the intestine, liver, and kidney. Ingestion of DON induced a significant increase in the antioxidant potential in the intestine, liver, and kidney. However, this effect was not able to prevent oxidative stress in the renal tissue. Taken together, our results showed a sex-related response in food intake, weight gain, and biochemical parameters in rats exposed to DON during the juvenile and peripubertal periods. In addition, we have verified that oxidative stress is an important mechanism in the nephrotoxicity of DON.

Identifiants

pubmed: 36272502
pii: S0041-0101(22)00295-1
doi: 10.1016/j.toxicon.2022.106944
pii:
doi:

Substances chimiques

deoxynivalenol JT37HYP23V
Trichothecenes 0
Mycotoxins 0

Types de publication

Randomized Controlled Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106944

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Ana Paula F.R.L. Bracarense reports financial support was provided by Coordination of Higher Education Personnel Improvement. Ana Paula F.R.L. Bracarense reports financial support was provided by National Council for Scientific and Technological Development.

Auteurs

J R Gerez (JR)

Laboratory of Animal Pathology, Universidade Estadual de Londrina, Londrina, Paraná, 86057-970, Brazil.

W A Verri (WA)

Laboratory of Pain, Inflammation, Neuropathy and Cancer, Universidade Estadual de Londrina, Londrina, Paraná, 86057-970, Brazil.

M S Hohmann (MS)

Laboratory of Pain, Inflammation, Neuropathy and Cancer, Universidade Estadual de Londrina, Londrina, Paraná, 86057-970, Brazil.

K M C Flaiban (KMC)

Laboratory of Clinical Pathology, Universidade Estadual de Londrina, Londrina, Paraná, 86057-970, Brazil.

A L Hasuda (AL)

Laboratory of Clinical Pathology, Universidade Estadual de Londrina, Londrina, Paraná, 86057-970, Brazil.

E M Gloria (EM)

Laboratory of Mycology, Universidade de São Paulo, São Paulo, Brazil.

A P R L Bracarense (APRL)

Laboratory of Animal Pathology, Universidade Estadual de Londrina, Londrina, Paraná, 86057-970, Brazil. Electronic address: anapaula@uel.br.

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Classifications MeSH