Cargando…

Lufenuron induces reproductive toxicity and genotoxic effects in pregnant albino rats and their fetuses

Insecticides and other agrochemicals have become indispensable components of the agricultural system to ensure a notable increase in crop yield and food production. As a natural consequence, chemical residues result in significantly increased contamination of both terrestrial and aquatic ecosystems....

Descripción completa

Detalles Bibliográficos
Autores principales: Basal, Wesam T., Ahmed, Abdel Rahman T., Mahmoud, Aya A., Omar, Amel R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658361/
https://www.ncbi.nlm.nih.gov/pubmed/33177580
http://dx.doi.org/10.1038/s41598-020-76638-6
_version_ 1783608653574569984
author Basal, Wesam T.
Ahmed, Abdel Rahman T.
Mahmoud, Aya A.
Omar, Amel R.
author_facet Basal, Wesam T.
Ahmed, Abdel Rahman T.
Mahmoud, Aya A.
Omar, Amel R.
author_sort Basal, Wesam T.
collection PubMed
description Insecticides and other agrochemicals have become indispensable components of the agricultural system to ensure a notable increase in crop yield and food production. As a natural consequence, chemical residues result in significantly increased contamination of both terrestrial and aquatic ecosystems. The present study evaluated the teratogenic, genotoxic, and oxidative stress effects of residual-level lufenuron exposure on pregnant rats during the organogenesis gestational period of both mother and fetus. The tested dams were divided into three groups; control (untreated), low-dose group (orally administered with 0.4 mg/kg lufenuron) and high-dose group (orally administered with 0.8 mg/kg lufenuron). The dams of the two treatment groups showed teratogenic abnormalities represented by the asymmetrical distribution of fetuses in both uterine horns, accompanied by observed resorption sites and intensive bleeding in the uterine horns, whereas their fetuses suffered from growth retardation, morphologic malformations, and skeletal deformations. Histologic examination of the liver and kidney tissues obtained from mothers and fetuses after lufenuron exposure revealed multiple histopathologic changes. DNA fragmentation and cell cycle perturbation were also detected in the liver cells of lufenuron-treated pregnant dams and their fetuses through comet assay and flow cytometry, respectively. Moreover, lufenuron-induced oxidative stress in the liver of mothers and fetuses was confirmed by the increased malondialdehyde levels and decreased levels of enzymatic antioxidants (glutathione peroxidase and superoxide dismutase). Taken together, it can be concluded that lufenuron has a great potential in exerting teratogenic, genotoxic, and oxidative stresses on pregnant rats and their fetuses upon chronic exposure to residual levels during the organogenesis gestational period. The obtained results in the present study imply that women and their fetuses may have the same risk.
format Online
Article
Text
id pubmed-7658361
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-76583612020-11-13 Lufenuron induces reproductive toxicity and genotoxic effects in pregnant albino rats and their fetuses Basal, Wesam T. Ahmed, Abdel Rahman T. Mahmoud, Aya A. Omar, Amel R. Sci Rep Article Insecticides and other agrochemicals have become indispensable components of the agricultural system to ensure a notable increase in crop yield and food production. As a natural consequence, chemical residues result in significantly increased contamination of both terrestrial and aquatic ecosystems. The present study evaluated the teratogenic, genotoxic, and oxidative stress effects of residual-level lufenuron exposure on pregnant rats during the organogenesis gestational period of both mother and fetus. The tested dams were divided into three groups; control (untreated), low-dose group (orally administered with 0.4 mg/kg lufenuron) and high-dose group (orally administered with 0.8 mg/kg lufenuron). The dams of the two treatment groups showed teratogenic abnormalities represented by the asymmetrical distribution of fetuses in both uterine horns, accompanied by observed resorption sites and intensive bleeding in the uterine horns, whereas their fetuses suffered from growth retardation, morphologic malformations, and skeletal deformations. Histologic examination of the liver and kidney tissues obtained from mothers and fetuses after lufenuron exposure revealed multiple histopathologic changes. DNA fragmentation and cell cycle perturbation were also detected in the liver cells of lufenuron-treated pregnant dams and their fetuses through comet assay and flow cytometry, respectively. Moreover, lufenuron-induced oxidative stress in the liver of mothers and fetuses was confirmed by the increased malondialdehyde levels and decreased levels of enzymatic antioxidants (glutathione peroxidase and superoxide dismutase). Taken together, it can be concluded that lufenuron has a great potential in exerting teratogenic, genotoxic, and oxidative stresses on pregnant rats and their fetuses upon chronic exposure to residual levels during the organogenesis gestational period. The obtained results in the present study imply that women and their fetuses may have the same risk. Nature Publishing Group UK 2020-11-11 /pmc/articles/PMC7658361/ /pubmed/33177580 http://dx.doi.org/10.1038/s41598-020-76638-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Basal, Wesam T.
Ahmed, Abdel Rahman T.
Mahmoud, Aya A.
Omar, Amel R.
Lufenuron induces reproductive toxicity and genotoxic effects in pregnant albino rats and their fetuses
title Lufenuron induces reproductive toxicity and genotoxic effects in pregnant albino rats and their fetuses
title_full Lufenuron induces reproductive toxicity and genotoxic effects in pregnant albino rats and their fetuses
title_fullStr Lufenuron induces reproductive toxicity and genotoxic effects in pregnant albino rats and their fetuses
title_full_unstemmed Lufenuron induces reproductive toxicity and genotoxic effects in pregnant albino rats and their fetuses
title_short Lufenuron induces reproductive toxicity and genotoxic effects in pregnant albino rats and their fetuses
title_sort lufenuron induces reproductive toxicity and genotoxic effects in pregnant albino rats and their fetuses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658361/
https://www.ncbi.nlm.nih.gov/pubmed/33177580
http://dx.doi.org/10.1038/s41598-020-76638-6
work_keys_str_mv AT basalwesamt lufenuroninducesreproductivetoxicityandgenotoxiceffectsinpregnantalbinoratsandtheirfetuses
AT ahmedabdelrahmant lufenuroninducesreproductivetoxicityandgenotoxiceffectsinpregnantalbinoratsandtheirfetuses
AT mahmoudayaa lufenuroninducesreproductivetoxicityandgenotoxiceffectsinpregnantalbinoratsandtheirfetuses
AT omaramelr lufenuroninducesreproductivetoxicityandgenotoxiceffectsinpregnantalbinoratsandtheirfetuses