Cargando…
Toxicity mechanisms of aflatoxin M(1) assisted with molecular docking and the toxicity-limiting role of trans-resveratrol
In this study, AFM(1) toxicity and the protective role of trans-resveratrol (t-rsv) against this toxicity were investigated with the help of multiple parameters in albino mice. As a result, AFM(1) (16 mg/kg b.w) administration caused a decrease in body, kidney and liver weights. This reduction was a...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411558/ https://www.ncbi.nlm.nih.gov/pubmed/36008536 http://dx.doi.org/10.1038/s41598-022-18791-8 |
_version_ | 1784775295967952896 |
---|---|
author | Güç, İlknur Yalçin, Emine Çavuşoğlu, Kültiğin Acar, Ali |
author_facet | Güç, İlknur Yalçin, Emine Çavuşoğlu, Kültiğin Acar, Ali |
author_sort | Güç, İlknur |
collection | PubMed |
description | In this study, AFM(1) toxicity and the protective role of trans-resveratrol (t-rsv) against this toxicity were investigated with the help of multiple parameters in albino mice. As a result, AFM(1) (16 mg/kg b.w) administration caused a decrease in body, kidney and liver weights. This reduction was associated with a decrease in feed consumption. AFM(1) induced an increase in AST and ALT enzyme parameters and BUN, creatinine and MDA levels and a decrease in GSH levels. These increases have been associated with liver and kidney cell damage. AFM(1) decreased MI and encouraged increases in MN and CAs numbers. The decrease in MI was correlated with AFM1-tubulin and the increase in CAs was associated with the AFM(1)-DNA interaction, which was demonstrated by molecular docking and spectral shifting. Besides, the decrease in DNA damage and amount was demonstrated by the comet assay technique. Administration of t-rsv (10 and 20 mg/kg b.w) reduced the toxic effects of AFM(1) and caused a dose-dependent improvement in all physiological, biochemical and cytogenetic parameter values studied. For this reason, foods containing t-rsv or food supplements should be consumed in the daily diet to reduce the effect of toxic agents. |
format | Online Article Text |
id | pubmed-9411558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94115582022-08-27 Toxicity mechanisms of aflatoxin M(1) assisted with molecular docking and the toxicity-limiting role of trans-resveratrol Güç, İlknur Yalçin, Emine Çavuşoğlu, Kültiğin Acar, Ali Sci Rep Article In this study, AFM(1) toxicity and the protective role of trans-resveratrol (t-rsv) against this toxicity were investigated with the help of multiple parameters in albino mice. As a result, AFM(1) (16 mg/kg b.w) administration caused a decrease in body, kidney and liver weights. This reduction was associated with a decrease in feed consumption. AFM(1) induced an increase in AST and ALT enzyme parameters and BUN, creatinine and MDA levels and a decrease in GSH levels. These increases have been associated with liver and kidney cell damage. AFM(1) decreased MI and encouraged increases in MN and CAs numbers. The decrease in MI was correlated with AFM1-tubulin and the increase in CAs was associated with the AFM(1)-DNA interaction, which was demonstrated by molecular docking and spectral shifting. Besides, the decrease in DNA damage and amount was demonstrated by the comet assay technique. Administration of t-rsv (10 and 20 mg/kg b.w) reduced the toxic effects of AFM(1) and caused a dose-dependent improvement in all physiological, biochemical and cytogenetic parameter values studied. For this reason, foods containing t-rsv or food supplements should be consumed in the daily diet to reduce the effect of toxic agents. Nature Publishing Group UK 2022-08-25 /pmc/articles/PMC9411558/ /pubmed/36008536 http://dx.doi.org/10.1038/s41598-022-18791-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Güç, İlknur Yalçin, Emine Çavuşoğlu, Kültiğin Acar, Ali Toxicity mechanisms of aflatoxin M(1) assisted with molecular docking and the toxicity-limiting role of trans-resveratrol |
title | Toxicity mechanisms of aflatoxin M(1) assisted with molecular docking and the toxicity-limiting role of trans-resveratrol |
title_full | Toxicity mechanisms of aflatoxin M(1) assisted with molecular docking and the toxicity-limiting role of trans-resveratrol |
title_fullStr | Toxicity mechanisms of aflatoxin M(1) assisted with molecular docking and the toxicity-limiting role of trans-resveratrol |
title_full_unstemmed | Toxicity mechanisms of aflatoxin M(1) assisted with molecular docking and the toxicity-limiting role of trans-resveratrol |
title_short | Toxicity mechanisms of aflatoxin M(1) assisted with molecular docking and the toxicity-limiting role of trans-resveratrol |
title_sort | toxicity mechanisms of aflatoxin m(1) assisted with molecular docking and the toxicity-limiting role of trans-resveratrol |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411558/ https://www.ncbi.nlm.nih.gov/pubmed/36008536 http://dx.doi.org/10.1038/s41598-022-18791-8 |
work_keys_str_mv | AT gucilknur toxicitymechanismsofaflatoxinm1assistedwithmoleculardockingandthetoxicitylimitingroleoftransresveratrol AT yalcinemine toxicitymechanismsofaflatoxinm1assistedwithmoleculardockingandthetoxicitylimitingroleoftransresveratrol AT cavusoglukultigin toxicitymechanismsofaflatoxinm1assistedwithmoleculardockingandthetoxicitylimitingroleoftransresveratrol AT acarali toxicitymechanismsofaflatoxinm1assistedwithmoleculardockingandthetoxicitylimitingroleoftransresveratrol |