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Combinatory Effects of Cerium Dioxide Nanoparticles and Acetaminophen on the Liver—A Case Study of Low-Dose Interactions in Human HuH-7 Cells

The interactions between pharmaceuticals and nanomaterials and its potentially resulting toxicological effects in living systems are only insufficiently investigated. In this study, two model compounds, acetaminophen, a pharmaceutical, and cerium dioxide, a manufactured nanomaterial, were investigat...

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Autores principales: Krause, Benjamin C., Kriegel, Fabian L., Tartz, Victoria, Jungnickel, Harald, Reichardt, Philipp, Singh, Ajay Vikram, Laux, Peter, Shemis, Mohamed, Luch, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268126/
https://www.ncbi.nlm.nih.gov/pubmed/34202329
http://dx.doi.org/10.3390/ijms22136866
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author Krause, Benjamin C.
Kriegel, Fabian L.
Tartz, Victoria
Jungnickel, Harald
Reichardt, Philipp
Singh, Ajay Vikram
Laux, Peter
Shemis, Mohamed
Luch, Andreas
author_facet Krause, Benjamin C.
Kriegel, Fabian L.
Tartz, Victoria
Jungnickel, Harald
Reichardt, Philipp
Singh, Ajay Vikram
Laux, Peter
Shemis, Mohamed
Luch, Andreas
author_sort Krause, Benjamin C.
collection PubMed
description The interactions between pharmaceuticals and nanomaterials and its potentially resulting toxicological effects in living systems are only insufficiently investigated. In this study, two model compounds, acetaminophen, a pharmaceutical, and cerium dioxide, a manufactured nanomaterial, were investigated in combination and individually. Upon inhalation, cerium dioxide nanomaterials were shown to systemically translocate into other organs, such as the liver. Therefore we picked the human liver cell line HuH-7 cells as an in vitro system to investigate liver toxicity. Possible synergistic or antagonistic metabolic changes after co-exposure scenarios were investigated. Toxicological data of the water soluble tetrazolium (WST-1) assay for cell proliferation and genotoxicity assessment using the Comet assay were combined with an untargeted as well as a targeted lipidomics approach. We found an attenuated cytotoxicity and an altered metabolic profile in co-exposure experiments with cerium dioxide, indicating an interaction of both compounds at these endpoints. Single exposure against cerium dioxide showed a genotoxic effect in the Comet assay. Conversely, acetaminophen exhibited no genotoxic effect. Comet assay data do not indicate an enhancement of genotoxicity after co-exposure. The results obtained in this study highlight the advantage of investigating co-exposure scenarios, especially for bioactive substances.
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spelling pubmed-82681262021-07-10 Combinatory Effects of Cerium Dioxide Nanoparticles and Acetaminophen on the Liver—A Case Study of Low-Dose Interactions in Human HuH-7 Cells Krause, Benjamin C. Kriegel, Fabian L. Tartz, Victoria Jungnickel, Harald Reichardt, Philipp Singh, Ajay Vikram Laux, Peter Shemis, Mohamed Luch, Andreas Int J Mol Sci Article The interactions between pharmaceuticals and nanomaterials and its potentially resulting toxicological effects in living systems are only insufficiently investigated. In this study, two model compounds, acetaminophen, a pharmaceutical, and cerium dioxide, a manufactured nanomaterial, were investigated in combination and individually. Upon inhalation, cerium dioxide nanomaterials were shown to systemically translocate into other organs, such as the liver. Therefore we picked the human liver cell line HuH-7 cells as an in vitro system to investigate liver toxicity. Possible synergistic or antagonistic metabolic changes after co-exposure scenarios were investigated. Toxicological data of the water soluble tetrazolium (WST-1) assay for cell proliferation and genotoxicity assessment using the Comet assay were combined with an untargeted as well as a targeted lipidomics approach. We found an attenuated cytotoxicity and an altered metabolic profile in co-exposure experiments with cerium dioxide, indicating an interaction of both compounds at these endpoints. Single exposure against cerium dioxide showed a genotoxic effect in the Comet assay. Conversely, acetaminophen exhibited no genotoxic effect. Comet assay data do not indicate an enhancement of genotoxicity after co-exposure. The results obtained in this study highlight the advantage of investigating co-exposure scenarios, especially for bioactive substances. MDPI 2021-06-25 /pmc/articles/PMC8268126/ /pubmed/34202329 http://dx.doi.org/10.3390/ijms22136866 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Krause, Benjamin C.
Kriegel, Fabian L.
Tartz, Victoria
Jungnickel, Harald
Reichardt, Philipp
Singh, Ajay Vikram
Laux, Peter
Shemis, Mohamed
Luch, Andreas
Combinatory Effects of Cerium Dioxide Nanoparticles and Acetaminophen on the Liver—A Case Study of Low-Dose Interactions in Human HuH-7 Cells
title Combinatory Effects of Cerium Dioxide Nanoparticles and Acetaminophen on the Liver—A Case Study of Low-Dose Interactions in Human HuH-7 Cells
title_full Combinatory Effects of Cerium Dioxide Nanoparticles and Acetaminophen on the Liver—A Case Study of Low-Dose Interactions in Human HuH-7 Cells
title_fullStr Combinatory Effects of Cerium Dioxide Nanoparticles and Acetaminophen on the Liver—A Case Study of Low-Dose Interactions in Human HuH-7 Cells
title_full_unstemmed Combinatory Effects of Cerium Dioxide Nanoparticles and Acetaminophen on the Liver—A Case Study of Low-Dose Interactions in Human HuH-7 Cells
title_short Combinatory Effects of Cerium Dioxide Nanoparticles and Acetaminophen on the Liver—A Case Study of Low-Dose Interactions in Human HuH-7 Cells
title_sort combinatory effects of cerium dioxide nanoparticles and acetaminophen on the liver—a case study of low-dose interactions in human huh-7 cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268126/
https://www.ncbi.nlm.nih.gov/pubmed/34202329
http://dx.doi.org/10.3390/ijms22136866
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