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Cadmium sulfide-induced toxicity in the cortex and cerebellum: In vitro and in vivo studies

Living organisms have an innate ability to regulate the synthesis of inorganic materials, such as bones and teeth in humans. Cadmium sulfide (CdS) can be utilized as a quantum dot that functions as a unique light-emitting semiconductor nanocrystal. The increased use in CdS has led to an increased in...

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Autores principales: Varmazyari, Atefeh, Taghizadehghalehjoughi, Ali, Sevim, Cigdem, Baris, Ozlem, Eser, Gizem, Yildirim, Serkan, Hacimuftuoglu, Ahmet, Buha, Aleksandra, Wallace, David R., Tsatsakis, Aristidis, Aschner, Michael, Mezhuev, Yaroslav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260592/
https://www.ncbi.nlm.nih.gov/pubmed/32489905
http://dx.doi.org/10.1016/j.toxrep.2020.04.011
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author Varmazyari, Atefeh
Taghizadehghalehjoughi, Ali
Sevim, Cigdem
Baris, Ozlem
Eser, Gizem
Yildirim, Serkan
Hacimuftuoglu, Ahmet
Buha, Aleksandra
Wallace, David R.
Tsatsakis, Aristidis
Aschner, Michael
Mezhuev, Yaroslav
author_facet Varmazyari, Atefeh
Taghizadehghalehjoughi, Ali
Sevim, Cigdem
Baris, Ozlem
Eser, Gizem
Yildirim, Serkan
Hacimuftuoglu, Ahmet
Buha, Aleksandra
Wallace, David R.
Tsatsakis, Aristidis
Aschner, Michael
Mezhuev, Yaroslav
author_sort Varmazyari, Atefeh
collection PubMed
description Living organisms have an innate ability to regulate the synthesis of inorganic materials, such as bones and teeth in humans. Cadmium sulfide (CdS) can be utilized as a quantum dot that functions as a unique light-emitting semiconductor nanocrystal. The increased use in CdS has led to an increased inhalation and ingestion rate of CdS by humans which requires a broader appreciation for the acute and chronic toxicity of CdS. We investigated the toxic effects of CdS on cerebellar cell cultures and rat brain. We employed a ‘green synthesis’ biosynthesis process to obtain biocompatible material that can be used in living organisms, such as Viridibacillus arenosi K64. Nanocrystal formation was initiated by adding CdCl(2) (1 mM) to the cell cultures. Our in vitro results established that increased concentrations of CdS (0.1 μg/mL) lead to decreased cell viability as assessed using 3-[4,5-dimethylthiazole-2-yl]-2,5-diphenyltetrazolium bromide (MTT), total antioxidant capacity (TAC), and total oxidant status (TOS). The in vivo studies showed that exposure to CdS (1 mg/kg) glial fibrillary acidic protein (GFAP) and 8-hydroxy-2' -deoxyguanosine (8-OHdG) were increased. Collectively, we describe a model system that addresses the process from the synthesis to the neurotoxicity assessment for CdS both in vitro and in vivo. These data will be beneficial in establishing a more comprehensive pathway for the understanding of quantum dot-induced neurotoxicity.
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spelling pubmed-72605922020-06-01 Cadmium sulfide-induced toxicity in the cortex and cerebellum: In vitro and in vivo studies Varmazyari, Atefeh Taghizadehghalehjoughi, Ali Sevim, Cigdem Baris, Ozlem Eser, Gizem Yildirim, Serkan Hacimuftuoglu, Ahmet Buha, Aleksandra Wallace, David R. Tsatsakis, Aristidis Aschner, Michael Mezhuev, Yaroslav Toxicol Rep Regular Article Living organisms have an innate ability to regulate the synthesis of inorganic materials, such as bones and teeth in humans. Cadmium sulfide (CdS) can be utilized as a quantum dot that functions as a unique light-emitting semiconductor nanocrystal. The increased use in CdS has led to an increased inhalation and ingestion rate of CdS by humans which requires a broader appreciation for the acute and chronic toxicity of CdS. We investigated the toxic effects of CdS on cerebellar cell cultures and rat brain. We employed a ‘green synthesis’ biosynthesis process to obtain biocompatible material that can be used in living organisms, such as Viridibacillus arenosi K64. Nanocrystal formation was initiated by adding CdCl(2) (1 mM) to the cell cultures. Our in vitro results established that increased concentrations of CdS (0.1 μg/mL) lead to decreased cell viability as assessed using 3-[4,5-dimethylthiazole-2-yl]-2,5-diphenyltetrazolium bromide (MTT), total antioxidant capacity (TAC), and total oxidant status (TOS). The in vivo studies showed that exposure to CdS (1 mg/kg) glial fibrillary acidic protein (GFAP) and 8-hydroxy-2' -deoxyguanosine (8-OHdG) were increased. Collectively, we describe a model system that addresses the process from the synthesis to the neurotoxicity assessment for CdS both in vitro and in vivo. These data will be beneficial in establishing a more comprehensive pathway for the understanding of quantum dot-induced neurotoxicity. Elsevier 2020-05-06 /pmc/articles/PMC7260592/ /pubmed/32489905 http://dx.doi.org/10.1016/j.toxrep.2020.04.011 Text en © 2020 Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Varmazyari, Atefeh
Taghizadehghalehjoughi, Ali
Sevim, Cigdem
Baris, Ozlem
Eser, Gizem
Yildirim, Serkan
Hacimuftuoglu, Ahmet
Buha, Aleksandra
Wallace, David R.
Tsatsakis, Aristidis
Aschner, Michael
Mezhuev, Yaroslav
Cadmium sulfide-induced toxicity in the cortex and cerebellum: In vitro and in vivo studies
title Cadmium sulfide-induced toxicity in the cortex and cerebellum: In vitro and in vivo studies
title_full Cadmium sulfide-induced toxicity in the cortex and cerebellum: In vitro and in vivo studies
title_fullStr Cadmium sulfide-induced toxicity in the cortex and cerebellum: In vitro and in vivo studies
title_full_unstemmed Cadmium sulfide-induced toxicity in the cortex and cerebellum: In vitro and in vivo studies
title_short Cadmium sulfide-induced toxicity in the cortex and cerebellum: In vitro and in vivo studies
title_sort cadmium sulfide-induced toxicity in the cortex and cerebellum: in vitro and in vivo studies
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260592/
https://www.ncbi.nlm.nih.gov/pubmed/32489905
http://dx.doi.org/10.1016/j.toxrep.2020.04.011
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