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Identification of potential biomarkers of gold nanoparticle toxicity in rat brains

BACKGROUND: Gold nanoparticles (AuNPs) are finding increased use in therapeutics and imaging. However, their toxic effects still remain to be elucidated. Therefore this study was undertaken to study the biochemical effects of AuNPs on rat brain and identify potential biomarkers of AuNP toxicity. MET...

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Autores principales: Siddiqi, Nikhat J, Abdelhalim, Mohamed Anwar K, El-Ansary, Afaf K, Alhomida, Abdullah S, Ong, W Y
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3423006/
https://www.ncbi.nlm.nih.gov/pubmed/22691312
http://dx.doi.org/10.1186/1742-2094-9-123
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author Siddiqi, Nikhat J
Abdelhalim, Mohamed Anwar K
El-Ansary, Afaf K
Alhomida, Abdullah S
Ong, W Y
author_facet Siddiqi, Nikhat J
Abdelhalim, Mohamed Anwar K
El-Ansary, Afaf K
Alhomida, Abdullah S
Ong, W Y
author_sort Siddiqi, Nikhat J
collection PubMed
description BACKGROUND: Gold nanoparticles (AuNPs) are finding increased use in therapeutics and imaging. However, their toxic effects still remain to be elucidated. Therefore this study was undertaken to study the biochemical effects of AuNPs on rat brain and identify potential biomarkers of AuNP toxicity. METHODS: Male Wister rats weighing 150–200 g were injected with 20 μg/kg body weight of 20-nm gold nanoparticles for 3 days through the intraperitoneal route. The rats were killed by carbon dioxide asphyxiation 24 h after the last dose of gold nanoparticle injection. The parameters studied included lipid peroxidation, glutathione peroxidase, 8- hydroxydeoxyguanosine, caspase-3, heat shock protein70, serotonin, dopamine, gamma amino-butyric acid and interferon-γ. RESULTS: In this study AuNPs caused generation of oxidative stress and a decrease of antioxidant enzyme, viz., glutathione peroxidase activity in rat brain. This was accompanied by an increase in 8-hydroxydeoxyguanosine, caspase-3 and heat shock protein70, which might lead to DNA damage and cell death. Gold nanoparticles also caused a significant decrease in the levels of neurotransmitters like dopamine and serotonin, indicating a possible change in the behavior of the treated animals. There was a significant increase in the cerebral levels of IFN-γ in treated animals. CONCLUSION: This study concludes that AuNPs cause generation of oxidative stress and an impairment of the antioxidant enzyme glutathione peroxidase in rat brain. AuNPs also cause generation of 8-hydroxydeoxyguanosine (8OHdG), caspase-3 and heat shock protein70 (Hsp70), and IFN-γ, which may lead to inflammation and DNA damage/cell death.
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spelling pubmed-34230062012-08-21 Identification of potential biomarkers of gold nanoparticle toxicity in rat brains Siddiqi, Nikhat J Abdelhalim, Mohamed Anwar K El-Ansary, Afaf K Alhomida, Abdullah S Ong, W Y J Neuroinflammation Research BACKGROUND: Gold nanoparticles (AuNPs) are finding increased use in therapeutics and imaging. However, their toxic effects still remain to be elucidated. Therefore this study was undertaken to study the biochemical effects of AuNPs on rat brain and identify potential biomarkers of AuNP toxicity. METHODS: Male Wister rats weighing 150–200 g were injected with 20 μg/kg body weight of 20-nm gold nanoparticles for 3 days through the intraperitoneal route. The rats were killed by carbon dioxide asphyxiation 24 h after the last dose of gold nanoparticle injection. The parameters studied included lipid peroxidation, glutathione peroxidase, 8- hydroxydeoxyguanosine, caspase-3, heat shock protein70, serotonin, dopamine, gamma amino-butyric acid and interferon-γ. RESULTS: In this study AuNPs caused generation of oxidative stress and a decrease of antioxidant enzyme, viz., glutathione peroxidase activity in rat brain. This was accompanied by an increase in 8-hydroxydeoxyguanosine, caspase-3 and heat shock protein70, which might lead to DNA damage and cell death. Gold nanoparticles also caused a significant decrease in the levels of neurotransmitters like dopamine and serotonin, indicating a possible change in the behavior of the treated animals. There was a significant increase in the cerebral levels of IFN-γ in treated animals. CONCLUSION: This study concludes that AuNPs cause generation of oxidative stress and an impairment of the antioxidant enzyme glutathione peroxidase in rat brain. AuNPs also cause generation of 8-hydroxydeoxyguanosine (8OHdG), caspase-3 and heat shock protein70 (Hsp70), and IFN-γ, which may lead to inflammation and DNA damage/cell death. BioMed Central 2012-06-12 /pmc/articles/PMC3423006/ /pubmed/22691312 http://dx.doi.org/10.1186/1742-2094-9-123 Text en Copyright ©2012 Siddiqi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Siddiqi, Nikhat J
Abdelhalim, Mohamed Anwar K
El-Ansary, Afaf K
Alhomida, Abdullah S
Ong, W Y
Identification of potential biomarkers of gold nanoparticle toxicity in rat brains
title Identification of potential biomarkers of gold nanoparticle toxicity in rat brains
title_full Identification of potential biomarkers of gold nanoparticle toxicity in rat brains
title_fullStr Identification of potential biomarkers of gold nanoparticle toxicity in rat brains
title_full_unstemmed Identification of potential biomarkers of gold nanoparticle toxicity in rat brains
title_short Identification of potential biomarkers of gold nanoparticle toxicity in rat brains
title_sort identification of potential biomarkers of gold nanoparticle toxicity in rat brains
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3423006/
https://www.ncbi.nlm.nih.gov/pubmed/22691312
http://dx.doi.org/10.1186/1742-2094-9-123
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