Cargando…

In vivo DNA damaging and apoptotic potential of silver nanoparticles in Swiss albino mice

Nanoparticles can potentially cause adverse effects on organs, tissue, cell levels, and protein levels because of their physicochemical properties. Silver nanoparticles (AgNPs) are being used on a wide scale in world consumer markets; their potential hazards for humans remain largely unknown. This s...

Descripción completa

Detalles Bibliográficos
Autores principales: Al Gurabi, Mohammed A, Ali, Daoud, Alkahtani, Saad, Alarifi, Saud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4321656/
https://www.ncbi.nlm.nih.gov/pubmed/25674004
http://dx.doi.org/10.2147/OTT.S77572
_version_ 1782356294354599936
author Al Gurabi, Mohammed A
Ali, Daoud
Alkahtani, Saad
Alarifi, Saud
author_facet Al Gurabi, Mohammed A
Ali, Daoud
Alkahtani, Saad
Alarifi, Saud
author_sort Al Gurabi, Mohammed A
collection PubMed
description Nanoparticles can potentially cause adverse effects on organs, tissue, cell levels, and protein levels because of their physicochemical properties. Silver nanoparticles (AgNPs) are being used on a wide scale in world consumer markets; their potential hazards for humans remain largely unknown. This study aimed to investigate the intraperitoneal toxicity of AgNPs (26 mg per kg of body weight, 52 mg per kg of body weight, and 78 mg per kg of body weight) over 72 hours in Swiss albino mice. AgNPs induced a significant increase in serum liver injury markers including alkaline phosphatase, alanine aminotransferase, and aspartate aminotransferase. Induction of DNA damage was also studied in mice injected with AgNPs. Apoptosis (detected by using the terminal deoxynucleotidyl transferase deoxyuridine triphosphatase nick end labeling assay method) in liver tissue and DNA strand breaks (detected by using the comet assay method) in lymphocytes revealed that a concentration of 78 mg of AgNPs per kg body weight can cause significant apoptosis and DNA damage. The DNA damage and apoptosis raise the concern about the safety associated with application of the AgNPs. Significantly more alterations were induced in the hepatocytes of animals exposed to AgNP doses than in the control animals. The induced histological and apoptotic changes may be due to AgNP toxicity. Immunohistochemical and ultrastructural of AgNP.
format Online
Article
Text
id pubmed-4321656
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-43216562015-02-11 In vivo DNA damaging and apoptotic potential of silver nanoparticles in Swiss albino mice Al Gurabi, Mohammed A Ali, Daoud Alkahtani, Saad Alarifi, Saud Onco Targets Ther Original Research Nanoparticles can potentially cause adverse effects on organs, tissue, cell levels, and protein levels because of their physicochemical properties. Silver nanoparticles (AgNPs) are being used on a wide scale in world consumer markets; their potential hazards for humans remain largely unknown. This study aimed to investigate the intraperitoneal toxicity of AgNPs (26 mg per kg of body weight, 52 mg per kg of body weight, and 78 mg per kg of body weight) over 72 hours in Swiss albino mice. AgNPs induced a significant increase in serum liver injury markers including alkaline phosphatase, alanine aminotransferase, and aspartate aminotransferase. Induction of DNA damage was also studied in mice injected with AgNPs. Apoptosis (detected by using the terminal deoxynucleotidyl transferase deoxyuridine triphosphatase nick end labeling assay method) in liver tissue and DNA strand breaks (detected by using the comet assay method) in lymphocytes revealed that a concentration of 78 mg of AgNPs per kg body weight can cause significant apoptosis and DNA damage. The DNA damage and apoptosis raise the concern about the safety associated with application of the AgNPs. Significantly more alterations were induced in the hepatocytes of animals exposed to AgNP doses than in the control animals. The induced histological and apoptotic changes may be due to AgNP toxicity. Immunohistochemical and ultrastructural of AgNP. Dove Medical Press 2015-01-29 /pmc/articles/PMC4321656/ /pubmed/25674004 http://dx.doi.org/10.2147/OTT.S77572 Text en © 2015 Al Gurabi et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Al Gurabi, Mohammed A
Ali, Daoud
Alkahtani, Saad
Alarifi, Saud
In vivo DNA damaging and apoptotic potential of silver nanoparticles in Swiss albino mice
title In vivo DNA damaging and apoptotic potential of silver nanoparticles in Swiss albino mice
title_full In vivo DNA damaging and apoptotic potential of silver nanoparticles in Swiss albino mice
title_fullStr In vivo DNA damaging and apoptotic potential of silver nanoparticles in Swiss albino mice
title_full_unstemmed In vivo DNA damaging and apoptotic potential of silver nanoparticles in Swiss albino mice
title_short In vivo DNA damaging and apoptotic potential of silver nanoparticles in Swiss albino mice
title_sort in vivo dna damaging and apoptotic potential of silver nanoparticles in swiss albino mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4321656/
https://www.ncbi.nlm.nih.gov/pubmed/25674004
http://dx.doi.org/10.2147/OTT.S77572
work_keys_str_mv AT algurabimohammeda invivodnadamagingandapoptoticpotentialofsilvernanoparticlesinswissalbinomice
AT alidaoud invivodnadamagingandapoptoticpotentialofsilvernanoparticlesinswissalbinomice
AT alkahtanisaad invivodnadamagingandapoptoticpotentialofsilvernanoparticlesinswissalbinomice
AT alarifisaud invivodnadamagingandapoptoticpotentialofsilvernanoparticlesinswissalbinomice