Cargando…

Silver nanoparticles cause complications in pregnant mice

BACKGROUND: Silver nanoparticles (AgNPs) have attracted much interest and have been used for antibacterial, antifungal, anticancer, and antiangiogenic applications because of their unique properties. The increased usage of AgNPs leads to a potential hazard to human health. However, the potential eff...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Xi-Feng, Park, Jung-Hyun, Choi, Yun-Jung, Kang, Min-Hee, Gurunathan, Sangiliyandi, Kim, Jin-Hoi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4654536/
https://www.ncbi.nlm.nih.gov/pubmed/26622177
http://dx.doi.org/10.2147/IJN.S95694
_version_ 1782402072491065344
author Zhang, Xi-Feng
Park, Jung-Hyun
Choi, Yun-Jung
Kang, Min-Hee
Gurunathan, Sangiliyandi
Kim, Jin-Hoi
author_facet Zhang, Xi-Feng
Park, Jung-Hyun
Choi, Yun-Jung
Kang, Min-Hee
Gurunathan, Sangiliyandi
Kim, Jin-Hoi
author_sort Zhang, Xi-Feng
collection PubMed
description BACKGROUND: Silver nanoparticles (AgNPs) have attracted much interest and have been used for antibacterial, antifungal, anticancer, and antiangiogenic applications because of their unique properties. The increased usage of AgNPs leads to a potential hazard to human health. However, the potential effects of AgNPs on animal models are not clear. This study was designed to investigate the potential impact of AgNPs on pregnant mice. METHODS: The synthesis of AgNPs was performed using culture extracts of Bacillus cereus. The synthesized AgNPs were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, and transmission electron microscopy. AgNPs were administrated into pregnant mice via intravenous infusion at 1.0 mg/kg doses at 6.5 days postcoitum (dpc). At 13.5, 15.5, and 17.5 dpc, the pregnant mice were euthanized, and the embryo and placenta were isolated. The meiotic status of oocytes was evaluated. DNA methylation studies were performed, and aberrant imprinting disrupted fetal, placental, and postnatal development. Quantitative real-time polymerase chain reaction analysis and Western blot were used to analyze various gene expressions. RESULTS: The synthesized AgNPs were uniformly distributed and were spherical in shape with an average size of 8 nm. AgNPs exposure increased the meiotic progression of female germ cells in the fetal mouse ovaries, and maternal AgNP exposure significantly disrupted imprinted gene expression in 15.5 dpc embryos and placentas, such as Ascl2, Snrpn, Kcnq1ot1, Peg3, Zac1, H19, Igf2r, and Igf2; DNA methylation studies revealed that AgNPs exposure significantly altered the methylation levels of differentially methylated regions of Zac1. CONCLUSION: The results from this study indicated that early exposure to AgNPs has the potential to disrupt fetal and postnatal health through epigenetic changes in the embryo and abnormal development of the placenta. These results can contribute to research involved in the safe use of various biomedical applications of AgNPs and improves the understanding of the development of AgNPs in biomedical applications.
format Online
Article
Text
id pubmed-4654536
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-46545362015-11-30 Silver nanoparticles cause complications in pregnant mice Zhang, Xi-Feng Park, Jung-Hyun Choi, Yun-Jung Kang, Min-Hee Gurunathan, Sangiliyandi Kim, Jin-Hoi Int J Nanomedicine Original Research BACKGROUND: Silver nanoparticles (AgNPs) have attracted much interest and have been used for antibacterial, antifungal, anticancer, and antiangiogenic applications because of their unique properties. The increased usage of AgNPs leads to a potential hazard to human health. However, the potential effects of AgNPs on animal models are not clear. This study was designed to investigate the potential impact of AgNPs on pregnant mice. METHODS: The synthesis of AgNPs was performed using culture extracts of Bacillus cereus. The synthesized AgNPs were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, and transmission electron microscopy. AgNPs were administrated into pregnant mice via intravenous infusion at 1.0 mg/kg doses at 6.5 days postcoitum (dpc). At 13.5, 15.5, and 17.5 dpc, the pregnant mice were euthanized, and the embryo and placenta were isolated. The meiotic status of oocytes was evaluated. DNA methylation studies were performed, and aberrant imprinting disrupted fetal, placental, and postnatal development. Quantitative real-time polymerase chain reaction analysis and Western blot were used to analyze various gene expressions. RESULTS: The synthesized AgNPs were uniformly distributed and were spherical in shape with an average size of 8 nm. AgNPs exposure increased the meiotic progression of female germ cells in the fetal mouse ovaries, and maternal AgNP exposure significantly disrupted imprinted gene expression in 15.5 dpc embryos and placentas, such as Ascl2, Snrpn, Kcnq1ot1, Peg3, Zac1, H19, Igf2r, and Igf2; DNA methylation studies revealed that AgNPs exposure significantly altered the methylation levels of differentially methylated regions of Zac1. CONCLUSION: The results from this study indicated that early exposure to AgNPs has the potential to disrupt fetal and postnatal health through epigenetic changes in the embryo and abnormal development of the placenta. These results can contribute to research involved in the safe use of various biomedical applications of AgNPs and improves the understanding of the development of AgNPs in biomedical applications. Dove Medical Press 2015-11-13 /pmc/articles/PMC4654536/ /pubmed/26622177 http://dx.doi.org/10.2147/IJN.S95694 Text en © 2015 Zhang 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
Zhang, Xi-Feng
Park, Jung-Hyun
Choi, Yun-Jung
Kang, Min-Hee
Gurunathan, Sangiliyandi
Kim, Jin-Hoi
Silver nanoparticles cause complications in pregnant mice
title Silver nanoparticles cause complications in pregnant mice
title_full Silver nanoparticles cause complications in pregnant mice
title_fullStr Silver nanoparticles cause complications in pregnant mice
title_full_unstemmed Silver nanoparticles cause complications in pregnant mice
title_short Silver nanoparticles cause complications in pregnant mice
title_sort silver nanoparticles cause complications in pregnant mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4654536/
https://www.ncbi.nlm.nih.gov/pubmed/26622177
http://dx.doi.org/10.2147/IJN.S95694
work_keys_str_mv AT zhangxifeng silvernanoparticlescausecomplicationsinpregnantmice
AT parkjunghyun silvernanoparticlescausecomplicationsinpregnantmice
AT choiyunjung silvernanoparticlescausecomplicationsinpregnantmice
AT kangminhee silvernanoparticlescausecomplicationsinpregnantmice
AT gurunathansangiliyandi silvernanoparticlescausecomplicationsinpregnantmice
AT kimjinhoi silvernanoparticlescausecomplicationsinpregnantmice