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Genotoxicity of synthetic amorphous silica nanoparticles in rats following short-term exposure. Part 1: Oral route

dc.contributor.authorTarantini, Adeline
dc.contributor.authorHuet, Sylvie
dc.contributor.authorJarry, Gérard
dc.contributor.authorMartine, Poul
dc.contributor.authorTavares, Ana
dc.contributor.authorVital, Nádia
dc.contributor.authorLouro, Henriqueta
dc.contributor.authorSilva, Maria João
dc.contributor.authorFessard, Valérie
dc.date.accessioned2015-06-26T13:24:26Z
dc.date.available2015-06-26T13:24:26Z
dc.date.issued2015-03
dc.description.abstractSynthetic amorphous silica (SAS) in its nanosized form is now used in food applications although the potential risks for human health have not been evaluated. In this study, genotoxicity and oxidative DNA damage of two pyrogenic (NM-202 and 203) and two precipitated (NM-200 and -201) nanosized SAS were investigated in vivo in rats following oral exposure. Male Sprague Dawley rats were exposed to 5, 10, or 20 mg/kg b.w./day for three days by gavage. DNA strand breaks and oxidative DNA damage were investigated in seven tissues (blood, bone marrow from femur, liver,spleen, kidney, duodenum, and colon) with the alkaline and the (Fpg)-modified comet assays, respectively. Concomitantly, chromosomal damage was investigated in bone marrow and in colon with the micronucleus assay. Additionally, malondialdehyde (MDA), a lipid peroxidation marker, was measured in plasma. When required, a histopathological examination was also conducted. The results showed neither obvious DNA strand breaks nor oxidative damage with the comet assay, irrespective of the dose and the organ investigated. Similarly, no increases in chromosome damage in bone marrow or lipid peroxidation in plasma were detected. However, although the response was not dose-dependent, a weak increase in the percentage of micronucleated cells was observed in the colon of rats treated with the two pyrogenic SAS at the lowest dose (5 mg/kg b.w./day). Additional data are required to confirm this result, considering in particular, the role of agglomeration/aggregation of SAS NMs in their uptake by intestinal cells.por
dc.description.sponsorshipNANOGENOTOX Joint Action program (European Union in the framework of the Health Program and co-funded by the Executive Agency for Health and Consumers, grant agreement 2009 21 01).por
dc.identifier.citationEnviron Mol Mutagen. 2015 Mar;56(2):218-27. doi: 10.1002/em.21935. Epub 2014 Dec 15por
dc.identifier.doi10.1002/em.21935
dc.identifier.issn0893-6692
dc.identifier.urihttp://hdl.handle.net/10400.18/3089
dc.language.isoporpor
dc.peerreviewedyespor
dc.publisherWileypor
dc.relation.publisherversionhttp://onlinelibrary.wiley.com/doi/10.1002/em.21935/abstract;jsessionid=D754FB6D0A9F4EED8476E674BCEABA76.f04t01por
dc.subjectGenotoxicidade Ambientalpor
dc.subjectGenotoxicitypor
dc.subjectSilica Nanomaterialspor
dc.subjectComet Assaypor
dc.subjectMicronucleus Assaypor
dc.subjectOxidative Stresspor
dc.titleGenotoxicity of synthetic amorphous silica nanoparticles in rats following short-term exposure. Part 1: Oral routepor
dc.typejournal article
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/EC/FP7/310584
oaire.citation.endPage227por
oaire.citation.startPage218por
oaire.citation.titleEnvironmental and Molecular Mutagenesispor
oaire.citation.volume56(2)por
oaire.fundingStreamFP7
project.funder.identifierhttp://doi.org/10.13039/501100008530
project.funder.nameEuropean Commission
rcaap.rightsembargoedAccesspor
rcaap.typearticlepor
relation.isProjectOfPublication2d38ab8a-f85d-4d44-95ed-3be9e1ba1508
relation.isProjectOfPublication.latestForDiscovery2d38ab8a-f85d-4d44-95ed-3be9e1ba1508

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