2009
DOI: 10.1186/1743-8977-6-20
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Maternal exposure to nanoparticulate titanium dioxide during the prenatal period alters gene expression related to brain development in the mouse

Abstract: Background: Nanotechnology is developing rapidly throughout the world and the production of novel man-made nanoparticles is increasing, it is therefore of concern that nanomaterials have the potential to affect human health. The purpose of this study was to investigate the effects of maternal exposure to nano-sized anatase titanium dioxide (TiO 2 ) on gene expression in the brain during the developmental period using cDNA microarray analysis combined with Gene Ontology (GO) and Medical Subject Headings (MeSH) … Show more

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Cited by 227 publications
(163 citation statements)
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“…In fact, TNPs were shown to be transferred from pregnant mice to their pups [70][71][72][73]. When pregnant mice were treated with TNPs via subcutaneous injection, the genital and cranial nerve systems of the male offspring were affected [70].…”
Section: Developmental Toxicitymentioning
confidence: 99%
“…In fact, TNPs were shown to be transferred from pregnant mice to their pups [70][71][72][73]. When pregnant mice were treated with TNPs via subcutaneous injection, the genital and cranial nerve systems of the male offspring were affected [70].…”
Section: Developmental Toxicitymentioning
confidence: 99%
“…Так, ранее было показано, что подкожное введение беременным самкам мышей НЧ TiO2 приводит к определенным повреждениям репродуктивных органов и нейронов центральной нервной системы потомства [22]. По данным этих авторов подкожная инъекция беременным самкам мышей наноформы диоксида титана вызывает изменение экспрессии генов, связанных с развитием мозга, гибелью нейронов, оксидативным стрессом и повышением активности митохондрий в головном мозге в перинатальный период.…”
Section: рисunclassified
“…Moreover, they depend on experimental conditions, the route of administration and NP type. However, recent studies imply that NP toxicity might be mediated by oxidative stress and inflammation (Shimizu et al 2009;Wang et al 2010), cell growth inhibition, enhanced apoptotic processes (Hsieh et al 2009;Guo et al 2011), necrosis (KingHeiden et al 2009), and/or DNA damage (Wang et al 2010).…”
Section: Effects Of Nanoparticles On Embryogenesismentioning
confidence: 99%
“…The human placental perfusion model was successfully used in NP transplacental transfer studies and the experimental conditions can be sufficiently maintained to obtain reproducible results, therefore the placental perfusion model could be standardized for the assessment of NP transplacental passage. However placental barrier physiology highly depends on the gestation period (Gude et al 2004;Shimizu et al 2009) what raises the need for other experimental models that would produce data on NP passage in early stages of embryogenesis.…”
Section: Effects Of Nanoparticles On Embryogenesismentioning
confidence: 99%