2010
DOI: 10.1016/j.reprotox.2010.06.002
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Reproductive and developmental toxicity studies of manufactured nanomaterials

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Cited by 225 publications
(135 citation statements)
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“…Several researchers have expressed concern about the possible adverse effects of nanoparticles on human health because of their ability to pass through biological membranes (132)(133)(134) and "translocate through the circulatory, lymphatic, and nervous systems to many tissues and organs" (132). Potential reproductive and developmental toxicity of manufactured nanomaterials was investigated in several experimental in vivo and in vitro studies reviewed by Ema et al (135). It was found that "high concentrations of TiO 2 nanoparticles affect the viability and proliferation of mouse Leydig cells, that gold nanoparticles reduced the motility of human sperm, that silver, aluminium, and molybdenum trioxide were toxic to mouse spermatogonia stem cells, that silica nanoparticles inhibited the differentiation of mouse embryonic stem cells and midbrain cells, respectively, and that cadmium selenium-core quantum dots inhibited pre-and postimplantation development of mouse embryos".…”
Section: Reproductive Effects Of Exposure To Metals As Nanoparticlesmentioning
confidence: 99%
“…Several researchers have expressed concern about the possible adverse effects of nanoparticles on human health because of their ability to pass through biological membranes (132)(133)(134) and "translocate through the circulatory, lymphatic, and nervous systems to many tissues and organs" (132). Potential reproductive and developmental toxicity of manufactured nanomaterials was investigated in several experimental in vivo and in vitro studies reviewed by Ema et al (135). It was found that "high concentrations of TiO 2 nanoparticles affect the viability and proliferation of mouse Leydig cells, that gold nanoparticles reduced the motility of human sperm, that silver, aluminium, and molybdenum trioxide were toxic to mouse spermatogonia stem cells, that silica nanoparticles inhibited the differentiation of mouse embryonic stem cells and midbrain cells, respectively, and that cadmium selenium-core quantum dots inhibited pre-and postimplantation development of mouse embryos".…”
Section: Reproductive Effects Of Exposure To Metals As Nanoparticlesmentioning
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%
“…This finding can be explained by changes in the expression of genes associated with CNS development and function [72]. Maternal intranasal instillation with respirable TNPs increased allergic susceptibility [73] and caused pathologic and functional disorders and reduced daily sperm production in offspring [70].…”
Section: Developmental Toxicitymentioning
confidence: 99%
“…After fusion of the gametes, a series of reprogramming events is activated, which includes DNA methylation, protamine exchange, histone marks, embryonic genome activation and degradation of maternal and paternal transcripts and proteins (Bermejo- Alvarez et al 2008, Kues et al 2008a. A well-orchestrated succession of these events is required to allow normal development, potentially making gametes and early embryos vulnerable to NPs, which may accumulate in the reproductive tract or which are intentionally added to spermatozoa in vitro (Bonde 2010, Ema et al 2010, Schrand et al 2010.…”
Section: Sperm Toxicity Of Aunpsmentioning
confidence: 99%