Hazardous impacts of silver nanoparticles on mouse oocyte maturation and fertilization and fetal development through induction of apoptotic processes

• Published in: Environmental toxicology Vol. 33; no. 10; pp. 1039 - 1049
• Main Authors: Huang, Chien-Hsun, Yeh, Jui-Ming, Chan, Wen-Hsiung
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.10.2018
• Subjects: Acetylcysteine; Antibacterial materials; Apoptosis; Biological fertilization; Blastocysts; Body weight; Cascades; Caspase; Cyclin-dependent kinase inhibitor p21; Embryogenesis; Embryonic development; Embryonic growth stage; Fetuses; Impairment; In vitro fertilization; In vivo methods and tests; Intravenous administration; Maturation; Nanoparticles; Oocytes; p53 Protein; Pretreatment; Reactive oxygen species; Regulatory mechanisms (biology); Silver; apoptosis; oocyte maturation; silver nanoparticles; embryonic development
• ISSN: 1520-4081; 1522-7278
• DOI: 10.1002/tox.22590

Silver nanoparticles (AgNPs) are antibacterial materials widely used in numerous products and medical supplies. Previously, we showed that AgNPs trigger apoptotic processes in mouse blastocysts, leading to a decrease in cell viability and impairment of preimplantation and postimplantation embryonic development in vitro and in vivo. In the present study, we further investigated the hazardous effects of AgNPs on mouse oocyte maturation, in vitro fertilization (IVF), and subsequent preimplantation and postimplantation development in vitro and in vivo. Data from in vitro experiments revealed that AgNPs impair mouse oocyte maturation, decrease IVF rates, and induce injury effects on subsequent embryonic development to a significant extent. In an animal model, intravenous injection of AgNPs (5 mg/kg body weight) led to a significant decrease in mouse oocyte maturation and IVF concomitant with impairment of early embryonic development in vivo. Importantly, pretreatment with N-acetylcysteine effectively prevented AgNP-triggered reactive oxygen species (ROS) production and apoptosis, clearly suggesting a critical role of ROS as an upstream initiator or key regulator of AgNP-induced hazardous effects on oocyte maturation and sequent embryonic development. Furthermore, preincubation of oocytes with Ac-DEVD-cho, a caspase-3-specific inhibitor, effectively prevented hazardous effects, highlighting the potential involvement of caspase-dependent apoptotic signaling cascades in AgNP-mediated events. Expression levels of p53 and p21 of blastocysts were upregulated upon preincubation of mouse oocytes with AgNPs. Our collective results imply that cell apoptosis in mouse blastocysts derived from the AgNP-pretreated oocytes via intracellular ROS generation, which is further mediated through p53-, p21-, and caspase-3-dependent regulatory mechanisms.