| Literature DB >> 28009471 |
Xiumei Jiang1, Liming Wang1, Yinglu Ji2, Jinglong Tang1, Xin Tian3, Mingjing Cao1, Jingxuan Li4, Shuying Bi4, Xiaochun Wu2, Chunying Chen1, Jun-Jie Yin3.
Abstract
As a widely used nanomaterial in daily life, silver nanomaterials may cause great concern to female reproductive system as they are found to penetrate the blood-placental barrier and gain access to the ovary. However, it is largely unknown about how silver nanomaterials influence ovarian physiology and functions such as hormone production. This study performs in vitro toxicology study of silver nanomaterials, focusing especially on cytotoxicity and steroidogenesis and explores their underlying mechanisms. This study exposes primary rat granulosa cells to gold nanorod core/silver shell nanostructures (Au@Ag NRs), and compares outcomes with cells exposed to gold nanorods. The Au@Ag NRs generate more reactive oxygen species and reduce mitochondrial membrane potential and less production of adenosine triphosphate. Au@Ag NRs promote steroidogenesis, including progesterone and estradiol, in a time- and dose-dependent manner. Chemical reactivity and transformation of Au@Ag NRs are then studied by electron spin resonance spectroscopy and X-ray absorption near edge structure, which analyze the generation of free radical and intracellular silver species. Results suggest that both particle-specific activity and intracellular silver ion release of Au@Ag NR contribute to the toxic response of granulosa cells.Entities:
Keywords: Au@Ag NRs; cell apoptosis; electron spin resonance; silver nanomaterials; steroidogenesis
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Year: 2016 PMID: 28009471 DOI: 10.1002/smll.201602855
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281