AI Article Synopsis

  • Graphene nanomaterials, particularly graphene quantum dots (GQDs), show promise in biomedical applications due to their exceptional properties, but concerns exist regarding their potential adverse effects on biological systems.
  • In vitro studies revealed that high dosages of GQDs hindered the maturation of mouse oocytes, causing issues like decreased polar body extrusion rates and damage to mitochondrial structures, likely due to DNA damage and reactive oxygen species accumulation.
  • In vivo experiments indicated that while high GQD exposure during pregnancy affected fetal growth, it did not impact the long-term health or reproductive success of subsequent generations, suggesting a need for continued research on GQDs for safe medical use.

Article Abstract

Recently, graphene nanomaterials have attracted tremendous attention and have been utilized in various fields because of their excellent mechanical, thermal, chemical, optical properties, and good biocompatibility, especially in biomedical aspects. However, there is a concern that the unique characteristics of nanomaterials may have undesirable effects. Therefore, in this study, we sought to systematically investigate the effects of graphene quantum dots (GQDs) on the maturation of mouse oocytes and development of the offspring via in vitro and in vivo studies. In vitro, we found that the first polar body extrusion rate in the high dosage exposure groups (1.0-1.5 mg/ml) decreased significantly and the failure of spindle migration and actin cap formation after GQDs exposure was observed. The underlying mechanisms might be associated with reactive oxygen species accumulation and DNA damage. Moreover, transmission electron microscope studies showed that GQDs may have been internalized into oocytes, tending to accumulate in the nucleus and severely affecting mitochondrial morphology, which included swollen and vacuolated mitochondria accompanied by cristae alteration with a lower amount of dense mitochondrial matrix. In vivo, when pregnant mice were exposed to GQDs at 8.5 days of gestation (GD, 8.5), we found that high dosage of GQD exposure (30 mg/kg) significantly affected mean fetal length; however, all the second generation of female mice grew up normal, attained sexual maturity, and gave birth to a healthy offspring after mating with a healthy male mouse. The results presented in this study are important for the future investigation of GQDs for the biomedical applications.

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Source
http://dx.doi.org/10.1002/jcp.28062DOI Listing

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