Effect of Cerium Oxide Nanoparticles on the Expression of Developmental and Apoptosis Genes of Testicular Tissue in 6-Day-Old NMRI Mice Fetuses

Biol Trace Elem Res. 2022 Jul;200(7):3265-3274. doi: 10.1007/s12011-021-02939-0. Epub 2021 Oct 1.

Abstract

Cerium oxide (CeO2) has potential applications in medicine and various consumer products. This study investigated the effect of CeO2 on the expression of genes associated with apoptosis and testicular development in mouse embryos. The experimental groups of pregnant mice were injected intraperitoneally with CeO2 at a concentration of 10 mg/kg on days 7 and 14 of pregnancy. Six days after birth, the testicles of neonatal male mice were collected for mRNA expression determination using real-time PCR, protein expression analysis by immunohistochemistry, and apoptotic cell population determination using the TUNEL assay. The results showed that the mRNA expression of the Bax, Caspase-3, and Gsk3-β genes, unlike the Bcl2 gene, decreased significantly in the experimental group compared to the control group. The expression ratio of Bax/Bcl2 in the experimental group was lower than in the control group. A similar trend was observed in the population of apoptotic cells. In the experimental group, the expression levels of, Gata4, Sox8, and Rad54 at both the mRNA and protein levels increased significantly compared to the control group. Based on the results of this study, CeO2 at a concentration of 10 mg/kg, in addition to producing anti-apoptotic effects on the testicular cells of neonatal mice, can increase the expression of genes involved in testicular development and performance. The current experimental study proved the protective effects of 10 mg/kg CeO2 in developmental and apoptosis genes of testicular tissue in 6-day-old NMRI mice fetuses; however, more experiments are required to evaluate the possible side effects and interactions.

Keywords: Apoptosis; Cerium oxide nanoparticles; Gene expression; Male mouse; Testis development.

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Cerium* / pharmacology
  • Female
  • Fetus / metabolism
  • Glycogen Synthase Kinase 3 / pharmacology
  • Male
  • Metal Nanoparticles*
  • Mice
  • Nanoparticles
  • Pregnancy
  • Proto-Oncogene Proteins c-bcl-2
  • RNA, Messenger / genetics
  • bcl-2-Associated X Protein / metabolism

Substances

  • Proto-Oncogene Proteins c-bcl-2
  • RNA, Messenger
  • bcl-2-Associated X Protein
  • Cerium
  • ceric oxide
  • Glycogen Synthase Kinase 3