CeO2NPs relieve radiofrequency radiation, improve testosterone synthesis, and clock gene expression in Leydig cells by enhancing antioxidation

Introduction: The ratio of Ce3+/Ce4+ in their structure confers unique functions on cerium oxide nanoparticles (CeO(2)NPs) containing rare earth elements in scavenging free radicals and protecting against oxidative damage. The potential of CeO(2)NPs to protect testosterone synthesis in primary mouse Leydig cells during exposure to 1,800 MHz radiofrequency (RF) radiation was examined in vitro. Methods: Leydig cells were treated with different concentrations of CeO(2)NPs to identify the optimum concentration for cell proliferation. The cells were pretreated with the optimum dose of CeO(2)NPs for 24 hrs and then exposed to 1,800 MHz RF at a power density of 200.27 mu W/cm(2) (specific absorption rate (SAR), 0.116 W/kg) for 1 hr, 2 hrs, or 4 hrs. The medium was used to measure the testosterone concentration. The cells were collected to determine the antioxidant indices (catalase inverted right perpendicularCATinverted left perpendicular, malondialdehyde inverted right perpendicularMDAinverted left perpendicular, and total antioxidant capacity [T-AOC]), and the mRNA expression of the testosterone synthase genes (Star, Cyp11a1, and Hsd-3 beta) and clock genes (Clock, Bmal1, and Ror alpha). Results: Our preliminary result showed that 128 mu g/mL CeO(2)NPs was the optimumdose for cell proliferation. Cells exposed to RF alone showed reduced levels of testosterone, T-AOC, and CAT activities, increased MDA content, and the downregulated genes expression of Star, Cyp11a1, Hsd-3 beta, Clock, Bmal1, and Rora. Pretreatment of the cells with 128 mu g/mL CeO(2)NPs for 24 hrs followed by RF exposure significantly increased testosterone synthesis, upregulated the expression of the testosterone synthase and clock genes, and increased the resistance to oxidative damage in Leydig cells compared with those in cells exposed to RF alone. Conclusion: Exposure to 1,800 MHz RF had adverse effects on testosterone synthesis, antioxidant levels, and clock gene expression in primary Leydig cells. Pretreatment with CeO(2)NPs prevented the adverse effects on testosterone synthesis induced by RF exposure by regulating their antioxidant capacity and clock gene expression in vitro. Further studies of the mechanism underlying the protective function of CeO(2)NPs against RF in the male reproductive system are required.