Platinum Nanoparticles Exposure: Implications for Ejaculated Rabbit Spermatozoa Functionality
Lucia Dianová1, Michal Benc2, Hana Greifová3
1AgroBioTech Research Center, Slovak University of Agriculture, Tr. A. Hlinku 2, 94976 Nitra, Slovak Republic; Institute of Applied Biology, Faculty of Biotechnology and Food Sciences, Slovak University of Agriculture, Tr. A. Hlinku 2, 94976 Nitra, Slovak Republic.
Abstract:
Research indicates that environmental contaminants resulting from anthropogenic activities can significantly disrupt the functional attributes of spermatozoa. The environmental burden and anthropogenic emissions of platinum nanoparticles (Pt NPs) are currently rising significantly. Small size (≤ 100nm) and high surface area allow NPs to cross biological barriers, posing significant environmental and cellular risks. This study aimed to investigate the modulatory effects of Pt NPs on rabbit spermatozoa in vitro. Ejaculates were diluted with selected Pt NPs concentrations (1, 30, 250, and 500µg/mL) and exposed to these concentrations for 4hours at 37 °C. Spermatozoa motility was analyzed using CASA at time intervals of 0, 2, and 4hours. Following the 4-hour exposure, mitochondrial activity, superoxide radical levels, and ProAKAP4 protein content were assessed. DNA fragmentation was examined using an immunofluorescence method to detect γH2AX, a marker of double-stranded breaks. Results of this study show that spermatozoa motility was adversely affected at all time periods, with motility declining with higher Pt NPs doses. Mitochondrial activity was significantly diminished at peak doses of Pt NPs. A similar effect was observed in the production of intracellular superoxide and the presence of γH2AX. However, this decrease was likely indicative of significant cellular lethality rather than a reduction in free radical production or DNA damage, respectively. ProAKAP4 protein levels, which serve as markers for spermatozoa motility and viability, progressively decreased with increasing Pt NPs concentrations, thereby reflecting a negative impact on spermatozoa motility and fertilization capability at the molecular level.

